Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/11688
Title: Hybrid macrocyclic receptors based on lower rim functionalised thiacalix[4]arene and amino acids: Synthesis, structure and binding properties towards metal ions
Authors: Sreeja, Thulasi
Ganga, Viswanathan Bhagavathy
Praveen, Lakshmananpillai
Varma, Ramavarma Luxmi
Issue Date: May-2011
Publisher: NISCAIR-CSIR, India
Abstract: Peptidothiacalixarene derivatives <b style="">4a-d </b>and<b style=""> 7a-d</b> have been synthesized in excellent yields by the reaction of methyl esters of glycine, l-alanine and d- and l-phenyl alanine with lower rim substituted 1,3-diacid chloride and tetraacid chloride derivatives of thiacalixarene. The conformational and hydrogen bonding properties of these conjugates have been investigated by means of <sup>1</sup>H NMR in the solution state and by X-ray crystallography in the solid state. Complexation studies performed by UV-Vis and <sup>1</sup>H NMR spectroscopy in acetonitrile solution show that the 1,3-disubstituted hybrids selectively bind Hg<sup>2+</sup> ions and the orientation of the substituent on the chiral carbon is found to have a significant effect on the binding.
Description: 704-714
URI: http://hdl.handle.net/123456789/11688
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.50B(05) [May 2011]

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