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Polypyridyl Complexes (polypyridyl + complex)
Selected AbstractsEffect of Electronic Structures of Enantiomers of Ruthenium(II) Polypyridyl Complexes on DNA Binding BehaviorsCHINESE JOURNAL OF CHEMISTRY, Issue 8 2010Haimei Luo Abstract A pair of Ru(II) complex enantiomers, , - and , -[Ru(bpy)2(p -mpip)]2+ {bpy=2,2,-bipyridine, p -mpip=2-(4-methylphenyl)imidazo[4,5-f]-1,10-phenanthroline} have been synthesized and structurally characterized. Both experimental results from crystallography, NMR, electrochemistry and theoretical calculations applying the density functional theory (DFT) method based on their crystal structures show that small difference in geometric structure existed can cause a considerable difference in electronic structure between enantiomers. In addition, the binding of the two enantiomers to calf thymus DNA (CT DNA) has been investigated with UV spectroscopy titration and viscosity measurements. It is very rare that the , enantiomer binds to DNA more strongly than the , enantiomer, which can be reasonably explained by their different electronic structures for the first time, suggesting that the dominant factor governing the stereoselectivity of DNA binding of Ru(II) complex may be the different electronic structures of its enantiomers. [source] Mixed iridium(III) and ruthenium(II) polypyridyl complexes containing poly(,-caprolactone)-bipyridine macroligandsJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 17 2004Veronica Marin Abstract A hydroxy-functionalized bipyridine ligand was polymerized with ,-caprolactone utilizing the controlled ring-opening polymerization of ,-caprolactone in the presence of stannous octoate. The resulting poly(,-caprolactone)-containing bipyridine was characterized by 1H NMR and IR spectroscopy, and gel permeation chromatography, as well as matrix-assisted laser desorption/ionization time-of-flight mass spectrometry, revealing the successful incorporation of the bipyridine ligand into the polymer chain. Coordination to iridium(III) and ruthenium(II) precursor complexes yielded two macroligand complexes, which were characterized by NMR, gel permeation chromatography, matrix-assisted laser desorption/ionization time-of-flight MS, cyclic voltammetry, and differential scanning calorimetry. In addition, both photophysical and electrochemical properties of the metal-containing polymers proved the formation of a trisruthenium(II) and a trisiridium(III) polypyridyl species, respectively. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 4153,4160, 2004 [source] The Effect of Heavy Atoms on Photoinduced Electron Injection from Nonthermalized and Thermalized Donor States of MII,Polypyridyl (M=Ru/Os) Complexes to Nanoparticulate TiO2 Surfaces: An Ultrafast Time-Resolved Absorption StudyCHEMISTRY - A EUROPEAN JOURNAL, Issue 2 2010Sandeep Verma Abstract We have synthesized ruthenium(II), and osmium(II),polypyridyl complexes ([M(bpy)2L]2+, in which M=OsII or RuII, bpy=2,2,-bipyridyl, and L=4-(2,2,-bipyridinyl-4-yl)benzene-1,2-diol) and studied the interfacial electron-transfer process on a TiO2 nanoparticle surface using femtosecond transient-absorption spectroscopy. Ruthenium(II)- and osmium(II)-based dyes have a similar molecular structure; nevertheless, we have observed quite different interfacial electron-transfer dynamics (both forward and backward). In the case of the RuII/TiO2 system, single-exponential electron injection takes place from photoexcited nonthermalized metal-to-ligand charge transfer (MLCT) states. However, in the case of the OsII/TiO2 system, electron injection takes place biexponentially from both nonthermalized and thermalized MLCT states (mainly 3MLCT states). Larger spin,orbit coupling for the heavier transition-metal osmium, relative to that of ruthenium, accounts for the more efficient population of the 3MLCT states in the OsII -based dye during the electron-injection process that yields biexponential dynamics. Our results tend to suggest that appropriately designed OsII,polypyridyl dye can be a better sensitizer molecule relative to its RuII analogue not only due to much broader absorption in the visible region of the solar-emission spectrum, but also on account of slower charge recombination. [source] CuI versus RuII: Dye-Sensitized Solar Cells and BeyondCHEMSUSCHEM CHEMISTRY AND SUSTAINABILITY, ENERGY & MATERIALS, Issue 12 2008Neil Robertson Dr. Copper for the scientist cunning at his trade: RuII complexes have long played the central role in the photochemical conversion of sunlight and dye-sensitized solar cells (DSSCs). Recently, however, the first examples of DSSCs sensitized by CuI polypyridyl complexes were reported. CuI complexes have comparable photophysical and electrochemical properties to RuII complexes and offer similar function with a cheaper and more abundant metal. [source] | ||||||||||