Synthesis and1H NMR study of some organotin derivatives of diethanolamines View Full Text


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Article Info

DATE

1994-04

AUTHORS

V. I. Shiryaev, E. M. Stepina, S. N. Tandura, E. A. Kovaleva, A. A. Grachev, S. I. Androsenko

ABSTRACT

A number of organotin derivatives of diethanolamines (stannocanes) R2Sn(OCH2CH2)2NR', O(SiMe2CH2)2Sn(OCH2CH2)2NR', and Sn[(OCH2CH2)2NR']2 (R = Ph,cyclo-Hex; R' = H, Me, Ph) were synthesized and studied by1H NMR spectroscopy. The effect of steric factors on the ability of molecules of stannocanes to form associates in solutions is discussed.

PAGES

666-670

References to SciGraph publications

  • 1983-06. The structure of 5-aza-2,8-dioxa-1-stanna(II)bicyclo[3.3.0]octane in JOURNAL OF CHEMICAL CRYSTALLOGRAPHY
  • 1977-03. Zur Kristallchemie der Triäthanolaminkomplexe in MONATSHEFTE FÜR CHEMIE - CHEMICAL MONTHLY
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    http://scigraph.springernature.com/pub.10.1007/bf00699845

    DOI

    http://dx.doi.org/10.1007/bf00699845

    DIMENSIONS

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