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.
引用
收藏
页码:2597 / 2605
页数:9
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