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Gold luminescence

Keywords Biolabeling Gold Luminescence Quantum clusters... [Pg.333]

N(C6H4-p-Me)Au[3 to aggregate through gold-gold intermolecular interactions forming these supramolecular arrays confers to its extraordinary luminescent properties which have been described by Balch as solvoluminescence [48]. [Pg.27]

Mohamed, A.A., Kani, I., Ramirez, A.O. and Fackler, J.P. Jr (2004) Synthesis, characterization, and luminescent properties of dinuclear gold(I) xanthate complexes X-ray structure of [Au2(nBu-xanthate)2j. Inorganic Chemistry, 43, 3833-3839. [Pg.39]

King, C., Wang, J.-C., Khan, M.N.l. and Fackler, J.P. Jr (1989) Luminescence and metal-metal interactions in binudear Gold(I) compounds. Inorganic Chemistry, 28, 2145-2149. [Pg.39]

Forward, J.M., Fackler, J.P. and Staples, R.J. (1995) Synthesis and structural characterization of the luminescent Gold(I) Complex [(MeTPAJjAulJIj. Use of NaBPha as a phenyl transfer reagent to form [(MeTPA)AuPh](BPh4) and (TPA) AuPh. Organometallics, 14, 4194—4198. [Pg.45]

An emerging class of luminescent materials. Gold Bulletin, 40, 172. [Pg.80]

When [AuTl(C6F5)2]n reacts with DMSO the complex [Tl2 Au(C6F5)2 2 lt-DMSO 3]n [126] is obtained. The crystal structure of this complex shows unsupported Au - Tl interactions that range from 3.2225(6) to 3.5182(8) A but there are no Tl- - - Tl interactions. There are Au- - - Au interactions of3.733 A and the gold centers are almost linearly coordinated to two pentafluorophenyl groups. The complex is strongly luminescent both at room temperature (emits at 440 nm (exc.390 nm)) and at 77 K (emits at 460 nm (exc. 360 nm)). [Pg.118]

Acetylenephosphino gold(l) derivatives structure, reactivity and luminescence properties. Journal of the Chemical Society, Dalton Transactions, (18), 3624-3629. [Pg.166]

Bardaji, M., Jones, P.G., Laguna, A., Villacampa, M.D. and Villaverde, N. (2003) Synthesis and structural characterization of luminescent gold(I) derivatives with an imsymmetric diphosphine. Dalton Transactions, (23), 4529-4536. [Pg.169]

Bardaji, M., Laguna, A., Orera, V.M. and Villacampa, M.D. (1998) Synthesis, Structural Characterization, and Luminescence Studies of Gold(l) and Gold(lll) Complexes with a Triphosphine Ligand. Inorganic Chemistry, 37(20), 5125-5130. [Pg.169]

Bardaji, M Laguna, A., Jones, P.G. and Fischer, A.K. (2000) Synthesis, Structural Characterization of Luminescent Trinuclear Gold(I) Complexes with Difhiocarbamates. Inorganic Chemistry, 39(16), 3560-3566. [Pg.170]

Fernandez, E.J., Laguna, A., Lopez-de-Luzuriaga, J.M., Montiel, M Olmos, M.E. and Perez, J. (2005) Dimethylsulfoxide gold-thaDium complexes. Effects of the metal-metal interactions on the luminescence. Inorganica Chimica Acta, 358(14), 4293 300. [Pg.171]

Zhang, H.-X. and Che, C.-M. (2001) Aurophilic Attraction and Luminescence of Binuclear Gold(I) Complexes with Bridging Phosphine Ligands ah initio Study. Chemistry - A European Journal, 7, 4887-4893. [Pg.233]

The discriminatory emission properties between two-coordinate d ° gold(I) complexes and their respective three-coordinate counterparts have been demonstrated in the literature [6, 10-13]. As discussed in the later sections, Che and coworkers have rationalized that the extraordinarily large Stokes shift of the visible emission of [Au2(diphosphine)2] from the [5da 6pa] transition is due to the exciplex formation ofthe excited state with solvent or counterions [6]. Fackler [14—16] reported the photophysical properties of monomeric [AUL3] complexes, which show visible luminescence with large Stokes shifts (typically lOOOOcm ), suggesting significant excited-state distortion. Gray et al. [10] examined the spectroscopic properties of... [Pg.249]


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See also in sourсe #XX -- [ Pg.87 ]




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