Properties Of Metals, Metalloids And Nonmetals - Wikipedia

Comparison of the properties of the three main categories in the periodic table
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The chemical elements can be broadly divided into metals, metalloids, and nonmetals according to their shared physical and chemical properties. All elemental metals have a shiny appearance (at least when freshly polished); are good conductors of heat and electricity; form alloys with other metallic elements; and have at least one basic oxide. Metalloids are metallic-looking, often brittle solids that are either semiconductors or semimetals, and have amphoteric or weakly acidic oxides. Typical elemental nonmetals have a dull, coloured or colourless appearance; are often brittle when solid; are poor conductors of heat and electricity; and have acidic oxides. Most or some elements in each category share a range of other properties; a few elements have properties that are either anomalous given their category, or otherwise extraordinary.

Properties

[edit]
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Metals

[edit]
Pure (99.97%+) iron chips, electrolytically refined, accompanied by a high-purity (99.9999% = 6N) 1 cm3 cube
Main article: Metal

Elemental metals appear lustrous (beneath any patina); form compounds (alloys) when combined with other elements; tend to lose or share electrons when they react with other substances; and each forms at least one predominantly basic oxide.

Most metals are silvery looking, high density metals which can be plastically deformed solids with good electrical and thermal conductivity, closely packed structures, low ionisation energies and electronegativities, and are found naturally in combined states.

Some metals appear coloured (Cu, Cs, Au), have low densities (e.g. Be, Al) or very high melting points (e.g. W, Nb), are liquids at or near room temperature (e.g. Hg, Ga), are brittle (e.g. Os, Bi), not easily machined (e.g. Ti, Re), or are noble (hard to oxidise, e.g. Au, Pt), or have nonmetallic structures (Mn and Ga are structurally analogous to, respectively, white P and I).

Metals comprise the large majority of the elements, and can be subdivided into several different categories. From left to right in the periodic table, these categories include the highly reactive alkali metals; the less-reactive alkaline earth metals, lanthanides, and radioactive actinides; the archetypal transition metals; and the physically and chemically weak post-transition metals. Specialized subcategories such as the refractory metals and the noble metals also exist.

Metalloids

[edit]
A shiny silver-white medallion with a striated surface, irregular around the outside, with a square spiral-like pattern in the middle
Tellurium, described by Dmitri Mendeleev as forming a transition between metals and nonmetals[1]
Main article: Metalloid

Metalloids are metallic-looking often brittle solids; tend to share electrons when they react with other substances; have weakly acidic or amphoteric oxides; and are usually found naturally in combined states.

Most are semiconductors or semimetals, moderate thermal conductors, and have structures that are more open than those of most metals.

Some metalloids (As, Sb) conduct electricity like metals.

The metalloids, as the smallest major category of elements, are not subdivided further.

Nonmetals

[edit]
25 ml of bromine, a dark red-brown liquid at room temperature
Main article: Nonmetal (chemistry)

Nonmetallic elements often have open structures; tend to gain or share electrons when they react with other substances; and do not form distinctly basic oxides.

Many are gases at room temperature; have relatively low densities; are poor electrical and thermal conductors; have relatively high ionisation energies and electronegativities; form acidic oxides; and are found naturally in uncombined states in large amounts.

Some nonmetals (black P, S, and Se) are brittle solids at room temperature (although each of these also have malleable, pliable or ductile allotropes).

From left to right in the periodic table, the nonmetals can be divided into the reactive nonmetals and the noble gases. The reactive nonmetals near the metalloids show some incipient metallic character, such as the metallic appearance of graphite, black phosphorus, selenium and iodine. The noble gases are almost completely inert.

