The molecular structure of the tris(2-mercapto-1-tolylimidazolyl)hydroborato zinc(2-mercapto-1-tolylimidazole) complex, [[Tm(p-Tol)]Zn(mim(p-Tol))][ClO4]: intermolecular N-H...OClO3versus intramolecular N-H...S hydrogen bonding interactions of the mercaptoimidazole ligand |
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Authors: | Morlok Melissa M Docrat Arefa Janak Kevin E Tanski Joseph M Parkin Gerard |
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Institution: | Department of Chemistry, Columbia University, New York, New York 10027, USA. |
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Abstract: | The molecular structure of the tris(2-mercapto-1-tolylimidazolyl)hydroborato complex Tm(p-Tol)]Zn(mim(p-Tol))]ClO(4)].3MeCN has been determined by X-ray diffraction, thereby demonstrating that the mim(p-Tol) ligand exhibits a N-H...O hydrogen bond with the ClO(4)](-) counterion, Tm(p-Tol)]Zn(mim(p-Tol))...(OClO(3))], rather than hydrogen bond with a sulfur of the Tm(p-Tol)] ligand. DFT calculations on a series of related complexes, namely Tm(Me)]Zn(mim(Me))](+), Tm(Me)]Zn(mim(Me))]...(OClO(3))], Tm(Me)]Zn(mim(Me))]...O(H)Me]](+), and Tm(Me)]Zn(mim(Me))]...(NCMe)](+) demonstrate that an intramolecular N-H...S hydrogen bond within Tm(Me)]Zn(mim(Me))](+) is also less favored than the corresponding hydrogen bonding interactions with MeCN, MeOH, and ClO(4)](-). The inability of the sulfur atoms of Tm(R)] ligand to act as an effective hydrogen bond acceptor is in marked contrast to the ability of sulfur atoms in thiolate ligands to participate in the formation of N-H...S hydrogen bonds, an observation that reflects the "thione"versus"thiolate" nature of the Tm(R)] ligand. |
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