
Journal of Organometallic Chemistry p. C9 - C11 (1983)
Update date:2022-08-04
Topics:
Czisch, Peter
Erker, Gerhard
Photolysis of the hydrozirconation product 1(E) of phenylacetylene yields a 70/30 mixture of (Z)- and (E)-β-styrylzirconocene chloride.Reaction of the 1(E)/1(Z) mixture with organolithium or Grignard reagents gives alkenylzirconocene complexes with a substantial excess of the (Z)-isomer.The photochemically induced geometrical isomerization of alkyl- and aryl(alkenyl)zirconocenes can also be observed, provided the decomposition rate of these organozirconium complexes is being sufficiently reduced by added triphenylphosphine or trimethylphosphite.
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Doi:10.1002/jps.2600710912
(1982)Doi:10.1016/S0040-4039(01)81294-6
(1984)Doi:10.1007/BF00950678
(1982)Doi:10.1016/j.ica.2004.07.032
(2005)Doi:10.1039/c39820000945
(1982)Doi:10.1246/cl.1982.1421
(1982)