Summary
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1.
A study has been made of the mass spectra of tricarbonyliron complexes of 1-sila-2,4-cyclohexadiene with various substituents on the silicon atom.
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2.
The main route of fragmentation of the tricarbonyliron complexes under electron impact is successive decarbonylation with subsequent elimination of an HR molecule with the participation of the iron atom.
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3.
Structures have been proposed for the ions C5H5SiRFe+, C5H5Si+, and C3H3Si+. In the decomposing C5H5SiRFe+ ions, interaction of the iron atom with the silicon atom takes place, whereas the nondecomposing ions probably have the structure of coordinated silabenzene. A pyramidal structure of the nido-cluster type is ascribed to the C5H5Si+ and C3H3Si+ ions.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 10, pp. 2243–2248, October, 1981.
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Nekrasov, Y.S., Afanasova, O.B., Sukharev, Y.N. et al. Mass spectrometry of π complexes of transition metals. 27. 1-sila-2,4-cyclohexadienetricarbonyliron complexes. Russ Chem Bull 30, 1841–1845 (1981). https://doi.org/10.1007/BF00963404
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DOI: https://doi.org/10.1007/BF00963404