Comparative photosensitised transformation of polychlorophenols with different sulphonated metallophthalocyanine complexes in aqueous medium

被引:95
作者
Ozoemena, K [1 ]
Kuznetsova, N [1 ]
Nyokong, T [1 ]
机构
[1] Rhodes Univ, Dept Chem, ZA-6140 Grahamstown, South Africa
关键词
aluminium; zinc; tin; silicon phthalocyanine; trichlorophenol; pentachlorophenol; photosensitization; singlet oxygen;
D O I
10.1016/S1381-1169(01)00243-6
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
The relative efficiencies for the oxidation of trichlorophenol (TCP) and pentachlorophenol (PCP), sensitised by sulphonated phthalocyanine complexes containing Zn, Al, Sn and Si as central metals, were studied in aqueous solutions. For the first time, sulphonated silicon and tin phthalocyanines were synthesised and their activity towards photosensitisation of singlet oxygen and photo-oxidation of polychlorophenols was examined. The efficiency of the sensitised photo-oxidative degradation of polychlorophenols depends not only on singlet oxygen quantum yield of sensitiser, but also on its stability. The influence of substrate structure and the pH of the solution on the photo-oxidation efficiency, as well as on the sensitiser photodegradation were studied. It was found that the contribution of the Type II (singlet oxygen-mediated) mechanism to the relative efficiency of the photosensitised photo-oxidation of the phenol, decreased from phenol top-chlorophenol, TCP and PCP, whereas Type I radical pathway increased. The results obtained for PCP give evidence that electron transfer from the excited sensitiser to the substrate in its unionised form is responsible for enhanced sensitiser photodegradation. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:29 / 40
页数:12
相关论文
共 50 条
[1]   BIODEGRADATION OF CHEMICALS OF ENVIRONMENTAL CONCERN [J].
ALEXANDER, M .
SCIENCE, 1981, 211 (4478) :132-138
[2]   PREPARATIVE, ANALYTICAL AND FLUORESCENCE SPECTROSCOPIC STUDIES OF SULFONATED ALUMINUM PHTHALOCYANINE PHOTOSENSITIZERS [J].
AMBROZ, M ;
BEEBY, A ;
MACROBERT, AJ ;
SIMPSON, MSC ;
SVENSEN, RK ;
PHILLIPS, D .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 1991, 9 (01) :87-95
[3]   PHTALOCYANINE IN WASSERIGER LOSUNG I [J].
BERNAUER, K ;
FALLAB, S .
HELVETICA CHIMICA ACTA, 1961, 44 (05) :1287-&
[4]   IUPAC REPORTS ON PESTICIDES .14. ENVIRONMENTAL CHEMISTRY OF PENTACHLOROPHENOL [J].
CROSBY, DG .
PURE AND APPLIED CHEMISTRY, 1981, 53 (05) :1051-1080
[5]   METAL PHTHALOCYANINES AND PORPHYRINS AS PHOTOSENSITIZERS FOR REDUCTION OF WATER TO HYDROGEN [J].
DARWENT, JR ;
DOUGLAS, P ;
HARRIMAN, A ;
PORTER, G ;
RICHOUX, MC .
COORDINATION CHEMISTRY REVIEWS, 1982, 44 (01) :83-126
[6]   EXCITED SINGLET AND TRIPLET-STATE ELECTRON-TRANSFER REACTIONS OF ALUMINUM(III) SULFONATED PHTHALOCYANINE [J].
DARWENT, JR ;
MCCUBBIN, I ;
PHILLIPS, D .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS II, 1982, 78 :347-357
[7]   Comparison of the photophysics of an aggregating and non-aggregating aluminium phthalocyanine system incorporated into unilamellar vesicles [J].
Dhami, S ;
Phillips, D .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1996, 100 (1-3) :77-84
[8]   COFACIAL ASSEMBLY OF PARTIALLY OXIDIZED METALLOMACROCYCLES AS AN APPROACH TO CONTROLLING LATTICE ARCHITECTURE IN LOW-DIMENSIONAL MOLECULAR-SOLIDS - CHEMICAL AND ARCHITECTURAL PROPERTIES OF THE FACE-TO-FACE POLYMERS [M(PHTHALOCYANINATO)O]N, WHERE M = SI, GE, AND SN [J].
DIRK, CW ;
INABE, T ;
SCHOCH, KF ;
MARKS, TJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1983, 105 (06) :1539-1550
[9]  
Edrei R, 1998, J PORPHYR PHTHALOCYA, V2, P191, DOI 10.1002/(SICI)1099-1409(199805/06)2:3<191::AID-JPP65>3.0.CO
[10]  
2-4