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Structure and Coordination Determination of Peptide-metal Complexes Using 1D and 2D 1H NMR
Published on: December 16, 2013
Lowering melting points in asymmetrically substituted Salen-copper(II) complexes exhibiting mesomorphic behavior.
Reinhard Paschke1, Dörte Balkow, E Sinn
1BioCenter of the Martin-Luther-University Halle-Wittenberg, 06099 Halle, Germany. paschke@biozentrum.uni-halle.de
Abstract:
In comparison with their symmetrical analogues, unsymmetrically substituted Cu-Salen complexes show mesophases with lowered melting points. For terminally substituted complexes, symmetrical ones (R(1) = R(2)) have only an S(A) phase, while for unsymmetrical alkoxy substitution a monotropic S(E) phase occurs and the melting temperature decreases with no loss in mesophase stability. Lateral substitution, when it is symmetrical (R(3) = R(4)), lowers mesophase stability but not melting temperature, and when it is unsymmetrical, it greatly lowers both mesophase stability and melting temperature compared with the parent compound. Substitution at the imine carbon (R(5), R(6)) also lowers chemical stability (decomposition) of the compounds. The structure of the 5-hexyloxy complex (R(1) = R(2) = OC(6)H(13), R(3) = R(4) = R(5) = H) shows the pre-mesophasic arrangement likely adopted after melting.
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