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Iodosilane

From Wikipedia, the free encyclopedia
Iodosilane
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/H3ISi/c1-2/h2H3
    Key: IDIOJRGTRFRIJL-UHFFFAOYSA-N
  • I[SiH3]
Properties
SiH3I
Molar mass158.014 g/mol
Appearancecolorless crystals[1]
Density2.070 g·cm−3 (0.5 °C)
2.035 g·cm−3 (14.8 °C)[2]
Melting point−56.6 °C (216.6 K)[3]
Boiling point45.8 °C (318.9 K)[3]
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Iodosilane is achemical compound ofsilicon,hydrogen, andiodine. It is a colorlessmonoclinic crystal of space group P21/c at −157 °C.[1]

Preparation

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Iodosilane is the first product of the reaction betweenmonosilane and iodine, the other products beingdi-,tri- and finally tetraiodosilane (silicon tetraiodide).

It can also be produced by the reaction ofphenylsilane orchlorophenylsilane withhydrogen iodide.[4]

ClC6H4SiH3+HIC6H5Cl+SiH3I{\displaystyle \mathrm {ClC_{6}H_{4}SiH_{3}+HI\longrightarrow C_{6}H_{5}Cl+SiH_{3}I} }

Properties

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At low temperatures, iodosilane quickly reacts with [Co(CO)4] to form SiH3Co(CO)4.[5]

Further reading

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References

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  1. ^abA. J. Blake, E. A. V. Ebsworth, S. G. D. Henderson, A. J. Welch (1988-08-15)."Structure of silyl iodide at 116 K".Acta Crystallographica Section C Crystal Structure Communications.44 (8):1337–1339.Bibcode:1988AcCrC..44.1337B.doi:10.1107/S0108270188001155. Archived fromthe original on 2018-06-02. Retrieved2019-02-25.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  2. ^H. J. Emeléus, A. G. Maddock, C. Reid (1941)."68. Derivatives of monosilane. Part II. The iodo-compounds".J. Chem. Soc.:353–358.doi:10.1039/JR9410000353.ISSN 0368-1769. Retrieved2019-02-25.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  3. ^abA. G. Maddock, C. Reid, H. J. Emelus (August 1939)."New Iodine and Fluorine Derivatives of Monosilane".Nature.144 (3642): 328.Bibcode:1939Natur.144Q.328M.doi:10.1038/144328a0.ISSN 0028-0836.S2CID 4118995.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  4. ^Handbuch der präparativen anorganischen Chemie / 1 (in German). Stuttgart. p. 686.ISBN 3-432-02328-6.OCLC 310719485.
  5. ^B. J. Aylett, J. M. Campbell (1965). "A volatile silicon–transition-metal compound".Chem. Commun. (11): 217.doi:10.1039/C19650000217.ISSN 0009-241X.


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