الجدول الدوري الممدد

الجدول الدوري الممتد اقترحه جلين تى سيبورج عام 1969 وهو إمتداد منطقى للنظريات التى تبعت الجدول الدوري القياسي ليضم العناصر التى لم تكتشف بعد . وتم تسمية العناصر التى لم تكتشف بعد عن طريق IUPAC لتسمية العناصر وتم وضع سم عام لها حتى يتم اكتشافها وتسميتها واعتماد هذا الإسم .

Elements beyond 118 will be placed in additional periods when discovered, laid out (as with the existing periods) to illustrate periodically recurring trends in the properties of the elements concerned. Any additional periods are expected to contain a larger number of elements than the seventh period, as they are calculated to have an additional so-called g-block, containing at least 18 elements with partially filled g-orbitals in each period. An eight-period table containing this block was suggested by Glenn T. Seaborg in 1969.^[1]^[2] The first element of the g-block may have atomic number 121, and thus would have the systematic name unbiunium. Despite many searches, no elements in this region have been synthesized or discovered in nature.^[3]

According to the orbital approximation in quantum mechanical descriptions of atomic structure, the g-block would correspond to elements with partially filled g-orbitals, but spin–orbit coupling effects reduce the validity of the orbital approximation substantially for elements of high atomic number. Seaborg's version of the extended period had the heavier elements following the pattern set by lighter elements, as it did not take into account relativistic effects. Models that take relativistic effects into account predict that the pattern will be broken. Pekka Pyykkö and Burkhard Fricke used computer modeling to calculate the positions of elements up to Z = 172, and found that several were displaced from the Madelung rule.^[4] As a result of uncertainty and variability in predictions of chemical and physical properties of elements beyond 120, there is currently no consensus on their placement in the extended periodic table.

Elements in this region are likely to be highly unstable with respect to radioactive decay and undergo alpha decay or spontaneous fission with extremely short half-lives, though element 126 is hypothesized to be within an island of stability that is resistant to fission but not to alpha decay. Other islands of stability beyond the known elements may also be possible, including one theorised around element 164, though the extent of stabilizing effects from closed nuclear shells is uncertain. It is not clear how many elements beyond the expected island of stability are physically possible, whether period 8 is complete, or if there is a period 9. The International Union of Pure and Applied Chemistry (IUPAC) defines an element to exist if its lifetime is longer than 10⁻¹⁴ seconds (0.01 picoseconds, or 10 femtoseconds), which is the time it takes for the nucleus to form an electron cloud.^[5]

As early as 1940, it was noted that a simplistic interpretation of the relativistic Dirac equation runs into problems with electron orbitals at Z > 1/α ≈ 137, suggesting that neutral atoms cannot exist beyond element 137, and that a periodic table of elements based on electron orbitals therefore breaks down at this point.^[6] On the other hand, a more rigorous analysis calculates the analogous limit to be Z ≈ 173 where the 1s subshell dives into the Dirac sea, and that it is instead not neutral atoms that cannot exist beyond element 173, but bare nuclei, thus posing no obstacle to the further extension of the periodic system. Atoms beyond this critical atomic number are called supercritical atoms.

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التاريخ

Heavier elements beyond the actinides were first proposed to exist as early as 1895, when the Danish chemist Hans Peter Jørgen Julius Thomsen predicted that thorium and uranium formed part of a 32-element period which would end at a chemically inactive element with atomic weight 292 (not far from the 294 known today for the first and only discovered isotope of oganesson). In 1913, the Swedish physicist Johannes Rydberg similarly predicted that the next noble gas after radon would have atomic number 118, and purely formally derived even heavier congeners of radon at Z = 168, 218, 290, 362, and 460, exactly where the Aufbau principle would predict them to be. Niels Bohr predicted in 1922 the electronic structure of this next noble gas at Z = 118, and suggested that the reason why elements beyond uranium were not seen in nature was because they were too unstable. The German physicist and engineer Richard Swinne published a review paper in 1926 containing predictions on the transuranic elements (he may have coined the term) in which he anticipated modern predictions of an island of stability: he first hypothesised in 1914 that half-lives should not decrease strictly with atomic number, but suggested instead that there might be some longer-lived elements at Z = 98–102 and Z = 108–110, and speculated that such elements might exist in the Earth's core, in iron meteorites, or in the ice caps of Greenland where they had been locked up from their supposed cosmic origin.^[7] By 1955, these elements were called superheavy elements.^[8]

The first predictions on properties of undiscovered superheavy elements were made in 1957, when the concept of nuclear shells was first explored and an island of stability was theorised to exist around element 126.^[9] In 1967, more rigorous calculations were performed, and the island of stability was theorised to be centered at the then-undiscovered flerovium (element 114); this and other subsequent studies motivated many researchers to search for superheavy elements in nature or attempt to synthesize them at accelerators.^[8] Many searches for superheavy elements were conducted in the 1970s, all with negative results. اعتبارا من أبريل 2022^[تحديث], synthesis has been attempted for every element up to and including unbiseptium (Z = 127), except unbitrium (Z = 123),^[10]^[11]^[12] with the heaviest successfully synthesized element being oganesson in 2002 and the most recent discovery being that of tennessine in 2010.^[10]

As some superheavy elements were predicted to lie beyond the seven-period periodic table, an additional eighth period containing these elements was first proposed by Glenn T. Seaborg in 1969. This model continued the pattern in established elements and introduced a new g-block and superactinide series beginning at element 121, raising the number of elements in period 8 compared to known periods.^[1]^[2]^[8] These early calculations failed to consider relativistic effects that break down periodic trends and render simple extrapolation impossible, however. In 1971, Fricke calculated the periodic table up to Z = 172, and discovered that some elements indeed had different properties that break the established pattern,^[4] and a 2010 calculation by Pekka Pyykkö also noted that several elements might behave differently than expected.^[13] It is unknown how far the periodic table might extend beyond the known 118 elements, as heavier elements are predicted to be increasingly unstable. Glenn T. Seaborg suggested that practically speaking, the end of the periodic table might come as early as around Z = 120 due to nuclear instability.^[14]

البنى المتوقعة لجدول دوري ممدد

There is currently no consensus on the placement of elements beyond atomic number 120 in the periodic table.

All of these hypothetically undiscovered elements are named by the International Union of Pure and Applied Chemistry (IUPAC) systematic element name standard which creates a generic name for use until the element has been discovered, confirmed, and an official name approved. These names are typically not used in the literature, and are referred to by their atomic numbers; hence, element 164 would usually not be called "unhexquadium" or "Uhq" (the IUPAC systematic name and symbol), but rather "element 164" with symbol "164", "(164)", or "E164".^[15]

مبدأ آوفباو

At element 118, the orbitals 1s, 2s, 2p, 3s, 3p, 3d, 4s, 4p, 4d, 4f, 5s, 5p, 5d, 5f, 6s, 6p, 6d, 7s and 7p are assumed to be filled, with the remaining orbitals unfilled. A simple extrapolation from the Aufbau principle would predict the eighth row to fill orbitals in the order 8s, 5g, 6f, 7d, 8p; but after element 120, the proximity of the electron shells makes placement in a simple table problematic. قالب:Extended periodic table (by Aufbau, 50 columns, compact)

پيكو

Not all models show the higher elements following the pattern established by lighter elements. Pekka Pyykkö, for example, used computer modeling to calculate the positions of elements up to Z = 172 and their possible chemical properties in an article published in 2011. He found that several elements were displaced from the Madelung energy-ordering rule as a result of overlapping orbitals; this is caused by the increasing role of relativistic effects in heavy elements.^[13]

Fricke

Burkhard Fricke et al., who carried out calculations up to element 184 in an article published in 1971, also found some elements to be displaced from the Aufbau principle as a consequence of relativistic effects.^[4]^[16]

H																			He
Li	Be													B	C	N	O	F	Ne
Na	Mg													Al	Si	P	S	Cl	Ar
K	Ca	Sc			Ti	V	Cr	Mn	Fe	Co	Ni	Cu	Zn	Ga	Ge	As	Se	Br	Kr
Rb	Sr	Y			Zr	Nb	Mo	Tc	Ru	Rh	Pd	Ag	Cd	In	Sn	Sb	Te	I	Xe
Cs	Ba	La		Ce–Lu	Hf	Ta	W	Re	Os	Ir	Pt	Au	Hg	Tl	Pb	Bi	Po	At	Rn
Fr	Ra	Ac		Th–Lr	Rf	Db	Sg	Bh	Hs	Mt	Ds	Rg	Cn	Nh	Fl	Mc	Lv	Ts	Og
119	120	121	122–141	142–155	156	157	158	159	160	161	162	163	164
165	166													167	168	169	170	171	172

Nefedov

ru (Vadim Nefedov), Trzhaskovskaya, and Yarzhemskii carried out calculations up to 164 (results published in 2006). Contrary to Pyykkö, as well as Fricke et al., they considered elements 158 through 164 to be homologues of groups 4 through 10, and not 6 through 12, noting similarities of electron configurations to the period 5 transition metals. Rg and Cn are given an asterisk to reflect differing configurations from Au and Hg (in the original publication they are drawn as being displaced in the third dimension); however, the difference in configuration between Pt and Ds is not marked.^[17]

Nefedov et al.'s suggested form (fragment)
Cs	Ba	La–Lu	Hf	Ta	W	Re	Os	Ir	Pt	Au	Hg	Tl	Pb	Bi	Po	At	Rn
Fr	Ra	Ac–Lr	Rf	Db	Sg	Bh	Hs	Mt	Ds	Rg*	Cn*	Nh	Fl	Mc	Lv	Ts	Og
119	120	121–157	158	159	160	161	162	163	164

كولشا

Computational chemist Andrey Kulsha has suggested two forms of the extended periodic table. Based on their likely chemical properties, elements 157–172 are placed as eighth-period congeners of yttrium through xenon in the fifth period;^[18] this accords with the 2006 calculations of Nefedov et al.^[17] In Kulsha's first suggestion (2011, after Pyykkö's paper was published),^[19] elements 121–138 and 139–156 are placed as two separate rows (together called "ultransition elements"), related by the addition of a 5g¹⁸ subshell into the core, as they respectively mimic lanthanides and actinides.^[18] In his second suggestion (2016), elements 121–142 form a g-block (as they have 5g activity), while elements 143–156 form an f-block placed under actinium through nobelium.^[20]

Kulsha's first suggested form

Kulsha's second suggested form

تصور قديم للجدول الدوري الممدد

ويوضح اللون الأزرق في أعلى كل عامود آخر مدار إلكتروني كبقا لشكل مولار ( لاحظ وجود إستثناءات مثل النحاس ). كما يوضح اللون الأحمر على يمين كل صف الدورة : اخر غلاف إلكتروني .

