The mechanisms of cyclisation and 1,2-bond-shift rearrangements of 2,2,4,4-tetramethylpentane on transition metal films
1982
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.
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