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91.
Dmitry I. Bugaenko Alexey A. Volkov Dr. Mikhail V. Livantsov Prof. Dr. Marina A. Yurovskaya Dr. Alexander V. Karchava 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(54):12502-12506
The visible-light-induced arylation of tertiary phosphines with aryl(mesityl)iodonium triflates to produce the quaternary phosphonium salts occurs under mild, metal, and catalyst-free conditions. Photo-excited EDA complexes between diaryliodonium salts and phosphines supposedly enable this transformation, which is difficult to achieve through the traditional ground-state reactions. Demonstrating high functional group tolerance, broad scope, and complete selectivity of the aryl group transfer, the method is particularly compatible with sterically congested phosphines, which are challenging under metal-based catalytic methods. 相似文献
92.
《Journal of polymer science. Part A, Polymer chemistry》2018,56(9):959-967
In this work, a novel synthetic path for preparing semi‐armotic components modified polyamide 6 was developed by caprolactam as solvent of purified terephthalic acid and 1,6‐hexanediamine. First, the ring opening reaction and poly‐addition of caprolactam were initiated by 1,6‐hexanediamine to generate a prepolymer containing amino groups in both ends, then followed by the poly‐condensation reaction with purified terephthalic acid, a long chain copolymer was produced, which the reaction time was reduced by 4 h compared with conventional hydrolytic ring‐opening polymerization of pure caprolactam. By varying the ratio of terephthalic acid and 1,6‐hexanediamine, a series of copolymers with different number average molecular weight and physical properties were prepared. Analytical results showed that the conversion percentage of caprolactam is significantly increased by the proposed method. Furthermore, this new copolymers exhibited excellent transparence and high decomposition temperature. Besides, the copolymers with average molecular weight ≥15,000 present good mechanical properties, making it a potentially useful application in plastics, textile yarn, and membranes. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018 , 56, 959–967 相似文献
93.
S. Karashima 《辐射效应与固体损伤》2013,168(1-3):215-219
Abstract The stopping power and range for Xe ions in high temperature matter (partially ionized plasmas) have been calculated using the dielectric response function method. Calculations have been made for a target matter Al (Z = 13) over a wide range of temperatures and densities considering a finite temperature model. The stopping powers obtained have smaller values in comparison with those of a zero temperature model. The stopping power strongly depends on the density and temperature of the target material, and the projectile ion energy. 相似文献
94.
95.
Xu‐Wen Li Alexandre Ear Lukas Roger Dr. Nassima Riache Alexandre Deville Dr. Bastien Nay 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(48):16389-16393
A bio‐inspired strategy was used to complete the formal synthesis of the antitubercular hirsutellone B and congeners A and C, through construction of its decahydrofluorene core from a linear polyene strand activated at both ends by a silyl enol ether and an allyl acetate. Our synthesis features a key electrophilic cyclization, starting with the remote activation (by [Yb(OTf)3] or BF3 ? OEt2) of the allyl acetate and stereoselectively affording the C ring. This was followed by an intramolecular Diels–Alder reaction to get the tricyclic core of the natural product. The stereoselective reduction of the resulting ketone towards the formal intermediate was critical to the success of this strategy. 相似文献
96.
97.
98.
Hanghang Wang Haiyan Li Yonggao Zheng Pengcheng Lian Prof. Dr. Xiaobing Wan 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(9):2195-2198
In this communication, an unprecedented interception of CnF2n+1(O)SO. radical with a copper-based carbene has been established. Distinguished by wide substrate scopes and mild reaction conditions, this novel radical–carbene coupling reaction (RCC reaction) provides a fundamentally different and mechanistically interesting strategy for the synthesis of perfluoroalkanesulfinate esters. 相似文献
99.
Monika Kořenková Dr. Ing. Martin Hejda Prof. Milan Erben Dr. Ing. Robert Jirásko Prof. Dr. Roman Jambor Prof. Aleš Růžička Dr. Elena Rychagova Prof. Sergey Ketkov Prof. Libor Dostál 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(56):12884-12888
The reaction of N,C,N-chelated stibinidene ArSb ( 1 ) (Ar=C6H3-2,6-(CH=NtBu)2) with selected N-alkyl/aryl-maleimides RN(C(O)CH)2 (R=Me, tBu, Ph) gave the addition products with bridged bicyclic [2.2.1] structure containing an antimony atom at the bridgehead position, fused with a 6-membered benzene and a 5-membered N-alkyl/aryl-pyrrolidine ring. These compounds were completely characterized. More importantly, additional studies showed that these reactions are reversible in solution, thereby representing an unprecedented reversible activation of a C=C bond by an antimony(I) compound. 相似文献
100.
Anwar Jacintomoreno Dr. Hemant K. Sharma Dr. Alejandro Metta-Magaña Prof. Dr. Keith H. Pannell 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(48):11302-11307
The reactions of the Mannich reagent Et3SiOCH2NMe2 ( 1 ) with a variety of anilines (mono-substituted RC6H4NH2, R=H, 4-CN, 4-NO2, 4-Ph, 4-Me, 4-MeO, 4-Me2N; di-substituted R2C6H3NH2, R2=3,5-(CH3)2, 3,5-(CF3)2; tri-substituted R3C6H2NH2, R3=3,5-Me2-4-Br and a “super bulky” aniline (Ar*NH2) [Ar*=2,6-bis(diphenylmethyl)-4-tert-butylphenyl]) led to the formation of a range of products dependent upon the substituent. With electron-withdrawing substituents, previously unknown diamines, RC6H4NH(CH2NMe2) [R=CN ( 2 a ), NO2 ( 2 b )] and R2C6H3NH(CH2NMe2) [R2=3,5-(CF3)2 ( 2 c) ] were formed. Further reaction of 2 a , b , c with 1 yielded the corresponding triamines RC6H4N(CH2NMe2)2 (R=CN ( 3 a ), NO2 ( 3 b ) and R2C6H3N(CH2NMe2)2, R2=3,5-(CF3)2 ( 3 c ). The new polyamines were characterized by NMR spectroscopy, and for 2 a , 2 c , and 3 c , by single crystal XRD. In the case of electron-donating groups, R=4-OMe, 4-NMe2, 4-Me, 3,5-Me2, 3,5-Me2-4-Br, and for R=4-Ph, the reactions with 1 immediately led to the formation of the related 1,3,5-triazines, R=4-MeO ( 5 a ), 4-Me2N ( 5 b ), 4-Me ( 5 c ), 3,5-Me2 ( 5 d ), 3,5-Me2-4-Br ( 5 e ), 4-Ph ( 5 f ), 4-Cl ( 5 g ). The “super bulky” aniline rapidly produced a single product, namely the corresponding imine Ar*N=CH2 ( 4 ) which was also characterized by single crystal XRD. Imine 4 is both thermally and oxidatively stable. All reactions are very fast, thus based upon the presence of Si we are tempted to denote the reactions of 1 as examples of “Silick” chemistry. 相似文献