The keto→enol photoisomerization of N‐salicilydenemethylfurylamine: Nonadiabatic ab initio dynamics simulation. Issue 16 (7th May 2018)

• Record Type: Journal Article
• Authors: Gao, Aihua; Wang, Meishan
• Is Part Of: International journal of quantum chemistry. Volume 118:Issue 16(2018)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2018-05-07
• Subjects: aromatic Schiff base -- conical intersection -- dynamics simulations -- keto‐enol photoisomerization -- Zhu–Nakamura theory; Quantum chemistry -- Periodicals; 541.28
• DOI: 10.1002/qua.25656
• Languages: English
• ISSNs: 0020-7608

Abstract

Abstract: The photoinduced isomerization of cis ‐keto and trans ‐keto isomers in N ‐salicilydenemethylfurylamine has been studied using the surface‐hopping approach at the CASSCF level of theory. After the cis ‐keto or trans ‐keto isomer is excited to S 1 state, the molecule initially moves to a excited‐state local minimum. The torsional motion around relative bonds in the chain drives the molecule to approach a keto‐form conical intersection and then nonadiabatic transition occurs. According to our full‐dimensional dynamics simulations, the trans ‐keto and enol photoproducts are responsible for the photochromic effect of cis ‐keto isomer excited to S 1 state, while no enol isomer was obtained in the photoisomerization of trans keto on excitation. The cis keto to enol and cis keto to trans keto isomerizations are reversible photochemical reactions. It is confirmed that this aromatic Schiff base is a potential molecular switch. Furthermore, the torsion of CN bond occurs in the radiationless decay of trans ‐keto isomer, while it is completely suppressed by an intramolecular hydrogen bonding interaction in the dynamics of cis ‐keto form. Moreover, the excited‐state lifetime of cis keto is longer than that of trans ‐keto form due to the O···HN hydrogen bond. Abstract : The photoinduced isomerization of cis ‐keto and trans ‐keto isomers in N ‐salicilydenemethylfurylamine has been studied using the surface‐hopping approach. The trans ‐keto and enol photoproducts are responsible for the photochromic effect of cis ‐keto isomer excited to S 1 state, while no enol isomer was obtained in the photoisomerization of trans keto on excitation. It is suggested that this aromatic Schiff base has potential applications as molecular switch.