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Syntheses and Molecular Structure of Dinuclear Transition Metal Complexes Bridged by Dipyridylamine Derivative Ligands
Authors:Gajendra Gupta  Sunhong Park  Shim Sung Lee  Prof Dr Jinkwon Kim
Institution:1. Department Of Chemistry, Kongju National University, 182 Shinkwan, Kongju‐Chungnam 314‐701, Republic of Korea;2. Department of Chemistry and Research Institute of Natural Science, Gyeongsang National University, Jinju 660‐701, Republic of Korea
Abstract:Stable dinuclear transition metal complexes,(η6‐C6H6)2Ru2(L1)Cl2]2+ ( 1 ), (η6piPrC6H4Me)2Ru2(L1)Cl2]2+ ( 2 ), (η6‐C6Me6)2Ru2(L1)Cl2]2+ ( 3 ), (η6‐C6H6)2Ru2(L2)Cl2]2+ ( 4 ),(η6piPrC6H4Me)2Ru2(L2)Cl2]2+ ( 5 ), (η6‐C6Me6)2Ru2(L2)Cl2]2+ ( 6 ), (η5‐C5Me5)2Rh2(L1)Cl2]2+ ( 7 ), (η5‐C5Me5)2Ir2(L1)Cl2]2+ ( 8 ),(η5‐C5Me5)2Rh2(L2)Cl2]2+ ( 9 ), and (η5‐C5Me5)2Rh2(L2)Cl2]2+ ( 10 ), with the bis‐bidentate ligands 1,3‐bis(di‐2‐pyridylaminomethyl)benzene (L1) and 1,4‐bis(di‐2‐pyridylaminomethyl)benzene (L2), which contain two chelating dipyridylamine units connected by an aromatic spacer, were synthesized. The cationic dinuclear complexes were isolated as their hexafluorophosphate salts and characterized by using a combination of NMR, IR, and UV/Vis spectroscopic methods and mass spectrometry. The solid‐state structure of complex 8 as a representative was determined by X‐ray structure analysis.
Keywords:Dipyridylamine ligands  Ruthenium  Rhodium  Iridium  Structure eludcidation
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