Issue 21, 1982

The mechanisms of cyclisation and 1,2-bond-shift rearrangements of 2,2,4,4-tetramethylpentane on transition metal films

Abstract

The cyclisation/rearrangement products 2,2,4,4-tetramethylpentane in deuterium on sintered films of Ir, Rh, Pd, and Pt, analysed by combined gas-liquid chromatography/mass spectrometry, show that chemisorbed carbene and carbyne species are not responsible.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1982, 1277-1279

The mechanisms of cyclisation and 1,2-bond-shift rearrangements of 2,2,4,4-tetramethylpentane on transition metal films

J. K. A. Clarke, O. E. Finlayson and J. J. Rooney, J. Chem. Soc., Chem. Commun., 1982, 1277 DOI: 10.1039/C39820001277

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