A new heterocyclic skeleton with highly tunable absorption/emission wavelength via H-bonding. Issue 115 (3rd November 2015)

• Record Type: Journal Article
• Authors: Tomashenko, Olesya A.; Khlebnikov, Alexander F.; Mosiagin, Ivan P.; Novikov, Mikhail S.; Grachova, Elena V.; Shakirova, Julia R.; Tunik, Sergey P.
• Is Part Of: RSC advances. Volume 5:Issue 115(2015)
• Page Start: 94551
• Page End: 94561
• Publication Date: 2015-11-03
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c5ra17755c
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : A new heterocyclic system, pyrido[2, 1- a ]pyrrolo[3, 2- c ]isoquinoline, showing stimuli responsive fluorescence, was synthesized via Pd-catalyzed intramolecular cyclization of 1-[1-benzyl-2-(2-bromophenyl)-1 H -pyrrol-3-yl]pyridin-1-ium bromides. Abstract : A new heterocyclic system, pyrido[2, 1- a ]pyrrolo[3, 2- c ]isoquinoline, was synthesized via Pd-catalyzed intramolecular cyclization of 1-[1-benzyl-2-(2-bromophenyl)-1 H -pyrrol-3-yl]pyridin-1-ium bromides. The heterocycles obtained display stimuli responsive fluorescence in solution depending on the nature of the solvent. The strongest blue shift of the emission maxima and growth in luminescence intensity was observed in protic solvents and upon addition of proton donors to solutions of compounds in aprotic solvents. The effect of proton donors on emission characteristics was explained by DFT calculations in terms of H-complex formation with the nucleophilic centres of the molecular skeleton.