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The first structural and spectroscopic characterisation of a ring-opened form of a 2H-naphtho[1,2-b]pyran: a novel photomerocyanine†
Stuart Aiken,Kathryn Booth,Christopher D. Gabbutt,B. Mark Heron,Craig R. Rice,Azzam Charaf-Eddin
Chemical Communications Pub Date : 06/05/2014 00:00:00 , DOI:10.1039/C4CC03435J
Abstract

Heating 4-methoxy-1-naphthol with a 1,1-diarylprop-2-yn-1-ol gave the 2,2-diaryl-6-methoxy-2H-naphtho[1,2-b]pyran together with the novel merocyanine, (E)-2-[3′,3′-bis(aryl)allylidene]-4-methoxynaphthalen-1(2H)-one. Brief UV-irradiation of the pyran favoured the formation of the (Z)-merocyanine with longer irradiation and/or acidic conditions favouring the (E)-isomer.

Graphical abstract: The first structural and spectroscopic characterisation of a ring-opened form of a 2H-naphtho[1,2-b]pyran: a novel photomerocyanine
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