Abstract
Several (η 8-alkenylbenzene)dicarbonylchromium complexes (arenechelate complexes) were prepared in fair yield by the photolysis in ether of the tricarbonylchromium complexes of benzonorbornadiene ( syn-isomer), dibenzobicyclo[2.2.2]octa-2,5,7-triene ( syn-isomer), 4-phenyl-1-butene, 4-phenyl-1-butene-4,4- d 2, 5-phenyl-1-pentene, allyl phenyl ether, and benzyl vinyl ether. All of these arenechelate complexes are relatively stable and their IR, NMR, and mass spectral data are presented. Photolysis of the tricarbonylchromium complexes of benzobicyclo[2.2.2]octa-2,5-diene ( syn-isomer), 1,4-dihydronaphthalene, 3-phenyl-1-propene, 6-phenyl-1-hexene, and benzyl acrylate lead to decomposition and no arenechelate complexes. It is concluded that this method of preparation of arenechelate complexes is fairly general but there are some limitations that are apparent from the tricarbonylchromium complexes studied which failed to produce arenechelate complexes.
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