Article ID Journal Published Year Pages File Type
1305513 Inorganica Chimica Acta 2015 6 Pages PDF
Abstract

•Optically active mixed-ligand cobalt(III) complex of penicillaminate was prepared.•Crystallization of the complex is considerably affected by counter anion.•Structure of the complex was determined by single crystal X-ray analysis.•The complex shows stereospecific intermolecular interactions.

The optically active mixed-ligand complex, [Co(d-pen)(bpma)]+ {pen = penicillaminate; bpma = bis(2-pyridylmethyl)amine}, and its enantiomer, [Co(l-pen)(bpma)]+, were prepared by the reactions of CoCl2·6H2O, bpma, and d-pen2− (or l-pen2−) under aerobic condition. The racemates, [Co(d-pen)(bpma)]0.5[Co(l-pen)(bpma)]0.5X·nH2O (dlCl: X = Cl, n = 0; dlNO3: X = NO3, n = 0; dlClO4·H2O: X = ClO4, n = 1) were also obtained by using dl-pen2− (1:1 mixture of d- and l-pen2−) instead of optically active d- or l-pen2− in the coexistences of the corresponding counter anions. In the presence of PF6− as a counter anion, contrary to the cases of Cl−, NO3−, and ClO4−, a similar reaction results in not racemate but mixture of chiral crystals accompanied by spontaneous crystallizations as chiral single crystals of [Co(d-pen)(bpma)]PF6·H2O (dPF6·H2O) or [Co(l-pen)(bpma)]PF6·H2O (lPF6·H2O). The crystal structures of racemates, dlCl, dlNO3, and dlClO4·H2O, were determined by X-ray crystallography, and compared with those of optically active dPF6·H2O and lPF6·H2O. In the racemic crystals of dlCl, dlNO3, and dlClO4·H2O, characteristic networks are built up by stereospecific π–π stacking and/or hydrogen bonding interactions between two enantiomeric complex cations attendant on auxiliary hydrogen bonds with counter anions. Contrary to dlCl, dlNO3, and dlClO4·H2O, the crystal structures of dPF6·H2O and lPF6·H2O are stabilized by the direct hydrogen-bonding networks between homochiral complex cations.

Graphical abstractNovel optically active mixed-ligand Co(III) complex with penicillaminate and bis(2-pyridylmethyl)amine was prepared. Counter-anion dependent assemblies between the complex and its enantiomer have been examined by means of single crystal X-ray diffraction analyses, electronic absorption and CD spectra.Figure optionsDownload full-size imageDownload as PowerPoint slide

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Physical Sciences and Engineering Chemistry Inorganic Chemistry
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