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Abstract

Two fluorophores bound with a short photoreactive bridge are fascinating structures and remained unexplored. To investigate the synthesis and photolysis of such dyes, we linked two rhodamine dyes via a diazoketone bridge (−COCN₂−) attached to position 5′ or 6′ of the pendant phenyl rings. For that, the mixture of 5′- or 6′-bromo derivatives of the parent dye was prepared, transformed into 1,2-diarylacetylenes, hydrated to 1,2-diarylethanones, and converted to diazoketones Ar¹COCN₂Ar². The high performance liquid chromatography (HPLC) separation gave four individual regioisomers of Ar1COCN₂Ar2. Photolysis of the model compound─C₆H₅COCN₂C₆H₅─in aqueous acetonitrile at pH 7.3 and under irradiation with 365 nm light provided diphenylacetic acid amide (Wolff rearrangement). However, under the same conditions, Ar1COCN₂Ar² gave mainly α-diketones Ar1COCOAr². The migration ability of the very bulky dye residues was low, and the Wolff rearrangement did not occur. We observed only moderate fluorescence increase, which may be explained by the insufficient quenching ability of diazoketone bridge (−COCN₂−) and its transformation into another (weaker) quencher, 1,2-diarylethane-1,2-dione.