There are many reports1 of the pyrolysis of fluorinated organic compounds, including the defluorination of cyclic fluorocarbons over iron to give aromatic compounds. Extending this technique we have investigated the flow pyrolysis of some readily accessible unsaturated fluorocarbons, such as I, II, and III, and found these to be synthetically useful routes to fluorinated dienes, cyclobutenes, and furans. Pyrolyses were carried out using a nitrogen flow over platinum, iron or caesium fluoride heated at 430–700°. The various products can all be rationalized in terms of intermediate allylic radicals, and the solid substrate influences which allylic radicals are formed.We are also investigating the chemistry of those now accessible compounds, such as IV, V, and VI, and some of the preliminary results are described. For example the fluoride ion induced dimerisation of IV gave two major products VII and VIII via a particular interesting mechanism.相似文献
The reactions of [Co(η-C5H5)(CO)(PR3)] or [Co(η-C5GH5)(CO)2]/R3P mixtures (R = alkyl or aryl) with CS2 in refluxing CS2 or CS2/toluene gives rise to [Co(η-C5H5)(PR3)(CS)], [Co(η-C5H5)(PR3)(CS2)], [Co(η-C5H5)(PR3)(CS3)], and [Co3(η-C5H5)3 (CS)(S)] in reasonable yields. The corresponding reactions using PhNCS give [Co(η-C5H5)(PPh3)(PhNCS)] and a polymeric species which appears to be [Co4(η-C5H5)4 (PhNCS)]. Similar products are obtained with [Co(η-C5H5)(CO)(CNR)] or [Co(η0C5H5)(CO)2]/RNC mixtures. 相似文献
Modified nuclear recoil techniques have been used to obtain accurate relative bimolecular rate coefficients for thermally induced hydrogen abstraction reactions by atomic fluorine. New results are reported for 12 hydrocarbons and partially fluorinated hydrocarbons studied at 303°K. 相似文献