2006
DOI: 10.1016/j.chemphys.2005.07.024
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Comparative study on the transition metal complexes of a novel thiacalix[4]arene derivative

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Cited by 9 publications
(6 citation statements)
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“…Higher charge transfer from ligand to Cu 2+ was presumably due to unfilled d orbitals. [ 35 ] Nevertheless, the higher selectivity for Zn 2+ predicted by DFT simulation was in complete agreement with the experimental observation for the competing ions experiments (Figures 3 and 5).…”
Section: Resultssupporting
confidence: 86%
“…Higher charge transfer from ligand to Cu 2+ was presumably due to unfilled d orbitals. [ 35 ] Nevertheless, the higher selectivity for Zn 2+ predicted by DFT simulation was in complete agreement with the experimental observation for the competing ions experiments (Figures 3 and 5).…”
Section: Resultssupporting
confidence: 86%
“…Thiacalixarenes have found considerable attention for its potential in further elaboration on both the aromatic rings and on the bridge atoms. 6, 65, 66, 112–115 The synthesis and properties of thiacalix[ n ]pyridine were therefore studied in detail 55–58. Thiacalix[3]pyridine was found adopting a C 3v symmetry when it binds a cation and has interesting catalytic properties,56–58 but little is known about the structure and conformational behavior of these compounds beyond that.…”
Section: Resultsmentioning
confidence: 99%
“…Also, theoretical calculations on the Zn(II) and Cu(II) complexation of parent thiacalix [4]arene and the methyl ester of 1 were done to obtain a deeper insight into the complexation ability of the disubstituted lower rim for the development of suitable supramolecular hosts/receptors with thiacalix [4]arene moieties. 19 In conclusion, we have described the suitability of thiacalix [4]arene derivatives with acid and amino surface groups as dendritic cores for the realization of novel lysine dendrimers up to the 3rd generation. Especially, the cone and 1,3-alternate thiacalix [4]arenes with amino surface groups were found useful as potential building blocks and molecular scaffolds in dendrimer chemistry.…”
Section: Org/njcmentioning
confidence: 92%