Comparison of properties

[edit] Physical and chemical properties[n 1]
Metals[2] Metalloids Nonmetals[2]
Form and structure
Colour
  • nearly all are shiny and grey-white
  • Cu, Cs, Au: shiny and golden[3]
  • shiny and grey-white[4]
  • most are colourless or dull red, yellow, green, or intermediate shades[5]
  • C, P, Se, I: shiny and grey-white
Reflectivity
  • intermediate to typically high[6][7]
  • intermediate[8][9]
  • zero or low (mostly)[10] to intermediate[11]
State of matter at STP
  • almost all solid
  • Rb, Cs, Fr, Ga, Hg: liquid at/near stp[12][13][n 2]
  • all solid[4]
  • most are gases[15]
  • C, P, S, Se, I: solid; Br: liquid
Density
  • generally high, with some exceptions such as the alkali metals[16]
  • lower than nearby metals but higher than nearby nonmetals[17]
  • often low
Deformability (as a solid)
  • most are ductile and malleable
  • some are brittle (Cr, Mn, Ga, Ru, W, Os, Bi)[18][n 3]
  • often brittle[21]
  • often brittle
  • some (C, P, S, Se) have non-brittle forms[n 4]
Poisson's ratio[n 5]
  • low to high[n 6]
  • low to intermediate[n 7]
  • low to intermediate[n 8]
Crystalline structure at freezing point[41]
  • most are hexagonal or cubic
  • Ga, U, Np: orthorhombic; In, Sn, Pa: tetragonal; Sm, Hg, Bi: rhombohedral; Pu: monoclinic
  • B, As, Sb: rhombohedral
  • Si, Ge: cubic
  • Te: hexagonal
  • H, He, C, N, Se: hexagonal
  • O, F, Ne, P, Ar, Kr, Xe, Rn: cubic
  • S, Cl, Br, I: orthorhombic
Packing & coordination number
  • close-packed crystal structures[42]
  • high coordination numbers
  • relatively open crystal structures[43]
  • medium coordination numbers[44]
  • open structures[45]
  • low coordination numbers
Atomic radius(calculated)[46]
  • intermediate to very large
  • 112–298 pm, average 187
  • small to intermediate: B, Si, Ge, As, Sb, Te
  • 87–123 pm, average 115.5 pm
  • very small to intermediate
  • 31–120 pm, average 76.4 pm
Allotropes[47][n 9]
  • around half form allotropes
  • one (Sn) has a metalloid-like allotrope (grey Sn, which forms below 13.2 °C[48])
  • all or nearly all form allotropes
  • some (e.g. red B, yellow As) are more nonmetallic in nature
  • some form allotropes
  • some (e.g. graphitic C, black P, grey Se) are more metalloidal or metallic in nature
Electron-related
Periodic table block
  • s, p, d, f[49]
  • p[50]
  • s, p[50]
Outer s and p electrons
  • few in number (1–3)
  • except 0 (Pd); 4 (Sn, Pb, Fl); 5 (Bi); 6 (Po)
  • medium number (3–7)
  • high number (4–8)
  • except 1 (H); 2 (He)
Electron bands: (valence, conduction)
  • nearly all have substantial band overlap
  • Bi: has slight band overlap (semimetal)
  • most have narrow band gap (semiconductors)
  • As, Sb are semimetals
  • most have wide band gap (insulators)
  • C (graphite): a semimetal
  • P (black), Se, I: semiconductors
Electron behaviour
  • "free" electrons (facilitating electrical and thermal conductivity)
  • valence electrons less freely delocalized; considerable covalent bonding present[51]
  • have Goldhammer-Herzfeld criterion[n 10] ratios straddling unity[55][56]
  • no, few, or directionally confined "free" electrons (generally hampering electrical and thermal conductivity)
Electrical conductivity
  • good to high[n 11]
  • intermediate[58] to good[n 12]
  • poor to good[n 13]
... as a liquid[64]
  • falls gradually as temperature rises[n 14]
  • most behave like metals[55][66]
  • increases as temperature rises
Thermodynamics
Thermal conductivity
  • medium to high[67]
  • mostly intermediate;[21][68] Si is high
  • almost negligible[69] to very high[70]
Temperature coefficient of resistance[n 15]
  • nearly all positive (Pu is negative)[71]
  • negative (B, Si, Ge, Te)[72] or positive (As, Sb)[73]
  • nearly all negative (C, as graphite, is positive in the direction of its planes)[74][75]
