Chiral lanthanoid dimers ligated by carbohydrate-based diketonates: catalytic and luminescent properties
Gee, William J., Hierold, Judith, MacLellan, Jonathan G., Andrews, Philip C., Lupton, David W., and Junk, Peter C. (2011) Chiral lanthanoid dimers ligated by carbohydrate-based diketonates: catalytic and luminescent properties. European Journal of Inorganic Chemistry, 2011 (25). pp. 3755-3760.
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Abstract
The reaction of hydrated lanthanoid chlorides (Ln = La, Eu) with chiral, carbohydrate-based diketonate ligands has yielded dimeric species with Ln2L6 composition as determined by MALDI mass spectrometry and single-crystal X-ray crystallography. The X-ray crystallographic analysis identified a chiral cavity formed by interligand repulsion able to coordinate dimethylformamide, prompting investigation of the catalytic properties of the dimers. Preliminary results indicate that the dimers display catalytic activity in thio-Michael addition reactions as well as metal-based luminescence in the case of europium.
Item ID: | 29659 |
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Item Type: | Article (Research - C1) |
ISSN: | 1099-0682 |
Keywords: | rare earths, lanthanoids, asymmetric catalysis, luminescence, enantioselectivity, lewis acids, diketonates |
Funders: | Australian Research Council (ARC), Monash University |
Date Deposited: | 02 Oct 2013 10:34 |
FoR Codes: | 03 CHEMICAL SCIENCES > 0302 Inorganic Chemistry > 030202 f-Block Chemistry @ 100% |
SEO Codes: | 97 EXPANDING KNOWLEDGE > 970103 Expanding Knowledge in the Chemical Sciences @ 100% |
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