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21.
Dr. Toshiro Takao Dr. Yuta Takahashi Masataka Kai 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(29):e202200327
A dicationic triruthenium complex containing a μ3-η3-C3 ring, [(Cp*Ru)3(μ3-η3-C3MeH2−)(μ3-CH)(μ-H)]2+ ( 1 a , Cp*=η5-C5Me5), reacted with ammonia to yield a μ-amido complex, [(Cp*Ru)3(μ3-η3-CHCMeCH) (μ3-CH)(μ-NH2)]2+ ( 5 ), via N−H bond scission. Subsequent treatment with base resulted in C−N bond formation to yield a μ3-η2:η2-1-azabutadien-4-yl complex, [(Cp*Ru)3(μ3-CH)(μ3-η2:η2-NH=CH−CMe=CH−)]+ ( 6 a ). The azaruthenacyclopentadiene skeleton was alternatively synthesized by the photolysis of mono-cationic complex [(Cp*Ru)3(μ3-η3-C3RH2−)(μ3-CH)]+ ( 2 a ; R=Me, 2 b ; R=H) in the presence of ammonia. The C3 ring skeleton was broken via the electron transfer to the π*(C−C) orbital in the C3 ring, and a transiently generated unsaturated μ3-allylic species can take up ammonia, resulting in N−H bond scission followed by C−N bond formation. 相似文献
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Polymerization of optically active disubstituted acetylene monomers by Pd catalyst bearing bulky phosphine ligand 下载免费PDF全文
Yuta Goto Yu Miyagi Natsuhiro Sano Fumio Sanda 《Journal of polymer science. Part A, Polymer chemistry》2017,55(18):3011-3016
Chloro- and aryl-substituted acetylene monomers having an optically active group were polymerized by a Pd catalyst [(tBu3P)PdMeCl] bearing a bulky phosphine ligand, and by MoCl5 for comparison. The corresponding disubstituted acetylene polymers with Mn's = 2000–19,500 and 6900–10,800 were obtained in 29–83% and 11–62% yields when the Pd and Mo catalysts were used, respectively. The formation of polyacetylenes, poly[(R)- 1p ], poly[(R)- 1m ], and poly[(S)- 2p ] were confirmed by SEC and the presence of a Raman scattering peak based on the alternating double bonds of the main chain. Pd-based poly[(R)- 1m ] exhibited CD signals around 350 nm assignable to a certain secondary structure, while Mo-based poly[(R)- 1m ] did not. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 3011–3016 相似文献
24.
Yuta Yamamoto Shogo Nakano Fumio Seki Yasuteru Shigeta Sohei Ito Hiroaki Tokiwa Makoto Takeda 《Molecules (Basel, Switzerland)》2021,26(5)
Infection of hosts by morbilliviruses is facilitated by the interaction between viral hemagglutinin (H-protein) and the signaling lymphocytic activation molecule (SLAM). Recently, the functional importance of the n-terminal region of human SLAM as a measles virus receptor was demonstrated. However, the functional roles of this region in the infection process by other morbilliviruses and host range determination remain unknown, partly because this region is highly flexible, which has hampered accurate structure determination of this region by X-ray crystallography. In this study, we analyzed the interaction between the H-protein from canine distemper virus (CDV-H) and SLAMs by a computational chemistry approach. Molecular dynamics simulations and fragment molecular orbital analysis demonstrated that the unique His28 in the N-terminal region of SLAM from Macaca is a key determinant that enables the formation of a stable interaction with CDV-H, providing a basis for CDV infection in Macaca. The computational chemistry approach presented should enable the determination of molecular interactions involving regions of proteins that are difficult to predict from crystal structures because of their high flexibility. 相似文献
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Mark Kristan Espejo Cabello Dr. Yuta Uetake Dr. Yu Yao Prof. Dr. Susumu Kuwabata Prof. Dr. Hidehiro Sakurai 《化学:亚洲杂志》2021,16(16):2280-2285
An aqueous colloidal dispersion of Pt nanoparticles (NPs) stabilized by fullerenol C60(OH)12 (Pt:C60(OH)12) was successfully synthesized via liquid-phase chemical reduction. The subsequent pyrolysis of Pt:C60(OH)12 at different temperatures was conducted to afford Pt-doped carbon with different chemical compositions (Pt:C60n). X-ray absorption spectroscopy (XAS) and Infrared (IR) absorption spectroscopy and thermogravimetric measurements revealed that the thus-prepared nanocomposite consists of Pt NPs and high valent Pt-C60(OH)12 complex. One distinct feature of C60(OH)12 matrix as catalyst support is the suppression of size growth of Pt NPs during the pyrolysis up to 300 °C. Electrochemical experiments using cyclic voltammetry (CV) and linear sweep voltammetry (LSV) were performed to find that Pt:C60300 (pyrolyzed at 300 °C) exhibited higher activity than others, that was attributed to the π-extended feature of the as-obtained carbon. 相似文献
27.