Melting point
  • mostly high
  • mostly high
  • mostly low
Melting behaviour
  • volume generally expands[76]
  • some contract, unlike (most)[77] metals[78]
  • volume generally expands[76]
Enthalpy of fusion
  • low to high
  • intermediate to very high
  • very low to low (except C: very high)
Elemental chemistry
Overall behaviour
  • metallic
  • nonmetallic[79]
  • nonmetallic
Ion formation
  • tend to form cations
  • some tendency to form anions in water[80]
  • solution chemistry dominated by formation and reactions of oxyanions[81][82]
  • tend to form anions
Bonds
  • seldom form covalent compounds
  • form salts as well as covalent compounds[83]
  • form many covalent compounds
Oxidation number
  • nearly always positive
  • positive or negative[84]
  • positive or negative
Ionization energy
  • relatively low
  • intermediate[85][86]
  • high
Electronegativity
  • usually low
  • close to 2,[87] i.e., 1.9–2.2[88][n 16]
  • high
Combined form chemistry
With metals
  • form alloys
  • can form alloys[83][91][92]
  • form ionic or interstitial compounds
With carbon
  • carbides and organometallic compounds
  • same as metals
  • carbon-nonmetal (e.g. CO2, CS2)[n 17] or organic (e.g. CH4, C6H12O6) compounds
With hydrogen (hydrides)
  • ionic, with alkali metals, alkaline earth metals
  • metallic, with transition metals
  • covalent, with post-transition metals
  • covalent, volatile hydrides[93]
  • covalent, gaseous or liquid hydrides
With oxygen (oxides)
  • nearly all solid (Mn2O7 is a liquid)
  • very few glass formers[94]
  • lower oxides: ionic and basic
  • higher oxides: more covalent, acidic
  • solid
  • glass formers (B, Si, Ge, As, Sb, Te)[95]
  • polymeric in structure;[96] tend to be amphoteric or weakly acidic[4][97]
  • solid, liquid or gaseous
  • few glass formers (P, S, Se)[98]
  • covalent, acidic
With sulfur (sulfates)
  • do form[n 18][n 19]
  • most form[n 20]
  • some form[n 21]
With halogens (halides, esp. chlorides) (see also[119])
  • typically ionic, involatile
  • generally insoluble in organic solvents
  • mostly water-soluble (not hydrolysed)
  • more covalent, volatile, and susceptible to hydrolysis[n 22] and organic solvents with higher halogens and weaker metals[120][121]
  • covalent, volatile[122]
  • usually dissolve in organic solvents[123]
  • partly or completely hydrolysed[124]
  • some reversibly hydrolysed[124]
  • covalent, volatile
  • usually dissolve in organic solvents
  • generally completely or extensively hydrolyzed
  • not always susceptible to hydrolysis if parent nonmetal at maximum covalency for period e.g. CF4, SF6 (then nil reaction)[125]
Environmental chemistry
Molar composition of Earth's ecosphere[n 23]
  • about 14%, mostly Al, Na, Mg, Ca, Fe, K
  • about 17%, mostly Si
  • about 69%, mostly O, H
Primary form on Earth
  • most occur in combined states, as carbonates, silicates, phosphates, oxides, sulfides, or halides
  • some (e.g. Au, Cu, Ag, Pt) occur in free or uncombined states[129]
  • all occur in combined states, as borates, silicates, sulfides, or tellurides
  • elemental C, N, O, S, noble gases are plentiful
  • H,[n 24] F[n 25], Se occur primarily in compounds
  • P, Cl, Br, I occur only in compounds, as phosphates, oxides, selenides or halides
Required by mammals
  • large amounts needed: Na, Mg, K, Ca
  • trace amounts needed of some others
  • trace amounts needed: B, Si, As
  • large amounts needed: H, C, N, O, P, S, Cl
  • trace amounts needed: Se, Br, I, possibly F
  • only noble gases not needed
Composition of the human body, by weight
  • about 1.5% Ca
  • traces of most others through 92U
  • trace amounts of B, Si, Ge, As, Sb, Te
  • about 97% O, C, H, N, P
  • others detectable except noble gases

