Synthesis and characterisation of heterometallic molecular triangles using ambidentate linker: self-selection of a single linkage isomers

被引:40
作者
Bar, Arun Kumar [2 ]
Chakrabarty, Rajesh [2 ]
Chi, Ki-Whan [1 ]
Batten, Stuart R. [3 ]
Mukherjeea, Partha Sarathi [2 ]
机构
[1] Univ Ulsan, Dept Chem, Ulsan 680749, South Korea
[2] Indian Inst Sci, Dept Inorgan & Phys Chem, Bangalore 560012, Karnataka, India
[3] Monash Univ, Sch Chem, Clayton, Vic 3800, Australia
关键词
HOST-GUEST CHEMISTRY; CRYSTAL-STRUCTURE; SOLID-STATE; RATIONAL DESIGN; SUPRAMOLECULAR CHEMISTRY; COORDINATION NETWORKS; MACROCYCLIC SQUARES; BUILDING-BLOCKS; OROTIC-ACID; GAS-PHASE;
D O I
10.1039/b900118b
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The coordination driven self-assembly of discrete molecular triangles from a non-symmetric ambidentate linker 5-pyrimidinecarboxylate (5-pmc) and Pd(II)/Pt(II) based 90 acceptors is presented. Despite the possibility of formation of a mixture of isomeric macrocycles (linkage isomers) due to different connectivity of the ambidentate linker, formation of a single and symmetrical linkage isomer in both the cases is an interesting observation. Moreover, the reported macrocycles represent the first example of discrete metallamacrocycles of bridging 5-pmc. While solution composition in both the cases was characterised by multinuclear NMR study and electrospray ionization mass spectrometry (ESI-MS), the identity of the assemblies in the solid state was established by X-ray single crystals structure analysis. Variable temperature NMR study clearly ruled out the formation of any other macrocycles by [4 + 4] or [2 + 2] self-assembly of the reacting components.
引用
收藏
页码:3222 / 3229
页数:8
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