Abstract
The thermally initiated
reaction of hexafluorobut-2-yne with (π-C5H5)Rh(CO)2 has been studied in detail, and it is
found that the nature and yields of the products are sensitive to the reaction
conditions. The known complexes (π-C5H5)Rh-[(C4F6)2CO] and (π-C5H5)Rh(C4F6)3 and the new organorhodium complexes (π-C5H5)2Rh2(CO)2(C4F6),
(.π-C5Hs)3Rh3(C4F6)2,
(π-C5H5)2Rh2(CO)(C4F6)2,
and (π-C5H5)3Rh3(CO)(C4F6)
have been isolated from the reaction system. Each organorhodium
complex has been characterized by elementary and mass spectral analysis, and reasonable
structures for all complexes have been predicted from the appropriate i.r. and N.M.R. data. The monoalkyne
complex (π-C5H5)2Rh2(CO)2(C4F6)
is an intermediate in the formation of the other organorhodium
complexes.
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