Recognition Properties and Self-assembly of Planar [M(2-pyridyl-1,2,3-triazole)2]2+ Metallo-ligands

被引:13
作者
Preston, Dan [1 ]
Findlay, James A. [1 ,2 ]
Crowley, James D. [1 ,2 ]
机构
[1] Univ Otago, Dept Chem, POB 56, Dunedin 9054, New Zealand
[2] MacDiarmid Inst Adv Mat & Nanotechnol, Dunedin, New Zealand
关键词
molecular recognition; metallo-ligands; palladium(II); platinum(II); -; interactions; PI-PI-STACKING; MOLECULAR RECOGNITION; SUPRAMOLECULAR RECOGNITION; INFINITE CHAINS; COMPLEXES; COORDINATION; CHEMISTRY; ARCHITECTURES; PALLADIUM(II); CONSTRUCTION;
D O I
10.1002/asia.201801132
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Molecular recognition continues to be an area of keen interest for supramolecular chemists. The investigated [M(L)(2)](2+) metallo-ligands (M=Pd-II, Pt-II, L=2-(1-(pyridine-4-methyl)-1H-1,2,3-triazol-4-yl)pyridine) form a planar cationic panel with vacant pyridyl binding sites. They interact with planar neutral aromatic guests through - and/or metallophilic interactions. In some cases, the metallo-ligands also interacted in the solid state with Ag-I either through coordination to the pendant pyridyl arms, or through metal-metal interactions, forming coordination polymers. We have therefore developed a system that reliably recognises a planar electron-rich guest in solution and in the solid state, and shows the potential to link the resultant host-guest adducts into extended solid-state structures. The facile synthesis and ready functionalisation of 2-pyridyl-1,2,3-triazole ligands through copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) click chemistry should allow for ready tuning of the electronic properties of adducts formed from these systems.
引用
收藏
页码:1136 / 1142
页数:7
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