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A luminescent supermolecule with gold(I) quinoline-8-thiolate: crystal structure, spectroscopic and photophysical properties.
Tzeng, Biing-Chiau; Yeh, Hsien-Te; Huang, Yung-Chi; Chao, Hsiu-Yi; Lee, Gene-Hsiang; Peng, Shie-Ming.
Afiliação
  • Tzeng BC; Department of Chemistry and Biochemistry, National Chung Cheng University, 160 San-Hsin, Min-Hsiung, Chia-Yi, Taiwan 621. chebct@ccu.edu.tw
Inorg Chem ; 42(19): 6008-14, 2003 Sep 22.
Article em En | MEDLINE | ID: mdl-12971771
ABSTRACT
The trinuclear complex [(8-QNS)(2)Au(AuPPh(3))(2)].BF(4) (8-QNS = quinoline-8-thiolate), with intramolecular gold(I)...gold(I) distances of 3.0952(4) and 3.0526(3) A, is aggregated to form a novel hexanuclear supermolecule, ([(8-QNS)2(Au(AuPPh3)2])2.(BF4)2, via a close intermolecular gold(I)...gold(I) contact of 3.1135(3) A. The beautiful hexanuclear supermolecule has an inversion center, and the six metal centers can be viewed as roughly coplanar. Six gold(I) ions are embedded in an ellipse and surrounded by 4 quinoline and 12 phenyl rings. The title compound shows interesting spectroscopic and luminescence properties dependent on the solvent polarity; i.e., it emits at ca. 440 and 636 nm in CH(2)Cl(2) and only at ca. 450 nm in CH(3)CN. The long-lived emission at ca. 636 nm (16.2 micros) in CH(2)Cl(2) is quenched by polar solvents such as CH(3)CN and CH(3)OH with quenching constants as 1.00 x 10(5) and 3.03 x 10(4) s(-1) M(-1), respectively, which is suggested to be related to the presence or absence of gold(I)...gold(I) interactions due to scrambling of the [AuPPh(3)]+ units, isolobal to H+.
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Base de dados: MEDLINE Idioma: En Ano de publicação: 2003 Tipo de documento: Article
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Base de dados: MEDLINE Idioma: En Ano de publicação: 2003 Tipo de documento: Article