Metal-Dependent Coordination Modes Displayed by Macrocyclic Polycarbene Ligands

被引:83
作者
Radloff, Christian [2 ]
Gong, Han-Yuan [1 ]
Brinke, Christian Schulte To [2 ]
Pape, Tania [2 ]
Lynch, Vincent M. [1 ]
Sessler, Jonathan L. [1 ,3 ]
Hahn, F. Ekkehardt [2 ]
机构
[1] Univ Texas Austin, Dept Chem & Biochem, Austin, TX 78712 USA
[2] Univ Munster, Inst Anorgan & Analyt Chem, D-48149 Munster, Germany
[3] Yonsei Univ, Seoul 120749, South Korea
基金
美国国家科学基金会;
关键词
coordination modes; macrocyclic ligands; palladium polycarbenes silver; HETEROCYCLIC CARBENE COMPLEXES; BIS(BENZIMIDAZOLIN-2-YLIDENE) PALLADIUM COMPLEXES; IMIDAZOLIUM-LINKED CYCLOPHANE; C COUPLING REACTIONS; TEMPLATE SYNTHESIS; STRUCTURAL-CHARACTERIZATION; CATALYTIC APPLICATIONS; RHODIUM; RECEPTORS; SILVER(I);
D O I
10.1002/chem.201002276
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Carbene-metal molecular box: Two imidazolium macrocycles, H 2-1(X)2 and H4-2(PF6)4, act as precursors for the formation of poly(NHC) ligands. The carbene ligands display metal-dependent conformations in forming organometallic complexes. In particular, they are capable of stabilizing boxlike structures such as syn-[Ag2(1)2]2+ and [Ag4(2) 2]4+ when exposed to linearly coordinated silver cations. In contrast, a monomeric species featuring a C-Pd-C angle of about 90° is formed between 1 and PdII. © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
引用
收藏
页码:13077 / 13081
页数:5
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