Spectrophotometric determination of conditional acidity constant as a function of β-cyclodextrin concentration for some organic acids using rank annihilation factor analysis

被引:39
作者
Afkhami, A [1 ]
Khalafi, L [1 ]
机构
[1] Bu Ali Sina Univ, Dept Chem, Fac Sci, Hamadan 65174, Iran
关键词
conditional acidity constant; spectrophotometry; beta-cyclodextrin; RAFA;
D O I
10.1016/j.aca.2006.03.054
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Rank annihilation factor analysis (RAFA) was used to the spectrophotometric studies of acid-base equilibria in the presence of beta-cyclodextrin (beta-CD). When the conditional acidity constants (beta-CD concentration dependent acidity constant) acts as an optimizing object, and simply combined with the pure spectrum of acidic and basic forms, the rank of original data matrix can be reduced. The residual standard deviation (R.S.D.) of the residual matrix after bilinearization of the background matrix is regarded as the valuation function. The performance of the method has been evaluated by using synthetic data. Spectrophotometrie studies of neutral red, 4-nitrophenol and 4-nitrocatechol in the presence of varying amounts of beta-CD are used as experimental model systems and the amounts of conditional acidity constants and formation constants of the inclusion complexes of beta-CD with acidic and basic forms are calculated. The conditional acidity constants increased by increasing beta-CD concentration for all three investigated acids. The calculated stability constants show that 4-nitrophenolate, 4-nitrocatecholate anions and basic form of neutral red (neutral form) form more stable inclusion complexes with beta-CD than their acidic forms. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:267 / 274
页数:8
相关论文
共 35 条
[1]   Rank annihilation factor analysis for spectrophotometric study of complex formation equilibria [J].
Abdollahi, H ;
Nazari, F .
ANALYTICA CHIMICA ACTA, 2003, 486 (01) :109-123
[2]  
Allinger NL, 1976, ORGANIC CHEM
[3]  
[Anonymous], 1987, BINDING CONSTANTS ME
[4]   Multivariate calibration of polycyclic aromatic hydrocarbon mixtures from excitation-emission fluorescence spectra [J].
Beltrán, JL ;
Ferrer, R ;
Guiteras, J .
ANALYTICA CHIMICA ACTA, 1998, 373 (2-3) :311-319
[5]   ACID-BASE AND DISTRIBUTION EQUILIBRIA OF 5,7-DICHLORO-2-METHYL-8-HYDROXYQUINOLINE IN BRIJ-35 MICELLAR MEDIA SOLUTIONS [J].
BELTRAN, JL ;
CODONY, R ;
GRANADOS, M ;
IZQUIERDO, A ;
PRAT, MD .
TALANTA, 1993, 40 (02) :157-165
[6]   DISPOSITION REQUIREMENTS FOR BINDING IN AQUEOUS-SOLUTION OF POLAR SUBSTRATES IN CYCLOHEXAAMYLOSE CAVITY [J].
BERGERON, RJ ;
CHANNING, MA ;
GIBEILY, GJ ;
PILLOR, DM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1977, 99 (15) :5146-5151
[7]   RANK ANNIHILATION WITH INCOMPLETE INFORMATION [J].
BURNS, DH ;
CALLIS, JB ;
CHRISTIAN, GD .
ANALYTICAL CHEMISTRY, 1986, 58 (13) :2805-2811
[8]   Functional parasagittal compartments in the rat cerebellar cortex: An in vivo optical imaging study using neutral red [J].
Chen, G ;
Hanson, CL ;
Ebner, TJ .
JOURNAL OF NEUROPHYSIOLOGY, 1996, 76 (06) :4169-4174
[9]   Cyclodextrins and their uses: a review [J].
Del Valle, EMM .
PROCESS BIOCHEMISTRY, 2004, 39 (09) :1033-1046
[10]   An automated procedure to predict the number of components in spectroscopic data [J].
Elbergali, A ;
Nygren, J ;
Kubista, M .
ANALYTICA CHIMICA ACTA, 1999, 379 (1-2) :143-158