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A tetra-nuclear nickel(II) complex, [Ni4(L)4](ClO4)4·C2H3N·2H2O, with an asymmetric Ni4O4 open-cubane-like core.
Patel, R N; Patel, S K; Patel, A K; Patel, N; Butcher, Ray J.
Afiliação
  • Patel RN; Department of Chemistry, APS University, Rewa 486003, India.
  • Patel SK; Department of Chemistry, APS University, Rewa 486003, India.
  • Patel AK; Department of Chemistry, APS University, Rewa 486003, India.
  • Patel N; Department of Chemistry, APS University, Rewa 486003, India.
  • Butcher RJ; Department of Chemistry, Howard University, 525 College Street NW, Washington DC 20059, USA.
Acta Crystallogr E Crystallogr Commun ; 78(Pt 2): 98-102, 2022 Jan 01.
Article em En | MEDLINE | ID: mdl-35145731
A tetra-nuclear complex with an open-cubane-like core structure was synthesized from 2-meth-oxy-6-(pyridin-2-yl-hydrazonometh-yl)phenol (HL), namely, cyclo-tetra-kis-(µ-2-meth-oxy-6-{[2-(pyridin-2-yl)hydrazin-1-yl-idene]meth-yl}pheno-lato)tetra-nickel(II) tetra-kis-(perchlorate) aceto-nitrile monosolvate dihydrate, [Ni4(C13H12N3O2)4](ClO4)4·C2H3N·2H2O, and characterized using micro-analytical and spectroscopic techniques. The crystal-structure determination reveals the formation of a distorted Ni4O4 cubane-like core architecture encapsulated by four hydrazone Schiff base (HL) mol-ecules. A open-cube tetra-nuclear architecture is created in which nickel(II) ions of the NiN2O3 unit are connected by µ2-O anions of the phenolate moiety of HL. In this complex, each Ni centre has a slightly distorted square-pyramidal coordination environment. The supra-molecular architectures are stabilized via the presence of various inter-molecular hydrogen bonds and (ar-yl-aryl, ar-yl-chelate and chelate-chelate) stacking inter-actions.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article