Notes

[edit]
  1. ^ At standard pressure and temperature, for the elements in their most thermodynamically stable forms, unless otherwise noted
  2. ^ Copernicium is reported to be the only metal known to be a gas at room temperature.[14]
  3. ^ Whether polonium is ductile or brittle is unclear. It is predicted to be ductile based on its calculated elastic constants.[19] It has a simple cubic crystalline structure. Such a structure has few slip systems and "leads to very low ductility and hence low fracture resistance".[20]
  4. ^ Carbon as exfoliated (expanded) graphite,[22] and as metre-long carbon nanotube wire;[23] phosphorus as white phosphorus (soft as wax, pliable and can be cut with a knife, at room temperature);[24] sulfur as plastic sulfur;[25] and selenium as selenium wires.[26]
  5. ^ For polycrystalline forms of the elements unless otherwise noted. Determining Poisson's ratio accurately is a difficult proposition and there could be considerable uncertainty in some reported values.[27]
  6. ^ Beryllium has the lowest known value (0.0476) among elemental metals; indium and thallium each have the highest known value (0.46). Around one third show a value ≥ 0.33.[28]
  7. ^ Boron 0.13;[29] silicon 0.22;[30] germanium 0.278;[31] amorphous arsenic 0.27;[32] antimony 0.25;[33] tellurium ~0.2.[34]
  8. ^ Graphitic carbon 0.25;[35] [diamond 0.0718];[36] black phosphorus 0.30;[37] sulfur 0.287;[38] amorphous selenium 0.32;[39] amorphous iodine ~0.[40]
  9. ^ At atmospheric pressure, for elements with known structures
  10. ^ The Goldhammer-Herzfeld criterion is a ratio that compares the force holding an individual atom's valence electrons in place with the forces, acting on the same electrons, arising from interactions between the atoms in the solid or liquid element. When the interatomic forces are greater than or equal to the atomic force, valence electron itinerancy is indicated. Metallic behaviour is then predicted.[52] Otherwise nonmetallic behaviour is anticipated. The Goldhammer-Herzfeld criterion is based on classical arguments.[53] It nevertheless offers a relatively simple first order rationalization for the occurrence of metallic character among the elements.[54]
  11. ^ Metals have electrical conductivity values of from 6.9 × 103 S•cm−1 for manganese to 6.3 × 105 for silver.[57]
  12. ^ Metalloids have electrical conductivity values of from 1.5 × 10−6 S•cm−1 for boron to 3.9 × 104 for arsenic.[59] If selenium is included as a metalloid the applicable conductivity range would start from ~10−9 to 10−12 S•cm−1.[60][61][62]
  13. ^ Nonmetals have electrical conductivity values of from ~10−18 S•cm−1 for the elemental gases to 3 × 104 in graphite.[63]
  14. ^ Mott and Davis[65] note however that 'liquid europium has a negative temperature coefficient of resistance' i.e. that conductivity increases with rising temperature
