Site specificity of metal ions in heterodinuclear complexes derived from an "end-off" compartmental ligand

Koji Abe, Kanako Matsufuji, Masaaki Ohba, Hisashi Okawa

研究成果: ジャーナルへの寄稿学術誌査読

38 被引用数 (Scopus)

抄録

A phenol-based "end-off" compartmental ligand, 2-{N-[2-(dimethylamino)ethyl]iminomethyl}-6-[N,N-di(2-pyridylmethyl) -aminomethyl]-4-methylphenol (HL), having a bidentate arm and a tridentate arm attached to the 2 and 6 positions of the phenolic ring, has afforded the following heterodinuclear MaIIMbII complexes: [CuM(L)(AcO)2]CIO4 (M = Mn (1), Fe (2), Co (3), Ni (4), Zn (5)), [ZnM(L)(AcO)2]CIO4 (M = Co (6), Ni (7)), and [CuNi(L)(AcO)(NCS)2] (8). 1·MeOH (1′), 2·MeOH (2′), 3·MeOH (3′), 4·MeOH (4′), 5·MeOH (5′), and 7·MeOH (7′) are isostructural and have a heterodinuclear core bridged by the phenolic oxygen atom of L- and two acetate groups. In 1′-5′ the CuII is bound to the bidentate arm and has a square-pyramidal geometry with one acetate oxygen at the apical site. The MII is bound to the tridentate arm and has a six-coordinate geometry together with two acetate oxygen atoms. In the case of 7′ the Zn is bound to the bidentate arm and the Ni is bound to the tridentate arm. 8·2-PrOH (8′) has a dinuclear core bridged by the phenolic oxygen atom of L- and one acetate group. The Cu bound to the bidentate arm has a square-pyramidal geometry with an isothiocyanate group at the apical site. The Ni bound to the tridentate arm has a six-coordinate geometry with further coordination of an isothiocyanate group. The site specificity of the metal ions is discussed together with the crystal structure of [Cu4(L)2(AcO)3] (CIO4)3·H2O (9) prepared in this work.

本文言語英語
ページ(範囲)4461-4467
ページ数7
ジャーナルInorganic chemistry
41
17
DOI
出版ステータス出版済み - 8月 26 2002

!!!All Science Journal Classification (ASJC) codes

  • 物理化学および理論化学
  • 無機化学

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