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Synthesis of an optically switchable salicylaldimine substituted naphthopyran for selective and reversible Cu2+ recognition in aqueous solution†
Priya Ranjan Sahoo,Satish Kumar
RSC Advances Pub Date : 02/01/2016 00:00:00 , DOI:10.1039/C5RA24857D
Abstract

A light controlled reversible switch for copper ion was synthesized by substituting photochromic naphthopyran with a salicylaldimine moiety. The naphthopyran based photoreversible receptor was characterized using IR, NMR, HRMS and single crystal X-ray crystallographic techniques. The photochromic properties of the receptor under light irradiation were investigated by UV-visible spectroscopy. The affinity towards transition metal ions in both closed and open forms were determined. The open form of the receptor displayed an increased affinity towards copper ions. A 3.25 × 104 fold difference in binding affinity for copper ions between the closed and open forms in aqueous methanol solution suggested that the receptor can act as a selective photoswitch for copper ions. Theoretical investigations at the molecular level supported the experimental observations.

Graphical abstract: Synthesis of an optically switchable salicylaldimine substituted naphthopyran for selective and reversible Cu2+ recognition in aqueous solution
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