Photophysical properties of highly luminescent copper(I) halide complexes chelated with 1,2-bis(diphenylphosphino)benzene

被引:327
作者
Tsuboyama, Akira [1 ]
Kuge, Katsuaki
Furugori, Manabu
Okada, Shinjiro
Hoshino, Mikio
Ueno, Kazunori
机构
[1] Canon Inc, Leading Edge Technol Dev Headquarters, Tokyo 1468501, Japan
[2] Inst Phys & Chem Res, Wako, Saitama 3510198, Japan
关键词
D O I
10.1021/ic0608086
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Studies on synthesis, structures, and photophysics have been carried out for a series of luminescent copper(I) halide complexes with the chelating ligand, 1,2-bis[diphenylphosphino]benzene (dppb). The complexes studied are halogen-bridged dinuclear complexes, [Cu(mu-X)dppb](2) (X = I (1), Br (2), Cl (3)), and a mononuclear complex, CuI(dppb)(PPh3) (4). These complexes in the solid state exhibit intense blue-green photoluminescence with microsecond lifetimes (emission peaks, lambda(max) = 492-533 nm; quantum yields, Phi = 0.6-0.8; and lifetimes, tau = 4.0-10.4 mu s) at 298 K. In 2-methyltetrahydrofuran (2mTHF) solutions at 298 K, only 1 and 4 show weaker emission (Phi = 0.009) with shorter lifetimes (tau = 0.35 and 0.23 mu s) and red-shifted spectra (lambda(max) = 543 and 546 nm). The emission in the solid state originates from the (M + X)LCT excited state with a distorted-tetrahedral conformation, in which emissive excited states, (1)(M + X)LCT and (3)(M + X)LCT, are in equilibrium with an energy difference of similar to 2 kcal/mol. On the other hand, the complexes in the 2mTHF solutions emit from the MLCT excited state with an energetically favorable flattened conformation in the temperature range of 298-130 K. The flattened geometry with equilibrated (MLCT)-M-1 and (MLCT)-M-3 states has a nonradiative rate at least 2 orders of magnitude larger than that of the distorted-tetrahedral geometry, leading to a much smaller emission quantum yield (Phi = 0.009) at 298 K. Since the flattening motion is markedly suppressed below 130 K, the emission observed in 2mTHF below 130 K is considered to occur principally from the (M + X)LCT state with a distorted-tetrahedral geometry. To interpret the photophysics of V 1 and 4 in both the solid and solution states, we have proposed the "2-conformations with 2-spin-states model (2C x 2S model)". The electroluminescence device using (1) as a green emissive dopant showed a moderate EL efficiency; luminous efficiency = 10.4 cd/A, power efficiency = 4.2 lm/W at 93 cd/m(2), and maximum external quantum efficiency = 4.8%.
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页码:1992 / 2001
页数:10
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共 48 条
[1]   Luminescence ranging from red to blue:: A series of copper(I)-halide complexes having rhombic {Cu2(μ-X)2} (X=Br and I) units with N-heteroaromatic ligands [J].
Araki, H ;
Tsuge, K ;
Sasaki, Y ;
Ishizaka, S ;
Kitamura, N .
INORGANIC CHEMISTRY, 2005, 44 (26) :9667-9675
[2]   Copper(I) halide complexes from cis-1,2-bis(diphenylphosphino) ethylene and some heterocyclic thiones [J].
Aslanidis, P ;
Cox, PJ ;
Divanidis, S ;
Karagiannidis, P .
INORGANICA CHIMICA ACTA, 2004, 357 (04) :1063-1076
[3]   Copper(I) halide complexes with 1,3-propanebis(diphenylphosphine) and heterocyclic thione ligands:: Crystal and electronic structures (DFT) of [CuCl(pymtH)(dppp)], (CuBr(pymtH)(dppp)], and [Cu(μ-I)(dppp)]2 [J].
Aslanidis, P ;
Cox, PJ ;
Divanidis, S ;
Tsipis, AC .
INORGANIC CHEMISTRY, 2002, 41 (25) :6875-6886
[4]   Designing dendrimers based on transition metal complexes. Light-harvesting properties and predetermined redox patterns [J].
Balzani, V ;
Campagna, S ;
Denti, G ;
Juris, A ;
Serroni, S ;
Venturi, M .
ACCOUNTS OF CHEMICAL RESEARCH, 1998, 31 (01) :26-34
[5]   Anion-controlled nuclearity and metal-metal distances in copper(I)-dppm complexes (dppm = bis(diphenylphosphino)methane) [J].
Bera, JK ;
Nethaji, M ;
Samuelson, AG .
INORGANIC CHEMISTRY, 1999, 38 (02) :218-228
[6]   Molecular and supramolecular sensitization of nanocrystalline wide band-gap semiconductors with mononuclear and polynuclear metal complexes [J].
Bignozzi, CA ;
Argazzi, R ;
Kleverlaan, CJ .
CHEMICAL SOCIETY REVIEWS, 2000, 29 (02) :87-96
[7]   SYNTHESIS AND SOLUTION MULTINUCLEAR NUCLEAR-MAGNETIC-RESONANCE STUDIES OF HOMOLEPTIC COPPER(I) COMPLEXES OF GROUP-15 DONOR LIGANDS [J].
BLACK, JR ;
LEVASON, W ;
SPICER, MD ;
WEBSTER, M .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1993, (20) :3129-3136
[8]   MLCT state structure and dynamics of a copper(I) diimine complex characterized by pump-probe X-ray and laser spectroscopies and DFT calculations [J].
Chen, LX ;
Shaw, GB ;
Novozhilova, I ;
Liu, T ;
Jennings, G ;
Attenkofer, K ;
Meyer, GJ ;
Coppens, P .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (23) :7022-7034
[9]   Cooperative substituent effects on the excited states of copper phenanthrolines [J].
Cunningham, CT ;
Cunningham, KLH ;
Michalec, JF ;
McMillin, DR .
INORGANIC CHEMISTRY, 1999, 38 (20) :4388-4392
[10]   Structural and photophysical studies of Cu(NN)2+ systems in the solid state.: Emission at last from complexes with simple 1,10-phenanthroline ligands [J].
Cunningham, CT ;
Moore, JJ ;
Cunningham, KLH ;
Fanwick, PE ;
McMillin, DR .
INORGANIC CHEMISTRY, 2000, 39 (16) :3638-3644