10403-47-1Relevant articles and documents
Effect of Hydrogen Bond on Second-Order Nonlinear Optical Property of 2-Alkylcarboxamido-4′-methoxy-4-nitrotolan Derivatives
Kato, Midori,Okunaka, Masaaki,Sugita, Nami,Kiguchi, Masashi,Taniguchi, Yoshio
, p. 583 - 585 (1997)
We have synthesized a series of 2-alkylcarboxamido-4′-methoxy-4-nitrotolan derivatives and studied the second-order nonlinear optical properties using the total reflection technique. We measured the infrared absorption spectra of the derivatives and examined the absorption peak of the N-H stretching vibration around 3300 cm-1, which is sensitive to hydrogen bonding. We observed that the peak frequencies of the nonlinear optical active materials were lower than those of the inactive ones, and thus found that for 2-alkylcarboxamido-4′-methoxy-4-nitrotolan derivatives the hydrogen bond plays an important role in activating the second-order optical nonlinearity of the material.
Iridium-catalyzed intramolecular C–N and C–O/S cross-coupling reactions: Preparation of benzoazole derivatives
Shi, Yajie,Zhou, Qifan,Du, Fangyu,Fu, Yang,Du, Yang,Fang, Ting,Chen, Guoliang
supporting information, (2019/09/10)
The irdium-catalyzed intramolecular arylcarbon-hetero cross-coupling reactions with o-haloarylamides or o-haloarylamidine have been effectively achieved using KOAc and just 1 mol% catalyst. The [Ir(cod)Cl]2 was proved to be more potential for smoothly assembling functional structures benzimidazoles, benzoxazoles and benzothiazoles, which was superior to Cu- and Pd-catalyzed systems. Simultaneously, a concise and efficient synthesis of tafamidis was developed in 5-g scale.
Polymer-anchored peroxo compounds of molybdenum and tungsten as efficient and versatile catalysts for mild oxidative bromination
Boruah, Jeena Jyoti,Das, Siva Prasad,Borah, Rupam,Gogoi, Sandhya Rani,Islam, Nashreen S.
, p. 246 - 254 (2013/05/23)
A polymer supported peroxomolybdate(VI) compound of the type [MoO 2(O2)(CN)2]-PAN [PAN = poly(acrylonitrile)] (PANMo) was obtained by reacting H2MoO4 with 30% H 2O2 and the macromolecular ligand, PAN at near neutral pH. The macrocomplex has been characterized by elemental analysis (CHN and EDX analysis), spectral (IR, UV-Vis and 13C NMR, 95Mo NMR), thermal (TGA-DTG) as well as SEM studies. The catalytic activity of PANMo and its previously reported tungsten containing analog PANW, in oxidative bromination of organic substrates has been explored. The supported complexes could serve as efficient heterogeneous catalysts for the oxidative bromination of a variety of structurally diverse aromatic compounds, with H 2O2 as terminal oxidant, to afford bromo organics in impressive yields under environmentally clean conditions. The catalysts afforded regeneration and could be reused for a minimum of six reaction cycles.
Effect of the electronic structure of the radical anions of 4-substituted 1,2-and 1,3-dinitrobenzenes on the regioselectivity of reduction of the nitro groups
Orlov,Begunov,Demidova,Rusakov
, p. 76 - 81 (2007/10/03)
Theoretical and experimental regularities of the regioselectivity of the reduction of one of the two nitro groups in unsymmetrical dinitrobenzenes were studied. It was found that the regioselectivity of the formation of isomeric nitroanilines depends on the structure of the substrate and the nature of the reducing agent. The reduction regioselectivity model was verified, according to which radical anion protonation is the major reaction direction. Pleiades Publishing, Inc. 2006.
