Indium trihydride

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Indium trihydride
Indigane-3D-balls.png
Names
Systematic IUPAC name
Indigane [1] (substitutive)
Trihydridoindium [1] (additive)
Other names
Indium(III) hydride
Indium trihydride
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
163932
PubChem CID
  • InChI=1S/In.3H Yes check.svgY
    Key: CXQHBGCUHODCNP-UHFFFAOYSA-N Yes check.svgY
  • [InH3]
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
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Yes check.svgY  verify  (what is  Yes check.svgYX mark.svgN ?)

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.

Contents

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

Structure of the adduct of
InH3 and tricyclohexylphosphine. Cy3PInH3.png
Structure of the adduct of InH3 and tricyclohexylphosphine.

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(−C6H4ortho-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]

Related Research Articles

<span class="mw-page-title-main">Diborane</span> Chemical compound

Diborane(6), commonly known as diborane, is the chemical compound with the formula B2H6. It is a toxic, colorless, and pyrophoric gas with a repulsively sweet odor. Given its simple formula, borane is a fundamental boron compound. It has attracted wide attention for its electronic structure. Several of its derivatives are useful reagents.

Borderline hydrides typically refer to hydrides formed of hydrogen and elements of the periodic table in group 11 and group 12 and indium (In) and thallium (Tl). These compounds have properties intermediate between covalent hydrides and saline hydrides. Hydrides are chemical compounds that contain a metal and hydrogen acting as a negative ion.

<span class="mw-page-title-main">Aluminium hydride</span> Chemical compound

Aluminium hydride (also known as alane and alumane) is an inorganic compound with the formula AlH3. Alane and its derivatives are common reducing (hydride addition) reagents in organic synthesis that are used in solution at both laboratory and industrial scales. In solution—typically in etherial solvents such tetrahydrofuran or diethyl ether—aluminium hydride forms complexes with Lewis bases, and reacts selectively with particular organic functional groups (e.g., with carboxylic acids and esters over organic halides and nitro groups), and although it is not a reagent of choice, it can react with carbon-carbon multiple bonds (i.e., through hydroalumination). Given its density, and with hydrogen content on the order of 10% by weight, some forms of alane are, as of 2016, active candidates for storing hydrogen and so for power generation in fuel cell applications, including electric vehicles. As of 2006 it was noted that further research was required to identify an efficient, economical way to reverse the process, regenerating alane from spent aluminium product.

<span class="mw-page-title-main">Dicobalt octacarbonyl</span> Chemical compound

Dicobalt octacarbonyl is an organocobalt compound with composition Co2(CO)8. This metal carbonyl is used as a reagent and catalyst in organometallic chemistry and organic synthesis, and is central to much known organocobalt chemistry. It is the parent member of a family of hydroformylation catalysts. Each molecule consists of two cobalt atoms bound to eight carbon monoxide ligands, although multiple structural isomers are known. Some of the carbonyl ligands are labile.

<span class="mw-page-title-main">Dihydrogen complex</span> Containing intact H2 as a ligand

Dihydrogen complexes are coordination complexes containing intact H2 as a ligand. They are a subset of sigma complexes. The prototypical complex is W(CO)3(PCy3)2(H2). This class of compounds represent intermediates in metal-catalyzed reactions involving hydrogen. Hundreds of dihydrogen complexes have been reported. Most examples are cationic transition metals complexes with octahedral geometry.

<span class="mw-page-title-main">Potassium nonahydridorhenate</span> Chemical compound

Potassium nonahydridorhenate(VII) is an inorganic compound having the formula K2ReH9. This colourless salt is soluble in water but only poorly soluble in most alcohols. The ReH2−
9
anion is a rare example of a coordination complex bearing only hydride ligands.

<span class="mw-page-title-main">Beryllium hydride</span> Chemical compound

Beryllium hydride is an inorganic compound with the chemical formula n. This alkaline earth hydride is a colourless solid that is insoluble in solvents that do not decompose it. Unlike the ionically bonded hydrides of the heavier Group 2 elements, beryllium hydride is covalently bonded.

Zinc hydride is an inorganic compound with the chemical formula ZnH2. It is a white, odourless solid which slowly decomposes into its elements at room temperature; despite this it is the most stable of the binary first row transition metal hydrides. A variety of coordination compounds containing Zn–H bonds are used as reducing agents, however ZnH2 itself has no common applications.

