Boyko, Y. D. and Sukhorukov, A. Yu. and Semakin, A. N. and Nelyubina, Y. V. and Ananyev, I. V. and Rangappa, K. S. and Ioffe, S. L. (2014) Synthesis, structure and dioxygen reactivity of Ni(II) complexes with mono-, bis-, tetra- and hexa-oxime ligands. Polyhedron, 71. pp. 24-33. ISSN 0277-5387
Full text not available from this repository. (Request a copy)Abstract
Four nickel complexes with β-(oximinoalkyl)amine ligands Ox nHn containing one (Ox1H1), two (Ox2H2), four (Ox4H4) and six (Ox6H6) oxime groups were synthesized and characterized by elemental analysis, FTIR, HRMS and single crystal X-ray diffraction. β-Oximinoalkylamines OxnHn act as polydentate ligands forming five-membered chelate rings, in which nickel is coordinated with both amine and oxime nitrogen atoms. In all structurally characterized complexes, OH-groups of oximes arms are involved in hydrogen bonding with counterions (Cl-), which are located in the inner or outer coordination sphere of the nickel atom. Two new structural types of pseudo-octahedral Ni(II) β-oximinoalkylamine complexes containing two ligands per one nickel ion (Ni(Ox1H1)2Cl2 and Ni(Ox 2H2)2Cl2) were identified. Dioxygen reactivity of the obtained complexes in aerobic oxidation of triphenylphosphine was studied. Bis-oxime complex Ni(Ox2H2) 2Cl2 was found to be the most active promoter of triphenylphosphine oxidation among the synthesized nickel complexes.
| Item Type: | Article |
|---|---|
| Subjects: | C Chemical Science > Chemistry |
| Divisions: | Department of > Chemistry |
| Depositing User: | Arshiya Kousar Library Assistant |
| Date Deposited: | 17 Jun 2019 05:21 |
| Last Modified: | 17 Jun 2019 05:21 |
| URI: | http://eprints.uni-mysore.ac.in/id/eprint/3177 |
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