Binary compounds of hydrogen

Binary compounds of hydrogen are binary chemical compounds containing just hydrogen and one other chemical element. By convention all binary hydrogen compounds are called hydrides even when the hydrogen atom in it is not an anion.[1][2][3][4] These hydrogen compounds can be grouped into several types.

Binary hydrogen compounds in group 1 are the ionic hydrides (also called saline hydrides) wherein hydrogen is bound electrostatically. Because hydrogen is located somewhat centrally in a electronegative sense, it is necessary for the counterion to be exceptionally electropositive for the hydride to possibly be accurately described as truly behaving ionic. Therefore, this category of hydrides contains only a few members.

Hydrides in group 2 are polymeric covalent hydrides. In these, hydrogen forms bridging covalent bonds, usually possessing mediocre degrees of ionic character, which make them difficult to be accurately described as either covalent or ionic. The one exception is beryllium hydride, which has definitively covalent properties.

Hydrides in the transition metals and Lanthanoids are also typically polymeric covalent hydrides. However, they usually possess only weak degrees of ionic character. Usually, these hydrides rapidly decompose into their component elements at ambient conditions. The results consist of metallic matrices with dissolved, often stoichiometric or near so, concentrations of hydrogen, ranging from negligible to substantial. Such a solid can be thought of as a solid solution and is alternately termed a metallic- or interstitial hydride. These decomposed solids are identifiable by their ability to conduct electricity and their magnetic properties (the presence of hydrogen is coupled with the delocalisation of the valence electrons of the metal), and their lowered density compared to the metal. Both the saline hydrides and the polymeric covalent hydrides typically react strongly with water and air.

It is possible to produce a metallic hydride without requiring decomposition as a necessary step. If a sample of bulk metal is subjected to any one of numerous hydrogen absorption techniques, the characteristics, such as luster and hardness of the metal is often retained to a large degree. Bulk actinoid hydrides are only known in this form. The affinity for hydrogen for most of the d-block elements are low. Therefore elements in this block do not form hydrides (the hydride gap) under standard temperature and pressure with the notable exception of palladium.[5] Palladium can absorb up to 900 times its own volume of hydrogen and is therefore actively researched in the field hydrogen storage.

Elements in group 13 to 17 (p-block) form covalent hydrides (or nonmetal hydrides). In group 12 zinc hydride is a common chemical reagent but cadmium hydride and mercury hydride are very unstable and esoteric. In group 13 boron hydrides exist as a highly reactive monomer BH3, as an adduct for example ammonia borane or as dimeric diborane and as a whole group of BH cluster compounds. Alane (AlH3) is a polymer. Gallium exists as the dimer digallane. Indium hydride is only stable below −90 °C (−130 °F).

In group 14 the total number of possible binary saturated compounds with carbon of the type CnH2n+2 is very large. Going down the group the number of binary silicon compounds (silanes) is small (straight or branched but rarely cyclic) for example disilane and trisilane. For germanium only 5 linear chain binary compounds are known as gases or volatile liquids. Examples are n-pentagermane, isopentagermane and neopentagermane. Of tin only the distannane is known. Plumbane is an unstable gas.

Non-classical hydrides are those in which extra hydrogen molecules are coordinated as a ligand on the central atoms. These are very unstable but some have been shown to exist.

The periodic table of the stable binary hydrides

The relative stability of binary hydrogen compounds and alloys at standard temperature and pressure can be inferred from their standard enthalpy of formation values.[6]