تم وضع الهيليوم بجوار الهيدروجين معا أعلى النيون لأنه جزء من مجموعة s² .

**الجدول الدوري الممتد للعناصر**
الدورة	s¹	s²
1	1 H	2 He																																											p¹	p²	p³	p⁴	p⁵	p⁶
2	3 Li	4 Be																																											5 B	6 C	7 N	8 O	9 F	10 Ne
3	11 Na	12 Mg																																	d¹	d²	d³	d⁴	d⁵	d⁶	d⁷	d⁸	d⁹	d¹⁰	13 Al	14 Si	15 P	16 S	17 Cl	18 Ar
4	19 K	20 Ca																																	21 Sc	22 Ti	23 V	24 Cr	25 Mn	26 Fe	27 Co	28 Ni	29 Cu	30 Zn	31 Ga	32 Ge	33 As	34 Se	35 Br	36 Kr
5	37 Rb	38 Sr																			f¹	f²	f³	f⁴	f⁵	f⁶	f⁷	f⁸	f⁹	f¹⁰	f¹¹	f¹²	f¹³	f¹⁴	39 Y	40 Zr	41 Nb	42 Mo	43 Tc	44 Ru	45 Rh	46 Pd	47 Ag	48 Cd	49 In	50 Sn	51 Sb	52 Te	53 I	54 Xe
6	55 Cs	56 Ba																			57 La	58 Ce	59 Pr	60 Nd	61 Pm	62 Sm	63 Eu	64 Gd	65 Tb	66 Dy	67 Ho	68 Er	69 Tm	70 Yb	71 Lu	72 Hf	73 Ta	74 W	75 Re	76 Os	77 Ir	78 Pt	79 Au	80 Hg	81 Tl	82 Pb	83 Bi	84 Po	85 At	86 Rn
7	87 Fr	88 Ra	g¹	g²	g³	g⁴	g⁵	g⁶	g⁷	g⁸	g⁹	g¹⁰	g¹¹	g¹²	g¹³	g¹⁴	g¹⁵	g¹⁶	g¹⁷	g¹⁸	89 Ac	90 Th	91 Pa	92 U	93 Np	94 Pu	95 Am	96 Cm	97 Bk	98 Cf	99 Es	100 Fm	101 Md	102 No	103 Lr	104 Rf	105 Db	106 Sg	107 Bh	108 Hs	109 Mt	110 Ds	111 Rg	112 Uub	113 Uut	114 Uuq	115 Uup	116 Uuh	117 Uus	118 Uuo
8	119 Uue	120 Ubn	121 Ubu	122 Ubb	123 Ubt	124 Ubq	125 Ubp	126 Ubh	127 Ubs	128 Ubo	129 Ube	130 Utn	131 Utu	132 Utb	133 Utt	134 Utq	135 Utp	136 Uth	137 Uts	138 Uto	139 Ute	140 Uqn	141 Uqu	142 Uqb	143 Uqt	144 Uqq	145 Uqp	146 Uqh	147 Uqs	148 Uqo	149 Uqe	150 Upn	151 Upu	152 Upb	153 Upt	154 Upq	155 Upp	156 Uph	157 Ups	158 Upo	159 Upe	160 Uhn	161 Uhu	162 Uhb	163 Uht	164 Uhq	165 Uhp	166 Uhh	167 Uhs	168 Uho
9	169 Uhe	170 Usn	171 Usu	172 Usb	173 Ust	174 Usq	175 Usp	176 Ush	177 Uss	178 Uso	179 Use	180 Uon	181 Uou	182 Uob	183 Uot	184 Uoq	185 Uop	186 Uoh	187 Uos	188 Uoo	189 Uoe	190 Uen	191 Ueu	192 Ueb	193 Uet	194 Ueq	195 Uep	196 Ueh	197 Ues	198 Ueo	199 Uee	200 Bnn	201 Bnu	202 Bnb	203 Bnt	204 Bnq	205 Bnp	206 Bnh	207 Bns	208 Bno	209 Bne	210 Bun	211 Buu	212 Bub	213 But	214 Buq	215 Bup	216 Buh	217 Bus	218 Buo

المستويات الفرعية
مستوى فرعي s	مستوى فرعي p	مستوى فرعي d	مستوى فرعي f	مستوى فرعي g

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البحث عن العناصر غير المكتشفة

المحاولات الاصطناعية

Unsuccessful attempts have been made to synthesise the period 8 elements up to unbiseptium, except unbitrium. Attempts to synthesise ununennium, the first period 8 element, are ongoing اعتبارا من 2024^[تحديث].

Ununennium (E119)

The synthesis of element 119 (ununennium) was first attempted in 1985 by bombarding a target of einsteinium-254 with calcium-48 ions at the superHILAC accelerator at Berkeley, California:

25499Es + 4820Ca → ³⁰²119* → no atoms

No atoms were identified, leading to a limiting cross section of 300 nb.^[21] Later calculations suggest that the cross section of the 3n reaction (which would result in ²⁹⁹119 and three neutrons as products) would actually be six hundred thousand times lower than this upper bound, at 0.5 pb.^[22]

From April to September 2012, an attempt to synthesize the isotopes ²⁹⁵119 and ²⁹⁶119 was made by bombarding a target of berkelium-249 with titanium-50 at the GSI Helmholtz Centre for Heavy Ion Research in Darmstadt, Germany.^[23]^[24] Based on the theoretically predicted cross section, it was expected that an ununennium atom would be synthesized within five months of the beginning of the experiment.^[25] Moreover, as berkelium-249 decays to californium-249 (the next element) with a short half-life of 327 days, this allowed elements 119 and 120 to be searched for simultaneously.^[26]

249Error in Template:ProtonsForElement: unknown element berkelium.Bk + 5022Ti → ²⁹⁹119* → ²⁹⁶119 + 3 10n

249Error in Template:ProtonsForElement: unknown element berkelium.Bk + 5022Ti → ²⁹⁹119* → ²⁹⁵119 + 4 10n

The experiment was originally planned to continue to November 2012,^[27] but was stopped early to make use of the ²⁴⁹Bk target to confirm the synthesis of tennessine (thus changing the projectiles to ⁴⁸Ca).^[28] This reaction between ²⁴⁹Bk and ⁵⁰Ti was predicted to be the most favorable practical reaction for formation of element 119,^[24] as it is rather asymmetrical,^[25] though also somewhat cold.^[28] (The reaction between ²⁵⁴Es and ⁴⁸Ca would be superior, but preparing milligram quantities of ²⁵⁴Es for a target is difficult.)^[25] Nevertheless, the necessary change from the "silver bullet" ⁴⁸Ca to ⁵⁰Ti divides the expected yield of element 119 by about twenty, as the yield is strongly dependent on the asymmetry of the fusion reaction.^[25]

Due to the predicted short half-lives, the GSI team used new "fast" electronics capable of registering decay events within microseconds.^[24] No atoms of element 119 were identified, implying a limiting cross section of 70 fb.^[28] The predicted actual cross section is around 40 fb, which is at the limits of current technology.^[25]

The team at the Joint Institute for Nuclear Research in Dubna, Russia, planned to begin experiments on the synthesis of elements 119 and 120 using the ²⁴⁹Bk+⁵⁰Ti and ²⁴⁹Cf+⁵⁰Ti reactions in 2019 using a new experimental complex.^[29]^[30] The team at RIKEN in Japan also planned to make attempts on these elements starting in 2018 with ²⁴⁸Cm targets using the ²⁴⁸Cm+⁵¹V^[31] and ²⁴⁸Cm+⁵⁴Cr reactions.^[32] The former was conducted from 2018^[31] to May 2019, and subsequently from 2020 to the end of 2021 using the upgraded facility.^[33]

Unbinilium (E120)

Following their success in obtaining oganesson by the reaction between ²⁴⁹Cf and ⁴⁸Ca in 2006, the team at the Joint Institute for Nuclear Research (JINR) in Dubna started similar experiments in March–April 2007, in hope of creating element 120 (unbinilium) from nuclei of ⁵⁸Fe and ²⁴⁴Pu.^[34]^[35] Isotopes of unbinilium are predicted to have alpha decay half-lives of the order of microseconds.^[36]^[37] Initial analysis revealed that no atoms of element 120 were produced, providing a limit of 400 fb for the cross section at the energy studied.^[38]

244Error in Template:ProtonsForElement: unknown element plutonium.Pu + 5826Fe → ³⁰²120* → no atoms

The Russian team planned to upgrade their facilities before attempting the reaction again.^[38]

In April 2007, the team at the GSI Helmholtz Centre for Heavy Ion Research in Darmstadt, Germany, attempted to create element 120 using uranium-238 and nickel-64:^[39]

23892U + 6428Ni → ³⁰²120* → no atoms

No atoms were detected providing a limit of 1.6 pb for the cross section at the energy provided. The GSI repeated the experiment with higher sensitivity in three separate runs in April–May 2007, January–March 2008, and September–October 2008, all with negative results, reaching a cross section limit of 90 fb.^[39]

In June–July 2010, and again in 2011, after upgrading their equipment to allow the use of more radioactive targets, scientists at the GSI attempted the more asymmetrical fusion reaction:^[40]

248Error in Template:ProtonsForElement: unknown element curium.Cm + 54Error in Template:ProtonsForElement: unknown element chromium.Cr → ³⁰²120 → no atoms

It was expected that the change in reaction would quintuple the probability of synthesizing element 120,^[41] as the yield of such reactions is strongly dependent on their asymmetry.^[25] Three correlated signals were observed that matched the predicted alpha decay energies of ²⁹⁹120 and its daughter ²⁹⁵Og, as well as the experimentally known decay energy of its granddaughter ²⁹¹Lv. However, the lifetimes of these possible decays were much longer than expected, and the results could not be confirmed.^[42]^[43]^[40]

In August–October 2011, a different team at the GSI using the TASCA facility tried a new, even more asymmetrical reaction:^[44]^[28]

