Hydrostannolysis a general method for establishing tin-metal bonds. by Henricus Maria Johannes Cornelis Creemers

Cover of: Hydrostannolysis | Henricus Maria Johannes Cornelis Creemers

Published by Schotanus & Jens Utrecht N.V. in Utrecht .

Written in English

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Subjects:

  • Tin compounds.,
  • Organotin compounds.,
  • Metal-metal bonds.

Edition Notes

Book details

ContributionsTin Research Institute.
Classifications
LC ClassificationsQD181.S7 C73
The Physical Object
Pagination125 p.
Number of Pages125
ID Numbers
Open LibraryOL5002525M
LC Control Number76510991

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If your time is valuable, this book is for you. First, you will not waste time searching the Internet while missing a lot of relevant published: 08 Oct,   Purchase Hydronephrosis - 1st Edition. Print Book & E-Book. ISBNBook Edition: 1. Diorganotin halide hydrides or carboxylate hydrides, R 2 SnXH, will bring about the hydrostannolysis of alkyl halides, or the hydrostannation of alkynes or of carbonyl compounds at or below room temperature.

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o At that time the mathematical characterization of heat flow was well developed, while. Hydrostannolysis.- Use of organotin hydrides in synthesis.- Compounds containing tin-tin bonds.- Derivatives of distannane.- Derivatives of hexa-alkyl or -aryl-ditin compounds.- Derivatives of higher stannanes.- Derivatives of the type (R2Sn)n.- Organotin-metal compounds.- Alkali-metal derivatives.- This book, in some sense, began to be.

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The mechanism of the reaction of organotin hydrides with compounds containing a tin element bond (Sn N, Sn P, Sn As, Sn O, Sn S) has been investigated using IR spectroscopic techniques. In reactions involving formation of a tin tin bond (hydrostannolysis reactions) a polar mechanism is operative as appears from the lack of activity of free radical generators or scavengers and from the.

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