2015
Synthesis of Photochromic Oligophenylenimines: Optical and Computational Studies, Armando I. Martínez Pérez, Oscar Coreño Alonso, Julián Cruz Borbolla, José M. Vásquez-Pérez, Juan Coreño Alonso, Karina Alemán Ayala, Gabriel Luna-Bárcenas, Thangarasu Pandiyan and Rosa A. Vázquez García, Molecules, 20 (4) (2015), 5440-5455; doi:10.3390/molecules20045440
Abstract
Phenyleneimine oligomers 4,4'-(((1E,1'E)-(((1E,1'E)-(1,4-phenylenebis-(azanylylidene))bis(methanylylidene))bis(2,5-bis(octyloxy)-4,1-phenylene))bis(methanylyl-idene))-bis(azanylylidene))dianiline (OIC1MS) and 7,7'-(((1E,1'E)-(((1E,1'E)-((9H-fluorene-2,7-diyl)bis(azanylylidene))bis(methanylylidene))bis(2,5-bis(octyloxy)-4,1phenylene))bis- (methanylylidene))bis(azanylylidene))bis(9H-fluoren-2-amine) (OIC2MS) were prepared by means of conventional and mechanochemical synthesis and characterized by FT-IR, 1H- and 13C-NMR techniques. The optical properties of the compounds were studied in solution by using UV-visible spectroscopy, and the optical effects were analyzed as a function of solvent. The results show that OIC2MS exhibits interesting photochromic properties. Furthermore, the structural and electronic properties of the compounds were analyzed by TD-DFT. It was found that the mechanosynthesis is an efficient method for the synthesis of both tetraimines.
Study on the intramolecular transannular chalcogentin interactions in dithiastannecine compounds.
Pyrite?Arsenopyrite Galvanic Interaction and Electrochemical Reactivity