865623-26-3Relevant academic research and scientific papers
Control of the equilibrium between 2-phosphinoazobenzenes and inner phosphonium salts by heat, solvent, acid, and photoirradiation
Yamamura, Masaki,Kano, Naokazu,Kawashima, Takayuki
, p. 110 - 123 (2012/03/07)
Several 2-phosphinoazobenzenes, which are in equilibrium with inner phosphonium salts, were synthesized. Effects of substituents, solvents, and acidic additives on their equilibria are described. Thermodynamic parameters of the equilibria in various solvents suggest that the acceptor character of the solvents is mainly responsible for the solvent effects. Addition of phenols changed the equilibria depending on their acidity. Substituents at the 4- and 4′-positions of the azobenzene also affected the equilibrium constants, which shifted the equilibrium toward the phosphonium salt in the order of their electron-withdrawing ability. Photoisomerization of the 2-phosphinoazobenzenes bearing electron-donating substituents at the 4- and 4′-positions, which shifted the equilibrium toward the 2-phosphinoazobenzene, proceeded successfully. While the phosphonium salt in equilibrium with the (E)-isomer of the 2-phosphinoazobenzene was protonated by perchlorophenol, the (Z)-isomer did not react with a proton source because it could not take on the form of an inner phosphonium salt. Thus, the properties and reactivity of the inner phosphonium salts in equilibrium with the phosphines can be successfully controlled by photoirradiation.
Thermal and photocontrol of the equilibrium between a 2-phosphinoazobenzene and an inner phosphonium salt
Yamamura, Masaki,Kano, Naokazu,Kawashima, Takayuki
, p. 11954 - 11955 (2007/10/03)
The reversible conversion between a phosphine and a phosphonium salt has been achieved by external stimuli of light and heat. Two 2-phosphinoazobenzenes were successfully synthesized by desulfurization of the corresponding phosphine sulfides. One of the p
