Iodosilane

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| ImageFile1 = Iodosilane Structure V.1.svg

| ImageFileL1 = Iodosilane-3D-vdW.png

| ImageFileR1 = Iodosilane-elpot-3D-vdW.png

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| Section1 = {{Chembox Identifiers

| CASNo = 13598-42-0

| ChemSpiderID = 123034

| PubChem = 139512

| SMILES = I[SiH3]

| StdInChI=1S/H3ISi/c1-2/h2H3

| StdInChIKey = IDIOJRGTRFRIJL-UHFFFAOYSA-N

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| Section2 = {{Chembox Properties

| Formula = SiH3I

| MolarMass = 158.014 g/mol

| Appearance = colorless crystals{{cite journal|journal=Acta Crystallographica Section C Crystal Structure Communications|volume=44|issue=8|date=1988-08-15|pages=1337–1339|doi=10.1107/S0108270188001155|url=http://scripts.iucr.org/cgi-bin/paper?S0108270188001155|title=Structure of silyl iodide at 116 K|accessdate=2019-02-25|author=A. J. Blake, E. A. V. Ebsworth, S. G. D. Henderson, A. J. Welch|archive-date=2018-06-02|archive-url=https://web.archive.org/web/20180602134825/http://scripts.iucr.org/cgi-bin/paper?S0108270188001155}}

| Density = 2.070 g·cm−3 (0.5 °C)
2.035 g·cm−3 (14.8 °C){{cite journal|journal=J. Chem. Soc.|language=en|issn=0368-1769|date=1941|pages=353–358|doi=10.1039/JR9410000353|url=http://xlink.rsc.org/?DOI=JR9410000353|title=68. Derivatives of monosilane. Part II. The iodo-compounds|accessdate=2019-02-25|author=H. J. Emeléus, A. G. Maddock, C. Reid}}

| MeltingPt = {{convert|-56.6|C|K}}{{cite journal|journal=Nature|volume=144|issue=3642|language=en|issn=0028-0836|date=August 1939|pages=328|doi=10.1038/144328a0|url=http://www.nature.com/articles/144328a0|title=New Iodine and Fluorine Derivatives of Monosilane|accessdate=2019-02-25|author=A. G. Maddock, C. Reid, H. J. Emelus|bibcode=1939Natur.144Q.328M |s2cid=4118995 |archive-date=2021-09-14|archive-url=https://web.archive.org/web/20210914070430/https://www.nature.com/articles/144328a0|doi-access=free}}

| BoilingPt = {{convert|45.8|C|K}}

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Iodosilane is a chemical compound of silicon, hydrogen, and iodine. It is a colorless monoclinic crystal of space group P21/c at −157 °C.

Preparation

Iodosilane is the first product of the reaction between monosilane and iodine, the other products being di-, tri- and finally tetraiodosilane (silicon tetraiodide).

It can also be produced by the reaction of phenylsilane or chlorophenylsilane with hydrogen iodide.{{cite book | title=Handbuch der präparativen anorganischen Chemie / 1. | publication-place=Stuttgart | isbn=3-432-02328-6 | oclc=310719485 | language=de | page=686}}

:\mathrm{ClC_6H_4SiH_3 + HI \longrightarrow C_6 H_5 Cl + SiH_3I}

Properties

At low temperatures, iodosilant quickly reacts with [Co(CO)4] to form SiH3Co(CO)4.{{cite journal|journal=Chem. Commun. (London)|issue=11|language=en|issn=0009-241X|date=1965|pages=217|doi=10.1039/C19650000217|title=A volatile silicon–transition-metal compound|author=B. J. Aylett, J. M. Campbell}}

Further reading

  • {{cite journal|last1=Nakagawa|first1=Jun|last2=Hayashi|first2=Michiro|date=1982|title=Microwave spectra in the ν3, 2ν3, and ν6 excited states of iodosilane|journal=Journal of Molecular Spectroscopy|volume=93|issue=2|pages=441–444|doi=10.1016/0022-2852(82)90181-3|bibcode=1982JMoSp..93..441N}}
  • {{cite book|last1=Ward|first1=Laird G. L.|last2=Norman|first2=Arlan D.|last3=Gondal|first3=S. K.|last4=MacDiarmid|first4=A. G.|date=1968|chapter=Bromosilane, iodosilane, and trisilylamine|editor-last=Jolly|editor-first=William L.|display-editors=etal|title=Inorganic Syntheses|volume=11|publisher=McGraw-Hill|pages=159–170|doi=10.1002/9780470132425.ch35|isbn=978-0-470-13170-1}}
  • {{cite journal|last1=Sharbaugh|first1=A. H.|last2=Heath|first2=G. A.|last3=Thomas|first3=L. F.|last4=Sheridan|first4=J.|date=1953|title=Microwave spectrum and structure of iodosilane|journal=Nature|volume=171|issue=4341|page=87|doi=10.1038/171087a0|bibcode=1953Natur.171...87S|s2cid=4178870|doi-access=free}}

References