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Luminescent Homo- and Heteropolynuclear Gold Complexes Stabilized by a Unique Acetylide Fragment
被引:55
作者:
Carmen Blanco, M.
[1
,4
]
Camara, Jessica
[1
]
Concepcion Gimeno, M.
[1
]
Jones, Peter G.
[3
]
Laguna, Antonio
[1
]
Lopez-de-Luzuriaga, Jose M.
[2
]
Elena Olmos, M.
[2
]
Dolores Villacampa, M.
[1
]
机构:
[1] Univ Zaragoza, CSIC, Dept Quim Inorgan, ISQCH, E-50009 Zaragoza, Spain
[2] Univ La Rioja, Dept Quim, Grp Sintesis Quim La Rioja, UA CSIC, Logrono 26004, Spain
[3] Tech Univ Carolo Wilhelmina Braunschweig, Inst Anorgan & Analyt Chem, D-38023 Braunschweig, Germany
[4] Acad Gen Mil, Ctr Univ Def, Zaragoza 50090, Spain
基金:
奥地利科学基金会;
关键词:
X-RAY-STRUCTURE;
CRYSTAL-STRUCTURE;
STRUCTURAL-CHARACTERIZATION;
ORGANOGOLD(I) COMPLEXES;
MOLECULAR-STRUCTURES;
CLUSTER COMPLEXES;
GROUP-1B METALS;
DONOR LIGANDS;
ALKYNYL;
CHEMISTRY;
D O I:
10.1021/om200397t
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
In this paper we describe the reactivity of the gold acetylide derivatives [Au(C CR)(PPh3)] (R = Ph, 2-py). Reactions of these complexes with fragments of the type [M(PPh3)(2)](+) (M = Au, Ag, Cu) afford a series of novel discrete molecules stabilized not only by interactions with the triple bond but also by the formation of strong metal-gold interactions. The crystal structures of the gold-gold and gold-silver species confirm their similar behavior, while X-ray diffraction establishes a different arrangement for the copper complex with pyridine acetylide as a consequence of the coordination of this metal center to the nitrogen atom of pyridine and to the carbons of the alkyne. The luminescent properties of the complexes were also studied.
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页码:2597 / 2605
页数:9
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