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Cyclometalating terdentate

The terdentate cyclometalated complexes [Ir(L)(L )]2+ and [Ir(L )2]1, L = 2,6-bis(7 -methyl-4 -phenyl-2 -quinoyl)pyridine (233), L = monoanion of L (234), luminesce at 77 K in MeOH/EtOH (lmax = 592 nm, r =20 ps) and at room temperature in deoxygenated acetonitrile (imax 620 nm, r = 325 ns).405 Both compounds undergo four reversible, ligand-centered, one-electron reduction processes. [Pg.191]

Fig. 18 Schematic structures of cyclometalated bis-terdentate complexes the two terdentate planar systems are roughly perpendicular to each other... Fig. 18 Schematic structures of cyclometalated bis-terdentate complexes the two terdentate planar systems are roughly perpendicular to each other...
Table 12 Photophysical properties of selected Ir(III) complexes of terdentate cyclometalating ligands3... [Pg.177]

A dimethylplatinum(ii) complex having monoimine of ethylenediamine with 9-phenanthraldehyde undergoes oxidative addition of Mel to afford dimethyl(iodo)platinum(iv) complex with terdentate C,jV,A-ligand. Complex 1029 with a six-membered cyclometallated imine ring and its isomer with a five-membered ring are obtained as a mixture (Equation (190)). ... [Pg.588]

The rates of chloride dissociation for triphenylphosphine substitution have been measured for a series of cyclometalated [Pt(N-N-C)Cl] complexes containing terdentate N-N-C anionic ligands derived from deprotonated alkyl-, phenyl-and benzyl-6-substituted 2,2 -bipyridines. The main factor controlling the rate is... [Pg.302]


See other pages where Cyclometalating terdentate is mentioned: [Pg.168]    [Pg.100]    [Pg.168]    [Pg.100]    [Pg.1010]    [Pg.143]    [Pg.153]    [Pg.186]    [Pg.198]    [Pg.206]    [Pg.212]    [Pg.255]    [Pg.256]    [Pg.258]    [Pg.327]    [Pg.260]    [Pg.104]    [Pg.113]    [Pg.285]    [Pg.144]   
See also in sourсe #XX -- [ Pg.176 ]




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Cyclometalations

Cyclometallation

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