Captodative substitution induced acceleration effect towards 4π electrocyclic ring-opening of substituted cyclobutenes. Issue 30 (8th March 2016)

• Record Type: Journal Article
• Authors: Sheikh, Nadeem S.
• Is Part Of: RSC advances. Volume 6:Issue 30(2016)
• Page Start: 25503
• Page End: 25510
• Publication Date: 2016-03-08
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c5ra26590h
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : Significance of quantum chemical calculations as a theoretical tool to identify the optimum substitution pattern for a rapid 4π electrocyclic ring-opening of substituted cyclobutenes is presented. Abstract : The captodative substitution effect towards 4π electrocyclic ring-opening of substituted cyclobutenes is investigated using the B3LYP/6-31+G(d) method. For most of the cases, the activation free energy for the ring-opening of substituted cyclobutenes is lower than for the unsubstituted cyclobutenes and for several captodative substitution patterns, it differs by more than 15.0 kcal mol −1 . The lowest activation energy barrier is computed for trans -3-C(O)CH3 –4-NH2 substituted cyclobutene, which is remarkably 23.7 kcal mol −1 lower than for the unsubstituted cyclobutene. In addition to this, an extra acceleration effect exerted by the captodative substitution is probed through energetic analyses.