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BPy

Abbreviations acac, acetylacetonate Aik, alkyl AN, acetonitrile bpy, 2,2 -bipyridine Bu, butyl cod, 1,5- or 1,4-cyclooctadiene coe, cyclooctene cot, cyclooctatetraene Cp, cyclopentadienyl Cp, pentamethylcyclopenladienyl Cy, cyclohexyl dme, 1,2-dimethoxyethane dpe, bis(diphenyl-phosphino)ethane dppen, cis-l,2-bis(di[Atenylphosphino)ethylene dppm, bis(diphenylphosphino) methane dppp, l,3-bis(diphenylphosphino)propane eda,ethylenediamine Et,ethyl Hal,halide Hpz, pyrazole HPz, variously substituted pyrazoles Hpz, 3,5-dimethylpyrazole Me, methyl Mes, mesityl nbd, notboma-2,5-diene OBor, (lS)-endo-(-)-bomoxy Ph, phenyl phen, LlO-phenanthroline Pr, f opyl py, pyridine pz, pyrazolate Pz, variously substituted pyrazolates pz, 3,5-dimethylpyrazolate solv, solvent tfb, tetrafluorobenzo(5,6]bicyclo(2.2.2]octa-2,5,7-triene (tetrafluorobenzobanelene) THE, tetrahydrofuran tht, tetrahydrothicphene Tol, tolyl. [Pg.157]

Polypyridine ruthenium (II) chelate complex [Ru (Bpy) ] is known to participate in a photoredox reaction on excitation with visible light, coupled with the... [Pg.257]

Tris(2,2 -bipyridine)ruthenium(II) complex (Ru(bpy)3+) has been most commonly employed as a chromophore in the studies of photoinduced ET. Electrostatic effects on the quenching of the emission from the Ru(II) complex covalently bound to polyeletrolytes have been studied by several groups [79-82]. [Pg.76]

Kaneko et al. [80, 81] prepared copolymers of AA (93.9-95.9 mol%) and vinylbipyridine (1.6-3.7 mol%) with pendant Ru(bpy)2+ (2.4-2.5 mol%) (25). The quenching of the excited state of the pendant Ru(II) complex by MV2+ was accelerated in alkaline aqueous solution owing to the electrostatic attraction of the cationic quencher. Interestingly, the quenching efficiency was dependent on the molecular weight of 25. The quenching of the polymer with MW 2100 occurred... [Pg.76]

Sassoon and Rabani [79, 83] constructed an intriguing photoinduced ET system in which the back ET was greatly retarded by the electrostatic repulsion between two different polycations. They prepared poly(3,3-ionene) covalently linked with Ru(bpy)f + (26) and with an iY,Af,/V, Ar -tetraalkyl-/>-phenylenediamine derivative (27). The latter is an electron donor quencher toward the photoexcited Ru(II) complex. [Pg.80]

The genes coding for CETP and PLTP belong to one gene family, which also includes lipopolysaccharide-binding-protein (LBP) and bactericidal/permeability-increasing-protein (BPI). This common descent not only becomes clear from a considerable sequence similarity (45-65% homology at the cDNA level), but also from substantial conservation of exon/intron transitions. [Pg.694]

Detailed protein structures have been reported for BPI and CETP. Given the aforementioned similarities within this gene family, these protein structures serve as a likely model for the protein structure of PLTP. CETP and BPI are elongated molecules, shaped like a boomerang. There are two domains with similar folds, and a central beta-sheet domain between these two domains. The molecules contain two lipid-binding sites, one in each domain near the interface of the barrels and the central beta-sheet. [Pg.694]

Beamer LJ, Carroll SF, Eisenberg D (1997) Crystal structure of human BPI and two bound phospholipids at 2.4 angstrom resolution. Science 276 1861—1864... [Pg.696]

The most common catalysts for ATRP are complexes based on a copper(T) halide and nitrogen based ligand(s). Various ligands have been employed and those most frequently encountered are summarized in Table 9.5. Typically, four nitrogens coordinate to copper. The bidentate bipyridyl (bpy) ligands 132-133 are known to form a 2 1 complex. The tetradentate ligands are expected to form a 1 1 complex. [Pg.493]


See other pages where BPy is mentioned: [Pg.508]    [Pg.511]    [Pg.155]    [Pg.267]    [Pg.528]    [Pg.528]    [Pg.561]    [Pg.223]    [Pg.209]    [Pg.209]    [Pg.128]    [Pg.129]    [Pg.45]    [Pg.543]    [Pg.544]    [Pg.544]    [Pg.171]    [Pg.436]    [Pg.139]    [Pg.23]    [Pg.23]    [Pg.24]    [Pg.295]    [Pg.702]    [Pg.176]    [Pg.221]    [Pg.252]    [Pg.252]    [Pg.252]    [Pg.257]    [Pg.257]    [Pg.259]    [Pg.120]    [Pg.694]    [Pg.489]    [Pg.493]   
See also in sourсe #XX -- [ Pg.14 ]

See also in sourсe #XX -- [ Pg.297 , Pg.312 ]




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