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TDDFT study of the UV-vis spectra of subporphyrazines and subphthalocyanines

AuthorsLamsabhi, A. M.; Yáñez, M.; Mó, O.; Trujillo, C.; Blanco, F.; Alkorta, Ibon ; Elguero, José ; Caballero, E.; Rodríguez-Morgade, M. Salomé; Claessen, C. G.; Torres, T.
Issue Date2011
PublisherJohn Wiley & Sons
CitationJournal of Porphyrins and Phthalocyanines 15: 1220- 1230 (2011)
AbstractThe UV-vis spectra of a series of subporphyrazines, SubPz(A,R), and subphthalocyanines, SubPc(A,R) (A = F, Cl; R = H, F, CH 3, C 3H 7, SCH 3, SC 2H 5 and SPh), where A is the substituent attached to the central boron atom and R is the substituent attached to the periphery of the molecule have been analyzed through the use of TDDFT calculations in vacuum and using chloroform as a solvent. The absorption spectra depend on both, the characteristics of the substituent attached to the periphery of the molecule and the extension of the π-system on going from SubPz to the SubPc analog. These latter effects lead to a red-shift of both the Q-band and the B-band, although the effect is larger for the former, mainly due to the increase of HOMOLUMO energy gap on going from the SubPz to the SubPc analog. The effect of the substituents R is more intricate, because the profile of the absorption spectra changes depending on whether both substituents are on the same side (uu or dd) or on opposite sides (ud) of the molecular cone. Since the three conformers are rather close in energy, the observed spectra correspond, very likely, to the sum of the spectra of all of them. © 2011 World Scientific Publishing Company.
Publisher version (URL)http://dx.doi.org/10.1142/S1088424611004154
Identifiersdoi: 10.1142/S1088424611004154
issn: 1088-4246
e-issn: 1099-1409
Appears in Collections:(IQM) Artículos
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