Abstract
A new triply-bridged dicopper(I) complex, [Cu2(μ-dppm)2(μ-HL)](NO3)2 (1), has been prepared via successive treatment of cupric nitrate trihydrate with bis(diphenylphosphino)methane (dppm) and 3,5-bis{6-(2,2′-dipyridyl)}pyrazole (HL) in 2 : 4 : 1 molar ratio in dichloromethane. X-ray diffraction analysis of 1 reveals that the two Cu(I)s are in highly distorted tetrahedral environments with a distance of 4.2775(10) Å, triply bridged by two dppm ligands and one HL chelate as a bis-bidentate bridging ligand through two bipyridyl moieties. Intermolecular N···H–C hydrogen bonding and π···H–C interactions assemble the [Cu2(μ-dppm)2(μ-HL)]2+ cations into a 3-D supramolecular architecture with extended channels along the b-axis, filled with methanol and anions. Complex 1 shows weak low-energy absorptions at 350–425 nm, tentatively ascribed to Cu(I) to HL metal-to-ligand charge-transfer (MLCT) transition, probably mixed with some ILCT character inside HL. The emission is observed at ambient temperature for 1, both in solution and in the solid state, originating from the MLCT excited states.
Acknowledgments
The authors thank the National Natural Science Foundation of China (No. 21001057), the Key Project of Chinese Ministry of Education (No. 211088), the Natural Science Foundations of Jiangxi Province (No. 2009GQH0038) and Fujian Province (No. 2008F3117), the Science Foundation of State Key Laboratory of Structural Chemistry (No. 20110015), the Science Foundation of Education Bureau of Jiangxi Province (No. GJJ10151), and the start-up fund of Jiangxi University of Science and Technology (No. 09162) for the financial support.