Zobrazeno 1 - 10 of 135 pro vyhledávání: '"Takeo Nakano"'
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Akademický článek
Study on Molecular Thermal Energy Transfer in a Lipid Bilayer
Autor: Takeo NAKANO, Taku OHARA, Gota KIKUGAWA
Publikováno v: Journal of Thermal Science and Technology, Vol 3, Iss 3, Pp 421-429 (2008)
Recently, lipid bilayers attract a great deal of interest as a material with nanoscale structure. Various devices utilizing lipid bilayers, which include some kinds of sensors and molecular sorting devices, have been proposed. Understanding of therma
Externí odkaz: https://doaj.org/article/64cb48522a454fd78239a4c30e377c44
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2
Aryl/Heteroaryl Substituted Boron-Difluoride Complexes Bearing 2-(Isoquinol-1-yl)pyrrole Ligands Exhibiting High Luminescence Efficiency with a Large Stokes Shift
Autor: Takeo Nakano, Shigenori Fujikawa
Publikováno v: The Journal of Organic Chemistry. 87:11708-11721
A series of 2-(isoquinol-1-yl)pyrrole-boron complexes possessing (hetero)aryl substituents on the pyrrole and/or isoquinoline moiety were prepared. These compounds exhibited the fluorescence emission character in both solution and solid state. In mos
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fee1715fbec6062d964951aae95c342
https://doi.org/10.1021/acs.joc.2c01343
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3
Synthesis and Self‐Aggregation of Chlorophyll‐ a Derivatives Possessing a Hydroxymethyl Group in the C20‐Substituent with Ethynylene and/or Phenylene Linkers
Autor: Takeo Nakano, Yuki Hashimoto, Hitoshi Tamiaki
Publikováno v: Photochemistry and Photobiology. 99:35-44
Chlorophyll(Chl)-a derivatives containing some rigid linkers in the C20 substituents, which were inserted between a hydroxymethyl group and the chlorin π-skeleton, were synthesized and their self-aggregation abilities were investigated. Measurements
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1a1a87a7210e1dd1447de4ff9e424c2
https://doi.org/10.1111/php.13655
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6
First synthesis of a chlorin skeleton containing thiazole and thiophene rings and its optical properties
Autor: Takeo Nakano, Shigenori Fujikawa
Publikováno v: Journal of Porphyrins and Phthalocyanines. 26:279-285
A novel macrocyclic [Formula: see text]-skeleton 1 containing thiazole and thiophene rings was synthesized via MacDonald [3+1]-type condensation, and its optical properties were investigated. Two sulfur atoms were effective for the bathochromic shift
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::47080f5edd34cf75079e6ec95170335d
https://doi.org/10.1142/s1088424622500110
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