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Methoxy-Substituted Transition Metal β-Diketonates: Synthesis and Properties Full article

Journal Journal of Structural Chemistry
ISSN: 1573-8779 , E-ISSN: 0022-4766
Output data Year: 2019, Volume: 60, Pages: 1635–1647 Pages count : DOI: 10.1134/S0022476619100093
Authors Urkasym kyzy S. 1 , Krisyuk V.V. 1 , Turgambaeva, A.E. 1 , Baidina I.A. 1 , Komarov V.Yu. 1 , Korotaev E.V. 1 , Korolkov I.V. 1
Affiliations
1 Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences, Novosibirsk, Russia

Abstract: Novel volatile complexes of Ni(II), Co(II), Mn(II), Zn(II) with methoxy-substituted β-diketonate ligands L = (CH3)2C(OCH3)-CO-CH-CO-C(CH3)3 and LF = (CH3)2C(OCH3)-CO-CH-CO-CF3 are obtained. The novel compounds are identified by a complex of techniques, including CHF elemental, mass spectrometric, and NMR spectroscopic analyses. According to the X-ray crystallographic analysis data, in the crystals, NiL2 and ZnL2 are asymmetric binuclear complexes in which metal atoms have a different coordination environment composed of ligand oxygen atoms (c.n.= 6 and 5) and are bridged by oxygen atoms, both chelate and from one of the methoxy groups. The mixed-ligand complex [NiL(dpm)]2 (dpm = dipivaloylmethanate: 2,2,6,6-tetramethyl-3,5-heptandionate) has a similar binuclear structure. It is found that complexes with non-fluorinated ligands pass to the gas phase as monomers whereas fluorine-containing complexes pass as dimers. The compounds are paramagnetic, except zinc complexes. In the binuclear complexes based on non-fluorinated ligands, a ferromagnetic exchange interaction of magnetic moments is observed while for fluorine-containing ligands it is antiferromagnetic.
Cite: Urkasym kyzy S. , Krisyuk V.V. , Turgambaeva, A.E. , Baidina I.A. , Komarov V.Y. , Korotaev E.V. , Korolkov I.V.
Methoxy-Substituted Transition Metal β-Diketonates: Synthesis and Properties
Journal of Structural Chemistry. 2019. V.60. P.1635–1647. DOI: 10.1134/S0022476619100093 WOS Scopus РИНЦ OpenAlex
Identifiers:
Web of science: WOS:000494481800009
Scopus: 2-s2.0-85074662144
Elibrary: 41685845
OpenAlex: W2985553047
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