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- W2146222421 endingPage "12117" @default.
- W2146222421 startingPage "12117" @default.
- W2146222421 abstract "Readily synthesised and functionalised di-1,2,3-triazole “click” ligands are shown to self-assemble into coordinatively saturated, quadruply stranded helical [Pd2L4](BF4)4 cages with Pd(II) ions. The cages have been fully characterised by elemental analysis, HR-ESMS, IR, 1H, 13C and DOSY NMR, DFT calculations, and in one case by X-ray crystallography. By exploiting the CuAAC “click” reaction we were able to rapidly generate a small family of di-1,2,3-triazole ligands with different core spacer units and peripheral substituents and examine how these structural modifications affected the formation of the [Pd2L4](BF4)4 cages. The use of both flexible (1,3-propyl) and rigid (1,3-phenyl) core spacer units led to the formation of discrete [Pd2L4](BF4)4 cage complexes. However, when the spacer unit of the di-1,2,3-triazole ligand was a 1,4-substituted-phenyl group steric interactions led to the formation of an oligomeric/polymeric species. By keeping the 1,3-phenyl core spacer constant the effect of altering the “click” ligands’ peripheral substituents was also examined. It was shown that ligands with alkyl, phenyl, electron-rich and electron-poor benzyl substituents all quantitatively formed [Pd2L4](BF4)4 cage complexes. The results suggest that a wide range of functionalised palladium(II) “click” cages could be rapidly generated. These novel molecules may potentially find uses in catalysis, molecular recognition and drug delivery." @default.
- W2146222421 created "2016-06-24" @default.
- W2146222421 creator A5006151763 @default.
- W2146222421 creator A5013502071 @default.
- W2146222421 creator A5018372186 @default.
- W2146222421 creator A5022871023 @default.
- W2146222421 creator A5075147918 @default.
- W2146222421 date "2011-01-01" @default.
- W2146222421 modified "2023-09-27" @default.
- W2146222421 title "Self-assembled palladium(ii) “click” cages: synthesis, structural modification and stability" @default.
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