Excited-state dynamics of 5,10,15,20-tetraphenyl-21H,23H-porphine manganese(III) chloride encapsulated in TiMCM-41 and MCM-41; Proved by fs-diffuse reflectance laser photolysis

Citation
Y. Kim et al., Excited-state dynamics of 5,10,15,20-tetraphenyl-21H,23H-porphine manganese(III) chloride encapsulated in TiMCM-41 and MCM-41; Proved by fs-diffuse reflectance laser photolysis, J PHYS CH B, 105(36), 2001, pp. 8513-8518
Citations number
51
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF PHYSICAL CHEMISTRY B
ISSN journal
15206106 → ACNP
Volume
105
Issue
36
Year of publication
2001
Pages
8513 - 8518
Database
ISI
SICI code
1520-6106(20010913)105:36<8513:EDO5M>2.0.ZU;2-C
Abstract
5,10,15,20-Tetraphenyl-21H,23H-porphine manganese(III) chloride ((MnTPP)-T- III(Cl)) was encapsulated into MCM-41 and TiMCM-41, and its photoinduced el ectron transfer had been studied by using femtosecond diffuse reflectance p hotolysis. Two different transient species (c.a. 10 ps and c.a. 80 ps) were observed. The shorter-lived species should be originated from relaxation o f a "tripmultiplet" state and the longer-lived species should be attributed to the spin-forbidden relaxation (slower than the spin-allowed decay of tr iptquintet) via a quintet CT state. After irradiation, MnTPPCI+. radicals a re detected in MCM-41 or TiMCM-41, indicating that the mesoporous silicate framework plays a good electron acceptor. Furthermore, it has been found th at the formation MnTPPCI+. is easier in TiMCM-41 than in MCM-41, indicating that framework modification by incorporating the Ti4+ into the MCM-41 enha nces the electron-accepting ability of the MCM-41 framework.