Role of the conformational changes brought in the arms of the 1,3-di-capped conjugate of calix[4]arene (L) in turning on the fluorescence of L by Hg 2+

Anilkumar Bandela; Jugun Prakash Chinta; Chebrolu P. Rao

doi:10.1039/c1dt11208b

Role of the conformational changes brought in the arms of the 1,3-di-capped conjugate of calix[4]arene (L) in turning on the fluorescence of L by Hg ²⁺

Anilkumar Bandela
, Jugun Prakash Chinta
, Chebrolu P. Rao

Research output: Contribution to journal › Article › peer-review

17 Scopus citations

Abstract

A new 1,3-di-capped calix[4]arene conjugate of salicylidene (L) has been synthesized, characterized and the structure has been established by single crystal XRD. L shows selectivity towards Hg ²⁺ in ethanol by turn-on fluorescence among the biologically important metal ions studied. The species of recognition has been modeled by DFT computational calculations to result in conformational changes in the arms that support the turn-on fluorescence behaviour.

Original language	English
Pages (from-to)	11367-11370
Number of pages	4
Journal	Dalton Transactions
Volume	40
Issue number	43
DOIs	https://doi.org/10.1039/c1dt11208b
State	Published - 21 Nov 2011
Externally published	Yes

ASJC Scopus subject areas

Inorganic Chemistry

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abstract = "A new 1,3-di-capped calix[4]arene conjugate of salicylidene (L) has been synthesized, characterized and the structure has been established by single crystal XRD. L shows selectivity towards Hg 2+ in ethanol by turn-on fluorescence among the biologically important metal ions studied. The species of recognition has been modeled by DFT computational calculations to result in conformational changes in the arms that support the turn-on fluorescence behaviour.",

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AU - Chinta, Jugun Prakash

AU - Rao, Chebrolu P.

PY - 2011/11/21

Y1 - 2011/11/21

N2 - A new 1,3-di-capped calix[4]arene conjugate of salicylidene (L) has been synthesized, characterized and the structure has been established by single crystal XRD. L shows selectivity towards Hg 2+ in ethanol by turn-on fluorescence among the biologically important metal ions studied. The species of recognition has been modeled by DFT computational calculations to result in conformational changes in the arms that support the turn-on fluorescence behaviour.

AB - A new 1,3-di-capped calix[4]arene conjugate of salicylidene (L) has been synthesized, characterized and the structure has been established by single crystal XRD. L shows selectivity towards Hg 2+ in ethanol by turn-on fluorescence among the biologically important metal ions studied. The species of recognition has been modeled by DFT computational calculations to result in conformational changes in the arms that support the turn-on fluorescence behaviour.

UR - https://www.scopus.com/pages/publications/80054984625

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DO - 10.1039/c1dt11208b

M3 - Article

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JF - Dalton Transactions

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ER -

Role of the conformational changes brought in the arms of the 1,3-di-capped conjugate of calix[4]arene (L) in turning on the fluorescence of L by Hg ²⁺

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