249Error in Template:ProtonsForElement: unknown element californium.Cf + 5022Ti → ²⁹⁹120* → no atoms

Because of its asymmetry,^[45] the reaction between ²⁴⁹Cf and ⁵⁰Ti was predicted to be the most favorable practical reaction for synthesizing unbinilium, although it is also somewhat cold. No unbinilium atoms were identified, implying a limiting cross-section of 200 fb.^[28] Jens Volker Kratz predicted the actual maximum cross-section for producing element 120 by any of these reactions to be around 0.1 fb;^[46] in comparison, the world record for the smallest cross section of a successful reaction was 30 fb for the reaction ²⁰⁹Bi(⁷⁰Zn,n)²⁷⁸Nh,^[25] and Kratz predicted a maximum cross-section of 20 fb for producing the neighbouring element 119.^[46] If these predictions are accurate, then synthesizing element 119 would be at the limits of current technology, and synthesizing element 120 would require new methods.^[46]

Unbiunium (E121)

The synthesis of element 121 (unbiunium) was first attempted in 1977 by bombarding a target of uranium-238 with copper-65 ions at the Gesellschaft für Schwerionenforschung in Darmstadt, Germany:

23892U + 6529Cu → ³⁰³121* → no atoms

No atoms were identified.^[11]

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Unbibium (E122)

The first attempts to synthesize element 122 (unbibium) were performed in 1972 by Flerov et al. at the Joint Institute for Nuclear Research (JINR), using the heavy-ion induced hot fusion reactions:^[10]

23892U + 66,6830Zn → ^{304, 306}122* → no atoms

These experiments were motivated by early predictions on the existence of an island of stability at N = 184 and Z > 120. No atoms were detected and a yield limit of 5 nb (5,000 pb) was measured. Current results (see flerovium) have shown that the sensitivity of these experiments were too low by at least 3 orders of magnitude.^[12]

In 2000, the Gesellschaft für Schwerionenforschung (GSI) Helmholtz Center for Heavy Ion Research performed a very similar experiment with much higher sensitivity:^[10]

23892U + 7030Zn → ³⁰⁸122* → no atoms

These results indicate that the synthesis of such heavier elements remains a significant challenge and further improvements of beam intensity and experimental efficiency is required. The sensitivity should be increased to 1 fb in the future for more quality results.

Another unsuccessful attempt to synthesize element 122 was carried out in 1978 at the GSI Helmholtz Center, where a natural erbium target was bombarded with xenon-136 ions:^[10]

nat68Er + 13654Xe → ^{298, 300, 302, 303, 304, 306}122* → no atoms

In particular, the reaction between ¹⁷⁰Er and ¹³⁶Xe was expected to yield alpha-emitters with half-lives of microseconds that would decay down to isotopes of flerovium with half-lives perhaps increasing up to several hours, as flerovium is predicted to lie near the center of the island of stability. After twelve hours of irradiation, nothing was found in this reaction. Following a similar unsuccessful attempt to synthesize element 121 from ²³⁸U and ⁶⁵Cu, it was concluded that half-lives of superheavy nuclei must be less than one microsecond or the cross sections are very small.^[47] More recent research into synthesis of superheavy elements suggests that both conclusions are true.^[25]^[48] The two attempts in the 1970s to synthesize element 122 were both propelled by the research investigating whether superheavy elements could potentially be naturally occurring.^[10]

Several experiments studying the fission characteristics of various superheavy compound nuclei such as ³⁰⁶122* were performed between 2000 and 2004 at the Flerov Laboratory of Nuclear Reactions. Two nuclear reactions were used, namely ²⁴⁸Cm + ⁵⁸Fe and ²⁴²Pu + ⁶⁴Ni.^[10] The results reveal how superheavy nuclei fission predominantly by expelling closed shell nuclei such as ¹³²Sn (Z = 50, N = 82). It was also found that the yield for the fusion-fission pathway was similar between ⁴⁸Ca and ⁵⁸Fe projectiles, suggesting a possible future use of ⁵⁸Fe projectiles in superheavy element formation.^[49]

Unbiquadium (E124)

Scientists at GANIL (Grand Accélérateur National d'Ions Lourds) attempted to measure the direct and delayed fission of compound nuclei of elements with Z = 114, 120, and 124 in order to probe shell effects in this region and to pinpoint the next spherical proton shell. This is because having complete nuclear shells (or, equivalently, having a magic number of protons or neutrons) would confer more stability on the nuclei of such superheavy elements, thus moving closer to the island of stability. In 2006, with full results published in 2008, the team provided results from a reaction involving the bombardment of a natural germanium target with uranium ions:

23892U + nat32Ge → ^{308, 310, 311, 312, 314}124* → fission

The team reported that they had been able to identify compound nuclei fissioning with half-lives > 10⁻¹⁸ s. This result suggests a strong stabilizing effect at Z = 124 and points to the next proton shell at Z > 120, not at Z = 114 as previously thought. A compound nucleus is a loose combination of nucleons that have not arranged themselves into nuclear shells yet. It has no internal structure and is held together only by the collision forces between the target and projectile nuclei. It is estimated that it requires around 10⁻¹⁴ s for the nucleons to arrange themselves into nuclear shells, at which point the compound nucleus becomes a nuclide, and this number is used by IUPAC as the minimum half-life a claimed isotope must have to potentially be recognised as being discovered. Thus, the GANIL experiments do not count as a discovery of element 124.^[10]

The fission of the compound nucleus ³¹²124 was also studied in 2006 at the tandem ALPI heavy-ion accelerator at the Laboratori Nazionali di Legnaro (Legnaro National Laboratories) in Italy:^[50]

232Error in Template:ProtonsForElement: unknown element thorium.Th + 8034Se → ³¹²124* → fission

Similarly to previous experiments conducted at the JINR (Joint Institute for Nuclear Research), fission fragments clustered around doubly magic nuclei such as ¹³²Sn (Z = 50, N = 82), revealing a tendency for superheavy nuclei to expel such doubly magic nuclei in fission.^[49] The average number of neutrons per fission from the ³¹²124 compound nucleus (relative to lighter systems) was also found to increase, confirming that the trend of heavier nuclei emitting more neutrons during fission continues into the superheavy mass region.^[50]

Unbipentium (E125)

The first and only attempt to synthesize element 125 (unbipentium) was conducted in Dubna in 1970 – 1971 using zinc ions and an americium-243 target:^[12]

243Error in Template:ProtonsForElement: unknown element americium.Am + 66, 6830Zn → ^{309, 311}125* → no atoms

No atoms were detected, and a cross section limit of 5 nb was determined. This experiment was motivated by the possibility of greater stability for nuclei around Z ~ 126 and N ~ 184,^[12] though more recent research suggests the island of stability may instead lie at a lower atomic number (such as copernicium, Z = 112), and the synthesis of heavier elements such as element 125 will require more sensitive experiments.^[25]

Unbihexium (E126)

The first and only attempt to synthesize element 126 (unbihexium), which was unsuccessful, was performed in 1971 at CERN (European Organization for Nuclear Research) by René Bimbot and John M. Alexander using the hot fusion reaction:^[10]

232Error in Template:ProtonsForElement: unknown element thorium.Th + 8436Kr → ³¹⁶126* → no atoms

High-energy (13–15 MeV) alpha particles were observed and taken as possible evidence for the synthesis of element 126. Subsequent unsuccessful experiments with higher sensitivity suggest that the 10 mb sensitivity of this experiment was too low; hence, the formation of element 126 nuclei in this reaction is highly unlikely.^[8]

Unbiseptium (E127)

The first and only attempt to synthesize element 127 (unbiseptium), which was unsuccessful, was performed in 1978 at the UNILAC accelerator at the GSI Helmholtz Center, where a natural tantalum target was bombarded with xenon-136 ions:^[10]

nat73Ta + 13654Xe → ^{316, 317}127* → no atoms

البحث في الطبيعة

A study in 1976 by a group of American researchers from several universities proposed that primordial superheavy elements, mainly livermorium, elements 124, 126, and 127, could be a cause of unexplained radiation damage (particularly radiohalos) in minerals.^[8] This prompted many researchers to search for them in nature from 1976 to 1983. A group led by Tom Cahill, a professor at the University of California at Davis, claimed in 1976 that they had detected alpha particles and X-rays with the right energies to cause the damage observed, supporting the presence of these elements. In particular, the presence of long-lived (on the order of 10⁹ years) nuclei of elements 124 and 126, along with their decay products, at an abundance of 10⁻¹¹ relative to their possible congeners uranium and plutonium, was conjectured.^[51] Others claimed that none had been detected, and questioned the proposed characteristics of primordial superheavy nuclei.^[8] In particular, they cited that any such superheavy nuclei must have a closed neutron shell at N = 184 or N = 228, and this necessary condition for enhanced stability only exists in neutron deficient isotopes of livermorium or neutron rich isotopes of the other elements that would not be beta-stable^[8] unlike most naturally occurring isotopes.^[52] This activity was also proposed to be caused by nuclear transmutations in natural cerium, raising further ambiguity upon this claimed observation of superheavy elements.^[8]

On April 24, 2008, a group led by Amnon Marinov at the Hebrew University of Jerusalem claimed to have found single atoms of ²⁹²122 in naturally occurring thorium deposits at an abundance of between 10⁻¹¹ and 10⁻¹² relative to thorium.^[53] The claim of Marinov et al. was criticized by a part of the scientific community. Marinov claimed that he had submitted the article to the journals Nature and Nature Physics but both turned it down without sending it for peer review.^[54] The ²⁹²122 atoms were claimed to be superdeformed or hyperdeformed isomers, with a half-life of at least 100 million years.^[10]

A criticism of the technique, previously used in purportedly identifying lighter thorium isotopes by mass spectrometry,^[55] was published in Physical Review C in 2008.^[56] A rebuttal by the Marinov group was published in Physical Review C after the published comment.^[57]

A repeat of the thorium-experiment using the superior method of Accelerator Mass Spectrometry (AMS) failed to confirm the results, despite a 100-fold better sensitivity.^[58] This result throws considerable doubt on the results of the Marinov collaboration with regard to their claims of long-lived isotopes of thorium,^[55] roentgenium^[59] and element 122.^[53] It is still possible that traces of unbibium might only exist in some thorium samples, although this is unlikely.^[10]

