期刊
INORGANICA CHIMICA ACTA
卷 549, 期 -, 页码 -出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.ica.2023.121408
关键词
Amino-phenolate ligands; Cobalt; X-ray crystallography; Acetato (OAc) complex; Radical polymerization
This study reports the synthesis and characterization of cobalt(II) and acetato cobalt(III) complexes with tripodal tetradentate diamino-bis(phenolate) ligands. The structures of the proligand and complexes were determined by X-ray crystallography. The complexes exhibited different coordination modes and were not efficient initiators or moderators for radical polymerization reactions.
The synthesis and characterization of cobalt(II) (3, 4) and acetato cobalt(III) (5) complexes with two tripodal tetradentate diamino-bis(phenolate) ligands (L1 and L2) are reported. The solid-state structures of proligand H2L1 and complexes 4 and 5 were determined by X-ray crystallography. Complex 4 crystallizes as a dimer via the formation of a Co2O2 core. Complex 5 is monomeric with a six-coordinated cobalt(III) center bearing a chelating acetate ligand. In both structures, the diamino-bis(phenolate) ligand (L1 or L2) is acting as a tetradentate dia-nionic kappa 4-(O2,N2) chelating ligand. The diamagnetic nature of complex 5 allowed its characterization by multinuclear NMR spectroscopic techniques. Complex 5 is not a competent unimolecular initiator for the radical polymerization of methyl acrylate or methyl methacrylate. Its cobalt(II) analog (3) did not act as an efficient OMRP moderator for the radical polymerization of activated (styrene, tert-butyl acrylate) and non-activated (vinyl acetate) monomers.
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