Indium trihydride
Indium trihydride is an inorganic compound with the chemical formula (InH3). It has been observed in matrix isolation and laser ablation experiments.[2][3] Gas phase stability has been predicted.[4] The infrared spectrum was obtained in the gas phase by laser ablation of indium in presence of hydrogen gas [5] InH3 is of no practical importance.
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Systematic IUPAC name | |
Other names
Indium(III) hydride Indium trihydride | |
Identifiers | |
3D model (JSmol) |
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ChEBI | |
ChemSpider | |
163932 | |
PubChem CID |
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Properties | |
InH3 | |
Molar mass | 117.842 g/mol |
Melting point | −90 °C (−130 °F; 183 K) (decomposes) |
Structure | |
Trigonal planar | |
Dihedral | |
Related compounds | |
Related metallanes |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references |
Chemical properties
Solid InH3 is a three-dimensional network polymeric structure, where In atoms are connected by In-H-In bridging bonds, is suggested to account for the growth of broad infrared bands when samples of InH3 and InD3 produced on a solid hydrogen matrix are warmed.[5] Such a structure is known for solid AlH3.[6] When heated above −90 °C, indium trihydride decomposes to produce indium–hydrogen alloy and elemental hydrogen. As of 2013, the only known method of synthesising indium trihydride is the autopolymerisation of indane below −90 °C.
Other indium hydrides
Several compounds with In-H bonds have been reported.[7] Examples of complexes with two hydride ligands replaced by other ligands are (K+)3[K((CH3)2SiO)+7][InH(CH2C(CH3)3)−3]4[8] and HIn(−C6H4−ortho-CH2N(CH3)2)2.
Although InH3 is labile, adducts are known with the stoichiometry InH3Ln (n = 1 or 2).[9] 1:1 amine adducts are made by the reaction of Li+[InH4]− (lithium tetrahydridoindate(III)) with a trialkylammonium salt. The trimethylamine complex is only stable below −30 °C or in dilute solution. The 1:1 and 1:2 complexes with tricyclohexylphosphine (PCy3) have been characterised crystallographically. The average In-H bond length is 168 pm.[7] Indium hydride is also known to form adducts with NHCs.[10]
References
- "Indigane (CHEBI:30429)". Chemical Entities of Biological Interest (ChEBI). UK: European Bioinformatics Institute.
- Pullumbi, P.; Bouteiller, Y.; Manceron, L.; Mijoule, C. (July 1994). "Aluminium, gallium and indium trihydrides. An IR matrix isolation and ab initio study". Chemical Physics. 185 (1): 25–37. Bibcode:1994CP....185...25P. doi:10.1016/0301-0104(94)00111-1.
- Aldridge, S.; Downs, A. J. (2001). "Hydrides of the Main-Group Metals: New Variations on an Old Theme". Chemical Reviews. 101 (11): 3305–65. doi:10.1021/cr960151d. PMID 11840988.
- Hunt, P.; Schwerdtfeger, P. (1996). "Are the Compounds InH3 and TlH3 Stable Gas Phase or Solid State Species?". Inorganic Chemistry. 35 (7): 2085–2088. doi:10.1021/ic950411u.
- Andrews, L.; Wang, X. (2004). "Infrared Spectra of Indium Hydrides in Solid Hydrogen and of Solid Indane". Angewandte Chemie International Edition. 43 (13): 1706–1709. doi:10.1002/anie.200353216. PMID 15038043.
- Turley, J. W.; Rinn, H. W. (1969). "The Crystal Structure of Aluminum Hydride". Inorganic Chemistry. 8 (1): 18–22. doi:10.1021/ic50071a005.
- Jones, C. (2001). "The stabilisation and reactivity of indium trihydride complexes". Chemical Communications (22): 2293–2298. doi:10.1039/b107285b. ISSN 1359-7345. PMID 12240044.
- Rowen Churchill, M.; Lake, C. H.; Chao, S.-H. L.; Beachley, O. T. (1993). "Silicone grease as a precursor to a pseudo crown ether ligand: crystal structure of [K+]3[K(Me2SiO)7+][InH(CH2CMe3)3–]4". Journal of the Chemical Society, Chemical Communications. 1993 (20): 1577–1578. doi:10.1039/C39930001577.
- Wang, X.; Andrews, L. (20 May 2004). "Infrared Spectra of Indium Hydrides in Solid Hydrogen and Neon". The Journal of Physical Chemistry A. 108 (20): 4440–4448. Bibcode:2004JPCA..108.4440W. doi:10.1021/jp037942l.
- Abernethy, C. D.; Cole, M. L.; Jones, C. (2000). "Preparation, Characterization, and Reactivity of the Stable Indium Trihydride Complex [InH3{IMes}]". Organometallics. 19 (23): 4852–4857. doi:10.1021/om0004951.