H2 0 He
LiH -91 BeH2 125 BH3 91 CH4 -74.8 NH3 -46.8 H2O -243 HF -272 Ne
NaH -57 MgH2 -75 AlH3 SiH4 -31 PH3 5.4 H2S -207 HCl -93 Ar
KH -58 CaH2 -174 ScH3 TiH1.7 VH CrH Mn Fe Co Ni CuH ZnH2 GaH3 GeH4 92 AsH3 67 H2Se 30 HBr -36.5 Kr
RbH -47 SrH2 -177 YH3 ZrH2 NbHx Mo Tc Ru Rh PdH Ag CdH2 InH3 SnH4 163 SbH3 146 H2Te 100 HI 26.6 Xe
CsH -50 BaH2 -172 HfH2 TaH W Re Os Ir Pt Au HgH Tl PbH4 252 BiH3 277 H2Po At Rn
Fr Ra Rf Db Sg Bh Hs Mt Ds Rg Cn Uut Uuq Uup Uuh Uus Uuo
↓
LaH2 CeH2 PrH2 NdH2 PmH2 SmH2 EuH2 GdH2 TbH2 DyH2 HoH2 ErH2 TmH2 YbH2 LuH2
Ac Th Pa U Np Pu Am Cm Bk Cf Es Fm Md No Lr
Binary compounds of hydrogen
Covalent hydrides metallic hydrides.
Ionic hydrides Intermediate hydrides.
Do not exist Not assessed

Molecular hydrides

Most monomeric hydrides are isolable only under extreme conditions (i.e. at cryogenic temperatures, and often embedded in a rare gas matrix). This is generally attributable to poor contribution of the atomic orbitals of the respective atoms with the s-orbital of hydrogen; and to the low activation enthalpies of autopolymerisation reactions, which electron-deficient monomers are prone to undergo. The table below shows the monomeric hydride for each element, which is closest to, but not surpassing its heuristic valence. A heuristic valence is the valence of an element that strictly obeys the octet, duodectet, and other valence rules. Where available, both the enthalpy of formation for each monomer and the enthalpy of formation for the hydride in its standard state is shown (in brackets) to give a rough indication of which monomers tend to undergo aggregation to lower enthalpic states. For example, monomeric lithium hydride has an enthalpy of formation of 139 kJ mol−1, whereas solid lithium hydride has an enthalpy of −91 kJ mol−1. This means that it is energetically favourable for a mole of monomeric LiH to aggregate into the ionic solid, losing 230 kJ as a consequence. Aggregation can occur as a chemical association, such as polymerisation, or it can occur as an electrostatic association, such as the formation of hydrogen-bonding in water.

Classical hydrides

Classical hydrides
1 2 3 4 5 6 5 4 3 2 1 2 3 4 3 2 1
H
2 0
LiH[7] 139
(−91)		 BeH
2[8] 123		 BH
3[9] 107
(41)		 CH
4 −75		 NH
3 −46		 H
2O −242
(−286)		 HF −273
NaH[10] 140
(−56)		 MgH
2 142
(−76)		 AlH
3[11] 123
(−46)		 SiH
4 34		 PH
3 5		 H
2S −21		 HCl −92
KH 132
(−58)		 CaH
2 192
(−174)		 ScH
3		 TiH
4		 VH
2[12]		 CrH
2[13]		 MnH
2[14]		 FeH
2[15] 324		 CoH
2[16]		 NiH
2[17]		 CuH[18] 278
(28)		 ZnH
2[19] 162		 GaH
3[20] 151		 GeH
4 92		 AsH
3 67		 H
2Se 30		 HBr −36
RbH 132
(−47)		 SrH
2 201
(−177)		 YH
3		 ZrH
4		 NbH
4[12]		 MoH
6[21]		 Tc RuH
2[15]		 RhH
2[22]		 PdH[23] 361 AgH[18] 288 CdH
2[19] 183		 InH
3[24] 222		 SnH
4 163		 SbH
3 146		 H
2Te 100		 HI 27
CsH 119
(−50)		 BaH
2 213
(−177)		 HfH
4		 TaH
4[12]		 WH
6[25] 586		 ReH
4[14]		 Os Ir PtH
2[26]		 AuH[18] 295 HgH
2[27] 101		 TlH
3[28] 293		 PbH
4 252		 BiH
3 247		 H
2Po 167		 HAt 88
Fr Ra Rf Db Sg Bh Hs Mt Ds Rg Cn Uut Fl Uup Lv Uus
↓
3 4 5 6 7 8 7 6 5 4 3 2 1 2 3
LaH
3		 CeH
4		 PrH
3		 NdH
4		 Pm SmH
4		 EuH
2[29]		 GdH
3		 TbH
3		 DyH
4		 HoH
3		 ErH
2		 TmH YbH
2		 LuH
3
Ac ThH
4[30]		 Pa UH
4[31]		 Np Pu Am Cm Bk Cf Es Fm Md No Lr
 Legend
Monomeric covalent hydride Oligomeric covalent hydride
Polymeric covalent hydride Ionic hydride
Unknown solid structure Not assessed

