A computational investigation towards substitution effects on 8π electrocyclisation of conjugated 1,3,5,7-octatetraenes

Nur Hazimah B Z Arfan; Malai Haniti S A Hamid; Nadeem S Sheikh

doi:10.1039/d3ra05127g

A computational investigation towards substitution effects on 8π electrocyclisation of conjugated 1,3,5,7-octatetraenes

RSC Adv. 2023 Oct 20;13(44):30787-30797. doi: 10.1039/d3ra05127g. eCollection 2023 Oct 18.

Authors

Nur Hazimah B Z Arfan¹, Malai Haniti S A Hamid¹, Nadeem S Sheikh¹

Affiliation

¹ Chemical Sciences, Faculty of Science, Universiti Brunei Darussalam Jalan Tungku Link, Gadong BE1413 Brunei Darussalam nadeem.sheikh@ubd.edu.bn.

Abstract

A computational investigation using M06-2X/6-31+G(d) method is reported for the substitution effects on 8π electrocyclisation of conjugated octatetraene. This systematic study describes the mono- and di-substitution effect across the 1,3,5,7-octatetraene skeleton. A general preference of the outward substitution over the inward, at C1 position of the monosubstituted system is observed. However, mesomerically electron donating group (-NH₂ and -OH) display an opposite effect with respect to secondary orbital interaction (SOI) between the lone pair on the substituent and the orbital. A comparative evaluation on the computed activation energies for the 1-, 2-, 3-, and 4-monosubstituted system showed an insignificant impact on the rate of the reaction, in contrast to the electrocyclic ring closure of the unsubstituted compound. Computations of disubstituted system are more pronounced, where a remarkable acceleration is observed for 2-NO₂-7-NO₂ substituted octatetraene at 4.9 kcal mol^-1, and a noticeable deceleration for 4-CH₃-5-CH₃ substituted octatetraene at 25.4 kcal mol^-1 from the parent molecule, 17.0 kcal mol^-1. A visible accelerated effects are commonly exhibited by the substitution on the terminal double bonds (C1, C2, C7, and C8), that are 1,2-, 1,7-, 1,8-, and 2,7-patterns, in regard to the greater orbital interaction for the new σ-bond formation. Despite the unfavourable steric clashes of the substituents in the 1,8-system, an apparent reduction in the energy barrier up to 7.4 kcal mol^-1 is computed for 1-NH₂-8-NO₂ system from 17.0 kcal mol^-1. This is due to the synergistic effect of the electron donor and electron acceptor, enhancing the stability of the transition structure. The electrocyclic ring closure involving vicinal substitution patterns, such as 1,2-, 2,3-, 3,4-, and 4,5-systems are critically dominated by steric crowding between the adjacent functional groups. In certain cases of the 1,2-substituted system, a noticeable accelerated effects are found for 1-NH₂-2-NH₂-substituted compound (9.7 kcal mol^-1) due to an increased in electronic density on the substituted terminal double bond (C1-C2), hence favouring the formation of the new σ-bond.