Tetranuclear (Phosphane)(thiolato)gold(I) Complexes: Synthesis, Characterization and Photoluminescent Properties
- Fernández, E.J. 1
- Laguna, A. 2
- López-de-Luzuriaga, J.M. 1
- Monge, M. 1
- Montiel, M. 1
- Olmos, M.E. 1
- Puelles, R.C. 1
- Sánchez-Forcada, E. 1
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1
Universidad de La Rioja
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2
Universidad de Zaragoza
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ISSN: 1434-1948
Année de publication: 2007
Volumen: 25
Pages: 4001-4005
Type: Article
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Résumé
The reactions of the tetraphosphane donor ligand (Ph2PCH 2)2NCH2CH2N(CH2PPh 2)2 with the gold precursors [AuCl(tht)] or [Au(C 6F5)(tht)] (tht = tetrahydrothiophene) leads to complexes [Au4R4{(Ph2PCH2)2NCH 2CH2N(CH2PPh2)2}] [R = Cl (1) or C6F5 (2)]. Further substitution of the chlorine atoms in 1 by the corresponding 4-substituted benzenethiolates gives rise to the tetranuclear (phosphane)fthiolato)gold(I) complexes [Au4(S-C 6H4-X)4{(Ph2PCH2) 2NCH2CH2N(CH2PPh2) 2}] [X = F (3), MeO (4), Me (5) and NO2 (6)]. Complexes 2 and 4 were characterized by X-ray diffraction studies showing Au-Au interactions in the case of complex 4. Complexes 3-6 display intense emissions in the solid state at 77 K with lifetimes in the microsecond range. The observed phosphorescent emissions are attributed to metal-to-ligand charge-transfer transitions. Nevertheless, the influence in the emission energies of gold-gold interactions or the contribution of the substituent in the 4-position of the benzenethiolate ring to the excited state cannot be neglected. © Wiley-VCH Verlag GmbH & Co. KGaA, 2007.