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111.
Terao J Kimura K Seki S Fujihara T Tsuji Y 《Chemical communications (Cambridge, England)》2012,48(10):1577-1579
We developed a new method for the synthesis of an organic-soluble insulated molecular wire (IMW) with permethylated cyclodextrin (PMCD); this method involves click polymerization of linked [2]rotaxane containing azide and alkynyl groups at both ends of a π-conjugated guest. 相似文献
112.
Preferentially, c-axis-oriented lithium-doped zinc oxide (ZnO:Li) thin films were prepared on Pyrex borosilicate glass substrates by a sol–gel method starting from zinc acetate dihydrate, lithium chloride, 2-methoxyethanol and monoethanolamine. Decomposition and crystallization behavior of dip-coated amorphous precursor films during post-annealing treatments were investigated by thermogravimetry–differential thermal analysis (TG–DTA), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), optical transmittance measurements, field emission scanning electron microscopy (FESEM) and atomic force microscopy (AFM). It was revealed that the films contained the organic compounds at temperatures up to 300°C, which was the key to the transformation from the amorphous to the crystalline state. Thermodynamical consideration of nucleation and crystal growth was made taking account of surface energies of the film and the glass substrate and an interfacial energy between them. Mechanisms underlying the c-axis orientation were proposed based upon the initial orientation due to nucleation and final growth orientation. 相似文献
113.
Prof. Dr. Kazuhiko Semba Naoto Bessho Prof. Dr. Tetsuaki Fujihara Prof. Dr. Jun Terao Prof. Dr. Yasushi Tsuji 《Angewandte Chemie (International ed. in English)》2014,53(34):9007-9011
Borylative allyl–allyl coupling using allenes, bis(pinacolato)diboron, and allyl phosphates has been developed in the presence of a copper catalyst bearing an N‐heterocyclic carbene ligand. The reaction affords boryl‐substituted 1,5‐diene derivatives in good to high yields with high regioselectivity and Z selectivity. 相似文献
114.
Kazuyuki Torii Atsushi Kawakubo Dr. Xianjin Lin Prof. Dr. Tetsuaki Fujihara Prof. Dr. Tatsuo Yajima Prof. Dr. Yasushi Obora 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(15):4888-4892
A highly regioselective and stereoselective difunctionalization reaction of 1,3-diene with amine and disilane to form C−N and C−Si bonds via a one-step Pd/Cu/O2 system is disclosed. The difunctionalization reaction affords allylic silanes, including the allylic amine moiety, in up to 92 % yield in the absence of any acid, base, or external ligand. The developed synthetic methodology can be scaled to 100 g in high yield with high Z-selectivity, which demonstrates the feasibility of the reaction for industrial applications. 相似文献
115.
116.
Keiko OkuzumiNoriyuki Hara Yoshinori Fujimoto Junko YamadaAtsuko Nakamura Kyoko TakahashiMasuo Morisaki 《Tetrahedron letters》2003,44(2):323-326
Feeding studies of six 13C-labeled sterols, including clerosterol, to hairy roots of Ajugareptans var. atropurpurea have established that clerosterol is a precursor of three phytoecdysteroids, cyasterone, isocyasterone and 29-norcyasterone. 相似文献
117.
118.
Yasumitsu Matsuo Yasuhito Tanaka Junko Hatori Seiichiro Ikehata 《Solid State Communications》2005,134(5):361-365
We have investigated the origin of the change in proton activity in the phase transition at TII-III (=369 K) in Cs3H(SeO4)2 from the viewpoint of its ferroelasticity by using 1H NMR and X-ray measurements. It is found that the second moment of the 1H NMR absorption line rapidly decreases at TII-III with increasing temperature. From this result, we conclude that the hopping motion of a proton, which is the precursor motion in the superprotonic phase, becomes more active above TII-III. This result is consistent with the fact that the electrical conductivity in phase II is larger than that in phase III. Furthermore, it is also found that the spontaneous strain decreases abruptly at TII-III. From these results, it is deduced that the decrease in the spontaneous strain at TII-III causes the increase in the proton activity at TII-III. In addition, it is deduced that the increase in proton activity and the decrease in the spontaneous strain at TII-III are closely related with the appearance of the superprotonic phase transition at TI-II (=456 K). 相似文献
119.
Junko Matsuda Marie T. Vanier Iuliana Popa Jacques Portoukalian Kunihiko Suzuki 《Proceedings of the Japan Academy. Series B, Physical and biological sciences》2006,82(6):189-196
Gangliosides in the brain of the knockout mouse deficient in the activity of β1,4 N-acetylgalactosaminyl transferase (β1,4 GalNAc-T)(GM2 synthase) consisted of nearly exclusively of GM3- and GD3-gangliosides as expected from the known substrate specificity of the enzyme and in confirmation of the initial reports from two laboratories that generated the mutant mouse experimentally. The total molar amount of gangliosides was approximately 30% higher in the mutant mouse brain than that in the wild-type brain. However, contrary to the initial reports, one-fourth of total GD3-ganglioside was O-acetylated. It reacted positively with an anti-O-acetylated GD3 monoclonal antibody and disappeared with a corresponding increase in GD3-ganglioside after mild alkaline treatment. The absence of O-acetylated GD3 in the initial reports can be explained by the saponification step included in their analytical procedures. Although quantitatively much less and identification tentative, we also detected GT3 and O-acetylated GT3. Anti-GD3 and anti-O-acetylated GD3 monoclonal antibodies gave positive reactions in the brain of mutant mouse as expected from the analytical results. Either antibody barely stained wild-type brain except for immunoreactivity of GD3 in the cerebellar Purkinje cells. The distributions of GD3 and O-acetylated GD3 in the brain of mutant mouse were similar but differential localization was noted in the cerebellar Purkinje cells and cerebral cortex. 相似文献
120.
The fundamental properties and extraction capability of an ionic liquid (IL), trioctylammonium nitrate ([HTOA][NO3]), for PdII and PtIV, are investigated. At room temperature, [HTOA][NO3] is a solid (melting point: 30.7 °C), but it becomes a liquid (melting point: 16.7 °C) when saturated with water. Water-saturated [HTOA][NO3] exhibits a viscosity of 267.1 mPa·s and an aqueous solubility of 2.821?×?10?4 mol·dm?3 at 25 °C, and can be used as an extraction solvent without dilution. [HTOA][NO3] exhibits an extremely high extraction capability for PdII and PtIV in dilute hydrochloric acid (0.1–2 mol·dm?3 HCl); the distribution ratio reaches 3 × 104 for both the metals. From electrospray ionization mass spectrometry analysis, the species extracted in the IL phase are [PdCl3]? and [PdCl2(NO3)]? for PdII and [PtCl6]2? and [PtCl5]? for PtIV. A majority of the other transition metals are considerably less or marginally extracted into [HTOA][NO3] from a 0.1 mol·dm?3 hydrochloric acid solution. The extraction capacity of [HTOA][NO3] is greater than that of other hydrophobic ILs such as [HTOA]Cl and bis(trifluoromethanesulfonyl)imide-based ILs. The metals extracted into the IL phase are quantitatively back-extracted using an aqueous solution containing thiourea and nitric acid. By controlling the thiourea concentration and shaking time, PdII and PtIV are mutually separated to some extent in the back extraction process. The IL phase used for the back extraction can be reused for the forward extraction of these metals after scrubbing it with an aqueous nitric acid solution. 相似文献