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Syntheses,Crystal Structures and Theoretical Calculation of Two Transition Metal Dinuclear Complexes

Syntheses,Crystal Structures and Theoretical Calculation of Two Transition Metal Dinuclear Complexes
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摘要 Two transition metal dinuclear complexes of [Mn2(OOCC6H4SSC6H4COO)- (Phen)2(H20)]n 1 and [CuE(OOCC6H4S)2(Phen)2] 2 were hydrothermally synthesized by the reaction of equivalent metal dichloride with 2,2'-dithiobis(benzoic acid) (HE-DTBB). Structure analysis indicates that each Mn2+ ion in I is coordinated by one chelate phen ligand, one bridging water molecule and three DTBB ligands forming Mn2+ dinuclear units which are further linked into one-dimensional chain by DTBB ligand. Under similar reaction conditions, the 2,2'-dithio- his(benzoic acid) ligand undergoes thiol reduction to form 2-mercaptobenzoic (H-2-MBA) in 2 where two Cu2+ ions are coordinated by phen and MBA ligands only constructing a dinuclear unit. Two transition metal dinuclear complexes of [Mn2(OOCC6H4SSC6H4COO)- (Phen)2(H20)]n 1 and [CuE(OOCC6H4S)2(Phen)2] 2 were hydrothermally synthesized by the reaction of equivalent metal dichloride with 2,2'-dithiobis(benzoic acid) (HE-DTBB). Structure analysis indicates that each Mn2+ ion in I is coordinated by one chelate phen ligand, one bridging water molecule and three DTBB ligands forming Mn2+ dinuclear units which are further linked into one-dimensional chain by DTBB ligand. Under similar reaction conditions, the 2,2'-dithio- his(benzoic acid) ligand undergoes thiol reduction to form 2-mercaptobenzoic (H-2-MBA) in 2 where two Cu2+ ions are coordinated by phen and MBA ligands only constructing a dinuclear unit.
出处 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2008年第11期1327-1332,共6页 结构化学(英文)
基金 Supported by the Natural Science Foundation of Henan Province (No. 0611011900)
关键词 coordination polymers crystal structure DINUCLEAR theoretical investigation coordination polymers, crystal structure, dinuclear, theoretical investigation
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  • 1Fei, B. L.; Sun, W. Y.; Okamura, T.; Tang, W. X.; Ueyama, N. New J. Chem. 2001, 25, 210-212.
  • 2Hawxwell, S. M.; Espallargas, G. M.; Bradshaw, D.; Rosseinsky, M. J.; Prior, T. J.; Florence, A. J.; Streek, J.; Brammer, L. Chem. Commun. 2007, 1532-1534.
  • 3Rao, C. N. R.; Natarajan, S.; Vaidhyanathan, R. Angew. Chem. Int. Ed. 2004, 43, 1466-1496.
  • 4Robin, A. Y.; Fromm, K. Coord. Chem. Rev. 2006, 250, 2127-2157.
  • 5Zhang, H. T.; Li, Y. Z.; Wang, H. Q.; Nfor, E. N.; You, X. Z. Cryst. Eng. Comm. 2005, 7, 578-585.
  • 6Horikoshi, R.; Mochida, T. Coord. Chem. Rev. 2006, 250, 2595-2609.
  • 7Tian, Y. P.; Zhu, Y. M.; Zhou, H. P.; Wang, P.; Wu, J. Y.; Tao, X. T.; Jiang, M. H. Eur.J. Inorg. Chem. 2007, 245-246.
  • 8Tao, J.; Tong, M. L.; Chen, X. M. J. Chem .Soc., Dalton Trans. 2000, 3669-3674.
  • 9Wang, X. L.; Qin, C.; Wang, E. B.; IA, Y. G.; Su, Z. M.; Xu, L.; Carlucci, L. Angew. Chem. Int. Ed. 2005, 44, 5824-5827.
  • 10Ghosh, S. K.; Ribas, .I.; Bharadwaj, P. K. Cryst. Growth Des. 2005, 5, 623-629.

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