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Relaxation Properties of Porphyrin, Diprotonated Porphyrin, and Isoelectronic Tetraoxaporphyrin Dication in the S2 state


Marcelli, Agnese; Foggi, Paolo; Moroni, Laura; Gellini, Cristina; Salvi, Pier Remigio; Jelovica Badovinac, Ivana
Relaxation Properties of Porphyrin, Diprotonated Porphyrin, and Isoelectronic Tetraoxaporphyrin Dication in the S2 state // Journal of physical chemistry A, 111 (2007), 12; 2276-2282 doi:10.1021/jp0686846 (međunarodna recenzija, članak, znanstveni)


Naslov
Relaxation Properties of Porphyrin, Diprotonated Porphyrin, and Isoelectronic Tetraoxaporphyrin Dication in the S2 state

Autori
Marcelli, Agnese ; Foggi, Paolo ; Moroni, Laura ; Gellini, Cristina ; Salvi, Pier Remigio ; Jelovica Badovinac, Ivana

Izvornik
Journal of physical chemistry A (1089-5639) 111 (2007), 12; 2276-2282

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Porphyrins; tetraoxaporphyrin dication; relaxation properties; fluorescence quantum yields and lifetimes

Sažetak
The fluorescence spectra of unsubstituted porphyrin (H2P), diprotonated porphyrin (H4P2+), and isoelectronic tetraoxaporphyrin dication (TOxP2+) have been measured in solution at room temperature. The S2 f S0 fluorescence has been observed, much more intense for TOxP2+ than for H4P2+ and H2P. In the TOxP2+ case, the S2 f S0 fluorescence spectrum is remarkably sharp and shows an excellent mirror symmetry with respect to S0 f S2 absorption. On the contrary, the spectra of H4P2+ and H2P are shifted and more extended with respect to the absorption counterparts. The differences have been attributed primarily to the change of the equilibrium geometry upon excitation, larger in H2P and H4P2+ than in TOxP2+ and in the case of H4P2+ to the nonplanar conformation of the macrocycle. Also the S1 f S0 spectra of H2P, H4P2+, and TOxP2+ have been measured and more qualitatively discussed. The S1 and S2 fluorescence decays have been observed for H4P2+ and TOxP2+ exciting with ultrashort pulses. The S2 lifetime of TOxP2+ is of the order of the temporal resolution of our experimental apparatus, whereas that of H4P2+ is shorter. The S2 f S0 quantum yield of TOxP2+ has been estimated to be 0.035, 3 orders of magnitude higher than that of H4P2+. It is proposed on the basis of ab initio model calculations that excited states of the H4P2+(CF3COO-)2 complex with chargetransfer character are responsible of the increased extension of the S2 f S0 spectrum with respect to that of H2P.

Izvorni jezik
Engleski

Znanstvena područja
Fizika



POVEZANOST RADA


Projekt / tema
316-0000000-3192 - Analiza složenih sustava spektroskopskim metodama (Nada Orlić, )

Ustanove
Sveučilište u Rijeci - Odjel za fiziku

Autor s matičnim brojem:
Ivana Jelovica Badovinac, (256993)

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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