✍ Scribed by H. Thun; F. Verbeek
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Metal ± ligand binding strength and selectivity result from antagonistic metal ± ligand M ± L attractions and ligand ± ligand L ± L repulsions. On the basis of quantum-mechanical (QM) calculations on lanthanide complexes, we show that this interplay determines the binding affinities in the gas phase
The hydration state of a series of [Ln(DO2A)(H 2 O) n ] + complexes in aqueous solution at pH = 6.4-7.0 was studied by measuring the lanthanide-induced 17 O shifts (LIS) of water [Ln includes elements from Ce to Yb; DO2A = 1,7-bis(carboxymethyl)-1,4,7,10-tetraazacyclododecane]. Their contact contrib
Correlated electronic structure calculations predict that computed relative stabilities of the mixed [R-I-CH 3 ] -ate anions of iodine (where R = phenyl, ethynyl, vinyl, ethyl, or [(CH 3 ) n+1 X] -methyl ate anions, where X is an element of the main groups 14, 15, 16, or 17 up to Bi, possess widely