Bar Arun Kumar, Chakrabarty Rajesh, Chi Ki-Whan, Batten Stuart R, Mukherjee Partha Sarathi
Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bangalore, 560012, India.
Dalton Trans. 2009 May 7(17):3222-9. doi: 10.1039/b900118b. Epub 2009 Mar 25.
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 degrees 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.
本文介绍了由不对称双齿连接体5-嘧啶羧酸酯(5-pmc)和基于Pd(II)/Pt(II)的90度受体通过配位驱动自组装形成离散分子三角形的过程。尽管由于双齿连接体的不同连接方式可能形成异构大环(连接异构体)混合物,但在两种情况下形成单一且对称的连接异构体是一个有趣的现象。此外,所报道的大环代表了桥连5-pmc的离散金属大环的首个实例。虽然两种情况下的溶液组成通过多核NMR研究和电喷雾电离质谱(ESI-MS)进行了表征,但固态组装体的身份通过X射线单晶结构分析得以确定。变温NMR研究明确排除了反应组分通过[4 + 4]或[2 + 2]自组装形成任何其他大环的可能性。