364595-57-3Relevant articles and documents
Syntheses and characterization of heterobimetallic complexes (dppf)Pt(dithiolate) (dppf: bis(diphenylphosphino)ferrocene); X-ray crystal structures of (dppf)PtL where L = dmit, phdt and i-mnt
Noh, Dong-Youn,Seo, Eun-Me,Lee, Ha-Jin,Jang, Hong-Young,Choi, Moon-Gun,Kim, Young Hwan,Hong, Jongki
, p. 1939 - 1945 (2008/10/08)
Hetrobimetallic complexes of the type (dppf)PtL (dppf = 1,1′-bis(diphenylphosphino)ferrocene; L = dmit (1,3-dithiole-2-thione-4,5-dithiolate), dddt (5,6-dihydro-1,4-dithiin-2,3-dithiolate), phdt (6-hydro-5-phenyl-1,4-dithiin-2,3-dithiolate), dphdt (5,6-diphenyl-1,4-dithiin-2,3-dithiolate), mtdt (1,2-bis(methylthio)ethylene-1,2-dithiolate), i-mnt (2,2-dicyano-1,1-ethylenedithiolate)) have been synthesized and studied by a high-resolution FAB-MS, cyclic voltammetry and 31P NMR. (Dppf)Pt(i-mnt) exhibits one reversible redox peak at E1/2 = 1.225 V and a strong Pt-P coupling constant (JPt-P = 3237 Hz) due to the electron-accepting property of i-mnt ligand. On the contrary, (dppf)Pt(mtdt) shows three reversible redox peaks corresponding to [dppf]0/+ (E1/21 = 0.470 V), [Pt(mtdt)]0/+ (E1/22 = 1.050 V) and [Pt(mtdt)]+/2+ (E1/23 = 1.405 V) processes and a weak Pt-P coupling constant (JPt-P = 2962 Hz) due to relatively strong electron-donor property of mtdt ligand. X-ray structural analyses were performed for the three complexes: (dppf)PtL where L = dmit, phdt and i-mnt. The P2PtS2 core shows a distorted square planar geometry for the three complexes with P(1)-Pt-P(2) bite angle being larger than 96°. The S(1)-Pt-S(2) bite angle of the i-mnt complex is the smallest (74.42°) because of the formation of the four-membered ring.