The possible extent of primordial superheavy elements on Earth today is uncertain. Even if they are confirmed to have caused the radiation damage long ago, they might now have decayed to mere traces, or even be completely gone.^[60] It is also uncertain if such superheavy nuclei may be produced naturally at all, as spontaneous fission is expected to terminate the r-process responsible for heavy element formation between mass number 270 and 290, well before elements beyond 120 may be formed.^[61]

A recent hypothesis tries to explain the spectrum of Przybylski's Star by naturally occurring flerovium and element 120.^[62]^[63]^[64]

الخصائص المتوقعة لعناصر الدورة الثامنة

Element 118, oganesson, is the heaviest element that has been synthesized. The next two elements, elements 119 and 120, should form an 8s series and be an alkali and alkaline earth metal respectively. Beyond element 120, the superactinide series is expected to begin, when the 8s electrons and the filling of the 8p_1/2, 7d_3/2, 6f, and 5g subshells determine the chemistry of these elements. Complete and accurate CCSD calculations are not available for elements beyond 122 because of the extreme complexity of the situation: the 5g, 6f, and 7d orbitals should have about the same energy level, and in the region of element 160, the 9s, 8p_3/2, and 9p_1/2 orbitals should also be about equal in energy. This will cause the electron shells to mix so that the block concept no longer applies very well, and will also result in novel chemical properties that will make positioning some of these elements in a periodic table very difficult.^[15]

Energy eigenvalues (in eV) for the outermost electrons of elements with Z = 100 through 172, predicted using Dirac–Fock calculations. The − and + signs refer to orbitals with decreased or increased azimuthal quantum number from spin–orbit splitting respectively: p− is p_1/2, p+ is p_3/2, d− is d_3/2, d+ is d_5/2, f− is f_5/2, f+ is f_7/2, g− is g_7/2, and g+ is g_9/2.^[16]

الخصائص الكيمياية والفيزيائية

العنصران 119 و 120

بعض الخصائص المتوقعة للعنصرين 119 و 120^[4]^[15]
الخاصية	119	120
Standard atomic weight	[322]	[325]
Group	1	2
Valence electron configuration	8s¹	8s²
Stable oxidation states	1, 3	2, 4
First ionization energy	463.1 kJ/mol	563.3 kJ/mol
Metallic radius	260 pm	200 pm
Density	3 g/cm³	7 g/cm³
Melting point	0–30 °C (32–86 °F)	680 °C (1,300 °F)
Boiling point	630 °C (1,200 °F)	1,700 °C (3,100 °F)

The first two elements of period 8 will be ununennium and unbinilium, elements 119 and 120. Their electron configurations should have the 8s orbital being filled. This orbital is relativistically stabilized and contracted; thus, elements 119 and 120 should be more like rubidium and strontium than their immediate neighbours above, francium and radium. Another effect of the relativistic contraction of the 8s orbital is that the atomic radii of these two elements should be about the same as those of francium and radium. They should behave like normal alkali and alkaline earth metals (albeit less reactive than their immediate vertical neighbours), normally forming +1 and +2 oxidation states respectively, but the relativistic destabilization of the 7p_3/2 subshell and the relatively low ionization energies of the 7p_3/2 electrons should make higher oxidation states like +3 and +4 (respectively) possible as well.^[4]^[15]

Superactinides

The superactinides may be considered to range from elements 121 through 157, which can be classified as the 5g and 6f elements of the eighth period, together with the first 7d element.^[17] In the superactinide series, the 7d_3/2, 8p_1/2, 6f_5/2 and 5g_7/2 shells should all fill simultaneously.^[16] This creates very complicated situations, so much so that complete and accurate CCSD calculations have been done only for elements 121 and 122.^[15] The first superactinide, unbiunium (element 121), should be similar to lanthanum and actinium:^[65] its main oxidation state should be +3, although the closeness of the valence subshells' energy levels may permit higher oxidation states, just as in elements 119 and 120.^[15] Relativistic stabilization of the 8p subshell should result in a ground-state 8s²8p¹ valence electron configuration for element 121, in contrast to the ds² configurations of lanthanum and actinium;^[15] nevertheless, this anomalous configuration does not appear to affect its calculated chemistry, which remains similar to that of actinium.^[66] Its first ionization energy is predicted to be 429.4 kJ/mol, which would be lower than those of all known elements except for the alkali metals potassium, rubidium, caesium, and francium: this value is even lower than that of the period 8 alkali metal ununennium (463.1 kJ/mol). Similarly, the next superactinide, unbibium (element 122), may be similar to cerium and thorium, with a main oxidation state of +4, but would have a ground-state 7d¹8s²8p¹ or 8s²8p² valence electron configuration,^[67] unlike thorium's 6d²7s² configuration. Hence, its first ionization energy would be smaller than thorium's (Th: 6.3 eV; element 122: 5.6 eV) because of the greater ease of ionizing unbibium's 8p_1/2 electron than thorium's 6d electron.^[15] The collapse of the 5g orbital itself is delayed until around element 125; the electron configurations of the 119-electron isoelectronic series are expected to be [Og]8s¹ for elements 119 through 122, [Og]6f¹ for elements 123 and 124, and [Og]5g¹ for element 125 onwards.^[68]

In the first few superactinides, the binding energies of the added electrons are predicted to be small enough that they can lose all their valence electrons; for example, unbihexium (element 126) could easily form a +8 oxidation state, and even higher oxidation states for the next few elements may be possible. Element 126 is also predicted to display a variety of other oxidation states: recent calculations have suggested a stable monofluoride 126F may be possible, resulting from a bonding interaction between the 5g orbital on element 126 and the 2p orbital on fluorine.^[69] Other predicted oxidation states include +2, +4, and +6; +4 is expected to be the most usual oxidation state of unbihexium.^[16] The superactinides from unbipentium (element 125) to unbiennium (element 129) are predicted to exhibit a +6 oxidation state and form hexafluorides, though 125F₆ and 126F₆ are predicted to be relatively weakly bound.^[68] The bond dissociation energies are expected to greatly increase at element 127 and even more so at element 129. This suggests a shift from strong ionic character in fluorides of element 125 to more covalent character, involving the 8p orbital, in fluorides of element 129. The bonding in these superactinide hexafluorides is mostly between the highest 8p subshell of the superactinide and the 2p subshell of fluorine, unlike how uranium uses its 5f and 6d orbitals for bonding in uranium hexafluoride.^[68]

Despite the ability of early superactinides to reach high oxidation states, it has been calculated that the 5g electrons will be most difficult to ionize; the 125⁶⁺ and 126⁷⁺ ions are expected to bear a 5g¹ configuration, similar to the 5f¹ configuration of the Np⁶⁺ ion.^[13]^[68] Similar behavior is observed in the low chemical activity of the 4f electrons in lanthanides; this is a consequence of the 5g orbitals being small and deeply buried in the electron cloud.^[13] The presence of electrons in g-orbitals, which do not exist in the ground state electron configuration of any currently known element, should allow presently unknown hybrid orbitals to form and influence the chemistry of the superactinides in new ways, although the absence of g electrons in known elements makes predicting superactinide chemistry more difficult.^[4]

Some predicted compounds of the superactinides (X = a halogen)^[13]^[68]^[70]
	121	122	123	124	125	126	127	128	129	132	142	143	144	145	146	148	153	154	155	156	157
Compound	121X₃	122X₄	123X₅	124X₆	125F 125F₆ 125O2+2	126F 126F₆ 126O₄	127F₆	128F₆	129F 129F₆		142X₄ 142X₆	143F₆	144X₆ 144O2+2 144F₈ 144O₄	145F₆		148O₆
Analogs	LaX₃ AcX₃	CeX₄ ThX₄			NpO2+2						ThF₄		UF₆ UO2+2 PuF₈ PuO₄			UO₆
Oxidation states	3	4	5	6	1, 6, 7	1, 2, 4, 6, 8	6	6	1, 6	6	4, 6	6, 8	3, 4, 5, 6, 8	6	8	12	3	0, 2	3, 5	2	3

In the later superactinides, the oxidation states should become lower. By element 132, the predominant most stable oxidation state will be only +6; this is further reduced to +3 and +4 by element 144, and at the end of the superactinide series it will be only +2 (and possibly even 0) because the 6f shell, which is being filled at that point, is deep inside the electron cloud and the 8s and 8p_1/2 electrons are bound too strongly to be chemically active. The 5g shell should be filled at element 144 and the 6f shell at around element 154, and at this region of the superactinides the 8p_1/2 electrons are bound so strongly that they are no longer active chemically, so that only a few electrons can participate in chemical reactions. Calculations by Fricke et al. predict that at element 154, the 6f shell is full and there are no d- or other electron wave functions outside the chemically inactive 8s and 8p_1/2 shells. This may cause element 154 to be rather unreactive with noble gas-like properties.^[4]^[15] Calculations by Pyykkö nonetheless expect that at element 155, the 6f shell is still chemically ionisable: 155³⁺ should have a full 6f shell, and the fourth ionisation potential should be between those of terbium and dysprosium, both of which are known in the +4 state.^[13]

Similarly to the lanthanide and actinide contractions, there should be a superactinide contraction in the superactinide series where the ionic radii of the superactinides are smaller than expected. In the lanthanides, the contraction is about 4.4 pm per element; in the actinides, it is about 3 pm per element. The contraction is larger in the lanthanides than in the actinides due to the greater localization of the 4f wave function as compared to the 5f wave function. Comparisons with the wave functions of the outer electrons of the lanthanides, actinides, and superactinides lead to a prediction of a contraction of about 2 pm per element in the superactinides; although this is smaller than the contractions in the lanthanides and actinides, its total effect is larger due to the fact that 32 electrons are filled in the deeply buried 5g and 6f shells, instead of just 14 electrons being filled in the 4f and 5f shells in the lanthanides and actinides respectively.^[4]

Pekka Pyykkö divides these superactinides into three series: a 5g series (elements 121 to 138), an 8p_1/2 series (elements 139 to 140), and a 6f series (elements 141 to 155), also noting that there would be a great deal of overlapping between energy levels and that the 6f, 7d, or 8p_1/2 orbitals could well also be occupied in the early superactinide atoms or ions. He also expects that they would behave more like "superlanthanides", in the sense that the 5g electrons would mostly be chemically inactive, similarly to how only one or two 4f electrons in each lanthanide are ever ionized in chemical compounds. He also predicted that the possible oxidation states of the superactinides might rise very high in the 6f series, to values such as +12 in element 148.^[13]

Andrey Kulsha has called the thirty-six elements 121 to 156 "ultransition" elements and has proposed to split them into two series of eighteen each, one from elements 121 to 138 and another from elements 139 to 156. The first would be analogous to the lanthanides, with oxidation states mainly ranging from +4 to +6, as the filling of the 5g shell dominates and neighbouring elements are very similar to each other, creating an analogy to uranium, neptunium, and plutonium. The second would be analogous to the actinides: at the beginning (around elements in the 140s) very high oxidation states would be expected as the 6f shell rises above the 7d one, but after that the typical oxidation states would lower and in elements in the 150s onwards the 8p_1/2 electrons would stop being chemically active. Because the two rows are separated by the addition of a complete 5g¹⁸ subshell, they could be considered analogues of each other as well.^[18]

As an example from the late superactinides, element 156 is expected to exhibit mainly the +2 oxidation state, on account of its electron configuration with easily removed 7d² electrons over a stable [Og]5g¹⁸6f¹⁴8s²8p21/2 core. It can thus be considered a heavier congener of nobelium, which likewise has a pair of easily removed 7s² electrons over a stable [Rn]5f¹⁴ core, and is usually in the +2 state (strong oxidisers are required to obtain nobelium in the +3 state).^[18] Its first ionization energy should be about 400 kJ/mol and its metallic radius approximately 170 picometers. With a relative atomic mass of around 445 u,^[4] it should be a very heavy metal with a density of around 26 g/cm³.