<span class="mw-page-title-main">Gallane</span> Chemical compound

Gallane, also systematically named trihydridogallium, is an inorganic compound of gallium with the chemical formula GaH
3
. It is a photosensitive, colourless gas that cannot be concentrated in pure form. Gallane is both the simplest member of the gallanes, and the prototype of the monogallanes. It has no economic uses, and is only intentionally produced for academic reasons.

Scandium trihydride is an unstable molecular chemical compound with the chemical formula ScH3. It has been formed as one of a number of other molecular scandium hydride products at low temperature using laser ablation and identified by infrared spectroscopy. Scandium trihydride has recently been the subject of Dirac–Hartree–Fock relativistic calculation studies, which investigate the stabilities, geometries, and relative energies of hydrides of the formula MH3, MH2, or MH.

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. These hydrogen compounds can be grouped into several types.

Cadmium hydride is an inorganic compound with the chemical formula (CdH
2
)
n
. It is a solid, known only as a thermally unstable, insoluble white powder.

Thallane is an inorganic compound with the empirical chemical formula TlH3. It has not yet been obtained in bulk, hence its bulk properties remain unknown. However, molecular thallane has been isolated in solid gas matrices. Thallane is mainly produced for academic purposes.

<span class="mw-page-title-main">Mercury(II) hydride</span> Chemical compound

Mercury(II) hydride is an inorganic compound with the chemical formula HgH
2
. It is both thermodynamically and kinetically unstable at ambient temperature, and as such, little is known about its bulk properties. However, it known as a white, crystalline solid, which is kinetically stable at temperatures below −125 °C (−193 °F), which was synthesised for the first time in 1951.

<span class="mw-page-title-main">Chromium(I) hydride</span> Chemical compound

Chromium(I) hydride, systematically named chromium hydride, is an inorganic compound with the chemical formula (CrH)
n
. It occurs naturally in some kinds of stars where it has been detected by its spectrum. However, molecular chromium(I) hydride with the formula CrH has been isolated in solid gas matrices. The molecular hydride is very reactive. As such the compound is not well characterised, although many of its properties have been calculated via computational chemistry.

Chromium(II) hydride, systematically named chromium dihydride and poly­(dihydridochromium) is pale brown solid inorganic compound with the chemical formula (CrH2)n. Although it is thermodynamically unstable toward decomposition at ambient temperatures, it is kinetically metastable.

Iron(II) hydride, systematically named iron dihydride and poly(dihydridoiron) is solid inorganic compound with the chemical formula (FeH
2
)
n
(also written ([FeH
2
]
)n or FeH
2
). ). It is kinetically unstable at ambient temperature, and as such, little is known about its bulk properties. However, it is known as a black, amorphous powder, which was synthesised for the first time in 2014.

Borane, also known as borine, is an unstable and highly reactive molecule with the chemical formula BH
3
. The preparation of borane carbonyl, BH3(CO), played an important role in exploring the chemistry of boranes, as it indicated the likely existence of the borane molecule. However, the molecular species BH3 is a very strong Lewis acid. Consequently, it is highly reactive and can only be observed directly as a continuously produced, transitory, product in a flow system or from the reaction of laser ablated atomic boron with hydrogen. It normally dimerizes to diborane in the absence of other chemicals.

<span class="mw-page-title-main">1,2-Dimethyldiborane</span> Chemical compound

1,2-Dimethyldiborane is an organoboron compound with the formula [(CH3)BH2]2. Structurally, it is related to diborane, but with methyl groups replacing terminal hydrides on each boron. It is the dimer of methylborane, CH3BH2, the simplest alkylborane. 1,2-Dimethyldiborane can exist in a cis- and a trans arrangement. 1,2-Dimethyldiborane is an easily condensed, colorless gas that ignites spontaneously in air.

Hydrogen compounds are compounds containg the element hydrogen. In these compounds, hydrogen can form in the +1 and -1 oxidation states. Hydrogen can form compounds both ionically and in covalent substances. It is a part of many organic compounds such as hydrocarbons as well as water and other organic substances. The H+ ion is often called a proton because it has one proton and no electrons, although the proton does not move freely. Brønsted–Lowry acids are capable of donating H+ ions to bases.

References

  1. 1 2 "Indigane (CHEBI:30429)". Chemical Entities of Biological Interest (ChEBI). UK: European Bioinformatics Institute.
  2. 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.
  3. 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.
  4. 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.
  5. 1 2 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.
  6. Turley, J. W.; Rinn, H. W. (1969). "The Crystal Structure of Aluminum Hydride". Inorganic Chemistry. 8 (1): 18–22. doi:10.1021/ic50071a005.
  7. 1 2 3 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.
  8. 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.
  9. 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.
  10. 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.