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Synthesis, Crystal Structure, and Electrochemical Behaviour of an Azido μ‐bridged Ni 2+ Complex
Author(s) -
Kurtaran Raif,
Arici Cengiz,
Emregül Kaan C.,
Ülkü Dinçer,
Atakol Orhan,
Taştekin Mustafa
Publication year - 2003
Publication title -
zeitschrift für anorganische und allgemeine chemie
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.354
H-Index - 66
eISSN - 1521-3749
pISSN - 0044-2313
DOI - 10.1002/zaac.200200372
Subject(s) - azide , monoclinic crystal system , crystal structure , crystallography , chemistry , cyclic voltammetry , octahedron , electrochemistry , pyridine , nitrogen , ion , infrared spectroscopy , group (periodic table) , ligand (biochemistry) , medicinal chemistry , electrode , organic chemistry , biochemistry , receptor
A homo‐dinuclear Ni II complex was prepared from 2, 6‐bis(3, 5‐dimethylpyrazolyl)pyridine (Me 4 ‐bpp) and azide ions in nonaqueous media. It was characterized by single crystal X‐ray structural analysis, IR spectroscopy, and elemental analysis. In addition, the electrochemical properties of the compound were determined with cyclic voltammetry in DMF. The title compound crystallizes in the P2 1 /n monoclinic space group, with unit cell parameters a = 8.978(1), b = 12.459(1), c = 17.764(1) Å, ß =100.603(3)°, V = 1953.0(3) Å 3 , Z = 2. The Ni 2+ ion has a distorted octahedral environment involving three nitrogen atoms of the Me 4 ‐bpp ligand, two nitrogen atoms from the bridged azide group, and one nitrogen atom from the terminal azide group. The Ni···Ni distance is 3.273(5) Å.

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