Elements 157 to 166

The 7d transition metals in period 8 are expected to be elements 157 to 166. Although the 8s and 8p_1/2 electrons are bound so strongly in these elements that they should not be able to take part in any chemical reactions, the 9s and 9p_1/2 levels are expected to be readily available for hybridization.^[4]^[15] These 7d elements should be similar to the 4d elements yttrium through cadmium.^[18] In particular, element 164 with a 7d¹⁰9s⁰ electron configuration shows clear analogies with palladium with its 4d¹⁰5s⁰ electron configuration.^[16]

The noble metals of this series of transition metals are not expected to be as noble as their lighter homologues, due to the absence of an outer s shell for shielding and also because the 7d shell is strongly split into two subshells due to relativistic effects. This causes the first ionization energies of the 7d transition metals to be smaller than those of their lighter congeners.^[4]^[15]^[16]

Theoretical interest in the chemistry of unhexquadium is largely motivated by theoretical predictions that it, especially the isotopes ⁴⁷²164 and ⁴⁸²164 (with 164 protons and 308 or 318 neutrons), would be at the center of a hypothetical second island of stability (the first being centered on copernicium, particularly the isotopes ²⁹¹Cn, ²⁹³Cn, and ²⁹⁶Cn which are expected to have half-lives of centuries or millennia).^[71]^[46]^[72]^[73]

Calculations predict that the 7d electrons of element 164 (unhexquadium) should participate very readily in chemical reactions, so that it should be able to show stable +6 and +4 oxidation states in addition to the normal +2 state in aqueous solutions with strong ligands. Element 164 should thus be able to form compounds like 164(CO)₄, 164(PF₃)₄ (both tetrahedral like the corresponding palladium compounds), and 164(CN)2−2 (linear), which is very different behavior from that of lead, which element 164 would be a heavier homologue of if not for relativistic effects. Nevertheless, the divalent state would be the main one in aqueous solution (although the +4 and +6 states would be possible with stronger ligands), and unhexquadium(II) should behave more similarly to lead than unhexquadium(IV) and unhexquadium(VI).^[15]^[16]

Element 164 is expected to be a soft Lewis acid and have Ahrlands softness parameter close to 4 eV. It should be at most moderately reactive, having a first ionization energy that should be around 685 kJ/mol, comparable to that of molybdenum.^[4]^[16] Due to the lanthanide, actinide, and superactinide contractions, element 164 should have a metallic radius of only 158 pm, very close to that of the much lighter magnesium, despite its expected atomic weight of around 474 u which is about 19.5 times the atomic weight of magnesium.^[4] This small radius and high weight cause it to be expected to have an extremely high density of around 46 g·cm⁻³, over twice that of osmium, currently the most dense element known, at 22.61 g·cm⁻³; element 164 should be the second most dense element in the first 172 elements in the periodic table, with only its neighbor unhextrium (element 163) being more dense (at 47 g·cm⁻³).^[4] Metallic element 164 should have a very large cohesive energy (enthalpy of crystallization) due to its covalent bonds, most probably resulting in a high melting point. In the metallic state, element 164 should be quite noble and analogous to palladium and platinum. Fricke et al. suggested some formal similarities to oganesson, as both elements have closed-shell configurations and similar ionisation energies, although they note that while oganesson would be a very bad noble gas, element 164 would be a good noble metal.^[16]

Elements 165 (unhexpentium) and 166 (unhexhexium), the last two 7d metals, should behave similarly to alkali and alkaline earth metals when in the +1 and +2 oxidation states respectively. The 9s electrons should have ionization energies comparable to those of the 3s electrons of sodium and magnesium, due to relativistic effects causing the 9s electrons to be much more strongly bound than non-relativistic calculations would predict. Elements 165 and 166 should normally exhibit the +1 and +2 oxidation states respectively, although the ionization energies of the 7d electrons are low enough to allow higher oxidation states like +3 for element 165. The oxidation state +4 for element 166 is less likely, creating a situation similar to the lighter elements in groups 11 and 12 (particularly gold and mercury).^[4]^[15] As with mercury but not copernicium, ionization of element 166 to 166²⁺ is expected to result in a 7d¹⁰ configuration corresponding to the loss of the s-electrons but not the d-electrons, making it more analogous to the lighter "less relativistic" group 12 elements zinc, cadmium, and mercury, which have essentially no transition-metal character.^[13]

Some predicted properties of elements 156–166
The metallic radii and densities are first approximations.^[4]^[13]^[15]
Most analogous group is given first, followed by other similar groups.^[16]
Property	156	157	158	159	160	161	162	163	164	165	166
Standard atomic weight	[445]	[448]	[452]	[456]	[459]	[463]	[466]	[470]	[474]	[477]	[481]
Group	Yb group (4)	3 (5)	4 (6)	5 (7)	6 (8)	7 (9)	8 (10)	9 (11)	10 (12, 14, 18)	11 (1, 13)	12 (2, 14)
Valence electron configuration	7d²	7d³	7d⁴	7d⁵	7d⁶	7d⁷	7d⁸	7d⁹	7d¹⁰	7d¹⁰ 9s¹	7d¹⁰ 9s²
Stable oxidation states	2	3	4	1, 5	2, 6	3, 7	4, 8	5	0, 2, 4, 6	1, 3	2
First ionization energy	400 kJ/mol	450 kJ/mol	520 kJ/mol	340 kJ/mol	420 kJ/mol	470 kJ/mol	560 kJ/mol	620 kJ/mol	690 kJ/mol	520 kJ/mol	630 kJ/mol
Metallic radius	170 pm	163 pm	157 pm	152 pm	148 pm	148 pm	149 pm	152 pm	158 pm	250 pm	200 pm
Density	26 g/cm³	28 g/cm³	30 g/cm³	33 g/cm³	36 g/cm³	40 g/cm³	45 g/cm³	47 g/cm³	46 g/cm³	7 g/cm³	11 g/cm³

Elements 167 to 172

The next six elements on the periodic table are expected to be the last main-group elements in their period,^[13] and are likely to be similar to the 5p elements indium through xenon.^[18] In elements 167 to 172, the 9p_1/2 and 8p_3/2 shells will be filled. Their energy eigenvalues are so close together that they behave as one combined p-subshell, similar to the non-relativistic 2p and 3p subshells. Thus, the inert-pair effect does not occur and the most common oxidation states of elements 167 to 170 are expected to be +3, +4, +5, and +6 respectively. Element 171 (unseptunium) is expected to show some similarities to the halogens, showing various oxidation states ranging from −1 to +7, although its physical properties are expected to be closer to that of a metal. Its electron affinity is expected to be 3.0 eV, allowing it to form H171, analogous to a hydrogen halide. The 171⁻ ion is expected to be a soft base, comparable to iodide (I⁻). Element 172 (unseptbium) is expected to be a noble gas with chemical behaviour similar to that of xenon, as their ionization energies should be very similar (Xe, 1170.4 kJ/mol; element 172, 1090 kJ/mol). The only main difference between them is that element 172, unlike xenon, is expected to be a liquid or a solid at standard temperature and pressure due to its much higher atomic weight.^[4] Unseptbium is expected to be a strong Lewis acid, forming fluorides and oxides, similarly to its lighter congener xenon.^[16] Because of the analogy of elements 165–172 to periods 2 and 3, Fricke et al. considered them to form a ninth period of the periodic table, while the eighth period was taken by them to end at the noble metal element 164. This ninth period would be similar to the second and third period in that it is expected to have no transition metals.^[16]

Some predicted properties of elements 167–172
The metallic or covalent radii and densities are first approximations.^[4]^[15]^[16]
Property	167	168	169	170	171	172
Standard atomic weight	[485]	[489]	[493]	[496]	[500]	[504]
Group	13	14	15	16	17	18
Valence electron configuration	9s² 9p¹	9s² 9p²	9s² 9p² 8p¹	9s² 9p² 8p²	9s² 9p² 8p³	9s² 9p² 8p⁴
Stable oxidation states	3	4	5	6	−1, 3, 7	0, 4, 6, 8
First ionization energy	620 kJ/mol	720 kJ/mol	800 kJ/mol	890 kJ/mol	984 kJ/mol	1090 kJ/mol
Metallic or covalent radius	190 pm	180 pm	175 pm	170 pm	165 pm	220 pm
Density	17 g/cm³	19 g/cm³	18 g/cm³	17 g/cm³	16 g/cm³	9 g/cm³

Beyond element 172

Beyond element 172, there is the potential to fill the 6g, 7f, 8d, 10s, 10p_1/2, and perhaps 6h_11/2 shells. These electrons would be very loosely bound, potentially rendering extremely high oxidation states reachable, though the electrons would become more tightly bound as the ionic charge rises. Thus, there will probably be another very long transition series, like the superactinides.^[16]

