Conclusions
We measured the intensity of the bands of the stretching vibrations of the Si-H bond in the IR spectra of the organosilicon derivatives of fluorene and the corresponding phenyl derivatives. A greater degree of dπ−pπ. interaction of the silicon atom with the aromatic rings was established in chlorosilafluorene than in diphenylchlorosilane. This is caused by the coplanarity of the rings of the fluorene fragment.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1604–1606, July, 1974.
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Egorochkin, A.N., Khorshev, S.Y., Ostasheva, N.S. et al. Intensity of bands of stretching vibrations of Si-H bond in IR spectra of silafluorenes and dπ-pπ interaction. Russ Chem Bull 23, 1524–1526 (1974). https://doi.org/10.1007/BF00929669
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DOI: https://doi.org/10.1007/BF00929669