2006
DOI: 10.1107/s1600536806044308
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{2-[(E)-(2-Chlorophenoxyacetyl)hydrazonomethyl]phenolato}(imidazolyl)nickel(II)

Abstract: Key indicatorsSingle-crystal X-ray study T = 295 K Mean (C-C) = 0.005 Å R factor = 0.033 wR factor = 0.085 Data-to-parameter ratio = 15.4For details of how these key indicators were automatically derived from the article, see

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Cited by 4 publications
(5 citation statements)
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“…The conclusion that the shift toward coplanarity of imidazole and nickel planes in the N 2 ONiN imid virtual complexes is a result of an internal electrostatic interaction is consistent with the experimental structures of a set of square planar Ni II complexes of tridentate, truncated Schiff base units that show greater variation in imidazole ligand orientation with respect to the tridentate ligand−metal plane. Ten such molecular structures are to be found in the Cambridge Crystallographic Database, six of which are shown in Figure ; four others are given in Supporting Information, Figure S9. None were characterized for imidazole fluxionality by VT NMR solution studies as in our study above. The Ni II −Schiff base complexes containing hard O-donors cis to the unsubstituted imidazole monodentate ligand, complexes (a) and (b) in Figure , find coplanarity in the nickel complex plane and the plane of the imidazole ligand.…”
Section: Resultsmentioning
confidence: 99%
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“…The conclusion that the shift toward coplanarity of imidazole and nickel planes in the N 2 ONiN imid virtual complexes is a result of an internal electrostatic interaction is consistent with the experimental structures of a set of square planar Ni II complexes of tridentate, truncated Schiff base units that show greater variation in imidazole ligand orientation with respect to the tridentate ligand−metal plane. Ten such molecular structures are to be found in the Cambridge Crystallographic Database, six of which are shown in Figure ; four others are given in Supporting Information, Figure S9. None were characterized for imidazole fluxionality by VT NMR solution studies as in our study above. The Ni II −Schiff base complexes containing hard O-donors cis to the unsubstituted imidazole monodentate ligand, complexes (a) and (b) in Figure , find coplanarity in the nickel complex plane and the plane of the imidazole ligand.…”
Section: Resultsmentioning
confidence: 99%
“…Ten such molecular structures are to be found in the Cambridge Crystallographic Database, six of which are shown in Figure 12; four others are given in Supporting Information, Figure S9. [33][34][35][36][37][38][39][40][41] None were characterized for imidazole fluxionality by VT NMR solution studies as in our study above. The Ni II -Schiff base complexes containing hard O-donors cis to the unsubstituted imidazole monodentate ligand, complexes (a) and (b) in Figure 12, find coplanarity in the nickel complex plane and the plane of the imidazole ligand.…”
Section: Resultsmentioning
confidence: 99%
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“…Long, and presumably weak, bonding interactions between Cu II and ether oxygen have also been encountered in the complex [Cu(dboa)(C 6 H 5 NH 2 )] 2 Á-C 6 H 5 NH 2 [H 2 dboa is 2,2 0 -(1,2-phenylenedioxy)diacetic acid], in which the corresponding distance is 2.484 Å (McCann et al, 1995). However, in reported metal-hydrazone complexes containing phenoxy groups, these potential donors have not been found to coordinate to the metal atoms (Chen, 2008;Chen & Liu, 2004, 2006Gao et al, 2004;Li & Liu, 2004;Sun et al, 2005;Wang & Lian, 2013;Xiao, 2009;Zhang, 2006). Furthermore, these hydrazone ligands tend to form discrete metal compounds.…”
Section: Resultsmentioning
confidence: 99%