4.5 Article

Coordinated cations in dipicolinato complexes of divalent metal ions

Journal

INORGANICA CHIMICA ACTA
Volume 363, Issue 7, Pages 1479-1487

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.ica.2010.01.025

Keywords

Dipicolinato complex; Coordination complex of nickel; Copper and zinc; Crystal structures; Mixed metal complexes; Organic ammonium cations; Metal oxides

Funding

  1. Department of Science and Technology (New Delhi, India)

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Several salts of alkali, alkaline earth metal and organic ammonium cations of a complex anion [ML2](2) {Where L = dipicolinato dianion, M = copper(II), nickel(II) and zinc(II)} are prepared. The coordination effect of [ML2](2) with the cations such as sodium, potassium, calcium, magnesium, and organic cations namely diammonium cation of 1,5-pentanediamine, diammonium cation of 1,8-octyldiamine, mono ammonium cation of 4-aminobenzylamine are studied by determining their X-ray crystal structures. Depending on the nature of cations, four different types of structures are obtained. When calcium is the cation a polymeric structure with calcium ions bridging the [ML2](2) is observed. The salts having sodium and potassium cations form polymeric chain like structures by oxo and aqua bridges. In the case of magnesium, the hydrated form of magnesium cations coordinates to [ML2](2). The organic ammonium salts of [ML2](2) have the structural features of conventional ionic complexes. These salts easily exchange cations. The organic ammonium salts of [ML2](2) decomposes to give the corresponding metal oxides at relatively low temperature range 300-450 degrees C. (C) 2010 Elsevier B.V. All rights reserved.

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