In element 173 (unsepttrium), the outermost electron might enter the 6g_7/2, 9p_3/2, or 10s subshells. Because spin–orbit interactions would create a very large energy gap between these and the 8p_3/2 subshell, this outermost electron is expected to be very loosely bound and very easily lost to form a 173⁺ cation. As a result, element 173 is expected to behave chemically like an alkali metal, and one that might be far more reactive than even caesium (francium and element 119 being less reactive than caesium due to relativistic effects):^[74]^[18] the calculated ionisation energy for element 173 is 3.070 eV, compared to the experimentally known 3.894 eV for caesium. Element 174 (unseptquadium) may add an 8d electron and form a closed-shell 174²⁺ cation; its calculated ionisation energy is 3.614 eV.^[75]

Element 184 (unoctquadium) was significantly targeted in early predictions, as it was originally speculated that 184 would be a proton magic number: it is predicted to have an electron configuration of [172] 6g⁵ 7f⁴ 8d³, with at least the 7f and 8d electrons chemically active. Its chemical behaviour is expected to be similar to uranium and neptunium, as further ionisation past the +6 state (corresponding to removal of the 6g electrons) is likely to be unprofitable; the +4 state should be most common in aqueous solution, with +5 and +6 reachable in solid compounds.^[4]^[16]^[76]

End of the periodic table

The number of physically possible elements is unknown. A low estimate is that the periodic table may end soon after the island of stability,^[14] which is expected to center on Z = 126, as the extension of the periodic and nuclides tables is restricted by the proton and the neutron drip lines and stability toward alpha decay and spontaneous fission.^[77] One calculation by Y. Gambhir et al., analyzing nuclear binding energy and stability in various decay channels, suggests a limit to the existence of bound nuclei at Z = 146.^[78] Other predictions of an end to the periodic table include Z = 128 (John Emsley) and Z = 155 (Albert Khazan).^[10]

Elements above the atomic number 137

It is a "folk legend" among physicists that Richard Feynman suggested that neutral atoms could not exist for atomic numbers greater than Z = 137, on the grounds that the relativistic Dirac equation predicts that the ground-state energy of the innermost electron in such an atom would be an imaginary number. Here, the number 137 arises as the inverse of the fine-structure constant. By this argument, neutral atoms cannot exist beyond atomic number 137, and therefore a periodic table of elements based on electron orbitals breaks down at this point. However, this argument presumes that the atomic nucleus is pointlike. A more accurate calculation must take into account the small, but nonzero, size of the nucleus, which is predicted to push the limit further to Z ≈ 173.^[79]

Bohr model

The Bohr model exhibits difficulty for atoms with atomic number greater than 137, for the speed of an electron in a 1s electron orbital, v, is given by

v=Z\alpha c\approx {\frac {Zc}{137.04}}

where Z is the atomic number, and α is the fine-structure constant, a measure of the strength of electromagnetic interactions.^[80] Under this approximation, any element with an atomic number of greater than 137 would require 1s electrons to be traveling faster than c, the speed of light. Hence, the non-relativistic Bohr model is inaccurate when applied to such an element.

Relativistic Dirac equation

Energy eigenvalues for the 1s, 2s, 2p_1/2 and 2p_3/2 shells from solutions of the Dirac equation (taking into account the finite size of the nucleus) for Z = 135–175 (–·–), for the Thomas-Fermi potential (—) and for Z = 160–170 with the self-consistent potential (---).^[4]

The relativistic Dirac equation gives the ground state energy as

E={\frac {mc^{2}}{\sqrt {1+{\dfrac {Z^{2}\alpha ^{2}}{{\bigg (}{n-\left(j+{\frac {1}{2}}\right)+{\sqrt {\left(j+{\frac {1}{2}}\right)^{2}-Z^{2}\alpha ^{2}}}{\bigg )}}^{2}}}}}},

where m is the rest mass of the electron.^[81] For Z > 137, the wave function of the Dirac ground state is oscillatory, rather than bound, and there is no gap between the positive and negative energy spectra, as in the Klein paradox.^[82] More accurate calculations taking into account the effects of the finite size of the nucleus indicate that the binding energy first exceeds 2mc² for Z > Z_cr ≈ 173. For Z > Z_cr, if the innermost orbital (1s) is not filled, the electric field of the nucleus will pull an electron out of the vacuum, resulting in the spontaneous emission of a positron.^[83]^[84] This diving of the 1s subshell into the negative continuum has often been taken to constitute an "end" to the periodic table, although more detailed treatments suggest a less bleak outcome.^[13]^[79]^[85]

Atoms with atomic numbers above Z_cr ≈ 173 have been termed supercritical atoms. Supercritical atoms cannot be totally ionised because their 1s subshell would be filled by spontaneous pair creation in which an electron-positron pair is created from the negative continuum, with the electron being bound and the positron escaping. However, the strong field around the atomic nucleus is restricted to a very small region of space, so that the Pauli exclusion principle forbids further spontaneous pair creation once the subshells that have dived into the negative continuum are filled. Elements 173–184 have been termed weakly supercritical atoms as for them only the 1s shell has dived into the negative continuum; the 2p_1/2 shell is expected to join around element 185 and the 2s shell around element 245. Experiments have so far not succeeded in detecting spontaneous pair creation from assembling supercritical charges through the collision of heavy nuclei (e.g. colliding lead with uranium to momentarily give an effective Z of 174; uranium with uranium gives effective Z = 184 and uranium with californium gives effective Z = 190).^[86]

Even if passing Z_cr is not an issue, the increasing concentration of the 1s density close to the nucleus would likely make these electrons more vulnerable to K electron capture as Z_cr is approached. For such heavy elements, these 1s electrons would likely spend a significant fraction of time so close to the nucleus that they are actually inside it. This may pose another limit to the periodic table.^[87]

Quark matter

It has also been posited that in the region beyond A > 300, an entire "continent of stability" consisting of a hypothetical phase of stable quark matter, comprising freely flowing up and down quarks rather than quarks bound into protons and neutrons, may exist. Such a form of matter is theorized to be a ground state of baryonic matter with a greater binding energy per baryon than nuclear matter, favoring the decay of nuclear matter beyond this mass threshold into quark matter. If this state of matter exists, it could possibly be synthesized in the same fusion reactions leading to normal superheavy nuclei, and would be stabilized against fission as a consequence of its stronger binding that is enough to overcome Coulomb repulsion.^[88]

Recent calculations^[89] suggest stability of up-down quark matter (udQM) nuggets against conventional nuclei beyond A ~ 266, and also show that udQM nuggets become supercritical earlier (Z_cr ~ 163, A ~ 609) than conventional nuclei (Z_cr ~ 177, A ~ 480).

الخصائص النووية

Predicted half-lives (top) and decay modes (bottom) of superheavy nuclei. The line of synthesized proton-rich nuclei is expected to be broken soon after Z = 120, because of half-lives shorter than 1 microsecond from Z = 121, the increasing contribution of spontaneous fission instead of alpha decay from Z = 122 onward until it dominates from Z = 125, and the proton drip line around Z = 130. The white rings denote the expected location of the island of stability; the two squares outlined in white denote ²⁹¹Cn and ²⁹³Cn, predicted to be the longest-lived nuclides on the island with half-lives of centuries or millennia.^[48] The black square near the bottom of the second picture is uranium-238, the heaviest confirmed primordial nuclide (a nuclide stable enough to have survived from the Earth's formation to the present day).

الأرقام السحرية وجزيرة الاستقرار

The stability of nuclei decreases greatly with the increase in atomic number after curium, element 96, so that all isotopes with an atomic number above 101 decay radioactively with a half-life under a day. No elements with atomic numbers above 82 (after lead) have stable isotopes.^[90] Nevertheless, because of reasons not very well understood yet, there is a slight increased nuclear stability around atomic numbers 110–114, which leads to the appearance of what is known in nuclear physics as the "island of stability". This concept, proposed by University of California professor Glenn Seaborg, explains why superheavy elements last longer than predicted.^[91]

Calculations according to the Hartree–Fock–Bogoliubov method using the non-relativistic Skyrme interaction have proposed Z = 126 as a closed proton shell. In this region of the periodic table, N = 184, N = 196, and N = 228 have been suggested as closed neutron shells. Therefore, the isotopes of most interest are ³¹⁰126, ³²²126, and ³⁵⁴126, for these might be considerably longer-lived than other isotopes. Element 126, having a magic number of protons, is predicted to be more stable than other elements in this region, and may have nuclear isomers with very long half-lives.^[60] It is also possible that the island of stability is instead centered at ³⁰⁶122, which may be spherical and doubly magic.^[46]

Taking nuclear deformation and relativistic effects into account, an analysis of single-particle levels predicts new magic numbers for superheavy nuclei at Z = 126, 138, 154, and 164 and N = 228, 308, and 318.^[9]^[71] Therefore, in addition to the island of stability centered at ²⁹¹Cn, ²⁹³Cn,^[25] and ²⁹⁸Fl, further islands of stability may exist around the doubly magic ³⁵⁴126 as well as ⁴⁷²164 or ⁴⁸²164.^[72]^[73] These nuclei are predicted to be beta-stable and decay by alpha emission or spontaneous fission with relatively long half-lives, and confer additional stability on neighboring N = 228 isotones and elements 152–168, respectively.^[92] On the other hand, the same analysis suggests that proton shell closures may be relatively weak or even nonexistent in some cases such as ³⁵⁴126, meaning that such nuclei might not be doubly magic and stability will instead be primarily determined by strong neutron shell closures.^[71] Additionally, due to the enormously greater forces of electromagnetic repulsion that must be overcome by the strong force at the second island (Z = 164),^[93] it is possible that nuclei around this region only exist as resonances and cannot stay together for a meaningful amount of time. It is also possible that some of the superactinides between these series may not actually exist because they are too far from both islands,^[93] in which case the periodic table might end around Z = 130.^[16]

Beyond element 164, the fissility line defining the limit of stability with respect to spontaneous fission may converge with the neutron drip line, posing a limit to the existence of heavier elements.^[92] Nevertheless, further magic numbers have been predicted at Z = 210, 274, and 354 and N = 308, 406, 524, 644, and 772,^[94] with two beta-stable doubly magic nuclei found at ⁶¹⁶210 and ⁷⁹⁸274; the same calculation method reproduced the predictions for ²⁹⁸Fl and ⁴⁷²164. (The doubly magic nuclei predicted for Z = 354 are beta-unstable, with ⁹⁹⁸354 being neutron-deficient and ¹¹²⁶354 being neutron-rich.) Although additional stability toward alpha decay and fission are predicted for ⁶¹⁶210 and ⁷⁹⁸274, with half-lives up to hundreds of microseconds for ⁶¹⁶210,^[94] there will not exist islands of stability as significant as those predicted at Z = 114 and 164. As the existence of superheavy elements is very strongly dependent on stabilizing effects from closed shells, nuclear instability and fission will likely determine the end of the periodic table beyond these islands of stability.^[16]^[78]^[92]

