New halogenated phenylbacteriochlorins and their efficiency in singlet-oxygen sensitization

被引:71
作者
Pineiro, M
Gonsalves, AMDR
Pereira, MM
Formosinho, SJ
Arnaut, LG
机构
[1] Univ Coimbra, Dept Quim, P-3049 Coimbra, Portugal
[2] Univ Catolica Portuguesa, P-3080 Figueira Da Foz, Portugal
关键词
D O I
10.1021/jp013678p
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Halogenated phenylbacteriochlorins are synthesized with high yields in a two-step procedure. They have strong absorbances in the red and are very stable to air and light at room temperature. Flash photolysis measurements show that the triplet states of these bacteriochlorins have 30 mus lifetimes in deaerated toluene, that are quenched with diffusion-controlled rate constants by molecular oxygen. Time-resolved photoacoustic measurements, with nanosecond and nanocalorie resolution, show that these bacteriochlorins sensitize the formation of singlet oxygen with nearly unity quantum yield. However, singlet-oxygen phosphorescence measurements indicate that physical quenching occurs before the singlet-oxygen molecules diffuse into solution, and nearly half of the sensitized singlet states are lost.
引用
收藏
页码:3787 / 3795
页数:9
相关论文
共 43 条
[11]   2,3-VIC-DIHYDROXY-MESO-TETRAPHENYLCHLORINS FROM THE OSMIUM-TETROXIDE OXIDATION OF MESO-TETRAPHENYLPORPHYRIN [J].
BRUCKNER, C ;
DOLPHIN, D .
TETRAHEDRON LETTERS, 1995, 36 (19) :3295-3298
[12]   C-H Bond activation by alumina:: facile hydroxylation of chlorins at their saturated β-carbon by molecular oxygen and alumina [J].
Burns, DH ;
Li, YH ;
Shi, DC ;
Delaney, MO .
CHEMICAL COMMUNICATIONS, 1998, (16) :1677-1678
[13]   UNEXPECTED ROUTES TO NAPHTHOPORPHYRIN DERIVATIVES [J].
CALLOT, HJ ;
SCHAEFFER, E ;
CROMER, R ;
METZ, F .
TETRAHEDRON, 1990, 46 (15) :5253-5262
[14]   A NOVEL METHOD OF FUNCTIONALIZING THE ETHYL CHAIN OF OCTAETHYLPORPHYRIN [J].
CHANG, CK ;
SOTIRIOU, C .
JOURNAL OF ORGANIC CHEMISTRY, 1987, 52 (05) :926-929
[15]   A CONNECTION BETWEEN INTRAMOLECULAR LONG-RANGE ELECTRON, HOLE, AND TRIPLET ENERGY TRANSFERS [J].
CLOSS, GL ;
JOHNSON, MD ;
MILLER, JR ;
PIOTROWIAK, P .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (10) :3751-3753
[16]   Singlet and triplet energies of α-oligothiophenes:: A spectroscopic, theoretical, and photoacoustic study:: Extrapolation to polythiophene [J].
de Melo, JS ;
Silva, LM ;
Arnaut, LG ;
Becker, RS .
JOURNAL OF CHEMICAL PHYSICS, 1999, 111 (12) :5427-5433
[17]   SOME NOVEL HYDROPORPHYRINS [J].
EISNER, U .
JOURNAL OF THE CHEMICAL SOCIETY, 1957, (AUG) :3461-3469
[18]   Meso-tetraphenylporphyrin dimer derivative as a potential photosensitizer in photodynamic therapy [J].
Faustino, MAF ;
Neves, MGPMS ;
Vicente, MGH ;
Cavaleiro, JAS ;
Neumann, M ;
Brauer, HD ;
Jori, G .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1997, 66 (04) :405-412
[19]  
Fischer H, 1940, LIEBIGS ANN CHEM, V544, P138
[20]  
FORMOSINHO SJ, 1997, PROG REACT KINET, V22, P1