The dual chromogenic and fluorogenic chemodosimetric behaviour of substituted 5-amino-1,2-dihydro-2methyl-1,6-naphthyridine-8-carbonitriles was investigated. The reaction-based indicators operate by an unusualr earrangementf ollowed by ring contraction to generate ap yrro-lopyridine, with a" naked-eye"r esponse and chromofluorogenic selectives ensing for Cu 2 + ions. The structure of the pyrrolopyridine was confirmed by single-crystal X-ray analysis.
Results and DiscussionThis report describes the design and synthesis of afluorometric assay towards the effective detection of Cu 2 + ions. We present, for the first time, [1,6]-naphthyridine derivatives as dosimeters with high sensitivity and selectivity,o wing to the surprising rearrangement andr ing contraction mediated by Cu 2 + ions. The dosimeters (1 and 2,S cheme 1) were synthesizedi no ne step according to our recently published work. [12] [a] P.