Issue 19, 1971

Nuclear magnetic resonance evidence for the formation of cis- and trans-σ-but-2-enyl and syn-π-(1-methylallyl) complexes in the hydrogenation of butadiene by pentacyanocobaltate(II)

Abstract

Formation of similar amounts of cis- and trans-σ-but-2-enyl pentacyanocobaltate(III) and of syn-π-(1-methylallyl)tetracyanocobaltate(III) in the hydrogenation of butadiene by pentacyanocobaltate(II) is demonstrated from the i.r. spectrum and the n.m.r. spectra at 60, 100, and 220 MHz.

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 1177-1178

Nuclear magnetic resonance evidence for the formation of cis- and trans-σ-but-2-enyl and syn-π-(1-methylallyl) complexes in the hydrogenation of butadiene by pentacyanocobaltate(II)

T. Funabiki and K. Tarama, J. Chem. Soc. D, 1971, 1177 DOI: 10.1039/C29710001177

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