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排序方式: 共有154条查询结果,搜索用时 717 毫秒
1.
Dr. Yu Harabuchi Dr. Hiroki Hayashi Dr. Hideaki Takano Prof. Tsuyoshi Mita Prof. Satoshi Maeda 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2023,135(1):e202211936
Systematic reaction path exploration revealed the entire mechanism of Knowles's light-promoted catalytic intramolecular hydroamination. Bond formation/cleavage competes with single electron transfer (SET) between the catalyst and substrate. These processes are described by adiabatic processes through transition states in an electronic state and non-radiative transitions through the seam of crossings (SX) between different electronic states. This study determined the energetically favorable SET path by introducing a practical computational model representing SET as non-adiabatic transitions via SXs between substrate's potential energy surfaces for different charge states adjusted based on the catalyst's redox potential. Calculations showed that the reduction and proton shuttle process proceeded concertedly. Also, the relative importance of SET paths (giving the product and leading back to the reactant) varies depending on the catalyst's redox potential, affecting the yield. 相似文献
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Use of atmospheric pressure solids analysis probe time‐of‐flight mass spectrometry to screen for plasticisers in gaskets used in contact with foods 下载免费PDF全文
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A fabrication process for growth of GaN lateral polarity junctions consisting of Ga-polar and N-polar domains grown simultaneously side-by-side on c-plane sapphire was developed using the polarity control scheme. An ammonia-annealing step following deposition and patterning of a thin low-temperature AlN nucleation layer played a crucial role in avoiding mixed-polarity growth of the remaining AlN nucleation layer, as well as in nitriding the bare sapphire surface to facilitate growth of N-polar GaN. The achievement of both polar domains, free from inversion domains within a contiguous domain, led to Ga-polar domain exhibiting featureless morphology with highly resistive characteristics, while N-polar domains exhibited hexagonally faceted morphology and were highly conductive. 相似文献
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Takaaki Takatsuka Hideki Tomita Tetsu Sonoda Volker Sonnenschein Chika Sakamoto Hiroki Mita Takuma Noto Chikara Ito Shigetaka Maeda Tetsuo Iguchi Michiharu Wada Klaus Wendt Iain Moore 《Hyperfine Interactions》2013,216(1-3):41-46
93Nb(n, n′)93mNb reaction allows retrospective estimation of integrated fast neutron dose in nuclear reactor. We proposed isomer-selective trace analysis of 93mNb by Resonance Ionization Mass Spectrometry (RIMS) combined with a gas-jet atomic source and an injection locked Ti:Sapphire laser system operated at several kHz. Resonant ionization spectroscopy of Nb in gas-jet using Ti:Sapphire laser was demonstrated. 相似文献
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Ohne Zusammenfassung 相似文献
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Akio Okamoto Eiichi Watanabe Itaru Mita 《Journal of polymer science. Part A, Polymer chemistry》1979,17(8):2483-2490
The deactivation of α-methylstyryl and styryl carbanions followed by spectral change and titration was studied kinetically. First-order rate constants were obtained for the deactivation of oligo-α-methylstyryl lithium, disodium, and dipotassium in tetrahydrofuran and of polystyryl potassium in varying degrees of polymerization in benzene that contained a small amount of tetrahydrofuran and n-hexane. It was observed that the addition of cryptate [222] exerts a significant effect on the system of oligo-α-methylstyryl disodium in tetrahydrofuran. The effect of dilution, degree of polymerization of the polymer, and counterions on the rate of deactivation of carbanions was discussed. 相似文献
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Normal and second excimer formation has been examined for poly(1-methoxy-4-vinylnaphthalane) (PMVN) in polystyrene solid films as a function of measurement temperature from 420 to 77 K and film casting temperature between 369 and 303 K. It became clear that the conformation of the second excimer forming site is different from that of the normal excimer forming site. The difference in energy between the most stable conformation and the excimer forming site is 2.0 kcal/mol for the normal excimer and less than 1 kcal/mol for the second excimer. Moreover the temperature dependence of the second excimer to monomer intensity ratio is found to give information about Tγ (γ dispersion temperature) of the host polystyrene films, below which the motion of phenyl rings is restricted. 相似文献
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Parallel G-quadruplexes formed from oligonucleotide sequences, d(TTAGn), where n = 3-5, have been shown to form a dimer through end-to-end stacking of 3'-terminal G-tetrads. The monomers and dimers of the G-quadruplexes are in dynamic equilibrium with an exchange rate of approximately 1 s-1. A thermodynamic study demonstrated that the dimerization of the G-quadruplexes is largely enthalpic in origin. 相似文献