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

Journal

DALTON TRANSACTIONS
Volume -, Issue 17, Pages 3222-3229

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/b900118b

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Funding

  1. Department of Science and Technology [SR/S1/IC-18/2008]
  2. CSIR, New Delhi, Govt. of India
  3. Pohang Accelerator Laboratory, Pohang [790-784]

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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.

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