Fiche publication
Date publication
avril 2016
Journal
Physical chemistry chemical physics : PCCP
Auteurs
Membres identifiés du Cancéropôle Est :
Dr ELHABIRI Mourad
Tous les auteurs :
Marchand G, Giraudeau P, Chen Z, Elhabiri M, Siri O, Jacquemin D
Lien Pubmed
Résumé
Understanding the chemical nature and spectroscopic signatures of a new class of organic molecules remains a strong challenge. Azacalixphyrin, the first member of a family of strongly aromatic macrocycles absorbing in the near infrared domain, can exist in several tautomeric forms. Here, we use DFT calculations and NMR measurements to propose the first in-depth investigation of proton exchanges occurring in two forms of azacalixphyrins (non-protonated and protonated). Our results reveal, on the one hand, a very effective solvent-assisted tautomerism in the non-protonated form whereas the intramolecular proton transfer is less probable, and, on the other hand, the presence of a mixture of almost isoenergetic tautomers differing in both their aromaticity and absorption profiles. This clearly indicates that smartly-designed chemical substitutions could alter the relative weights of the different tautomers, and consequently tune the optical signatures of these new macrocycles in a versatile and efficient way. For the protonated form, rotations of the NH2 groups take place rather than the chemical exchange.
Référence
Phys Chem Chem Phys. 2016 Apr 14;18(14):9608-15
