Photophysics of novel 22 pi porphyrinoids.

• Autores: Martire, Daniel Osvaldo; Russell, Sigrid; Dietrich, Hans Jürgen; Cobos, Carlos Jorge; Braslavsky, Silvia E.
• Año de publicación: 2012
• Idioma: inglés
• Tipo de recurso: artículo
• Materia: Porphycenes; Porphyrins; Singlet Molecular Oxygen; Near-Infrared Emission
• Institución: Consejo Nacional de Investigaciones Científicas y Técnicas

The photophysical properties of toluene solutions of two new 22! expanded porphycene compounds were measured using a combination of various steady-state and time-resolved techniques. The determined triplet energy (ET = 109 ± 3) kJ.mol–1, coincident with the calculated ET = (96.0 ±! expanded porphycene compounds were measured using a combination of various steady-state and time-resolved techniques. The determined triplet energy (ET = 109 ± 3) kJ.mol–1, coincident with the calculated ET = (96.0 ±ET = 109 ± 3) kJ.mol–1, coincident with the calculated ET = (96.0 ± 10) kJ.mol–1, of both red absorbing compounds is higher than the energy required to excite ground state molecular oxygen to singlet molecular oxygen. However, the intersystem crossing yield is very low (ca. 10−2), which makes these compounds poor photosensitizers. The triplet state yield of the two expanded 22! porphyrinoid compounds is much lower than that of the parent porphycene, whereas their fluorescence is as high (ca. 30%) as the value for porphycene. The slower than diffusional quenching rate constant of a porphycene triplet state by the two new compounds reflects a steric hindering factor of the exothermic energy transfer.–1, of both red absorbing compounds is higher than the energy required to excite ground state molecular oxygen to singlet molecular oxygen. However, the intersystem crossing yield is very low (ca. 10−2), which makes these compounds poor photosensitizers. The triplet state yield of the two expanded 22! porphyrinoid compounds is much lower than that of the parent porphycene, whereas their fluorescence is as high (ca. 30%) as the value for porphycene. The slower than diffusional quenching rate constant of a porphycene triplet state by the two new compounds reflects a steric hindering factor of the exothermic energy transfer.ca. 10−2), which makes these compounds poor photosensitizers. The triplet state yield of the two expanded 22! porphyrinoid compounds is much lower than that of the parent porphycene, whereas their fluorescence is as high (ca. 30%) as the value for porphycene. The slower than diffusional quenching rate constant of a porphycene triplet state by the two new compounds reflects a steric hindering factor of the exothermic energy transfer.! porphyrinoid compounds is much lower than that of the parent porphycene, whereas their fluorescence is as high (ca. 30%) as the value for porphycene. The slower than diffusional quenching rate constant of a porphycene triplet state by the two new compounds reflects a steric hindering factor of the exothermic energy transfer.ca. 30%) as the value for porphycene. The slower than diffusional quenching rate constant of a porphycene triplet state by the two new compounds reflects a steric hindering factor of the exothermic energy transfer.
Fil: Martire, Daniel Osvaldo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina
Fil: Russell, Sigrid. Institut Max Planck fuer Bioanorganische Chemie; Alemania
Fil: Dietrich, Hans Jürgen. Universitat zu Köln; Alemania
Fil: Cobos, Carlos Jorge. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina
Fil: Braslavsky, Silvia E.. Institut Max Planck fuer Bioanorganische Chemie; Alemania