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Synthesis and 13C, 29Si, 199Hg nuclear magnetic resonance spectroscopy of alkynyl(trimethylsilyl)mercurials

โœ Scribed by Angelika Sebald; Bernd Wrackmeyer


Publisher
Elsevier Science
Year
1986
Tongue
English
Weight
370 KB
Volume
42
Category
Article
ISSN
1386-1425

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โœฆ Synopsis


Alkynyl(trimethylsilyl)

mercuriaB are formed by a fast and quantitative reaction between bis(alkynyl)-and bis(trimethylsilyl)me.rcury in chloroform or benzene at ambient temperature. They decompose slowly in solution to alkynyltrimethylsilanes and mercury. r3C, x%i, rg9Hg NMR data serve for the characterization. The polarixability of the Hg-Si bond and the great polarizing ability of the alkynyl group is clearly reflected by the NMR data.


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13C and 199Hg nuclear magnetic resonance
โœ Angelika Sebald; Bernd Wrackmeyer ๐Ÿ“‚ Article ๐Ÿ“… 1982 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 912 KB

Alkynyl mercury compounds of the type Hg(C=C-R)r (I), R'-Hg-C=C-R (II) and R'-Hg-GC-Hg-R' (III) have been studied by 'H, 13C and lPHg NMR. Chemical shifts (6'H, S"C, SIWHg) and coupling constants J(lWHg'H), J('99Hg'3C), J(13C'H) and J('3C5'3C) (in natural abundance) are reported. The changes in magn

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