View : 354 Download: 0
Evidence for a Catalytic Six-Membered Cyclic Transition State in Aminolysis of 4-Nitrophenyl 3,5-Dinitrobenzoate in Acetonitrile: Comparative Bronsted-Type Plot, Entropy of Activation, and Deuterium Kinetic Isotope Effects
- Evidence for a Catalytic Six-Membered Cyclic Transition State in Aminolysis of 4-Nitrophenyl 3,5-Dinitrobenzoate in Acetonitrile: Comparative Bronsted-Type Plot, Entropy of Activation, and Deuterium Kinetic Isotope Effects
- Um, Ik-Hwan; Kim, Min-Young; Bae, Ae-Ri; Dust, Julian M.; Buncel, Erwin
- Ewha Authors
- SCOPUS Author ID
- Issue Date
- Journal Title
- JOURNAL OF ORGANIC CHEMISTRY
- JOURNAL OF ORGANIC CHEMISTRY vol. 80, no. 1, pp. 217 - 222
- AMER CHEMICAL SOC
- SCIE; SCOPUS
- Document Type
Show the fulltext
- A kinetic study for reactions of 4-nitrophenyl 3,5-dinitrobenzoate (1a) with a series of cyclic secondary amines in acetonitrile is reported. Plots of the pseudo-first-order rate constant (k(obsd)) vs [amine] curve upward, while those of k(obsd) /[amine] vs [amine] exhibit excellent linear correlations with positive intercepts, indicating that the reaction proceeds through both uncatalyzed and catalyzed routes. Bronsted-type plots for uncatalyzed and catalyzed reactions are linear with beta(nuc) = 1.03 and 0.69, respectively. The Delta H double dagger and Delta S double dagger values measured for the catalytic reaction with morpholine are -0.80 kcal/mol and -61.7 cal/(mol K), respectively. The negative Delta H double dagger with a large negative Delta S double dagger suggests that the reaction proceeds through a highly ordered transition state (i.e., a six-membered cyclic transition state, which includes a second amine molecule that accepts a proton from the aminium moiety of the zwitterionic tetrahedral intermediate and simultaneously donates a proton to the aryloxyl oxygen of the nucleofuge with concomitant C-OAr bond scission). This proposal is consistent with the smaller beta(nuc) value for the catalyzed reaction as compared to the uncatalyzed reaction. An inverse deuterium kinetic isotope effect (DKIE) value of 0.93 and a contrasting normal primary DKIE value of 3.23 for the uncatalyzed and catalyzed routes, respectively, also support the proposed cyclic transition state.
- Appears in Collections:
- 자연과학대학 > 화학·나노과학전공 > Journal papers
- Files in This Item:
There are no files associated with this item.
- RIS (EndNote)
- XLS (Excel)
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.