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61.
Dalili S  Yudin AK 《Organic letters》2005,7(6):1161-1164
[reaction: see text] Straightforward methods for palladium-catalyzed alkenylation of aziridines with alkenyl halides and copper-catalyzed alkenylation of aziridines with alkenyl boronic acids have been developed. This methodology offers attractive alternatives to the known methods requiring activated alkenyl halides and acetylenes. A wide variety of N-alkenyl aziridines containing substituents other than electron-withdrawing substituents such as cyano groups and sulfones have been synthesized in good yields. Furthermore, these N-alkenyl aziridines exhibit quite a different reactivity from conventional enamines, as demonstrated by their reactivity.  相似文献   
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[reaction: see text] The combination of diethyl phosphite and DMAP as ligands for nickel in an 8:1 THF-N-ethylpyrrolidinone (NEP) mixture allows a very efficient cross-coupling reaction to be performed between various functionalized arylzinc halides and aryl bromides, triflates and activated chlorides. The reaction proceeds at 25 degrees C within 1-48 h and requires only 0.05 mol % of the nickel catalyst.  相似文献   
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Solid fuels represent one of the most used sources of energy in many countries. In terms of ranking for the coal deposits, Romania occupies the 26th place in the world, and the 11th place in Europe, with reserves of 22 million tones of bituminous coal (BC) and 472 million tones of lignite. The National Bituminous Coal Company extracts the most significant amount of BC from the Jiu Valley area, a Subcharpatian basin in the Parang Mountains. In the present article, the BC extracted from the Livezeni depth mine next to Petro?ani city is investigated from the microstructural, thermal, and kinetic point of view, in comparison with a sample from Ural Mountains in Russia. Scanning electron microscopy, FTIR spectroscopy, and thermal analysis (TG/DSC/DTA in air and inert atmosphere) measurements were performed. The KAS isoconversional kinetic method was applied for the in-depth understanding of thermal decompositions and burning processes that occur. Even if the thermal behavior of the two samples is generally similar, the non-isothermal kinetic study revealed important differences in the pathways of the oxidative decomposition of volatiles and formation of coke. Also, the kinetics of coke burning depends only on the amount of fix carbon, regardless of the provenience of BC.  相似文献   
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Novel semiflexible polyazomethines containing chromophoric units into azomethine mesogenic core have been synthesised by condensation of a flexible dialdehyde with mesogenic diamines containing fluorene, antraquinone, pyrimidine, azobenzene and benzophenone. The thermotropic behaviour of the resulting polyazomethines was assessed by differential scanning calorimetry, polarised light microscopy and investigations of the miscibility relations. While the pure polyazomethines showed a birefringent viscous texture difficult to be ascribed, by mixing with a liquid crystal dimer, clear Schlieren or marbled textures were observed, indicating a nematic mesophase. The polymers exhibited violet, blue or yellow light emission.  相似文献   
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The three‐dimensional (3D) confinement effect on the microphase‐separated structure of a diblock copolymer was investigated both experimentally and computationally. Block copolymer nanoparticles were prepared by adding a poor solvent into a block copolymer solution and subsequently evaporating the good solvent. The 3D structures of the nanoparticles were quantitatively determined with transmission electron microtomography (TEMT). TEMT observations revealed that various complex structures, including tennis‐ball, mushroom‐like, and multipod structures, were formed in the 3D confinement. Detailed structural analysis, showed that one block of the diblock copolymer slightly prefers to segregate into the particle surface compared with the other block. The observed structures were further elaborated using cell dynamics computer simulation. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016 , 54, 1702–1709  相似文献   
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