SOLVENT INDEPENDENT TRANSITION-STATE STRUCTURES .3. SULFONYL TRANSFER-REACTIONS

被引:12
作者
TARKKA, RM
PARK, WKC
LIU, P
BUNCEL, E
HOZ, S
机构
[1] BAR ILAN UNIV,DEPT CHEM,IL-52100 RAMAT GAN,ISRAEL
[2] QUEENS UNIV,DEPT CHEM,KINGSTON K7L 3N6,ON,CANADA
来源
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2 | 1994年 / 12期
关键词
D O I
10.1039/p29940002439
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A-kinetic spectrophotometric study has been performed on the reactions of p-nitrophenyl benzenesulfonate (PNPBS) with m-chlorophenoxide, p-chlorophenoxide, phenoxide, p-methylphenoxide and p-methoxyphenoxide ions in DMSO-H2O mixtures at 25.0 degrees C. Systematic variation of the DMSO content showed that the second-order rate constants (k(2)) changed only moderately upon addition of DMSO up to 20 mol% for reaction of p-chlorophenoxide, phenoxide and p-methylphenoxide. On the other hand, the rates of reaction for all of the phenoxide ions studied increased markedly in solvent compositions greater than 40 mol% DMSO. The nature of the transition state (TS) for these reactions was probed via Bronsted-type linear free energy relationships (LFERs). Traditional Bronsted-type plots (method 'A'), in which the remote substituent on the aryloxide was varied and the solvent composition was held constant, were constructed for the reactions of the phenoxides with PNPBS in each of the following solvent compositions: 40%. 50%, 70% and 90% DMSO by mole. Novel Bronsted-type plots (method 'B'), in which variation in phenoxide pK(a) was imparted through solvent changes while the remote substituent was held constant, were also constructed for the reactions of each of the five phenoxide nucleophiles. Method A yielded a set of lines whose slopes (beta(nuc) values) decreased steadily from 0.75 in 40 mol% DMSO to 0.60 in 90 mol% DMSO. Method B yielded a single straight line, beta(nuc) = 0.60, with satisfactory linearity for all data points (r(2) = 0.995, 95% Cl = +/- 0.021), although closer examination suggested slight curvature with beta(nuc) varying from 0.54 for p-CH3O to 0.66 for m-Cl. These results point to a discrepancy in the traditional view that Bronsted-type LFERs can be directly translated into a TS structure. Considerations based on the Marcus equation suggest that linearity in a Bronsted-type plot may result for a set of reaction series with differing intrinsic barriers provided that Delta G(0)(#), varies linearly with Delta G(0).
引用
收藏
页码:2439 / 2444
页数:6
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