This table includes the thermally unstable dihydrogen complexes for the sake of completeness. As with the above table, only the complexes with the most complete valence is shown, to the negligence of the most stable complex.

Non-classical covalent hydrides

Non-classical covalent hydrides
8 18 8
LiH(H
2)
2[7]		 Be BH
3(H
2)
Na MgH
2(H
2)
n[32]		 AlH
3(H
2)
K Ca[33] ScH
3(H
2)
6[34][35]		 TiH
2(H
2)[36]		 VH
2(H
2)[12]		 CrH2(H2)2 Mn FeH
2(H
2)
3[37]		 CoH(H
2)		 Ni(H
2)
4		 CuH(H2) ZnH
2(H
2)		 GaH
3(H
2)
Rb Sr[33] YH
2(H
2)
3		 Zr NbH
4(H
2)
4		 Mo Tc RuH
2(H
2)
4[38]		 RhH3(H2) Pd(H
2)
3		 AgH(H2) CdH(H
2)		 InH
3(H
2)[39]
Cs Ba[33] Hf TaH
4(H
2)
4		 WH
4(H
2)
4		 Re Os Ir PtH(H
2)		 AuH
3(H
2)		 Hg Tl
Fr Ra Rf Db Sg Bh Hs Mt Ds Rg Cn Uut
↓
32 18
LaH
2(H
2)
2		 CeH
2(H
2)		 PrH
2(H
2)
2		 Nd Pm Sm Eu GdH
2(H
2)		 Tb Dy Ho Er Tm Yb Lu
Ac ThH4(H2)4 Pa UH
4(H
2)
6[31]		 Np Pu Am Cm Bk Cf Es Fm Md No Lr
 Legend
Assessed Not assessed

Hydrogen solutions

Hydrogen has a highly variable solubility in the elements. When the continuous phase of the solution is a metal, it is called a metallic hydride or interstitial hydride, on account of the position of the hydrogen within the crystal structure of the metal. In solution, hydrogen can occur in either the atomic or molecular form. For some elements, when hydrogen content exceeds its solubility, the excess precipitates out as a stoichiometric compound. The table below shows the solubility of hydrogen in each element as a molar ratio at 25 °C (77 °F) and 100 kPa.

He
LiH
<1×10−4
[nb 1][40]		 Be B C N O F Ne
NaH
<8×10−7
[nb 2][41]		 MgH
<0.010
[nb 3][42]		 AlH
<2.5×10−8
[nb 4][43]		 Si P S Cl Ar
KH
<<0.01
[nb 5][44]		 CaH
<<0.01
[nb 6][45]		 ScH
≥1.86
[nb 7][46]		 TiH
2.00
[nb 8][47]		 VH
1.00
[nb 9][48]		 Cr MnH
<5×10−6
[nb 10][49]		 FeH
3×10−8
[50]		 Co NiH
3×10−5
[51]		 CuH
<1×10−7
[nb 11][52]		 ZnH
<3×10−7
[nb 12][53]		 Ga Ge As Se Br Kr
RbH
<<0.01
[nb 13][54]		 Sr YH
≥2.85
[nb 14][55]		 ZrH
≥1.70
[nb 15][56]		 NbH
1.1
[nb 16][57]		 Mo Tc Ru Rh PdH
0.724
[58]		 AgH
3.84×10−14
[59]		 Cd In Sn Sb Te I Xe
CsH
<<0.01
[nb 17][60]		 Ba Hf TaH
0.79
[nb 18][61]		 W Re Os Ir Pt AuH
3.06×10−9
[58]		 HgH
5×10−7
[62]		 Tl Pb Bi Po At Rn
Fr Ra Rf Db Sg Bh Hs Mt Ds Rg Cn Uut Fl Uup Lv Uus Uuo
↓
LaH
≥2.03
[nb 19][63]		 CeH
≥2.5
[nb 20][64]		 Pr Nd Pm SmH
3.00
[65]		 Eu Gd Tb Dy Ho Er Tm Yb Lu
Ac Th Pa UH
≥3.00
[nb 21][66]		 Np Pu Am Cm Bk Cf Es FM Md No Lr
 Legend
Miscible Undetermined

