The Effect of Medium on the a aa a-Effect: Nucleophilic Substitution Reaction of p-Nitrophenyl Diphenyl Phosphinate with Butane-2,3-dione Monoximate and Substituted Phenoxides in Cationic Micelles

Bulletin of the Korean chemical society

Jin-Kyung Limb¹  Ik-Hwan Um¹  Sang-Eun Jeon¹  Seung-Eun Lee¹ 

关键词: The a-effect;    Micellar effect;    Basicity;    Nucleophilicity;    Br©ªnsted equation;   

DOI  :  

学科分类：化学（综合）

来源: Korean Chemical Society

【 摘 要 】

Pseudo-first-order rate constants (k_obs) have been determined for the nucleophilic substitution reactions of p-nitrophenyl diphenyl phosphinate (PNPDPP) with substituted phenoxides (XC₆H₄O - ) and butane-2,3-dione monoximate (Ox^- ) in 0.1 M borate buffer (pH = 10.0) at 25.0 �? 0.1�?. The k_obs value increases sharply upon addition of cethyltrimethylammonium bromide (CTAB) to the reaction medium up to near 7 �? 10^-4 M CTAB and then decreases smoothly upon further addition of CTAB. The rate enhancement upon the addition of CTAB is most significant for the reaction with ^-O₂CC₆H₄O^- and least significant for the one with C₆H₅O^- , indicating that the reactivity of these aryloxides in the presence of CTAB cannot be determined by the basicity alone. The strength of the interaction of these anionic aryloxides with the positively charged micellar aggregates has been suggested to be an important factor to determine the reactivity in the presence of CTAB. The k_obs value for the reaction with Ox^- increases also upon the addition of CTAB. However, the increase in the k_obs value is much more significant for the reaction with Ox^- than for the one with ClC₆H₄O^- , indicating that Ox^- is less strongly solvated than ClC₆H₄O^- in H₂O. The �?-effect shown by Ox^- in H₂O has been attributed to the ground-state solvation difference between Ox^- and ClC₆H₄O^- .

【 授权许可】

Unknown