Department of Chemistry
Cobalt and iron complexes of chiral C1- and C2-terpyridines: Synthesis, characterization and use in catalytic asymmetric cyclopropanation of styrenes
Optically pure C1- and C2-terpyridine ligands (L) form cobalt(II) and iron(II) complexes of formula [Co(L)Cl2] and [Fe(L)Cl2], respectively, and Iron(III) complexes of formulas [Fe(L)Cl3]. Structures of three new chiral cobalt(II) and one iron(III) complexes were analysed using X-ray crystal structure analysis. These complexes were shown to be precursor of efficient catalyst for cyclopropanation. Reaction with AgOTf converted the complex to active catalyst, which gave enantioselectivities of up to 76% ee for the trans-isomers and 83% ee for the cis-isomers of styrene cyclopropanes with ethyl diazoacetate. Hammett studies showed the active species for both cobalt and iron complexes to have a non-linear relationship to σp constant. © 2009 Elsevier B.V. All rights reserved.
Asymmetric catalysis, Chiral terpyridine, Cobalt, Cyclopropanation, Iron
Source Publication Title
Inorganica Chimica Acta
Link to Publisher's Edition
Yeung, Chi-Tung, Kiu-Chor Sham, Wing-Sze Lee, Wing-Tak Wong, Wai-Yeung Wong, and Hoi-Lun Kwong. "Cobalt and iron complexes of chiral C1- and C2-terpyridines: Synthesis, characterization and use in catalytic asymmetric cyclopropanation of styrenes." Inorganica Chimica Acta 362.9 (2009): 3267-3273.