Loos Robert, Kobayashi Shinjiro, Mayr Herbert
Department Chemie der Ludwig-Maximilians-Universität München, Butenandtstrasse 5-13 (Haus F), D-81377 Münich, Germany.
J Am Chem Soc. 2003 Nov 19;125(46):14126-32. doi: 10.1021/ja037317u.
Laser flash photolysis and stopped-flow methods have been employed to determine the kinetics of the reactions of benzhydrylium ions with both termini of the thiocyanate ion. In contrast to previous investigations which reported sulfur/nitrogen ratios of k(S)/k(N) = 2-10 for the reactions of carbocations with SCN(-), values of k(S)/k(N) = 10(3)-10(4) are now derived from absolute rate constants. This discrepancy is explained by the fact that the data determined in this investigation are the first which refer to activation-controlled attack of carbocations at both termini of the thiocyanate ion, while previous reactivity ratios included diffusion-controlled reactions. It is concluded that the selectivities of the reactions of carbocations with the thiocyanate ion cannot be explained by the hard soft acid base principle.
采用激光闪光光解和停流方法来测定二苯甲基离子与硫氰酸根离子两端的反应动力学。与之前报道碳正离子与SCN(-)反应的硫/氮比率k(S)/k(N)=2 - 10的研究不同,现在从绝对速率常数得出k(S)/k(N)=10³ - 10⁴的值。这种差异的解释是,本研究中确定的数据是首次涉及碳正离子对硫氰酸根离子两端的活化控制进攻,而之前的反应活性比率包括扩散控制反应。得出的结论是,碳正离子与硫氰酸根离子反应的选择性不能用硬软酸碱原理来解释。