Search

Your search keyword '"Yoshinori Sato"' showing total 4 results
Start Over Author "Yoshinori Sato" Journal bulletin of the chemical society of japan
4 results on '"Yoshinori Sato"'

2. Large-Scale Production of Ba2+–Alginate-Coated Vesicles of Carbon Nanofibers for DNA-Interactive Pollutant Elimination

Author

Ken Ichiro Shibata, Yoshinobu Nodasaka, Masanobu Shindoh, Yoshinori Sato, Bunshi Fugetsu, Taeko Mizutani, Shuya Satoh, Norio Nishi, Keiji Yamazaki, Kazuyuki Tohji, Kiyoko Shimizu, Fumio Watari, and Toshikazu Shiba

Subjects
Pollutant, chemistry.chemical_compound, chemistry, Chemical engineering, Carbon nanofiber, Coated vesicle, Nanotechnology, General Chemistry, DNA
Abstract

Ba2+–alginate coated vesicles (Ba2+–ALG) containing highly dispersed carbon nanofibers (CNFs) were successfully produced for the first time using an encapsulation technique. These Ba2+–ALG/CNFs com...

Published
2004
Full Text
View/download PDF

3. Unusual Effects of the Reaction Temperature on the Catalytic Activity of Rh/Active-Carbon for Ethylene Hydroformylation

Author

Yoshinori Sato, Takahiro Uchiumi, Nobuo Takahashi, and Kazuo Ogawa

Subjects
Ethylene, Pentanal, Inorganic chemistry, chemistry.chemical_element, Propionaldehyde, General Chemistry, Activation energy, Medicinal chemistry, Catalysis, Rhodium, chemistry.chemical_compound, chemistry, Hydroformylation, Carbon monoxide
Abstract

The apparent activation energies for propionaldehyde and ethane formation from C2H4, CO, and H2 on a Rh/active-carbon catalyst, once used for a reaction at 453 K, were found to be 40 and 76 kJ mol−...

Published
1993
Full Text
View/download PDF

4. The Preparation of Protoheme Mono-N-[5-(2-methyl-1-imidazolyl)pentyl]amide and Its Oxygenation

Author

Eishun Tsuchida, Manabu Kaneda, Hiroyuki Nishide, and Yoshinori Sato

Subjects
Aqueous solution, Protoporphyrin IX, chemistry.chemical_element, General Chemistry, Oxygenation, Ethyl ester, Medicinal chemistry, Oxygen, Adduct, chemistry.chemical_compound, chemistry, Amide, Organic chemistry, Heme
Abstract

Iron(II)protoporphyrin IX N-[5-(2-methyl-1-imidazolyl)pentyl]amide ethyl ester (1) and its derivatives (2–4) were prepared. They predominantly form pentacoordinate heme complexes in organic and aqueous solutions, based on their 2-methylimidazole-ligand and spacer N-pentylamide groups. Oxygen adducts of 1–4 were rapidly formed on exposure to oxygen in N,N-dimethylformamide (DMF) at −30 °C, and their life-times were more than 30 min.

Published
1982
Full Text
View/download PDF

Catalog

Books, media, physical & digital resources
See catalog results