Abstract

Abstract Six new structures of Cd(II) complexes containing Hdpa ligands have been determined. With chloride and bromide, Cd(II) ions produce halide-bridged dinuclear units 1 and 2 while CdI2 produces mononuclear unit 3 without halide-bridging. Cd(II) ions produce mono-Hdpa complex 4 with chelating benzoate, di-Hdpa complex 5 with coordinating NO 3 - anion, and tri-Hdpa complexes 6 and 7 with non-coordinating ClO 4 - and BF 4 - anions. One-, two-, or three-dimensional structures of Cd(II)–Hdpa complexes can be produced by hydrogen bonding interactions and π–π interactions. The compounds 4, 5, and 6 catalyzed efficiently the transesterification of a variety of esters with methanol, while 1, 2, 3 and 7 have displayed a very slow conversion. The transesterification reactivity shown by the catalyst 6 is very efficient and the best among the compounds 1–7. In addition, all compounds 1–7 and ligand (Hdpa) have shown the similar luminescent properties at λmax = 352 nm which suggest that their emissions seem to be attributed to the π–π∗ intraligand fluorescence.

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