Dinuclear zinc(ii) pyrazolates with different degrees of ring-fluorination and their use in zinc(ii) mediated olefin aziridination†‡
Abstract
Zinc complexes [{(3,5-(CF3)2Pz)ZnEt}2(μ-THF)] (1), [{(3-(CF3),5-(t-Bu)Pz)ZnEt}2(μ-THF)] (2), and [{(3,5-(i-Pr)2Pz)ZnEt}2(μ-THF)] (3) adopt dinuclear structures with zinc sites bridged by a THF molecule and two pyrazolate ligands. The zinc complex 1 that features the weakest donating pyrazolate is the best catalyst among the three for the aziridination of styrene and cis-cyclooctene with PhI![[double bond, length as m-dash]](https://www.rsc.org/images/entities/char_e001.gif) NTs.
NTs.
- This article is part of the themed collection: Philip Power at 65: an icon of organometallic chemistry
 
                




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