The solvation of acetonitrile

被引:245
作者
Reimers, JR [1 ]
Hall, LE [1 ]
机构
[1] Univ Sydney, Sch Chem, Sydney, NSW 2006, Australia
关键词
D O I
10.1021/ja983878n
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Acetonitrile is an extremely important solvent and cosolvent. Despite this, we have no general picture of the nature of mixed liquids containing acetonitrile applicable across-solvent families. We consider the properties of acetonitrile dissolved in 33 solvents, focusing on interpretation of the environment-sensitive solvent shift, Delta upsilon, of its CN stretch frequency, upsilon(2). The two major models (dispersive and specific solvation) which have been proposed to interpret Delta upsilon are based on diverse experiments with incompatible conclusions. We ascertain the robust features of these models and combine them into a new one in which solvent-solvent and solvent-solute forces compete to determine the structure of the solution and hence Delta upsilon. First, Delta upsilon is analyzed in terms of solvent repulsive and dielectric effects combined with specific solvation effects. To interpret this specific solvation, 95 MP2 or B3LYP calculations are performed to evaluate structures and CN frequency shifts for CH3CN complexed with one molecule of either water, methanol, ethanol, 2-propanol, tert-butyl alcohol, phenol, benzyl alcohol, acetic acid, trifluoroacetic acid, 2,2,2-trifluoroethanol, 1,1,1,3,3,3-hexafluoro-2-propanol, acetonitrile, chloroform, carbon tetrachloride, tetrahydrofuran, formamide, pyridine, or Cl-, as well as 45 parallel calculations for the solvent monomers or dimers. The results are then convolved using known structural properties of the various solutions and/or related neat liquids, leading to an interpretation of the observed solvent shifts. Also, we measure Delta upsilon for acetonitrile in aqueous solution using Fourier transform Raman spectroscopy and show that the results are consistent with, but require modification of, microheterogeneity theories for the structure of acetonitrile-water solutions. Although such theories are still in their infancy, we suggest that microheterogeneity could also account for most known properties of acetonitrile-alcohol solutions and, in fact, be a quite general phenomenon.
引用
收藏
页码:3730 / 3744
页数:15
相关论文
共 87 条
[1]   SOLVENT-INDUCED SHIFT OF THE RAMAN-SPECTRA IN SUPERCRITICAL FLUIDS [J].
AKIMOTO, S ;
KAJIMOTO, O .
CHEMICAL PHYSICS LETTERS, 1993, 209 (03) :263-268
[2]   THERMODYNAMIC ULTRASONIC SPECTROSCOPIC AND MISCIBILITY STUDIES OF WATER+METHYL CYANIDE SOLUTIONS [J].
ARMITAGE, DA ;
BLANDAMER, MJ ;
FOSTER, MJ ;
HIDDEN, NJ ;
MORCOM, KW ;
SYMONS, MCR ;
WOOTTEN, MJ .
TRANSACTIONS OF THE FARADAY SOCIETY, 1968, 64 (545P) :1193-+
[3]   MALONONITRILE IN AROMATIC SOLVENTS - GEOMETRY OF SOLVATION [J].
ARONEY, MJ ;
PATSALIDES, E ;
PIERENS, RK .
AUSTRALIAN JOURNAL OF CHEMISTRY, 1985, 38 (03) :507-512
[4]   INTERMOLECULAR INTERACTIONS IN WATER+ACETONITRILE MIXTURES - EVIDENCE FROM THE COMPOSITION VARIATION OF SOLVENT POLARITY PARAMETERS [J].
BALAKRISHNAN, S ;
EASTEAL, AJ .
AUSTRALIAN JOURNAL OF CHEMISTRY, 1981, 34 (05) :943-947
[5]   ALPHA-ACETONITRILE AT 215-K [J].
BARROW, MJ .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 1981, 37 (DEC) :2239-2242
[6]   SOLVENT AND PRESSURE-INDUCED PERTURBATIONS OF THE VIBRATIONAL POTENTIAL SURFACE OF ACETONITRILE [J].
BENAMOTZ, D ;
LEE, MR ;
CHO, SY ;
LIST, DJ .
JOURNAL OF CHEMICAL PHYSICS, 1992, 96 (12) :8781-8792
[7]   Ultrafast Raman echo measurements of vibrational dephasing and the nature of solvent-solute interactions [J].
Berg, M ;
VandenBout, DA .
ACCOUNTS OF CHEMICAL RESEARCH, 1997, 30 (02) :65-71
[8]   THE ANHARMONIC-FORCE CONSTANT K234 OF CH3CN IN DIFFERENT PHASES, SOLVENTS AND COMPLEXES WITH LEWIS-ACIDS [J].
BERTRAN, JF ;
LASERNA, B .
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 1986, 42 (09) :955-958
[9]   RAMAN-SPECTROSCOPIC STUDIES ON THE DYNAMIC AND EQUILIBRIUM PROCESSES IN BINARY-MIXTURES CONTAINING METHANOL AND ACETONITRILE [J].
BESNARD, M ;
CABACO, MI ;
STREHLE, F ;
YARWOOD, J .
CHEMICAL PHYSICS, 1992, 163 (01) :103-114
[10]   EXCESS MOLAR GIBBS ENERGIES OF MIXING OF WATER AND 1,1,1,3,3,3-HEXAFLUOROPROPAN-2-OL MIXTURES AT 298.15-K - COMPARISON OF THERMODYNAMIC PROPERTIES AND INVERSE KIRKWOOD-BUFF INTEGRAL-FUNCTIONS FOR BINARY AQUEOUS MIXTURES FORMED BY ETHANOL, PROPAN-2-OL, 2,2,2-TRIFLUOROETHANOL AND 1,1,1,3,3,3-HEXAFLUOROPROPAN-2-OL [J].
BLANDAMER, MJ ;
BURGESS, J ;
COONEY, A ;
COWLES, HJ ;
HORN, IM ;
MARTIN, KJ ;
MORCOM, KW ;
WARRICK, P .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1990, 86 (12) :2209-2213