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排序方式: 共有525条查询结果,搜索用时 11 毫秒
521.
Y. Satou T. Nakamura N. Fukuda T. Sugimoto Y. Kondo N. Matsui Y. Hashimoto T. Nakabayashi T. Okumura M. Shinohara T. Motobayashi Y. Yanagisawa N. Aoi S. Takeuchi T. Gomi Y. Togano S. Kawai H. Sakurai H.J. Ong T.K. Onishi S. Shimoura M. Tamaki T. Kobayashi H. Otsu Y. Matsuda N. Endo M. Kitayama M. Ishihara 《Physics letters. [Part B]》2008
The neutron-rich carbon isotopes 19,17C have been investigated via proton inelastic scattering on a liquid hydrogen target at 70 MeV/nucleon. The invariant mass method in inverse kinematics was employed to reconstruct the energy spectrum, in which fast neutrons and charged fragments were detected in coincidence using a neutron hodoscope and a dipole magnet system. A peak has been observed with an excitation energy of 1.46(10) MeV in 19C, while three peaks with energies of 2.20(3), 3.05(3), and 6.13(9) MeV have been observed in 17C. Deduced cross sections are compared with microscopic DWBA calculations based on p-sd shell model wave functions and modern nucleon–nucleus optical potentials. Jπ assignments are made for the four observed states as well as the ground states of both nuclei. 相似文献
522.
Tomoya Shinke Mayu Itoh Takuma Wada Assist. Prof. Yuma Morimoto Assoc. Prof. Sachiko Yanagisawa Assoc. Prof. Hideki Sugimoto Prof. Minoru Kubo Prof. Shinobu Itoh 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(59):14730-14737
Mechanistic studies are performed on the alkane hydroxylation with m-CPBA (m-chloroperbenzoic acid) catalyzed by nickel(II) complexes, NiII(L). In the oxidation of cycloalkanes, NiII(TPA) acts as an efficient catalyst with a high yield and a high alcohol selectivity. In the oxidation of adamantane, the tertiary carbon is predominantly oxidized. The reaction rate shows first-order dependence on [substrate] and [NiII(L)] but is independent on [m-CPBA]; vobs=k2[substrate][NiII(L)]. The reaction exhibited a relatively large kinetic deuterium isotope effect (KIE) of 6.7, demonstrating that the hydrogen atom abstraction is involved in the rate-limiting step of the catalytic cycle. Furthermore, NiII(L) supported by related tetradentate ligands exhibit apparently different catalytic activity, suggesting contribution of the NiII(L) in the catalytic cycle. Based on the kinetic analysis and the significant effects of O2 and CCl4 on the product distribution pattern, possible contributions of (L)NiII−O. and the aroyloxyl radical as the reactive oxidants are discussed. 相似文献
523.
Summary: A novel quantitative method using isothermal titration calorimeter (ITC) for the estimation of the distribution of carboxyl groups within polymer particles has been proposed. The method has been employed to clarify the difference in the distribution between the particles prepared by batch emulsion copolymerization of styrene and methacrylic acid under inefficient and efficient stirring conditions. At inefficient stirring, monomer was floating as a layer on the aqueous medium, whereas at efficient stirring, the monomer phase was dispersed as droplets. Under inefficient stirring, methacrylic acid (MAA) polymerized faster than styrene (S) due to a slower diffusion rate of S than MAA into the aqueous medium, while under efficient stirring, S and MAA copolymerized at similar rates. ITC measurement showed that under inefficient stirring, the carboxyl groups were distributed mainly in the center of the particles, and their number decreased toward the surface. On the other hand, under efficient stirring, carboxyl groups were distributed homogeneously inside the particle. 相似文献
524.
Hao K. Shen Kiyoshi Morishita Dr. P. K. Hashim Prof. Dr. Kou Okuro Daiki Kashiwagi Ayumi Kimura Dr. Haruaki Yanagisawa Prof. Dr. Masahide Kikkawa Prof. Dr. Tatsuya Niwa Prof. Dr. Hideki Taguchi Prof. Dr. Takuzo Aida 《Angewandte Chemie (International ed. in English)》2023,62(31):e202304894
Herein, we report an ATP-responsive nanoparticle (GroELNP) whose surface is fully covered with the biomolecular machine “chaperonin protein GroEL”. GroELNP was synthesized by DNA hybridization between a gold NP with DNA strands on its surface and GroEL carrying complementary DNA strands at its apical domains. The unique structure of GroELNP was visualized by transmission electron microscopy including under cryogenic conditions. The immobilized GroEL units retain their machine-like function and enable GroELNP to capture denatured green fluorescent protein and release it in response to ATP. Interestingly, the ATPase activity of GroELNP per GroEL was 4.8 and 4.0 times greater than those of precursor cysGroEL and its DNA-functionalized analogue, respectively. Finally, we confirmed that GroELNP could be iteratively extended to double-layered NP. 相似文献
525.
Prof. Ryo Ohtani Jianeng Xu Dr. Junichi Yanagisawa Yuudai Iwai Takumi Ehara Dr. Kiyoshi Miyata Prof. Ken Onda Dr. Jenny Pirillo Prof. Yuh Hijikata Tomoaki Hiraoka Prof. Shinya Hayami Dr. Benjamin Le Ouay Prof. Masaaki Ohba 《Angewandte Chemie (International ed. in English)》2023,62(32):e202306853
We synthesized a (1-propylpyridinium)2[ReN(CN)4]-type organic–inorganic hybrid exhibiting water-vapor-induced drastic structural changes of the [ReN(CN)4]2− assemblies. Specifically, upon exposure to water vapor, dehydrated nitrido-bridged chains were converted to hydrated cyanido-bridged tetranuclear clusters via rearrangements of large molecular building units in the crystals. These switchable assembly forms display substantially different photo-physical properties, although in both cases the emission is caused by a metal-centered d–d transition. The nitrido-bridged chain exhibited a near-infrared (749 nm) emission, which blue-shifted as the temperature increased, while a visible (561 nm) emission and its red shift was demonstrated by the cyanido-bridged cluster. 相似文献