| Literature DB >> 29185729 |
Alena N Kulakova1,2, Alexey N Bilyachenko1,2, Mikhail M Levitsky1, Victor N Khrustalev2, Alexander A Korlyukov1,3, Yan V Zubavichus4, Pavel V Dorovatovskii4, Frédéric Lamaty5, Xavier Bantreil5, Benoît Villemejeanne5, Jean Martinez5, Lidia S Shul'pina1, Elena S Shubina1, Evgeniy I Gutsul1, Igor A Mikhailov6, Nikolay S Ikonnikov1, Ul'yana S Tsareva1, Georgiy B Shul'pin6,7.
Abstract
The synthesis, composition, and catalytic properties of a new family of hexanuclear Cu(II)-based phenylsilsesquioxanes are described here. Structural studies of 17 synthesized compounds revealed the general principle underlying their molecular topology: viz., a central metal oxide layer consisting of two Cu3 trimers is coordinated by two cyclic [PhSiO1.5]5 siloxanolate ligands to form a skewed sandwich architecture with the composition [(PhSiO1.5)10(CuO)6]2+. In addition to this O ligation by the siloxanolate rings, two opposite copper ions are additionally coordinated by the nitrogen atoms of corresponding N ligand(s), such as 2,2'-bipyridine (compounds 1-9), 1,10-phenanthroline (compounds 10-13), mixed 1,10-phenanthroline/2,2'-bipyridine (compound 14), or bathophenanthroline (compounds 15-17). Finally, the charge balance is maintained by two HO- (compounds 1-7, 10-13, and 15-17), two H3CO- (compound 8), or two CH3COO- (compounds 9 and 14) anions. Complexes 1 and 10 exhibited a high activity in the oxidative amidation oxidation of alcohols. Compounds 1, 10, and 15 are very efficient homogeneous catalysts in the oxidation of alkanes and alcohols with peroxides.Entities:
Year: 2017 PMID: 29185729 DOI: 10.1021/acs.inorgchem.7b02320
Source DB: PubMed Journal: Inorg Chem ISSN: 0020-1669 Impact factor: 5.165