Notes

  1. ↑ Upper limit imposed by phase diagram, taken at 454 K.
  2. ↑ Upper limit imposed by phase diagram, taken at 383 K.
  3. ↑ Upper limit imposed by phase diagram, taken at 650 K and 25 MPa.
  4. ↑ Upper limit imposed by phase diagram, taken at 556 K.
  5. ↑ Upper limit imposed by phase diagram.
  6. ↑ Upper limit imposed by phase diagram, taken at 500 K.
  7. ↑ Lower limit imposed by phase diagram.
  8. ↑ Limit imposed by phase diagram.
  9. ↑ Limit imposed by phase diagram.
  10. ↑ Upper limit imposed by phase diagram, taken at 500 K.
  11. ↑ Upper limit imposed by phase diagram, taken at 1000 K.
  12. ↑ Upper limit at 500 K.
  13. ↑ Upper limit imposed by phase diagram.
  14. ↑ Lower limit imposed by phase diagram.
  15. ↑ Lower limit imposed by phase diagram.
  16. ↑ Limit imposed by phase diagram.
  17. ↑ Upper limit imposed by phase diagram.
  18. ↑ Limit imposed by phase diagram.
  19. ↑ Lower limit imposed by phase diagram.
  20. ↑ Lower limit imposed by phase diagram.
  21. ↑ Lower limit imposed by phase diagram.

