C. Roberts, J. Walton
Jun 9, 1981
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0
Influential Citations
8
Citations
Journal
Journal of The Chemical Society-perkin Transactions 1
Abstract
Pent-2-en-4-ynyl radicals were generated from pent-1-en-4-yne and cis- and trans-1-bromopent-2-en-4-yne and observed in the trans(4) and cis(5) conformations by e.s.r. spectroscopy. The rate constant for the isomerization (5)→(4) was determined by kinetic e.s.r. to be given by equation (i) and for the isomerization (4)→(5) the log k1=(13.2 ± 1.3)–(47.5 ± 8.0 kJ mol–1/2.3RT) s–1(i) rate constant was found to be given by equation (ii). From the observed barriers to rotation the methane based log k–1=(13.0 ± 1.3)–(49.2 ± 8.0 kJ mol–1/2.3RT) s–1(ii) stabilization energies of (4) and (5) were estimated to be 112 and 110 kJ mol–1. E.s.r. spectra were also recorded for the 1-trimethylsiloxy-derivatives of (4) and (5), pent-2-en-4-ynyl radicals, 1-trimethylsiloxypent-2-en-4-ynyl radicals, and penta-1,4-diynyl radicals. The enthalpies of formation, structures, and stabilization energies of the hydrocarbon radicals were computed using the MINDO/3 method. The conformational interconversion of radicals (4) and (5) was also examined by MINDO/3.