Singlet oxygen quantum yields of different photosensitizers in polar solvents and micellar solutions

被引:2
作者
Spiller, W
Kliesch, H
Wöhrle, D
Hackbarth, S
Röder, B
Schnurpfeil, G
机构
[1] Univ Bremen, Inst Organ & Macromol Chem, Dept 2, Fachberiech 2, D-28334 Bremen, Germany
[2] Humboldt Univ, Inst Phys, D-10115 Berlin, Germany
关键词
singlet oxygen; porphyrazines; porphyrins; micellar solution; 1,3-diphenylisobenzofuran; bilirubin ditaurate;
D O I
10.1002/(SICI)1099-1409(199803/04)2:2<145::AID-JPP60>3.0.CO;2-2
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The singlet oxygen luminescence method and the photochemical methods using 1,3-diphenylisobenzofuran (DPBF) or bilirubin ditaurate (BDT) as chemical quenchers were employed to determine the single oxygen quantum yields (Phi(Delta)) of different phthalocyanines and tris(2,2'-bipyridyl)ruthenium(II) dichloride in dimethylformamide (DMF) or aqueous micellar solution of 0.1 M CTAC (cetyltrimethylammonium chloride). Additionally, a perylenetetracarboxylic acid diimide derivative was examined in DMF. In a series of tetrasulfonated phthalocyanines (PTS) the following order was found: ZnPTS > GaPTS > AIPTS approximate to H2PTS > CoPTS. In general, he singlet oxygen quantum yields are higher in DMF than in 0.1 M CTAC/H2O. The results obtained with the photochemical systems are comparable with those obtained by the photophysical method. The photochemical DPBF method results in absolute values of Phi(Delta). However, in micellar solution, chain reactions occur when DPBF is used as chemical quencher in the photo-oxidative process. This problem can be overcome by adding sodium thiosulphate which is able to destroy the endoperoxide initially formed. BDT can be used as quencher in different solvents to determine Phi(Delta) relative to a photosensitizer with known singlet oxygen quantum yield in the respective solvent. In comparison to the chemical methods the luminescence method exhibits the advantage that side reactions of the quencher are excluded. But normally the Phi(Delta) values obtained are relative to a reference, since absolute determinations need much larger efforts. (C) 1998 John Wiley & Sons, Ltd.
引用
收藏
页码:145 / 158
页数:14
相关论文
共 94 条
[1]   LIFETIME OF SINGLET OXYGEN IN LIQUID SOLUTION [J].
ADAMS, DR ;
WILKINSON, F .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS II, 1972, 68 (04) :586-+
[2]   A SIMPLIFIED SYNTHESIS FOR MESO-TETRAPHENYLPORPHIN [J].
ADLER, AD ;
LONGO, FR ;
FINARELLI, JD ;
GOLDMACH.J ;
ASSOUR, J ;
KORSAKOF.L .
JOURNAL OF ORGANIC CHEMISTRY, 1967, 32 (02) :476-+
[3]   Water-soluble 1,3-diphenylisobenzofuran derivatives. Synthesis and evaluation as singlet molecular oxygen acceptors for biological systems [J].
AmatGuerri, F ;
Lempe, E ;
Lissi, EA ;
Rodriguez, FJ ;
Trull, FR .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1996, 93 (01) :49-56
[4]   THE PHOTOPHYSICAL PROPERTIES OF PORPHYCENES - POTENTIAL PHOTODYNAMIC THERAPY AGENTS [J].
ARAMENDIA, PF ;
REDMOND, RW ;
NONELL, S ;
SCHUSTER, W ;
BRASLAVSKY, SE ;
SCHAFFNER, K ;
VOGEL, E .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1986, 44 (05) :555-559
[5]  
ARAMENDIA PF, 1994, NEWSLETTER, V52, P6
[6]  
Bailey P. S., 1978, OZONATION ORGANIC CH, V1
[7]  
BAILEY PS, 1908, OLEFINIC COMPOUNDS O, V39
[8]  
Balzani V., 1978, TOP CURR CHEM, P1, DOI [10.1007/BFb0048835, DOI 10.1007/BFB0048835]
[9]   PHTHALOCYANINE-INDUCED PHOTOHEMOLYSIS - STRUCTURE-ACTIVITY RELATIONSHIP AND THE EFFECT OF FLUORIDE [J].
BENHUR, E ;
MALIK, Z ;
DUBBELMAN, TMAR ;
MARGARON, P ;
ALI, H ;
VANLIER, JE .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1993, 58 (03) :351-355
[10]   PHTALOCYANINE IN WASSERIGER LOSUNG I [J].
BERNAUER, K ;
FALLAB, S .
HELVETICA CHIMICA ACTA, 1961, 44 (05) :1287-&