排序方式: 共有101条查询结果,搜索用时 46 毫秒
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Tsubasa Matsumoto Hiromitsu Kato Norio Tokuda Toshiharu Makino Masahiko Ogura Daisuke Takeuchi Hideyo Okushi Satoshi Yamasaki 《固体物理学:研究快报》2014,8(2):137-140
The contact resistance between heavily phosphorus doped n‐type (n+‐type) diamond (111) layers and graphite electrodes was investigated. To analyze the contact resistance properties in detail in the low‐voltage region, the transfer length method including nonlinear terms with a constant current was analyzed based on the double Schottky contact configuration. Using this method, we have revaluated the metal contact resistance reported previously. Using the graphite electrodes, the linearity of current‐voltage characteristics was improved. The contact resistance was reduced by a factor of ten compared to that of conventional Ti/Pt/Au electrodes. The graphite electrodes were formed directly by thermal annealing at 1300 °C for 10 min from an n+‐type diamond surface. (© 2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
84.
Symmetric quantum games for 2-player, 2-qubit strategies are analyzed in detail by using a scheme in which all pure states in the 2-qubit Hilbert space are utilized for strategies. We consider two different types of symmetric games exemplified by the familiar games, the Battle of the Sexes (BoS) and the Prisoners’ Dilemma (PD). These two types of symmetric games are shown to be related by a duality map, which ensures that they share common phase structures with respect to the equilibria of the strategies. We find eight distinct phase structures possible for the symmetric games, which are determined by the classical payoff matrices from which the quantum games are defined. We also discuss the possibility of resolving the dilemmas in the classical BoS, PD, and the Stag Hunt (SH) game based on the phase structures obtained in the quantum games. It is observed that quantization cannot resolve the dilemma fully for the BoS, while it generically can for the PD and SH if appropriate correlations for the strategies of the players are provided. 相似文献
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Dr. Yasuhiro Yamashita Dr. Hirotsugu Suzuki Io Sato Tsubasa Hirata Prof. Dr. Shū Kobayashi 《Angewandte Chemie (International ed. in English)》2018,57(23):6896-6900
Catalytic addition reactions of very weakly acidic nonactivated alkylarenes such as toluene and its derivatives were developed by using a strongly basic mixed catalyst system under mild reaction conditions. The addition reactions with imines and alkenes proceeded smoothly under proton‐transfer conditions to afford the desired products in good to high yields, and high levels of regio‐ and stereoselectivity were achieved. It was also revealed that the asymmetric addition reaction of an alkylarene was possible. 相似文献
86.
Molecular Recognition by a Short Partial Peptide of the Adrenergic Receptor: A Bottom‐Up Approach
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Tsubasa Sekiguchi Masato Tamura Hikari Oba Dr. Pierre Çarçarbal Dr. Rolando Rafael Lozada‐Garcia Prof. Dr. Anne Zehnacker‐Rentien Dr. Gilles Grégoire Prof. Dr. Shun‐ichi Ishiuchi Prof.Dr. Masaaki Fujii 《Angewandte Chemie (International ed. in English)》2018,57(20):5626-5629
Receptor–neurotransmitter molecular recognition is key for neurotransmission. Although crystal structures of the receptors are known, the mechanism for recognition is not clear. Reported here is the ultraviolet (UV) and infrared (IR) spectra of complexes between a partial peptide (SIVSF), mimicking the binding motif of a catechol ring in the adrenergic receptor, and various ligands. The UV spectra show that two isomers coexist in the complex of SIVSF with properly recognized ligands, such as protonated adrenaline (adrenalineH+). From IR spectra, they are assigned to catechol‐ and amino‐bound structures. The catechol‐bound structure is not observed when the ligand is replaced by nonproper molecules, such as noradrenalineH+. The results suggest that SIVSF not only recognizes the catechol ring but can distinguish differences in the amine side chain. The method provides a new possibility for screening molecules as potential therapeutics for activating the receptor. 相似文献
87.
Inside Cover: Molecular Recognition by a Short Partial Peptide of the Adrenergic Receptor: A Bottom‐Up Approach (Angew. Chem. Int. Ed. 20/2018)
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Nanami Uemura Tsubasa Kobayashi Shintaro Yoshida Ya‐xin Li Karel Goossens Xiangbing Zeng Go Watanabe Takahiro Ichikawa 《Angewandte Chemie (International ed. in English)》2020,59(22):8445-8450
We report a new molecular‐design principle for creating double‐gyroid nanostructured molecular assemblies based on atropisomerization. Ionic amphiphiles containing two imidazolium rings close to each other were designed and synthesized. NMR data revealed that the rotation of the imidazolium rings is restricted, with an activation energy as high as 63 kJ mol?1 in DMSO‐d6 solution (DFT prediction for a model compound in the vacuum: 90–100 kJ mol?1). Due to the restricted rotation, the amphiphiles feature “double” atropisomeric axes in their ionic segments and form three stable atropisomers: meso, R, and S. These isomers co‐organize into ‐type bicontinuous cubic liquid‐crystalline mesophases through nanosegregation of the ionic and non‐ionic parts. Considering the intrinsic characteristic of ‐type bicontinuous cubic structures that they are composed of intertwined right‐ and left‐handed single gyroids, we propose that the simultaneous presence of both R‐ and S‐atropisomers is an important contributor to the formation of double‐gyroid structures. 相似文献
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Minato Egashira Yuji Yamamoto Tsubasa Fukutake Nobuko Yoshimoto Masayuki Morita 《Journal of fluorine chemistry》2006,127(9):1261-1264
A new method for the preparation of substituted imidazolium tetrafluoroborate salt, some of which are known as versatile room temperature ionic liquids, is proposed. The new method based on N-methylation of imidazole provided tetrafluoroborate derivatives containing no counterions, with shorter time and lower cost than conventional ion-exchange method. 相似文献
90.
Enantiodivergent Atroposelective Synthesis of Chiral Biaryls by Asymmetric Transfer Hydrogenation: Chiral Phosphoric Acid Catalyzed Dynamic Kinetic Resolution
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Prof. Dr. Keiji Mori Tsubasa Itakura Prof. Dr. Takahiko Akiyama 《Angewandte Chemie (International ed. in English)》2016,55(38):11642-11646
Reported herein is an enantiodivergent synthesis of chiral biaryls by a chiral phosphoric acid catalyzed asymmetric transfer hydrogenation reaction. Upon treatment of biaryl lactols with aromatic amines and a Hantzsch ester in the presence of chiral phosphoric acid, dynamic kinetic resolution (DKR) involving a reductive amination reaction proceeded smoothly to furnish both R and S isomers of chiral biaryls with excellent enantioselectivities by proper choice of hydroxyaniline derivative. This trend was observed in wide variety of substrates, and various chiral biphenyl and phenyl naphthyl adducts were synthesized with satisfactory enantioselectivities in enantiodivergent fashion. The enantiodivergent synthesis of synthetically challenging, chiral o‐tetrasubstituted biaryls were also accomplished, and suggests high synthetic potential of the present method. 相似文献