  15. ^ At or near room temperature
  16. ^ Chedd[89] defines metalloids as having electronegativity values of 1.8 to 2.2 (Allred-Rochow scale). He included boron, silicon, germanium, arsenic, antimony, tellurium, polonium and astatine in this category. In reviewing Chedd's work, Adler[90] described this choice as arbitrary, given other elements have electronegativities in this range, including copper, silver, phosphorus, mercury, and bismuth. He went on to suggest defining a metalloid simply as, 'a semiconductor or semimetal' and 'to have included the interesting materials bismuth and selenium in the book'.
  17. ^ Phosphorus is known to form a carbide in thin films.
  18. ^ See, for example, the sulfates of the transition metals,[99] the lanthanides[100] and the actinides.[101]
  19. ^ Sulfates of osmium have not been characterized with any great degree of certainty.[102]
  20. ^ Common metalloids: Boron is reported to be capable of forming an oxysulfate (BO)2SO4,[103] a bisulfate B(HSO4)3[104] and a sulfate B2(SO4)3.[105] The existence of a sulfate has been disputed.[106] In light of the existence of silicon phosphate, a silicon sulfate might also exist.[107] Germanium forms an unstable sulfate Ge(SO4)2 (d 200 °C).[108] Arsenic forms oxide sulfates As2O(SO4)2 (= As2O3.2SO3)[109] and As2(SO4)3 (= As2O3.3SO3).[110] Antimony forms a sulfate Sb2(SO4)3 and an oxysulfate (SbO)2SO4.[111] Tellurium forms an oxide sulfate Te2O3(SO)4.[112] Less common: Polonium forms a sulfate Po(SO4)2.[113] It has been suggested that the astatine cation forms a weak complex with sulfate ions in acidic solutions.[114]
  21. ^ Hydrogen forms hydrogen sulfate H2SO4. Carbon forms (a blue) graphite hydrogen sulfate C+24HSO–4 • 2.4H2SO4.[115] Nitrogen forms nitrosyl hydrogen sulfate (NO)HSO4 and nitronium (or nitryl) hydrogen sulfate (NO2)HSO4.[116] There are indications of a basic sulfate of selenium SeO2.SO3 or SeO(SO4).[117] Iodine forms a polymeric yellow sulfate (IO)2SO4.[118]
  22. ^ layer-lattice types often reversibly so
  23. ^ Based on a table of the elemental composition of the biosphere, and lithosphere (crust, atmosphere, and seawater) in Georgievskii,[126] and the masses of the crust and hydrosphere give in Lide and Frederikse.[127] The mass of the biosphere is negligible, having a mass of about one billionth that of the lithosphere.[citation needed] "The oceans constitute about 98 percent of the hydrosphere, and thus the average composition of the hydrosphere is, for all practical purposes, that of seawater."[128]
  24. ^ Hydrogen gas is produced by some bacteria and algae and is a natural component of flatus. It can be found in the Earth's atmosphere at a concentration of 1 part per million by volume.
  25. ^ Fluorine can be found in its elemental form, as an occlusion in the mineral antozonite[130]

