Abstract
A new Schiff base compound 4((o-tolylimino)methyl)-3-methyl-1-phenyl-1H-pyrazol-5-ol(4TM-MPP) was synthesized and characterized by elemental analyses, LC-MS, FTIR, and 1H-NMR spectra. The compound exhibits photochromic property under 365 nm UV-light irradiation, which can be observed with solid state reflectance spectra. It suggests that the photoisomerization is due to photoinduced intermolecular hydrogen bond, which results in enol to keto transformation. The chemionics study is carried out using (Ni+2, H+), (Ag+, H+), and (Na+, H+, and OH−) using the UV absorption spectra in solution, which shows logic behavior of INHIBIT, NOR, and XOR, respectively.
Sign-in/Register to access full text options 
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
