A novel series of Schiff-base-substituted ruthenium carbene complexes have been prepared by the treatment of RuCl 2 ( CHPh)(PCy 3 ) 2 with a variety of Schiff-base ligands as the thallium salts. Modification of the Schiff-base electronic and/or structural substituents allowed for the tuning of the complexes activities in olefin metathesis reactions. The structures of the complexes were unambiguously characterized by NMR studies and X-ray analysis. These newly prepared complexes are highly stable to air, moisture, and temperature and even exhibit catalytic activity in polar protic solvents.
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Chang et al. (1998) studied this question.
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