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111.
In the presence of zeolites, moderately deactivated arenes such as 1-nitronaphthalene, naphthonitriles, and methylated benzonitriles can be smoothly nitrated at room temperature by the combined action of nitrogen dioxide and molecular oxygen. The regioselectivity is considerably improved as compared with the conventional nitration methodology based on nitric and sulfuric acids. In some cases, the minor isomer became favoured to a significant extent, resulting in the reversal of ordinary isomer ratios of nitration products. 相似文献
112.
113.
Yasuo Koma Naoyuki Koide Akira Tanaka Kazuyoshi Iimura Masatami Takeda 《Journal of polymer science. Part A, Polymer chemistry》1979,17(2):465-471
The complex of acrylonitrile (AN) with trimethylaluminum (AlMe3) was successfully isolated as a white needlelike crystal with a melting point of 42.5°C. In this article the preparation of the complex is described in detail. Cryoscopic and spectral investigations indicated that the complex is formed by an equimolar ratio of AN and AlMe3. From the measurement of the x-ray diffraction photograph of the crystal the repeat period was determined to be 9.47 ± 0.05 Å. 相似文献
114.
115.
Onodera Risako Sakai Aiko Tokuda Azumi Higashi Taishi Motoyama Keiichi 《Journal of inclusion phenomena and macrocyclic chemistry》2022,102(1-2):143-149
Journal of Inclusion Phenomena and Macrocyclic Chemistry - Among gynaecological cancers, ovarian cancer is known to be highly sensitive to chemotherapy. However, it is often detected at an advanced... 相似文献
116.
117.
In this article, we consider the maximum cocliques of the 211: M24 ‐graph Λ. We show that the maximum cocliques of size 24 of Λ can be obtained from two Hadamard matrices of size 24, and that there are exactly two maximum cocliques up to equivalence. We verify that the two nonisomorphic designs with parameters 5‐(24,9,6) can be constructed from the maximum cocliques of Λ, and that these designs are isomorphic to the support designs of minimum weights of the ternary extended quadratic residue and Pless symmetry [24,12,9] codes. Further, we give a new construction of Λ from these 5‐(24,9,6) designs. © 2009 Wiley Periodicals, Inc. J Combin Designs 17: 323–332, 2009 相似文献
118.
Koji Ishizu Naoyuki Kobayakawa Satoshi Takano Yoko Tokuno Masaaki Ozawa 《Journal of polymer science. Part A, Polymer chemistry》2007,45(9):1771-1777
The crosslinked polystyrene particles possessing photofunctional N,N‐diethyldithiocarbamate groups on their surface were prepared by free‐radical emulsion copolymerization of a mixture of styrene, divinylbenzene and 4‐vinylbenzyl N,N‐diethyldithiocarbamate with redox system as an initiator under UV irradiation. In this copolymerization, the inimer 4‐vinylbenzyl N,N‐diethyldithiocarbamate acted the formation of hyperbranched structures by living radical photopolymerization. The particle sizes (number‐average particle diameter = 214–523 nm) were controlled by varying the feed amount of surfactant and size distributions were relatively narrow. Subsequently, core–shell particles were synthesized by photoinduced atom transfer radical polymerization approach of methyl methacrylate initiated by photofunctional polystyrene particles as a macroinitiator. Such core–shell particles were stabilized sterically by grafted chains in organic solvents. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 1771–1777, 2007 相似文献
119.
Dr. Naoyuki Toriumi Kazuya Yamashita Prof. Dr. Nobuharu Iwasawa 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(49):12635-12641
A metal-free photoredox-catalyzed hydrodefluorination of fluoroarenes was achieved by using N,N,N’,N’-tetramethyl-para-phenylenediamine ( 1 ) as a strong photoreduction catalyst. This reaction was applicable not only to electron-rich monofluoroarenes but also to polyfluoroarenes to afford non-fluorinated arenes. The experimental mechanistic studies indicated that the amide solvent NMP plays an important role for regeneration of the photocatalyst, enabling additive-free photoreduction catalysis. 相似文献