
Journal of the American Chemical Society p. 5190 - 5195 (1981)
Update date:2022-08-17
Topics:
Baird, Mark S.
Dunkin, Ian R.
Hacker, Nigel
Poliakoff, Martyn
Turner, James J.
Diazocyclopentadiene (1) was photolyzed in N2, CO, and other low-temperature matrices.The resulting carbene, cyclopentadienylidene (2), was characterized by its UV and IR spectra, and its thermal dimerization and reaction with CO were observed.Photolysis of 1 with plane-polarized light gave matrices exhibiting linear dichroism.Comparison of dichroic IR and UV spectra revealed that the photolysis proceeds via an excited A1 state of the diazo compound.Plane-polarized irradiation of the corresponding ketene (4) in CO matrices resulted in photoreorientation of the molecules of 4 without significant loss.
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