Reversible Switching Based on Truly Intramolecular Long-Range Proton Transfer─Turning the Theoretical Concept into Experimental Reality

Herein, we demonstrate a working prototype of a conjugated proton crane, a reversible tautomeric switching molecule in which truly intramolecular long-range proton transfer occurs in solution at room temperature. The system consists of a benzothiazole rotor attached to a 7-hydroxy quinoline stator. According to the experimental and theoretical results, the OH proton is delivered under […]

Union of Scientists in Bulgaria Grand Prize for PhD thesis awarded to Dr Silvia Hristova

We are proud to announce that Dr Silvia Hristova, who defended her PhD thesis in our group last year, was awarded by The Union of Scientists in Bulgaria for best PhD thesis in 2020. The thesis of Silvia considers the possibility of using controlled proton transfer as an elementary process in the molecular machinery. The […]

7-OH quinoline Schiff bases: are they the long awaited tautomeric bistable switches?

Two novel, 7-hydroxyquinoline based, Schiff bases have been synthesized and their spectral properties have been investigated by combined use of optical and NMR spectroscopy and theoretical DFT calculations. The results indicate that 8-((phenylimino)methyl)quinolin-7-ol exists as a mixture of enol and two keto tautomers in solution, while 8-(((pentarfluorophenyl)imino)methyl)quinolin-7-ol is presented as a single enol form. Upon […]

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