Yuta Hirosawa Hiroaki Imoto Kensuke Naka 《Journal of polymer science. Part A, Polymer chemistry》2024,62(3):564-571
Cage silsesquioxanes, also known as polyhedral oligomeric silsesquioxanes (POSS), serve as crucial building blocks in crafting precisely designed organic–inorganic hybrid materials, given that their well-defined silsesquioxane clusters can be adorned with organic substituents. While polymers with POSS in their main chains have been thoroughly examined, analyzing the correlation between cage structure and material properties in main-chain-type polymers remains challenging. This difficulty stems from the limited range of organic substituents on traditional POSS monomers, thereby precluding comparisons between polymers with unified substituents and different cage structures. In this study, we synthesized double-decker silsesquioxane (DDSQ) and side-opened POSS (SO-POSS) monomers, both featuring phenyl groups. Subsequent platinum-catalyzed hydrosilylation polymerization yielded main-chain-polymers. Both the cage and linker structures influence thermal stability and the glass transition temperature, while the hardness was primarily determined by the linker structure. This research is the first to elucidate the impact of cage structure on the material properties of main-chain-type POSS polymers. 相似文献
28.
Prof. Dr. Michio Yamada Yuta Uokawa Shino Sasaki Naohiro Iha Yoshihisa Hashimoto Yuya Nagasaki Prof. Dr. Yutaka Maeda Prof. Dr. Mitsuaki Suzuki 《European journal of organic chemistry》2023,26(35):e202300633
The physicochemical properties of fullerene-based materials typically vary depending on the type and mode of addition of functional groups; therefore, developing fullerene derivatives with novel structures is imperative for further progress in materials science. In this study, we develop an efficient one-step strategy for synthesizing cyclobutene-annulated fullerene derivatives (cyclobutenofullerenes) and characterize their electronic properties. Despite the steric strain, cyclobutenofullerenes can be easily prepared via a one-step reaction of C60 with a secondary propargylic phosphate. Structural analysis of the reaction intermediates suggests that the cascade reaction proceeds through a formal [2+2] cycloaddition of C60 with an allene, caused by the 1,3-migration of the propargylic phosphate, followed by an additional 1,3-migration and the subsequent 1,2-elimination of the phosphodiester moiety. 相似文献
29.
Formation of iminophosphoranes from tetrazolopolyazines and triphenylphosphine has been studied kinetically in various solvents, and the mechanism explained as nucleophilic attack of the phosphine moiety on the trazolo ring. In the equilibrium system of tetrazolopolyazine (9) and azidopyrazine (9a) in chloroform, it is concluded that tetrazolo and azido moieties react competitively with triphenylphosphine. The mechanism of the reaction of tetrazolopolyazines with triphenylphosphine in chloroform is discussed on a phosphinium radical cation intermediate proposed. 相似文献
30.
Ambrose D Arroyo C Bachman M Connor D Eckhause M Graessle S Hancock AD Hartman K Hebert M Hoff CH Hoffmann GW Irwin GM Kane JR Kanematsu N Kuang Y Lang K Lee R Martin RD McDonough J Milder A Molzon WR Pommot-Maia M Riley PJ Ritchie JL Rubin PD Vassilakopoulos VI 《Physical review letters》2000,84(7):1389-1392
We report results from Experiment 871, performed at the BNL AGS, of a measurement of the branching ratio K(0)(L)-->&mgr;(+)&mgr;(-) with respect to the CP-violating mode K(0)(L)-->pi(+)pi(-). This experiment detected over 6200 candidate &mgr;(+)&mgr;(-) events, a factor of 6 more than that seen in all previous measurements combined. The resulting branching ratio gamma(K(0)(L)-->&mgr;(+)&mgr;(-))/gamma(K(0)(L)-->pi(+)pi(-)) = (3. 474+/-0.057)x10(-6) leads to a branching fraction B(K(0)(L)-->&mgr;(+)&mgr;(-)) = (7.18+/-0.17)x10(-9), which is consistent with the current world average, and reduces the uncertainty in this decay mode by a factor of 3. 相似文献