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171.
Krzysztof Ejsmont Jean‐Pierre Joly Emmanuel Wenger Benoit Guillot Christian Jelsch 《Acta Crystallographica. Section C, Structural Chemistry》2009,65(7):o342-o344
The structural model for the title compound, C16H12N2O2, was refined using a multipolar atom model transferred from an experimental electron‐density database. The refinement showed some improvements of crystallographic statistical indices when compared with a conventional spherical neutral‐atom refinement. The title compound adopts a half‐chair conformation. The amide N atom lies almost in the plane defined by the three neighbouring C atoms. In the crystal structure, molecules are linked by weak intermolecular C—H...O and C—H...π hydrogen bonds. 相似文献
172.
Krzysztof Kempa 《固体物理学:研究快报》2013,7(12):1112-1112
In the Letter by K. Kempa, the definitions of two auxiliary constants in Eqs. (10) and (11) were incorrectly given by the author. He now wishes to correct these equations. (© 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
173.
Explicit results of the van der Pauw method for a sample containing an isolated hole are presented together with experimental confirmation. Results of measurements and numerical analysis strongly suggest that four probe resistivities obey inequality similar in the form to the famous van der Pauw equation. The inequality seems to be valid for any sample with an isolated hole and contacts located on the same edge, however rigorous proof is not given. The inequality can be used for experimental detection of the sample quality. 相似文献
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Jacek Ścianowski Zbigniew Rafiński Andrzej Wojtczak Krzysztof Burczyński 《Tetrahedron: Asymmetry》2009,20(24):2871-2879
A convenient method for the synthesis of optically active trans-hydroxyselenides and trans-hydroxydiselenides from the bicyclic terpene group based on the reactions of sodium selenide or sodium diselenide with cis- and trans-(+)-3-carane, trans-(+)-2-carane and (?)-β-pinane epoxides is described. The corresponding cis-hydroxy and cis-methoxydiselenides were obtained in the reaction of sodium diselenide with β-hydroxy- and β-methoxytosylates. The influence of a hydroxy group at the β-position on the diastereomeric ratio of the products of the asymmetric methoxyselenenylation of styrene has been established by composition of the products, crystal structure analyses, and theoretical calculations using a DFT method on the B3LYP level (6-311G(d)). 相似文献
180.
Shin‐Ichi Yamamoto Joanna Pietrasik Krzysztof Matyjaszewski 《Journal of polymer science. Part A, Polymer chemistry》2008,46(1):194-202
Statistical copolymers of di(ethylene glycol) methyl ether methacrylate (MEO2MA) and tri(ethylene glycol) methyl ether methacrylate (MEO3MA) were synthesized by atom transfer radical polymerization (ATRP) providing copolymers with controlled composition and molecular weights ranging from Mn = 8,300–56,500 with polydispersity indexes (Mw/Mn) between 1.19 and 1.28. The lower critical solution temperature (LCST) of the copolymers increased with the mole fraction of MEO3MA in the copolymer over the range from 26 to 52 °C. The average hydrodynamic diameter, measured by dynamic light scattering, varied with temperature above the LCST. These two monomers were also block copolymerized by ATRP to form polymers with molecular weight of Mn = 30,000 and Mw/Mn from 1.12 to 1.21. The LCST of the block copolymers shifted toward the LCST of the major segment, as compared to the value measured for the statistical copolymers at the same composition. As temperature increased, micelles, consisting of aggregated PMEO2MA cores and PMEO3MA shell, were formed. The micelles aggregated upon further heating to precipitate as larger particles. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 194–202, 2008 相似文献