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Nitrogen-containing organosilicon compounds. 150. Synthesis and chromatographic and 1H, 13C, 15N, and 29Si NMR spectroscopic investigation of substituted (piperidinoalkyl)silanes

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Substituted (piperidinoalkyl)silanes were synthesized and investigated by means of multinuclear NMR spectroscopy and GLC. The data obtained indicate an additional N-Si interaction in α-aminomethylsilanes that depends substantially on the properties of the substituents attached to the silicon atom. The effect of the R1R2R3Si substituent on the capacity of the nitrogen atom for intermolecular interactions is not restricted to steric effects but also has electronic character.

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Authors and Affiliations

  1. Institute of Organic Synthesis, Latvian Academy of Sciences, 226006, Riga

    É. Lukevits, I. Sleiksha, É. Liepin'sh, V. D. Shat-ts, I. Zitsmane & A. Purvinya

Authors
  1. É. Lukevits
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  2. I. Sleiksha
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  3. É. Liepin'sh
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  4. V. D. Shat-ts
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  5. I. Zitsmane
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  6. A. Purvinya
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Additional information

See [1] for communication 149.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1644–1652, December, 1991.

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Lukevits, É., Sleiksha, I., Liepin'sh, É. et al. Nitrogen-containing organosilicon compounds. 150. Synthesis and chromatographic and 1H, 13C, 15N, and 29Si NMR spectroscopic investigation of substituted (piperidinoalkyl)silanes. Chem Heterocycl Compd 27, 1319–1327 (1991). https://doi.org/10.1007/BF00515577

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  • DOI: https://doi.org/10.1007/BF00515577

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