References

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  6. ↑ Data in KJ/mole gas-phase source: Modern Inorganic Chemistry W.L. Jolly
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    2    (H
    2    )    , NbH
    4    , and TaH
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    2    , CH
    4    , CH
    3    D    , CH
    2    D
    2    , CHD
    3    , CD
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    2    , M
    2    H    , M
    2    H−
    , and (H
    2    )CuHCu     in solid argon, neon, and hydrogen"    . The Journal of Physical Chemistry A (American Chemical Society) 107 (41): 8492–8505. doi:10.1021/jp0354346. Retrieved 24 September 2013.
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    2    H
    2,4,6    , and the GaH−
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  25. ↑ Wang, Xuefeng; Andrews, Lester (29 June 2002). "Neon Matrix Infrared Spectra and DFT Calculations of Tungsten Hydrides WH
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    2     Polymers". Inorganic Chemistry (ACS Publications) 43 (22): 7146–7150. doi:10.1021/ic049100m.
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    4    (H
    2    )
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    4    (H
    2    )
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    2    (H
    2    )
    4     complex in solid hydrogen". Organometallics (American Chemical Society) 27 (17): 4273–4276. doi:10.1021/om800507u.
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  51. ↑ Wayman, M. L.; Weatherly, G. C. (1 October 1989). "The H−Ni (Hydrogen-Nickel) System". Bulletin of Alloy Phase Diagrams (Springer US) 10 (5): 569–580. doi:10.1007/BF02882416.
  52. ↑ Predel, B. (1994). "Cu-H (Copper-Hydrogen)". In Madelung, O. Cr-Cs – Cu-Zr. Springer Berlin Heidelberg. pp. 1–3. ISBN 978-3-540-47417-3.
  53. ↑ San-Martin, A.; Manchester, F. D. (1 December 1989). "The H-Zn (Hydrogen-Zinc) System". Bulletin of Alloy Phase Diagrams (Springer US) 10 (6): 664–666. doi:10.1007/BF02877640.
  54. ↑ Sangster, J.; Pelton, A. D. (1 February 1994). "The H-Rb (Hydrogen-Rubidium) System". Journal of Phase Equilibria (Springer-Verlag) 15 (1): 87–89. doi:10.1007/BF02667687.
  55. ↑ Khatamian, D.; Manchester, F. D. (1 June 1988). "The H−Y (Hydrogen-Yttrium) System". Bulletin of Alloy Phase Diagrams (Springer US) 9 (3): 252–260. doi:10.1007/BF02881276.
  56. ↑ Zuzek, E.; Abriata, J. P.; San-Martin, A.; Manchester, F. D. (1 August 1990). "The H-Zr (Hydrogen-Zirconium) System". Bulletin of Alloy Phase Diagrams (Springer-Verlag) 11 (4): 385–395. doi:10.1007/BF02843318.
  57. ↑ Okamoto, H. (1 April 2013). "H-Nb (Hydrogen-Niobium)". Journal of Phase Equilibria and Diffusion (Springer US) 34 (2): 163–164. doi:10.1007/s11669-012-0165-2.
  58. 1 2 Materials Science International Team (2006). "Au-H-Pd (Gold - Hydrogen - Palladium)". In Effenberg, G.; Ilyenko, S. Noble Metal Systems. Selected Systems from Ag-Al-Zn to Rh-Ru-Sc. Berlin: Springer Berlin Heidelberg. pp. 1–8. ISBN 978-3-540-46994-0.
  59. ↑ Subramanian, P.R (1 December 1991). "The Ag-H (Silver-Hydrogen) System". Journal of Phase Equilibria (Springer-Verlag) 12 (6): 649–651. doi:10.1007/BF02645164.
  60. ↑ Songster, J.; Pelton, A. D. (1 February 1994). "The H-Cs (Hydrogen-Cesium) System". Journal of Phase Equilibria (Springer-Verlag) 15 (1): 84–86. doi:10.1007/BF02667686.
  61. ↑ San-Martin, A.; Manchester, F. D. (1 June 1991). "The H-Ta (Hydrogen-Tantalum) System". Journal of Phase Equilibria (Springer-Verlag) 12 (3): 332–343. doi:10.1007/BF02649922.
  62. ↑ Guminski, C. (1 October 2002). "The H-Hg (Hydrogen-Mercury) System". Journal of Phase Equilibria (Springer-Verlag) 23 (5): 448–450. doi:10.1361/105497102770331460.
  63. ↑ Khatamian, D.; Manchester, F. D. (1 February 1990). "The H-La (Hydrogen-Lanthanum) System". Bulletin of Alloy Phase Diagrams (Springer-Verlag) 11 (1): 90–99. doi:10.1007/BF02841589.
  64. ↑ Manchester, F. D.; Pitre, J. M. (1 February 1997). "The Ce-H (Cerium-Hydrogen) system". Journal of Phase Equilibria (Springer-Verlag) 18 (1): 63–77. doi:10.1007/BF02646759.
  65. ↑ Zinkevich, M.; Mattern, N.; Handstein, A.; Gutfleisch, O. (13 June 2002). "Thermodynamics of Fe–Sm, Fe–H, and H–Sm Systems and its Application to the Hydrogen–Disproportionation–Desorption–Recombination (HDDR) Process for the System Fe
    17    Sm
    2    –H
    2    ". Journal of Alloys and Compounds (Elsevier) 339 (1-2): 118–139. doi:10.1016/S0925-8388(01)01990-9.
  66. ↑ Manchester, F. D.; San-Martin, A. (1 June 1995). "The H-U (Hydrogen-Uranium) System". Journal of Phase Equilibria (Springer-Verlag) 16 (3): 263–275. doi:10.1007/BF02667312.
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