Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Shinya Muto"'
Publikováno v:
Journal of Colloid and Interface Science. 49:173-176
Critical micelle concentrations (CMC) of dodecylammonium acetate, propionate, butyrate, caprylate, caprate, and laurate were determined from spectral changes based on the solubilization of 7,7,8,8-tetracyanoquinodimethane (TCNQ). When TCNQ was solubi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6440847a2e29452b85f3505a489a9ab1
https://doi.org/10.1016/0021-9797(74)90349-x
https://doi.org/10.1016/0021-9797(74)90349-x
Publikováno v:
Synthesis. 1989:929-932
A series of di- 3 and triorganotin esters 2 of aromatic selenocarboxylic acid were synthesized and characterized. The organotin esters 2 and 3 are stable thermally, but labile towards moisture and oxygen. They readily reacted with benzyl bromide in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b7afc84a714af71ff5340b59f040d3e
https://doi.org/10.1055/s-1989-27432
https://doi.org/10.1055/s-1989-27432
Publikováno v:
NIPPON KAGAKU KAISHI. :2246-2249
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2479e460d70f3a3c7835fd7d646b8b98
https://doi.org/10.1246/nikkashi.1974.2246
https://doi.org/10.1246/nikkashi.1974.2246
Publikováno v:
Bulletin of the Chemical Society of Japan. 44:2087-2090
The absorption spectra of 7,7,8,8-tetracyanoquinodimethane (TCNQ) solubilized in surfactant solutions were found to be influenced by day light (hereafter referred to as light). The formation of the monomer band of TCNQ, anion radical in the aqueous s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::941589828391e1725260ea01a3808688
https://doi.org/10.1246/bcsj.44.2087
https://doi.org/10.1246/bcsj.44.2087
Autor:
Shinya Muto, Kenjiro Meguro
Publikováno v:
Bulletin of the Chemical Society of Japan. 46:1316-1320
Extra absorption spectra appeared when 7,7,8,8-tetracyanoquinodimethane (TCNQ) was solubilized into surfactant organic solvent solutions above the critical micelle concentration (CMC). It was found also that extra absorption spectra appeared when iod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::faea91fa17356c3a1799ac87d1b19d97
https://doi.org/10.1246/bcsj.46.1316
https://doi.org/10.1246/bcsj.46.1316
Publikováno v:
Journal of Colloid and Interface Science. 37:109-114
It was found that extra absorption spectra appear when 7,7,8,8-tetracyanoquino-dimethane (TCNQ), which is a strong π-acid, was solubilized into surfactant solutions above the critical micelle concentration (cmc). The extra absorption bands are cause
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de8a5f85803e6c2e333e5dad93a40b80
https://doi.org/10.1016/0021-9797(71)90270-0
https://doi.org/10.1016/0021-9797(71)90270-0
Publikováno v:
Journal of Japan Oil Chemists' Society. 15:26-29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1590a90f8d04392475bd64718633a166
https://doi.org/10.5650/jos1956.15.26
https://doi.org/10.5650/jos1956.15.26
Publikováno v:
NIPPON KAGAKU KAISHI. :2013-2016
The absorption spectra of iodine dissolved in aqueous solutions of heptaethyleneglycol dodecyl ether (C12E7) exhibit two extra bands at about 295 nm and 386 nm, when the concentration of C12E7 exceeds than its critical micelle concentration (CMC). Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a073e4696d62ab1d1ee6bee36e86729
https://doi.org/10.1246/nikkashi.1972.2013
https://doi.org/10.1246/nikkashi.1972.2013
Publikováno v:
NIPPON KAGAKU KAISHI. :1572-1575
The interaction between pentaethylene glycol-dodecyl ether(C12E5) and sodium dodecyl sulfate (SDS) was investigated from the spectra of iodine in aqueous solution containing C12E5 and SDS. When SDS is added in the aqueous solution of C12E5 and iodine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c91d020a8efd28522ed18900cc650fe
https://doi.org/10.1246/nikkashi.1972.1572
https://doi.org/10.1246/nikkashi.1972.1572
Publikováno v:
Synthesis. 1986:128-130
Les composes du titre sont prepares a partir de diacyl diseleniures et de piperidine; par action du bromures de phenacyle sur les selenoarenoates de piperidinium, on obtient les esters de phenacyle des acides selenoarenoiques
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0d4349890e56f772915a49fd84485ca
https://doi.org/10.1055/s-1986-31494
https://doi.org/10.1055/s-1986-31494