120837-75-4Relevant academic research and scientific papers
A Dynamic and Responsive Host in Action: Light-Controlled Molecular Encapsulation
Ryan, Seán T. J.,del Barrio, Jesús,Suardíaz, Reynier,Ryan, Daniel F.,Rosta, Edina,Scherman, Oren A.
, p. 16096 - 16100 (2016)
The rational design of a flexible molecular box, oAzoBox4+, incoporating both photochromic and supramolecular recognition motifs is described. We exploit the E?Z photoisomerization properties of azobenzenes to alter the shape of the cavity of t
Conformational changes of DNA by photoirradiation of DNA-bis(Zn II-cyclen)-azobenzene complex
Maie, Kenji,Nakamura, Mitsunobu,Yamana, Kazushige
, p. 453 - 462 (2006)
Bis(ZnII-cyclen)-azobenzene derivative, which has two Zn II-macrocyclic tetraamine complexes connected through azobenzene spacer, has been synthesized as a cross-linking agent for double stranded DNA in aqueous solution. The ZnI
Light-Controlled Regioselective Synthesis of Fullerene Bis-Adducts
Dor?evi?, Luka,Arcudi, Francesca,Baroncini, Massimo,Casimiro, Lorenzo,Credi, Alberto,Demitri, Nicola,Prato, Maurizio,Silvi, Serena
, p. 313 - 320 (2021)
Multi-functionalization and isomer-purity of fullerenes are crucial tasks for the development of their chemistry in various fields. In both current main approaches—tether-directed covalent functionalization and supramolecular masks—the control of regiosel
Electrosynthesis of Azobenzenes Directly from Nitrobenzenes
Ma, Yanfeng,Wu, Shanghui,Jiang, Shuxin,Xiao, Fuhong,Deng, Guo-Jun
, p. 3334 - 3338 (2021/10/29)
The electrochemical reduction strategy of nitrobenzenes is developed. The chemistry occurs under ambient conditions. The protocol uses inert electrodes and the solvent, DMSO, plays a dual role as a reducing agent. Its synthetic value has been demonstrated by the highly efficient synthesis of symmetric, unsymmetric and cyclic azo compounds.