The International Union of Pure and Applied Chemistry (IUPAC) defines an element to exist if its lifetime is longer than 10⁻¹⁴ seconds, which is the time it takes for the nucleus to form an electron cloud. However, a nuclide is generally considered to exist if its lifetime is longer than about 10⁻²² seconds, which is the time it takes for nuclear structure to form. Consequently it is possible that some Z values can only be realised in nuclides and that the corresponding elements do not exist.^[87]

It is also possible that no further islands actually exist beyond 126, as the nuclear shell structure gets smeared out (as the electron shell structure already is expected to be around oganesson) and low-energy decay modes become readily available.^[95]

خصائص الاضمحلال المتوقعة للعناصر غير المكتشفة

As the main island of stability is thought to lie around ²⁹¹Cn and ²⁹³Cn, undiscovered elements beyond oganesson may be very unstable and undergo alpha decay or spontaneous fission in microseconds or less. The exact region in which half-lives exceed one microsecond is unknown, though various models suggest that isotopes of elements heavier than unbinilium that may be produced in fusion reactions with available targets and projectiles will have half-lives under one microsecond and therefore may not be detected.^[48] It is consistently predicted that there will exist regions of stability at N = 184 and N = 228, and possibly also at Z ~ 124 and N ~ 198. These nuclei may have half-lives of a few seconds and undergo predominantly alpha decay and spontaneous fission, though minor beta-plus decay (or electron capture) branches may also exist.^[96] Outside these regions of enhanced stability, fission barriers are expected to drop significantly due to loss of stabilization effects, resulting in fission half-lives below 10⁻¹⁸ seconds, especially in even–even nuclei for which hindrance is even lower due to nucleon pairing.^[92] In general, alpha decay half-lives are expected to increase with neutron number, from nanoseconds in the most neutron-deficient isotopes to seconds closer to the beta-stability line.^[37] For nuclei with only a few neutrons more than a magic number, binding energy substantially drops, resulting in a break in the trend and shorter half-lives.^[37] The most neutron deficient isotopes of these elements may also be unbound and undergo proton emission. Cluster decay (heavy particle emission) has also been proposed as an alternative decay mode for some isotopes,^[97] posing yet another hurdle to identification of these elements.

Electron configurations

The following are expected electron configurations of elements 119–174 and 184. The symbol [Og] indicates the probable electron configuration of oganesson (Z = 118), which is currently the last known element. The configurations of the elements in this table are written starting with [Og] because oganesson is expected to be the last prior element with a closed-shell (inert gas) configuration, 1s² 2s² 2p⁶ 3s² 3p⁶ 3d¹⁰ 4s² 4p⁶ 4d¹⁰ 4f¹⁴ 5s² 5p⁶ 5d¹⁰ 5f¹⁴ 6s² 6p⁶ 6d¹⁰ 7s² 7p⁶. Similarly, the [172] in the configurations for elements 173, 174, and 184 denotes the likely closed-shell configuration of element 172.

Beyond element 123, no complete calculations are available and hence the data in this table must be taken as tentative.^[16]^[74]^[98] In the case of element 123, and perhaps also heavier elements, several possible electron configurations are predicted to have very similar energy levels, such that it is very difficult to predict the ground state. All configurations that have been proposed (since it was understood that the Madelung rule probably stops working here) are included.^[98]^[67]^[99]

The predicted block assignments up to 172 are Kulsha's,^[20] following the expected available valence orbitals. There is, however, not a consensus in the literature as to how the blocks should work after element 138.

Chemical element			Block	Predicted electron configurations^[15]^[16]^[74]^[17]
119	Uue	Ununennium	s-block	[Og] 8s¹
120	Ubn	Unbinilium	s-block	[Og] 8s²
121	Ubu	Unbiunium	g-block	[Og] 8s² 8p11/2^[67]
122	Ubb	Unbibium	g-block	[Og] 8s² 8p21/2^[67] [Og] 7d¹ 8s² 8p11/2
123	Ubt	Unbitrium	g-block	[Og] 6f¹ 8s² 8p21/2^[100] [Og] 6f¹ 7d¹ 8s² 8p11/2^[98]^[67] [Og] 6f² 8s² 8p11/2 [Og] 8s² 8p21/2 8p13/2^[98]
124	Ubq	Unbiquadium	g-block	[Og] 6f² 8s² 8p21/2^[67]^[100] [Og] 6f³ 8s² 8p11/2
125	Ubp	Unbipentium	g-block	[Og] 6f⁴ 8s² 8p11/2^[67] [Og] 5g¹ 6f² 8s² 8p21/2^[100] [Og] 5g¹ 6f³ 8s² 8p11/2 [Og] 8s² 0.81(5g¹ 6f² 8p21/2) + 0.17(5g¹ 6f¹ 7d² 8p11/2) + 0.02(6f³ 7d¹ 8p11/2)
126	Ubh	Unbihexium	g-block	[Og] 5g¹ 6f⁴ 8s² 8p11/2^[67] [Og] 5g² 6f² 8s² 8p21/2^[100] [Og] 5g² 6f³ 8s² 8p11/2 [Og] 8s² 0.998(5g² 6f³ 8p11/2) + 0.002(5g² 6f² 8p21/2)
127	Ubs	Unbiseptium	g-block	[Og] 5g² 6f³ 8s² 8p21/2^[67] [Og] 5g³ 6f² 8s² 8p21/2^[100] [Og] 8s² 0.88(5g³ 6f² 8p21/2) + 0.12(5g³ 6f¹ 7d² 8p11/2)
128	Ubo	Unbioctium	g-block	[Og] 5g³ 6f³ 8s² 8p21/2^[67] [Og] 5g⁴ 6f² 8s² 8p21/2^[100] [Og] 8s² 0.88(5g⁴ 6f² 8p21/2) + 0.12(5g⁴ 6f¹ 7d² 8p11/2)
129	Ube	Unbiennium	g-block	[Og] 5g⁴ 6f³ 7d¹ 8s² 8p11/2 [Og] 5g⁴ 6f³ 8s² 8p21/2^[67]^[100] [Og] 5g⁵ 6f² 8s² 8p21/2 [Og] 5g⁴ 6f³ 7d¹ 8s² 8p11/2
130	Utn	Untrinilium	g-block	[Og] 5g⁵ 6f³ 7d¹ 8s² 8p11/2 [Og] 5g⁵ 6f³ 8s² 8p21/2^[67]^[100] [Og] 5g⁶ 6f² 8s² 8p21/2 [Og] 5g⁵ 6f³ 7d¹ 8s² 8p11/2
131	Utu	Untriunium	g-block	[Og] 5g⁶ 6f³ 8s² 8p21/2^[67]^[100] [Og] 5g⁷ 6f² 8s² 8p21/2 [Og] 8s² 0.86(5g⁶ 6f³ 8p21/2) + 0.14(5g⁶ 6f² 7d² 8p11/2)
132	Utb	Untribium	g-block	[Og] 5g⁷ 6f³ 8s² 8p21/2^[100] [Og] 5g⁸ 6f² 8s² 8p21/2
133	Utt	Untritrium	g-block	[Og] 5g⁸ 6f³ 8s² 8p21/2^[100]
134	Utq	Untriquadium	g-block	[Og] 5g⁸ 6f⁴ 8s² 8p21/2^[100]
135	Utp	Untripentium	g-block	[Og] 5g⁹ 6f⁴ 8s² 8p21/2^[100]
136	Uth	Untrihexium	g-block	[Og] 5g¹⁰ 6f⁴ 8s² 8p21/2^[100]
137	Uts	Untriseptium	g-block	[Og] 5g¹¹ 6f⁴ 8s² 8p21/2^[100]
138	Uto	Untrioctium	g-block	[Og] 5g¹² 6f⁴ 8s² 8p21/2^[100] [Og] 5g¹² 6f³ 7d¹ 8s² 8p21/2
139	Ute	Untriennium	g-block	[Og] 5g¹³ 6f³ 7d¹ 8s² 8p21/2^[100] [Og] 5g¹³ 6f² 7d² 8s² 8p21/2
140	Uqn	Unquadnilium	g-block	[Og] 5g¹⁴ 6f³ 7d¹ 8s² 8p21/2^[100] [Og] 5g¹⁵ 6f¹ 8s² 8p21/2 8p23/2
141	Uqu	Unquadunium	g-block	[Og] 5g¹⁵ 6f² 7d² 8s² 8p21/2^[100]
142	Uqb	Unquadbium	g-block	[Og] 5g¹⁶ 6f² 7d² 8s² 8p21/2^[100]
143	Uqt	Unquadtrium	f-block	[Og] 5g¹⁷ 6f² 7d² 8s² 8p21/2^[100]
144	Uqq	Unquadquadium	f-block	[Og] 5g¹⁸ 6f² 7d² 8s² 8p21/2^[100] [Og] 5g¹⁸ 6f¹ 7d³ 8s² 8p21/2 [Og] 5g¹⁷ 6f² 7d³ 8s² 8p21/2 [Og] 8s² 0.95(5g¹⁷ 6f² 7d³ 8p21/2) + 0.05(5g¹⁷ 6f⁴ 7d¹ 8p21/2)
145	Uqp	Unquadpentium	f-block	[Og] 5g¹⁸ 6f³ 7d² 8s² 8p21/2^[100]
146	Uqh	Unquadhexium	f-block	[Og] 5g¹⁸ 6f⁴ 7d² 8s² 8p21/2^[100]
147	Uqs	Unquadseptium	f-block	[Og] 5g¹⁸ 6f⁵ 7d² 8s² 8p21/2^[100]
148	Uqo	Unquadoctium	f-block	[Og] 5g¹⁸ 6f⁶ 7d² 8s² 8p21/2^[100]
149	Uqe	Unquadennium	f-block	[Og] 5g¹⁸ 6f⁶ 7d³ 8s² 8p21/2^[100]
150	Upn	Unpentnilium	f-block	[Og] 5g¹⁸ 6f⁶ 7d⁴ 8s² 8p21/2 [Og] 5g¹⁸ 6f⁷ 7d³ 8s² 8p21/2^[100]
151	Upu	Unpentunium	f-block	[Og] 5g¹⁸ 6f⁸ 7d³ 8s² 8p21/2^[100]
152	Upb	Unpentbium	f-block	[Og] 5g¹⁸ 6f⁹ 7d³ 8s² 8p21/2^[100]
153	Upt	Unpenttrium	f-block	[Og] 5g¹⁸ 6f¹⁰ 7d³ 8s² 8p21/2 [Og] 5g¹⁸ 6f¹¹ 7d² 8s² 8p21/2^[100]
154	Upq	Unpentquadium	f-block	[Og] 5g¹⁸ 6f¹¹ 7d³ 8s² 8p21/2 [Og] 5g¹⁸ 6f¹² 7d² 8s² 8p21/2^[100]
155	Upp	Unpentpentium	f-block	[Og] 5g¹⁸ 6f¹² 7d³ 8s² 8p21/2 [Og] 5g¹⁸ 6f¹³ 7d² 8s² 8p21/2^[100]
156	Uph	Unpenthexium	f-block	[Og] 5g¹⁸ 6f¹³ 7d³ 8s² 8p21/2 [Og] 5g¹⁸ 6f¹⁴ 7d² 8s² 8p21/2^[100]
157	Ups	Unpentseptium	d-block	[Og] 5g¹⁸ 6f¹⁴ 7d³ 8s² 8p21/2^[100]
158	Upo	Unpentoctium	d-block	[Og] 5g¹⁸ 6f¹⁴ 7d⁴ 8s² 8p21/2^[100]
159	Upe	Unpentennium	d-block	[Og] 5g¹⁸ 6f¹⁴ 7d⁵ 8s² 8p21/2 [Og] 5g¹⁸ 6f¹⁴ 7d⁴ 8s² 8p21/2 9s¹^[100]
160	Uhn	Unhexnilium	d-block	[Og] 5g¹⁸ 6f¹⁴ 7d⁶ 8s² 8p21/2 [Og] 5g¹⁸ 6f¹⁴ 7d⁵ 8s² 8p21/2 9s¹^[100]
161	Uhu	Unhexunium	d-block	[Og] 5g¹⁸ 6f¹⁴ 7d⁷ 8s² 8p21/2 [Og] 5g¹⁸ 6f¹⁴ 7d⁶ 8s² 8p21/2 9s¹^[100]
162	Uhb	Unhexbium	d-block	[Og] 5g¹⁸ 6f¹⁴ 7d⁸ 8s² 8p21/2 [Og] 5g¹⁸ 6f¹⁴ 7d⁷ 8s² 8p21/2 9s¹^[100]
163	Uht	Unhextrium	d-block	[Og] 5g¹⁸ 6f¹⁴ 7d⁹ 8s² 8p21/2 [Og] 5g¹⁸ 6f¹⁴ 7d⁸ 8s² 8p21/2 9s¹^[100]
164	Uhq	Unhexquadium	d-block	[Og] 5g¹⁸ 6f¹⁴ 7d¹⁰ 8s² 8p21/2^[100]
165	Uhp	Unhexpentium	d-block	[Og] 5g¹⁸ 6f¹⁴ 7d¹⁰ 8s² 8p21/2 9s¹^[100]
166	Uhh	Unhexhexium	d-block	[Og] 5g¹⁸ 6f¹⁴ 7d¹⁰ 8s² 8p21/2 9s²^[100]
167	Uhs	Unhexseptium	p-block	[Og] 5g¹⁸ 6f¹⁴ 7d¹⁰ 8s² 8p21/2 9s² 9p11/2 [Og] 5g¹⁸ 6f¹⁴ 7d¹⁰ 8s² 8p21/2 8p13/2 9s²^[100]
168	Uho	Unhexoctium	p-block	[Og] 5g¹⁸ 6f¹⁴ 7d¹⁰ 8s² 8p21/2 9s² 9p21/2 [Og] 5g¹⁸ 6f¹⁴ 7d¹⁰ 8s² 8p21/2 8p23/2 9s²^[100]
169	Uhe	Unhexennium	p-block	[Og] 5g¹⁸ 6f¹⁴ 7d¹⁰ 8s² 8p21/2 8p13/2 9s² 9p21/2 [Og] 5g¹⁸ 6f¹⁴ 7d¹⁰ 8s² 8p21/2 8p33/2 9s²^[100]
170	Usn	Unseptnilium	p-block	[Og] 5g¹⁸ 6f¹⁴ 7d¹⁰ 8s² 8p21/2 8p23/2 9s² 9p21/2 [Og] 5g¹⁸ 6f¹⁴ 7d¹⁰ 8s² 8p21/2 8p43/2 9s²^[100]
171	Usu	Unseptunium	p-block	[Og] 5g¹⁸ 6f¹⁴ 7d¹⁰ 8s² 8p21/2 8p33/2 9s² 9p21/2 [Og] 5g¹⁸ 6f¹⁴ 7d¹⁰ 8s² 8p21/2 8p43/2 9s² 9p11/2^[100]
172	Usb [ك‍]	Unseptbium	p-block	[Og] 5g¹⁸ 6f¹⁴ 7d¹⁰ 8s² 8p21/2 8p43/2 9s² 9p21/2^[100]
173	Ust	Unsepttrium	?	[172] 6g¹ [172] 9p13/2 [172] 10s¹^[75]
174	Usq	Unseptquadium	?	[172] 8d¹ 10s¹^[75]
...	...	...	...	...
184	Uoq	Unoctquadium	?	[172] 6g⁵ 7f⁴ 8d³

