| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 7751346 | Inorganica Chimica Acta | 2013 | 6 Pages | 
Abstract
												Two 1:2 nickel(II) complexes, [Ni(HLL-phe)2]·MeOH·3H2O (1) using an optically pure tridentate ligand of 5-methylimidazol-4-yl-methylidene-L-phenylalanine (H2LL-phe) and [Ni(HLDL-phe)2]·6H2O (2) using its racemic ligand (H2LDL-phe) were synthesized and the crystal structures were determined. Both nickel(II) ion is coordinated by (N2O)2 donor atoms from two tridentate ligands and has an octahedral coordination environment. Complex 1 crystallized in an acentrosymmetric monoclinic space group, P21 (No. 4). In the crystal, 1 contains only the l-isomer and forms a homochiral 2D structure through hydrogen bonding between the adjacent complex molecules. In contrast, Complex 2 crystallized into a centrosymmetric monoclinic space group P21/c (No. 14). In the crystal, 2 consists of [Ni(HLd-phe)2] and [Ni(HLl-phe)2] molecule that are related and forms a heterochiral 3D structure via hydrogen bonding through the crystal solvents.
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											Authors
												Seira Shintoyo, Suguru Yamauchi, Tomohiro Oishi, Naohide Matsumoto, Takeshi Fujinami, 
											