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Reactions of bis(hexamethylbenzene)iron(0) with carbon monoxide and with unsaturated hydrocarbons

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1977

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Journal of Organometallic Chemistry. 1977, 127(1), pp. 45-54. ISSN 0022-328X. Available under: doi: 10.1016/S0022-328X(00)84196-0

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Thermal decomposition of bis(hexamethylbenzene)iron(0) in the presence of carbon monoxide yields a novel carbonyl iron complex, [C6(CH3)6]Fe(CO)2. The cyclohexadiene complex [C6(CH3)6]Fe(C6H8) is obtained from reaction of bis(hexamethylbenzene)iron(0) with either 1,3-cyclohexadiene or benzene, and the yield is much greater in the presence of hydrogen gas. Interaction of bis-(hexamethylbenzene)iron(0) with 2-butyne induces a catalytic cyclotrimerization to give more hexamethylbenzene. Kinetic and isotope distribution studies indicate that the primary step in these reactions is not a direct loss of one ring ligand, but rather an insertion of the iron center into one of the ligand methyl C-H bonds, leading to a benzyl hydride complex species. Mechanisms for the subsequent reactions of this iron hydride species are proposed.

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ISO 690WEBER, Sharon R., Hans-Herbert BRINTZINGER, 1977. Reactions of bis(hexamethylbenzene)iron(0) with carbon monoxide and with unsaturated hydrocarbons. In: Journal of Organometallic Chemistry. 1977, 127(1), pp. 45-54. ISSN 0022-328X. Available under: doi: 10.1016/S0022-328X(00)84196-0
BibTex
@article{Weber1977React-23865,
  year={1977},
  doi={10.1016/S0022-328X(00)84196-0},
  title={Reactions of bis(hexamethylbenzene)iron(0) with carbon monoxide and with unsaturated hydrocarbons},
  number={1},
  volume={127},
  issn={0022-328X},
  journal={Journal of Organometallic Chemistry},
  pages={45--54},
  author={Weber, Sharon R. and Brintzinger, Hans-Herbert}
}
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    <dcterms:abstract xml:lang="eng">Thermal decomposition of bis(hexamethylbenzene)iron(0) in the presence of carbon monoxide yields a novel carbonyl iron complex, [C&lt;sub&gt;6&lt;/sub&gt;(CH&lt;sub&gt;3&lt;/sub&gt;)&lt;sub&gt;6&lt;/sub&gt;]Fe(CO)&lt;sub&gt;2&lt;/sub&gt;. The cyclohexadiene complex [C&lt;sub&gt;6&lt;/sub&gt;(CH&lt;sub&gt;3&lt;/sub&gt;)&lt;sub&gt;6&lt;/sub&gt;]Fe(C&lt;sub&gt;6&lt;/sub&gt;H&lt;sub&gt;8&lt;/sub&gt;) is obtained from reaction of bis(hexamethylbenzene)iron(0) with either 1,3-cyclohexadiene or benzene, and the yield is much greater in the presence of hydrogen gas. Interaction of bis-(hexamethylbenzene)iron(0) with 2-butyne induces a catalytic cyclotrimerization to give more hexamethylbenzene. Kinetic and isotope distribution studies indicate that the primary step in these reactions is not a direct loss of one ring ligand, but rather an insertion of the iron center into one of the ligand methyl C-H bonds, leading to a benzyl hydride complex species. Mechanisms for the subsequent reactions of this iron hydride species are proposed.</dcterms:abstract>
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