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排序方式: 共有239条查询结果,搜索用时 25 毫秒
1.
Li-Ngee Ho Tasuku Ikegawa Hiroyasu Nishiguchi Katsutoshi Nagaoka Yusaku Takita 《Applied Surface Science》2006,252(18):6260-6268
A synthesis of molybdenum incorporated mesoporous aluminophosphate with long-chain n-alkylamine as template material had been prepared under non-aqueous condition. These materials were extensively characterized by using X-ray diffraction (XRD), nitrogen sorption isotherms, nuclear magnetic resonance of 27Al and 31P (NMR), inductive coupled plasma (ICP), electron spin resonance (ESR), Fourier transform infrared (FTIR) and thermogravimetric-differential thermal analysis (TG-DTA). Morphology of the materials had been observed by using transmission electron microscope (TEM) that revealed the mesoporous materials possessed wormhole-like structures. Alkaline solvent extraction using n-butylamine/ethanol had been efficiently removed the n-alkylamine from the mesoporous samples which yielded BET surface areas around 550-730 m2/g. BJH analysis showed a narrow pore size distribution which increased with increasing of the carbon chain length of alkylamine (template). Valence state and coordination of the molybdenum in the obtained samples were investigated by using ESR and FTIR where it was found that Mo4+ and Mo6+ molybdenum species existed in the molybdenum incorporated mesoporous aluminophosphate in tetrahedral coordination. 相似文献
2.
D. Kawamura A. Takita Y. Hayasaki N. Nishida 《Applied Physics A: Materials Science & Processing》2006,85(1):39-43
The morphology of a glass surface having a transparent coating processed with focused femtosecond laser pulses is investigated. The transparent coating is formed of poly-methyl methacrylate (PMMA). When the glass was coated with a PMMA film with a thickness of 2.8 μm, bumps were formed over a wide range of axial focus positions. The same laser pulse energy produced cavities when processing bare glass with no coating. The bumps were formed as a result of suppressing material emission from the glass surface by a shielding effect of plasma generated by ablation of the PMMA film and by physical blocking of the PMMA film. A thinner film with a thickness of 0.7 μm produced a reduced shielding effect, forming an exploded bump with a small pit at its center and debris around the periphery. PACS 44.10.+i; 61.80.Ba; 79.20.Ds 相似文献
3.
Hiroyasu Nishiguchi Hiroshi Yamada Masaru Ogura Tatsumi Ishihara Yusaku Takita 《Research on Chemical Intermediates》2003,29(7-9):755-760
The oxygen storage capacity of CeO2, Ce0.9Pr0.1O2, Pt?Rh/CeO2 and Pt?Rh/Ce0.9Pr0.1O2 was investigated by conventional GC pulse method and transient pulse techniques. It is shown that incorporation of PrOy into CeO2 matrix strongly promotes oxygen storage capacity (OSC) measured using the transient pulse technique. The improvement of OSC at low temperature is observed in Pt?Rh loaded onto CeO2 and Ce?Pr catalysts. 相似文献
4.
Dedicated to Professor John C. Sheehan on the occasion of his sixty-fifth birthday. Chemical and biological modifications of bleomycin, an antitumor glycopeptide antibiotic, have been achieved by three procedures analogous to the modifications of penicillin. 相似文献
5.
6.
T. Ishihara K. Nishida H. Nishiguchi Y. Takita K. Chaki 《Research on Chemical Intermediates》2006,32(3-4):253-262
A new reforming process was studied using Ni/SiO2 with a hydrogen-permeating membrane reactor. Nickel catalyst supported on SiO2 is highly active for CH4?H2O?O2 reaction in membrane reactor and the reaction close to CH4+0.35O2+1.3H2O→CO2+3.3H2 proceeds at 873 K. Since the selectivity to carbon and CO2 increased and decreased with decreasing contact time respectively, it is considered that the reaction was started by decomposition of CH4 followed by oxidation of C and water shift reaction. Therefore, the reaction mechanism was different from so-called autothermal reforming (ATR) reaction. 相似文献
7.
Hamao Umezawa Tomohisa Takita Yukio Sugiura Masami Otsuka Susumu Kobayashi Masaji Ohno 《Tetrahedron》1984,40(3):501-509
Biosynthetic intermediates and synthetic analogues of bleomycin (BLM) have been investigated for their metal binding, dioxygen activation, and DNA cleavage. Molecular O2 was activated by the Fe(II) complex of a synthetic model ligand. Nucleotide sequence specificities in DNA cleavage by the BLM-Fe(II) and deglyco-BLM-Fe(II) complexes were almost identical. It has been shown that (1) the β-aminoalanine-pyrimidine-β-hydroxyhistidine portion of BLM is essential for the metal binding and dioxygen activation and (2) the bithiazole moiety contributes to the specific binding to guanine base of DNA. 相似文献
8.
Transition of the radial electric field by electron cyclotron heating in the CHS heliotron/torsatron
9.
Majima K Takita R Okada A Ohshima T Shibasaki M 《Journal of the American Chemical Society》2003,125(51):15837-15845
We describe the development of a general catalytic asymmetric Michael reaction of acyclic beta-keto esters to cyclic enones, in which asymmetric induction occurs at the beta-position of the acceptors. Among the various asymmetric catalyst systems examined, the newly developed La-NR-linked-BINOL complexes (R = H or Me) afforded the best results in terms of reactivity and selectivity. In general, the NMe ligand 2 was suitable for the combination of small enones and small beta-keto esters, and the NH ligand 1 was suitable for bulkier substrates (steric tuning of the catalyst). Using the La-NMe-linked-BINOL complex, the Michael reaction of methyl acetoacetate (8a) to 2-cyclohexen-1-one (7b) gave the corresponding Michael adduct 9ba in 82% yield and 92% ee. The linker heteroatom in linked-BINOL is crucial for achieving high reactivity and selectivity in the Michael reaction of beta-keto esters. The amine moiety in the NR-linked-BINOL can also tune the Lewis acidity of the central metal (electronic tuning of the catalyst), which was supported by density functional studies and experimental results. Another advantage of the NR-linked-BINOL ligand as compared with O-linked-BINOL is the ease of modifying a substituent on the amine moiety, making it possible to synthesize a variety of NR-linked-BINOL ligands for further improvement or development of new asymmetric catalyses by introducing additional functionality on the linker with the amine moiety. The efficiency of the present asymmetric catalysis was demonstrated by the synthesis of the key intermediate of (-)-tubifolidine and (-)-19,20-dihydroakuammicine in only five steps compared to the nine steps required by the original process from the Michael product of malonate. This strategy is much more atom economical. On the basis of the results of mechanistic studies, we propose that a beta-keto ester serves as a ligand as well as a substrate and at least one beta-keto ester should be included in the active catalyst complex. Further improvement of the reaction by maintaining an appropriate ratio of the La-NMe-linked-BINOL complex and beta-keto esters is also described. 相似文献
10.
Mori M Oyama Y Suzuki A Takahashi K Yamada M Miyano K Miyata H Takei H Hirata KS Kajita T Kihara K Nakahata M Nakamura K Ohara S Sato N Suzuki Y Totsuka Y Yaginuma Y Koshiba M Suda T Tajima T Fukuda Y Nagashima Y Takita M Kaneyuki K Tanimori T Beier EW Frank ED Frati W Kim SB Mann AK Newcomer FM Van Berg R Zhang W 《Physical review D: Particles and fields》1991,43(9):2843-2846