Kinetics of the solvolyses of benzhydryl derivatives: Basis for the construction of a comprehensive nucleofugality scale

被引:75
作者
Denegri, B [1 ]
Streiter, A [1 ]
Juric, S [1 ]
Ofial, AR [1 ]
Kronja, O [1 ]
Mayr, H [1 ]
机构
[1] Univ Zagreb, Fac Pharm & Biochem, Zagreb 10000, Croatia
关键词
carbocations; kinetics; nucleophilic substitution; reaction mechanisms; solvent effects;
D O I
10.1002/chem.200500845
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of 21 benzhydrylium ions (diarylmethylium ions) are proposed as reference electrofuges for the development of a general nucleofugality scale, where nucleofugality refers to a combination of leaving group and solvent. A total of 167 solvolysis rate constants of benzhydrylium tosylates, bromides, chlorides, trifluoroacetates, 3,5-dinitrobenzoates, and 4-nitrobenzoates, two-thirds of which have been determined during this work, were subjected to a least-squares fit according to the correlation equation logk(25 degrees C) = s(f)(N-f + E-f), where s(f) and N-f are nucleofuge-specific parameters and Ef is an electrofuge-specific parameter. Although nucleofuges and electrofuges characterized in this way cover more than 12 orders of magnitude, a single set of the parameters, namely s(f), N-f, and E-f, is sufficient to calculate the solvolysis rate constants at 25 degrees C with an accuracy of +/- 16%. Because s(f)approximate to 1 for all nucleofuges, that is, leaving group/ solvent combinations, studied so far, qualitative discussions of nucleofugality can be based on N-f.
引用
收藏
页码:1648 / 1656
页数:9
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