Citations

[edit]
  1. ^ Mendeléeff 1897, p. 274
  2. ^ a b Kneen, Rogers & Simpson, 1972, p. 263. Columns 2 (metals) and 4 (nonmetals) are sourced from this reference unless otherwise indicated.
  3. ^ Russell & Lee 2005, p. 147
  4. ^ a b c Rochow 1966, p. 4
  5. ^ Pottenger & Bowes 1976, p. 138
  6. ^ Askeland, Fulay & Wright 2011, p. 806
  7. ^ Born & Wolf 1999, p. 746
  8. ^ Lagrenaudie 1953
  9. ^ Rochow 1966, pp. 23, 25
  10. ^ Burakowski & Wierzchoń 1999, p. 336
  11. ^ Olechna & Knox 1965, pp. A991‒92
  12. ^ Stoker 2010, p. 62
  13. ^ Chang 2002, p. 304. Chang speculates that the melting point of francium would be about 23 °C.
  14. ^ New Scientist 1975; Soverna 2004; Eichler, Aksenov & Belozeroz et al. 2007; Austen 2012
  15. ^ Hunt 2000, p. 256
  16. ^ Sisler 1973, p. 89
  17. ^ Hérold 2006, pp. 149–150
  18. ^ Russell & Lee 2005
  19. ^ Legit, Friák & Šob 2010, p. 214118-18
  20. ^ Manson & Halford 2006, pp. 378, 410
  21. ^ a b McQuarrie & Rock 1987, p. 85
  22. ^ Chung 1987;[broken footnote] Godfrin & Lauter 1995[broken footnote]
  23. ^ Cambridge Enterprise 2013[broken footnote]
  24. ^ Faraday 1853, p. 42;[broken footnote] Holderness & Berry 1979, p. 255[broken footnote]
  25. ^ Partington 1944, p. 405
  26. ^ Regnault 1853, p. 208[broken footnote]
  27. ^ Christensen 2012, p. 14
  28. ^ Gschneidner 1964, pp. 292‒93.
  29. ^ Qin et al. 2012, p. 258
  30. ^ Hopcroft, Nix & Kenny 2010, p. 236
  31. ^ Greaves et al. 2011, p. 826
  32. ^ Brassington et al. 1980
  33. ^ Martienssen & Warlimont 2005, p. 100
  34. ^ Witczak 2000, p. 823
  35. ^ Marlowe 1970, p. 6;Slyh 1955, p. 146
  36. ^ Klein & Cardinale 1992, pp. 184‒85
  37. ^ Appalakondaiah et al. 2012, pp. 035105‒6
  38. ^ Sundara Rao 1950; Sundara Rao 1954; Ravindran 1998, pp. 4897‒98
  39. ^ Lindegaard & Dahle 1966, p. 264
  40. ^ Leith 1966, pp. 38‒39
  41. ^ Donohoe 1982; Russell & Lee 2005
  42. ^ Gupta et al. 2005, p. 502
  43. ^ Walker, Newman & Enache 2013, p. 25
  44. ^ Wiberg 2001, p. 143
  45. ^ Batsanov & Batsanov 2012, p. 275
  46. ^ Clementi & Raimondi 1963; Clementi, Raimondi & Reinhardt 1967
  47. ^ Addison 1964; Donohoe 1982
  48. ^ Vernon 2013, p. 1704[broken footnote]
  49. ^ Parish 1977, pp. 34, 48, 112, 142, 156, 178
  50. ^ a b Emsley 2001, p. 12
  51. ^ Russell 1981, p. 628
  52. ^ Herzfeld 1927; Edwards 2000, pp. 100–103
  53. ^ Edwards 1999, p. 416
  54. ^ Edwards & Sienko 1983, p. 695
  55. ^ a b Edwards & Sienko 1983, p. 691
  56. ^ Edwards et al. 2010
  57. ^ Desai, James & Ho 1984, p. 1160; Matula 1979, p. 1260
  58. ^ Choppin & Johnsen 1972, p. 351
  59. ^ Schaefer 1968, p. 76; Carapella 1968, p. 30
  60. ^ Glazov, Chizhevskaya & Glagoleva 1969 p. 86
  61. ^ Kozyrev 1959, p. 104
  62. ^ Chizhikov & Shchastlivyi 1968, p. 25
  63. ^ Bogoroditskii & Pasynkov 1967, p. 77; Jenkins & Kawamura 1976, p. 88
  64. ^ Rao & Ganguly 1986
  65. ^ Mott & Davis 2012, p. 177
  66. ^ Antia 1998
  67. ^ Cverna 2002, p.1
  68. ^ Cordes & Scaheffer 1973, p. 79
  69. ^ Hill & Holman 2000, p. 42
  70. ^ Tilley 2004, p. 487
  71. ^ Russell & Lee 2005, p. 466
  72. ^ Orton 2004, pp. 11–12
  73. ^ Zhigal'skii & Jones 2003, p. 66: 'Bismuth, antimony, arsenic and graphite are considered to be semimetals ... In bulk semimetals ... the resistivity will increase with temperature ... to give a positive temperature coefficient of resistivity ...'
