Zobrazeno 1 - 10
of 121
pro vyhledávání: '"Michler's ketone"'
Publikováno v:
New Journal of Chemistry. 43:10859-10867
Interaction of Michler's ketone–benzimidazole derivatives (MK-1 and MK-2) with serum albumin proteins was examined by absorption, steady-state, time-resolved fluorescence, molecular docking and circular dichroism methods. In the presence of albumin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69e8f4eaaca20e5405f41b998027d6e2
https://doi.org/10.1039/c9nj01972c
https://doi.org/10.1039/c9nj01972c
Autor:
Bernadette Graff, Didier Gigmes, Tayssir Hamieh, Jacques Lalevée, Frédéric Dumur, Jean Pierre Fouassier, Cédric R. Mayer, Haifaa Mokbel, Joumana Toufaily
Publikováno v:
Macromolecular Chemistry and Physics. 215:783-790
Four new push-pull dyes derived from Michler's ketones are investigated. These dyes, based on a donor-π-acceptor (D-π-A) structure, exhibit a tunable character according to the electron- withdrawing ability of the acceptor used. The new proposed st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cd6aec35b15c13393e97169a2a4f23a
https://doi.org/10.1002/macp.201300779
https://doi.org/10.1002/macp.201300779
Publikováno v:
Textile Research Journal. 84:808-818
A new photoactive antimicrobial agent was synthesized by introducing a reactive functional group (–CH2CH2OH) to 4,4′-bis(dimethylamino)benzophenone (Michler’s ketone) that could enhance the fixation of benzophenone derivatives to cotton fabric.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aff802503227af8a2cef59509924dfb9
https://doi.org/10.1177/0040517513509872
https://doi.org/10.1177/0040517513509872
Publikováno v:
Advanced Materials Research. 818:54-57
Two novel reactive Michlers ketones were designed and easily synthesized in moderate yields. UV-absorption spectra showed that the reactive Michlers ketones absorbed light more efficiently than their bromide reactants. In practice, the Michlers keton
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5e2341614b7c1ad6bbab40c3450a25d
https://doi.org/10.4028/www.scientific.net/amr.818.54
https://doi.org/10.4028/www.scientific.net/amr.818.54
Autor:
Steven P. Fisher, Eric W. Reinheimer
Publikováno v:
Journal of Chemical Crystallography. 43:478-483
Trimeric perfluoro-ortho-phenylenemercury (o-(C6F4Hg)3) has been identified as one of the simplest Lewis acidic host molecules due to its proximity of Hg(II) atoms, electron-withdrawing properties and inherent accessibility to electrophilic sites on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::750100fc3c6a1a602268e1bf8b549171
https://doi.org/10.1007/s10870-013-0446-6
https://doi.org/10.1007/s10870-013-0446-6
Autor:
Artur K. Mailyan, Alexey A. Shimkin, M. M. Krayushkin, Andrey G. Lvov, Dmitry V. Lonshakov, Valerii Z. Shirinian
Publikováno v:
Synthesis. 2012:527-531
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b837f4847745e28f0178e011ba866157
https://doi.org/10.1055/s-0031-1289623
https://doi.org/10.1055/s-0031-1289623
Publikováno v:
Polymers for Advanced Technologies. 22:598-604
A series of amphiphilic polymeric Michler's ketone (MK) photoinitiators (APMKs) were synthesized by incorporating PEO short chain, MK moiety, and coinitiator amine into the same polymeric chain. APMKs possess good amphiphilic ability and become water
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c39f7cfbeb5db28d63eaec3d2aee6986
https://doi.org/10.1002/pat.1552
https://doi.org/10.1002/pat.1552
Autor:
Stefan Spange, Susann Anders, Lysann Kaßner, Wolfgang Dr Schrepp, Walter Hoyer, Andreas Pohlers
Publikováno v:
Macromolecular Chemistry and Physics. 211:1550-1558
A procedure for synthesis aromatic-aliphatic PAK, completely functionalized with p-fluorophenyl terminal groups, is presented. This synthesis uses the nucleophilic aromatic substitution of DFB with various secondary aliphatic diamines [CH 3 -NH-(CH 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cb5e6abd449abd37b05553274331fcf
https://doi.org/10.1002/macp.201000071
https://doi.org/10.1002/macp.201000071
Publikováno v:
Progress in Organic Coatings. 66:65-72
Through introducing Michler's ketone (MK) moiety and diglycidyl ether monomers of different molecular chain into the same polymeric chain, polymeric photoinitiators of different chain flexibility, PMKPR, PMKPG and PMKPP were synthesized. These polyme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a003dc7381357c8ff1e12d3b040860c6
https://doi.org/10.1016/j.porgcoat.2009.06.003
https://doi.org/10.1016/j.porgcoat.2009.06.003
Publikováno v:
Journal of the Chinese Chemical Society. 56:729-740
The TiO2/UV photocatalytic degradation of Michler’s Ketone (MK) has been investigated in aqueous heterogeneous suspensions. Results obtained show rapid and complete oxidation of MK after 24-h, and more than 97.5% of MK was mineralized after a 32-h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98cb123dbc657423409ae1a34b47549a
https://doi.org/10.1002/jccs.200900109
https://doi.org/10.1002/jccs.200900109