A study of the strongly fluorescent species formed by the interaction of the dye 1,4-dihydroxyanthraquinone (quinizarin) with Al(III)

被引:31
作者
Quinti, L
Allen, NS
Edge, M
Murphy, BP
Perotti, A
机构
[1] Manchester Metropolitan Univ, Dept Chem & Mat, Manchester M1 5GD, Lancs, England
[2] Univ Pavia, Dipartimento Chim Gen, I-27100 Pavia, Italy
基金
英国工程与自然科学研究理事会;
关键词
quinizarin; hydroxyanthraquinones; aluminium; fluorescence; supramolecular complexes;
D O I
10.1016/S1010-6030(02)00360-X
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
Strongly fluorescent species form when Al(111) ions interact with 1,4-dihydroxyanthraquinone (quinizarin, QNZ), in aqueous and non-aqueous media. Speciation studies suggest the supramolecular and/or polymeric nature of these complexes as both their absorbance and fluorescence intensity increase proportionally to the Al(111) equivalents up to 60/1 Al(111)/QNZ and in certain cases even further. iso-Propanol is the solvent that yields the highest quantum yield of fluorescence (Phi = 0.51 for QNZ/Al(111) 1/75). Counterion effects were also studied and Al(acac)(3) was found to be the compound with which the highest quantum yield values were obtained, suggesting an active role for acac(-) in the stabilisation of the QNZ/Al(111) fluorescent species. Potentiometric studies, performed between pH 3 and 6 in dioxane/water 80/20, suggest the formation of 2/1 QNZ/Al(111) species, having global stability constant of 10(40). Studies at higher ratios of Al(111) were precluded by precipitations. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:79 / 91
页数:13
相关论文
共 22 条
[1]   SPECTROSCOPIC, PHOTOCHEMICAL AND PHOTOCONDUCTIVE PROPERTIES OF A NOVEL FLUORESCENT POLYMERIC COMPLEX OF QUINIZARIN AND ALUMINUM [J].
ALLEN, NS ;
RICHARDS, AM .
EUROPEAN POLYMER JOURNAL, 1990, 26 (11) :1229-1235
[2]   SPECTROSCOPIC PROPERTIES OF A NOVEL FLUORESCENT COMPLEX OF ALUMINUM AND QUINIZARIN [J].
ALLEN, NS ;
HAYES, G ;
RILEY, PNK ;
RICHARDS, AM .
JOURNAL OF PHOTOCHEMISTRY, 1987, 38 :365-373
[3]   STUDY OF 1,4-DIHYDROXYANTHRAQUINONE AS AN ACID-BASE INDICATOR IN ISOPROPYL-ALCOHOL MEDIUM - EVALUATION OF COLOR-CHANGE LIMITS THROUGH COMPLEMENTARY CHROMATICITY PARAMETERS [J].
BARBOSA, J ;
SANCHEZ, J ;
BOSCH, E .
TALANTA, 1984, 31 (04) :279-282
[4]   REDOX CHEMISTRY OF 1,4-DIHYDROXY-9,10-ANTHRAQUINONE (QUINIZARINE) AND ITS MANGANESE(II) COMPLEXES IN DIMETHYLSULFOXIDE [J].
BODINI, ME ;
ARANCIBIA, V .
POLYHEDRON, 1991, 10 (16) :1929-1937
[5]   THERMAL AND SPECTRAL STUDIES OF SOME DIVALENT METAL-CHELATES OF QUINIZARIN [J].
BOTTEI, RS ;
LUSARDI, DA .
THERMOCHIMICA ACTA, 1981, 43 (03) :355-363
[6]   SOME OBSERVATIONS ON THE USE OF 1,4-DIHYDROXYANTHRAQUINONE AS A FLUOROMETRIC REAGENT FOR TRACES OF LITHIUM [J].
CEBA, MR ;
FERNANDEZGUTIERREZ, A ;
SANCHEZ, CM .
MICROCHEMICAL JOURNAL, 1985, 32 (03) :286-292
[7]   CHELATE POLYMERS OF COPPER(II) WITH VARIOUS DIHYDROXYQUINOID LIGANDS [J].
COBLE, HD ;
HOLTZCLA.HF .
JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1974, 36 (05) :1049-1053
[8]  
DEMAS JN, 1971, J PHYS CHEM-US, V75, P991, DOI 10.1021/j100678a001
[9]   Spectroscopic studies on iron complexes of different anthracyclines in aprotic solvent systems [J].
Drechsel, H ;
Fiallo, M ;
Garnier-Suillerot, A ;
Matzanke, BF ;
Schünemann, V .
INORGANIC CHEMISTRY, 2001, 40 (21) :5324-5333
[10]   SPECTROFLUORIMETRIC DETERMINATION OF INORGANIC ANIONS - A REVIEW [J].
GOMEZHENS, A ;
VALCARCEL, M .
ANALYST, 1982, 107 (1274) :465-494