  74. ^ Jauncey 1948, p. 500: 'Nonmetals mostly have negative temperature coefficients. For instance, carbon ... [has a] resistance [that] decreases with a rise in temperature. However, recent experiments on very pure graphite, which is a form of carbon, have shown that pure carbon in this form behaves similarly to metals in regard to its resistance.'
  75. ^ Reynolds 1969, pp. 91–92
  76. ^ a b Wilson 1966, p. 260
  77. ^ Wittenberg 1972, p. 4526
  78. ^ Habashi 2003, p. 73
  79. ^ Bailar et al. 1989, p. 742
  80. ^ Cox 2004, p. 27
  81. ^ Hiller & Herber 1960, inside front cover; p. 225
  82. ^ Beveridge et al. 1997, p. 185
  83. ^ a b Young & Sessine 2000, p. 849
  84. ^ Bailar et al. 1989, p. 417
  85. ^ Metcalfe, Williams & Castka 1966, p. 72
  86. ^ Chang 1994, p. 311
  87. ^ Pauling 1988, p. 183
  88. ^ Mann et al. 2000, p. 2783
  89. ^ Chedd 1969, pp. 24–25
  90. ^ Adler 1969, pp. 18–19
  91. ^ Hultgren 1966, p. 648
  92. ^ Bassett et al. 1966, p. 602
  93. ^ Rochow 1966, p. 34
  94. ^ Martienssen & Warlimont 2005, p. 257
  95. ^ Sidorov 1960
  96. ^ Brasted 1974, p. 814
  97. ^ Atkins 2006 et al., pp. 8, 122–23
  98. ^ Rao 2002, p. 22
  99. ^ Wickleder, Pley & Büchner 2006; Betke & Wickleder 2011
  100. ^ Cotton 1994, p. 3606
  101. ^ Keogh 2005, p. 16
  102. ^ Raub & Griffith 1980, p. 167
  103. ^ Nemodruk & Karalova 1969, p. 48
  104. ^ Sneed 1954, p. 472; Gillespie & Robinson 1959, p. 407
  105. ^ Zuckerman & Hagen 1991, p. 303
  106. ^ Sanderson 1967, p. 178
  107. ^ Iler 1979, p. 190
  108. ^ Sanderson 1960, p. 162; Greenwood & Earnshaw 2002, p. 387
  109. ^ Mercier & Douglade 1982
  110. ^ Douglade & Mercier 1982
  111. ^ Wiberg 2001, p. 764
  112. ^ Wickleder 2007, p. 350
  113. ^ Bagnall 1966, pp. 140−41
  114. ^ Berei & Vasáros 1985, pp. 221, 229
  115. ^ Wiberg 2001, p. 795
  116. ^ Lidin 1996, pp. 266, 270; Brescia et al. 1975, p. 453
  117. ^ Greenwood & Earnshaw 2002, p. 786
  118. ^ Furuseth et al. 1974
  119. ^ Holtzclaw, Robinson & Odom 1991, pp. 706–07; Keenan, Kleinfelter & Wood 1980, pp. 693–95
  120. ^ Kneen, Rogers & Simpson 1972, p. 278
  121. ^ Heslop & Robinson 1963, p. 417
  122. ^ Rochow 1966, pp. 28–29
  123. ^ Bagnall 1966, pp. 108, 120; Lidin 1996, passim
  124. ^ a b Smith 1921, p. 295; Sidgwick 1950, pp. 605, 608; Dunstan 1968, pp. 408, 438
  125. ^ Dunstan 1968, pp. 312, 408
  126. ^ Georgievskii 1982, p. 58
  127. ^ Lide & Frederikse 1998, p. 14–6
  128. ^ Hem 1985, p. 7
  129. ^ Perkins 1998, p. 350
  130. ^ Sanderson 2012

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Periodic table
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Periodic table
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18
1 H He
2 Li Be B C N O F Ne
3 Na Mg Al Si P S Cl Ar
4 K Ca Sc Ti V Cr Mn Fe Co Ni Cu Zn Ga Ge As Se Br Kr
5 Rb Sr Y Zr Nb Mo Tc Ru Rh Pd Ag Cd In Sn Sb Te I Xe
6 Cs Ba La Ce Pr Nd Pm Sm Eu Gd Tb Dy Ho Er Tm Yb Lu Hf Ta W Re Os Ir Pt Au Hg Tl Pb Bi Po At Rn
7 Fr Ra Ac Th Pa U Np Pu Am Cm Bk Cf Es Fm Md No Lr Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
s-block f-block d-block p-block

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