Luminescent metal complexes: Diversity of excited states

被引:157
作者
Vogler, A [1 ]
Kunkely, H [1 ]
机构
[1] Univ Regensburg, Inst Anorgan Chem, D-93040 Regensburg, Germany
来源
TRANSITION METAL AND RARE EARTH COMPOUNDS: EXCITED STATES, TRANSITION, INTERACTIONS I | 2001年 / 213卷
关键词
metal complexes; luminescence; excited states;
D O I
10.1007/3-540-44447-5_3
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The photoluminescence of metal complexes has attracted much recent interest since it can be utilized for a variety of applications such as optical sensors and LEDs. Moreover, the emission behavior provides a probe for the investigation of photoreactions including artificial photosynthesis. In this review, emitting compounds are classified according to the nature of their excited states: metal-centered, ligand-to-metal charge transfer, metal-to-ligand charge transfer, ligand-to-ligand charge transfer, metal-to-metal charge transfer, ligand-centered (or intra ligand), and intraligand charge transfer excited states. Complexes of transition metals (d(n) with n = 0-10), main group metals (s(2)),lanthanides and actinides (f(n)) are included in our discussion. However, this review does not cover the photoluminescence of metal complexes comprehensively, but illustrates this subject by selected examples. The viewpoint is that of a coordination chemist and not of a spectroscopist. Accordingly, molecular complexes which emit under ambient conditions are preferably chosen.
引用
收藏
页码:143 / 182
页数:40
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共 195 条
[1]  
Adamson A. W., 1975, CONCEPTS INORGANIC P
[2]   CONTINUOUS-WAVE LASER OPERATION AND QUANTUM EFFICIENCY OF TITANIUM-DOPED SAPPHIRE [J].
ALBERS, P ;
STARK, E ;
HUBER, G .
JOURNAL OF THE OPTICAL SOCIETY OF AMERICA B-OPTICAL PHYSICS, 1986, 3 (01) :134-139
[3]   Experimental and theoretical investigation of the molecular and electronic structure of [Zn4(μ4-S){μ-S2As(CH3)2}6] and [Cd4(μ4-S){μ-S2As(CH3)2}6]:: Two possible molecular models of extended metal chalcogenide semiconductors [J].
Albinati, A ;
Casarin, M ;
Maccato, C ;
Pandolfo, L ;
Vittadini, A .
INORGANIC CHEMISTRY, 1999, 38 (06) :1145-1152
[4]   EXCITATION POLARIZATION OF LUMINESCENT IRIDIUM(I) AND RHODIUM(I) PHOSPHINE COMPLEXES [J].
ANDREWS, LJ .
INORGANIC CHEMISTRY, 1978, 17 (11) :3180-3182
[5]  
[Anonymous], Z PHYS C
[6]   First-order Jahn-Teller effect, not metal-metal bonding, is responsible for structural distortion in Sn6(μ3-O)4(μ3-OR)4 excited states [J].
Arnold, FP ;
Burdett, JK ;
Sita, LR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (07) :1637-1638
[7]   STRUCTURES AND SPECTROSCOPIC PROPERTIES OF GOLD(I) COMPLEXES OF 1,3,5-TRIAZA-7-PHOSPHAADAMANTANE (TPA) .2. MULTIPLE-STATE EMISSION FROM (TPA)AUX (X=CL, BR, I) COMPLEXES [J].
ASSEFA, Z ;
MCBURNETT, BG ;
STAPLES, RJ ;
FACKLER, JP .
INORGANIC CHEMISTRY, 1995, 34 (20) :4965-4972
[8]   PREPARATION AND CHARACTERIZATION OF QUANTUM SIZE ZINC-OXIDE - A DETAILED SPECTROSCOPIC STUDY [J].
BAHNEMANN, DW ;
KORMANN, C ;
HOFFMANN, MR .
JOURNAL OF PHYSICAL CHEMISTRY, 1987, 91 (14) :3789-3798
[9]   CONSTRUCTION OF SMALL POLYNUCLEAR COMPLEXES WITH TRIFUNCTIONAL PHOSPHINE-BASED LIGANDS AS BACKBONES [J].
BALCH, AL .
PROGRESS IN INORGANIC CHEMISTRY, VOL 41, 1994, 41 :239-329
[10]   Very high-efficiency green organic light-emitting devices based on electrophosphorescence [J].
Baldo, MA ;
Lamansky, S ;
Burrows, PE ;
Thompson, ME ;
Forrest, SR .
APPLIED PHYSICS LETTERS, 1999, 75 (01) :4-6