انظر أيضاً

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للاستزادة

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المصادر

ويكيبيديا الإنجليزية.

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v t e الجدول الدوري
Standard form	Periodic table (18 columns) With large cells 18 columns wide 32 columns wide
Extended form	Extension beyond the 7th period Fricke model Pyykkö model Extended form, large cells
Alternative structure	Alternatives Chemical Galaxy Janet's Left Step table
Groups	1 (Alkali metals) 2 (Alkaline earth metals) 3 4 5 6 7 8 9 10 11 12 13 (Boron group) 14 (Carbon group) 15 (Pnictogens) 16 (Chalcogens) 17 (Halogens) 18 (Noble gases)
Periods	1 2 3 4 5 6 7 8 9
Blocks	s-block p-block d-block f-block g-block
Metals–nonmetals	Metals Metalloids dividing line Nonmetals Subgroups: Alkali metals Alkaline earth metals Lanthanides Actinides Superactinides Eka-superactinides Transition metals Other metals Metalloids Polyatomic nonmetals Diatomic nonmetals Noble gases
History	History of the periodic table Element discoveries Mendeleev's predictions Name etymology controversies places scientists
Element properties	Atomic weights Crystal structure Dietary elements Electron affinities Electron configurations Electronegativity by Allen scale Electronegativity by Pauling scale Goldschmidt classification Maximum valences Nutritional elements Platinum group metals (PGM) Rare earth elements Refractory metals
قائمة العناصر حسب	الوفرة (في البشر) الخصائص الذرية الاستقرار النووي الانتاج الرمز
صفحات بيانات	Abundances Atomic radii Boiling points Critical points Densities Elastic properties Electrical resistivities Electron affinities Electron configurations Electronegativities Hardnesses Heat capacities Heats of fusion Heats of vaporization Ionization energies Melting points Oxidation states Speeds of sound Thermal conductivities Thermal expansion coefficients Vapor pressures
انظر أيضاً	Names for sets of chemical elements IUPAC nomenclature systematic element name Trivial name Dmitri Mendeleev Periodic table (simplified Chinese) Periodic table (traditional Chinese)
Book Category Chemistry Portal

v t e الجداول الدورية
الصيغ القياسية	الجدول الدوري مضغوط ممتد f-block in-line, large
الصيغة الممتدة	Extension beyond the 7th period Pyykkö model compact Extended form, large Pyykkö model
البنية البديلة	البدائ مجرة كيميائية جدول جانت مضغوط
خصائص العنصر	الوزن الذري البنية البلورية Dietary elements Electron affinities Electron configurations Electronegativity by Allen scale Electronegativity by Pauling scale Goldschmidt classification Maximum valences Nutritional elements Platinum group metals (PGM) العناصر الأرضية النادرة Refractory metals
قائمة العناصر الكيميائية حسب	التوافر (في البشر) الخصائص الذرية الاستقرار الذري الانتاج الرمز
صفحات بيانات	التوافر نصف القطر الذري نقاط الغليان النقاط الحرجة الكثافة خصائص المرونة المقاومة الكهربية إنجذابات الإلكترون الموصلات الإلكترونية السلببة الكهربية الصلابة قدرات الحرارة حرارة الانصهار حرارة البخر طاقات التأين نقاط الانصهار حالات الأكسدة سرعة الصوت موصلات حرارية معاملات التمدد الحراري ضغط البخار
المجموعات	1 (فلزات قلوية) 2 (فلزات قلوية ترابية) 3 4 5 6 7 8 9 10 11 12 13 (مجموعة بورون) 14 (مجموعة كربون) 15 (Pnictogens) 16 (Chalcogens) 17 (هالوجينات) 18 (غازات نبيلة)
الفلزات–اللافلزات	الفلزات أشباه الفلزات الخط الفاصل اللافلزات مجموعات فرعية: الفلزات القلوية الفلزات القلوية الترابية اللانثنيدات الأكتينيدات الفوق أكتينيدات Eka-superactinides الفلزات الإنتقالية Metalloids الفلزات الضعيفة Polyatomic nonmetals Diatomic nonmetals الغازات النبيلة
المستويات	عناصر مستوى فرعي s عناصر مستوى فرعي p عناصر مستوى فرعي d عناصر مستوى فرعي f عناصر مستوى فرعي g
الدورات	1 2 3 4 5 6 7 8 9
أبجديات أخرى	الجدول الدوري (الصينية المبسطة) الجدول الدوري (الصينية التقليدية)
التاريخ	اكتشافات العناصر تاريخ الجدول الدوري أصل التسمية جدل أماكن علماء
انظر أيضاً	دميتري مندليڤ Collective names of groups of like elements ايوپاك مسميات الوحدات اسم عنصر قياسي Trivial name
كتب تصنيف بوابة الكيمياء