SOLVENT EFFECT ON DI-TERT-BUTYL NITROXIDE - DIPOLE-DIPOLE MODEL FOR POLAR SOLUTES IN POLAR-SOLVENTS

被引:98
作者
REDDOCH, AH
KONISHI, S
机构
[1] Division of Chemistry, National Research Council of Canada, Ottawa
[2] Department of Chemistry, Tohoku University, Sendai
关键词
D O I
10.1063/1.437756
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
New measurements of the solvent effect on the nitrogen hyperfine coupling constant of di-tert-butyl nitroxide are reported. These, together with literature data, are used to test various models for the solvent effect. At the Hückel level of approximation, aN is a linear function of the applied electric field. Thus various reaction field theories may be considered. The widely used Onsager reaction field does not account for the effects of the more polar solvents or for the differences between polar and nonpolar solvents. The Wertheim and Block-Walker reaction fields are better, especially for very polar solvents. However none of these continuum reaction fields is entirely satisfactory theoretically or experimentally. We propose a dipole-dipole model for polar solvents which is superior to the continuum models. From the dipole-dipole model, we suggest that the quantity μρ/M is a convenient linear parameter for polar solvent effects, the factors being solvent dipole moment, density, and molecular weight. The dipole-dipole model should apply to a wide range of polar solutes. Some special situations are not explained by the model, including hydrogen-bonding solvents, halogenated aromatics, and solvents with more than one conformation. The temperature dependence of the solvent effect is also considered. © 1979 American Institute of Physics.
引用
收藏
页码:2121 / 2130
页数:10
相关论文
共 44 条
[1]   REGARDING A GENERALIZED SCALE OF SOLVENT POLARITIES [J].
ABBOUD, JL ;
TAFT, RW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1977, 99 (25) :8325-8327
[2]   APPLICATION OF REACTION FIELD-THEORY TO CALCULATION OF SOLVENT EFFECTS ON TERT BUTYL CHLORIDE SOLVOLYSIS, AND ON ME4N+CL-ION PAIR [J].
ABRAHAM, MH ;
ABRAHAM, RJ .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1974, (01) :47-52
[3]   AN ELECTRON DIFFRACTION INVESTIGATION OF MOLECULAR STRUCTURE OF DI-T-BUTYLNITROXIDE FREE RADICAL IN VAPOUR PHASE [J].
ANDERSEN, B ;
ANDERSEN, P .
ACTA CHEMICA SCANDINAVICA, 1966, 20 (10) :2728-&
[4]   MODIFICATION OF ONSAGER THEORY FOR A DIELECTRIC [J].
BLOCK, H ;
WALKER, SM .
CHEMICAL PHYSICS LETTERS, 1973, 19 (03) :363-364
[5]  
BOTTCHER CJF, 1973, THEORY ELECTRIC POLA
[6]   NITROGEN-14 AND OXYGEN-17 HYPERFINE INTERACTIONS IN PERTURBED NITROXIDES [J].
COHEN, AH ;
HOFFMAN, BM .
JOURNAL OF PHYSICAL CHEMISTRY, 1974, 78 (13) :1313-1321
[7]  
DAVIES OL, 1972, STATISTICAL METHODS
[8]   NONEMPIRICAL CALCULATIONS ON CONFORMATION AND HYPERFINE-STRUCTURE OF NITROXIDE AND KETYL GROUPS - CONSEQUENCES OF OUT-OF-PLANE BENDING ON HYPERFINE INTERACTIONS [J].
ELLINGER, Y ;
SUBRA, R ;
RASSAT, A ;
DOUADY, J ;
BERTHIER, G .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1975, 97 (03) :476-479
[9]   USE OF NITROSO COMPOUNDS AS SCAVENGERS FOR STUDY OF SHORT-LIVED FREE RADICALS IN ORGANIC REACTIONS [J].
FORSHULT, S ;
LAGERCRANTZ, C .
ACTA CHEMICA SCANDINAVICA, 1969, 23 (02) :522-+
[10]   REACTION, CAVITY, AND DIPOLE FIELDS IN A DISCRETE LATTICE [J].
FULTON, RL .
JOURNAL OF CHEMICAL PHYSICS, 1975, 62 (09) :3676-3682