Classification of Organic Solvents Revisited by Using the COSMO-RS Approach

被引:44
作者
Durand, Morgan [1 ]
Molinier, Valerie [1 ]
Kunz, Werner [2 ]
Aubry, Jean-Marie [1 ]
机构
[1] Univ Lille Nord France, USTL, ENSCL, EA Chim Mol & Formulat 4478, F-59652 Villeneuve Dascq, France
[2] Univ Regensburg, Inst Phys & Theoret Chem, D-93040 Regensburg, Germany
关键词
classification; COSMO-RS; organic solvents; solubilisation; solvent design; SOLVATOCHROMIC COMPARISON METHOD; PHYSICOCHEMICAL PROPERTIES; PARTITION-COEFFICIENTS; SCREENING MODEL; REAL SOLVENTS; PARAMETERS; SCALE; DESCRIPTORS; PREDICTION; POLARITY;
D O I
10.1002/chem.201001743
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new approach for the classification of solvents is proposed, based solely on the solvent molecular structure and relying on the "COnductor-like Screening MOdel for Real Solvents" (COSMO-RS), in which solvents are considered in their liquid state. This approach provides an a priori classification without requiring the knowledge of any experimental data. The theoretical descriptors of the proposed classification are generated through the analysis of the COSMORS s-potential profiles. By applying a two-step statistical procedure to the descriptors generated for a set of 153 representative solvents, a clustering into 10 classes leads to an optimal classification that is compared to the classical Chastrette's classification. The investigation of nitrocellulose solubility allows a validation of the proposed classification, which can be extended also to solvent mixtures. This new approach for solvent classification, thus, appears as a consistent tool for the design of new solvents and their formulation.
引用
收藏
页码:5155 / 5164
页数:10
相关论文
共 45 条
[2]   ELECTRONIC-STRUCTURE CALCULATIONS ON WORKSTATION COMPUTERS - THE PROGRAM SYSTEM TURBOMOLE [J].
AHLRICHS, R ;
BAR, M ;
HASER, M ;
HORN, H ;
KOLMEL, C .
CHEMICAL PHYSICS LETTERS, 1989, 162 (03) :165-169
[3]  
Ahlrichs R., 2002, Turbomole Version 5
[4]   DENSITY-FUNCTIONAL EXCHANGE-ENERGY APPROXIMATION WITH CORRECT ASYMPTOTIC-BEHAVIOR [J].
BECKE, AD .
PHYSICAL REVIEW A, 1988, 38 (06) :3098-3100
[5]   OCTANOL WATER PARTITION-COEFFICIENTS EXPRESSED IN TERMS OF SOLUTE MOLECULAR-SURFACE AREAS AND ELECTROSTATIC POTENTIALS [J].
BRINCK, T ;
MURRAY, JS ;
POLITZER, P .
JOURNAL OF ORGANIC CHEMISTRY, 1993, 58 (25) :7070-7073
[6]   The theory of the acid-base-function. [J].
Bronsted, JN .
BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1928, 61 :2049-2063
[7]   ELECTRONIC DESCRIPTORS IN QUANTITATIVE STRUCTURE-ACTIVITY-RELATIONSHIPS [J].
CARTIER, A ;
RIVAIL, JL .
CHEMOMETRICS AND INTELLIGENT LABORATORY SYSTEMS, 1987, 1 (04) :335-347
[8]   APPROACH TO A GENERAL CLASSIFICATION OF SOLVENTS USING A MULTIVARIATE STATISTICAL TREATMENT OF QUANTITATIVE SOLVENT PARAMETERS [J].
CHASTRETTE, M ;
RAJZMANN, M ;
CHANON, M ;
PURCELL, KF .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1985, 107 (01) :1-11
[9]   STATISTICAL STUDY OF SOLVENT EFFECTS .2. ANALYSIS OF SOME EMPIRICAL PARAMETERS OF SOLVENT POLARITY [J].
CHASTRETTE, M ;
CARRETTO, J .
TETRAHEDRON, 1982, 38 (11) :1615-1618
[10]   STATISTICAL STUDY OF EFFECTS OF SOLVENT .1. PRINCIPLES AND APPLICATIONS TO EVALUATION OF SOLVENT PARAMETERS AND CLASSIFICATION [J].
CHASTRETTE, M .
TETRAHEDRON, 1979, 35 (11) :1441-1448