Abstract

Diels Alder reaction is employed to prepare a new cyclic imide. The structure of synthesized cyclic imide (11aR)-2-(2-nitrophenyl)-2,3,5,6,11,11a-hexahydro-1H-6,11-[1,2] benzen-ebenzo [5,6] cyclohepta [1,2-c]pyridine-1,4(4aH)-dione (A3) is characterized by FTIR, Mass, 1D and 2D NMR spectra. Theoretical calculations are performed using density functional theory (DFT) to investigate the possibility of nonlinear optical (NLO) behavior. The NLO properties of the cyclic imide are studied via the calculation of the nonlinear refraction index (NLRI) using diffraction patterns (DPs) and Z-scan. The all-optical switching (AOS) of the prepared cyclic imide is studied using two laser beams.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call