Structural and electronic properties of 1,2-bis(5-methyl-[2,2′-bithiophen]-4-yl)cyclopent-1-ene in closed form and open form under various external electric field with strengths, 0, 10 × 10−4, 20 × 10−4, 30 × 10−4, 40 × 10−4, and 50 × 10−4 a.u., were studied using the DFT-B3LYP/6-31G* method. As a positive index, structural parameters, length of the photoisomers, and the electronic spatial extents are almost stable at different external electric fields. The UV-Vis electronic spectrum based on time-dependent density functional theory indicated that the HOMO → LUMO transition in the closed form under different electric field strengths is strongly allowed, whereas is very weak in the open form. Electronic response parameters such as the HOMO−LUMO gap, electric dipole moment, and polarizability showed that electric conductivity of the closed form at different field strengths is greater than in the open form. Results of electronic density of states show that at high external electric field, the conductivity of the open form and closed form will be probably equal and switching behavior cannot be observed. Isomerization of the closed form to the open form at different external electric fields can be considered as exothermic and spontaneous.
Solving the self-interaction problem in Kohn–Sham density functional theory: Application to atoms