Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Susanne M. Fischer"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 1689-1697 (2021)
Electron-rich triarylphosphines, namely 4-(methoxyphenyl)diphenylphosphine (MMTPP) and tris(4-trimethoxyphenyl)phosphine (TMTPP), outperform commonly used triphenylphosphine (TPP) in catalyzing oxa-Michael additions. A matrix consisting of three diff
Externí odkaz:
https://doaj.org/article/4d674867da724cc98016243fb167e176
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 154:443-458
Poly(ether)s represent an important class of polymers and are typically formed by ring-opening polymerization, Williamson ether synthesis, or self-condensation of alcohols. The oxa-Michael reaction presents another method to form poly(ether)s with ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8acbc70d655c388cd2f35f1a854b869
https://doi.org/10.1007/s00706-023-03049-4
https://doi.org/10.1007/s00706-023-03049-4
Autor:
Karin Ratzenböck, Johanna M. Uher, Susanne M. Fischer, David Edinger, Viktor Schallert, Ema Žagar, David Pahovnik, Christian Slugovc
Publikováno v:
Polymer Chemistry. 14:651-661
The dynamic nature of oxa-Michael derived bonds in polymers is studied in this work. Brønsted base catalysis allows for reprocessing polymer networks at temperatures around 140 °C.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a274f1cdbc658ccacb58d13545b67e5
https://doi.org/10.1039/d2py01345b
https://doi.org/10.1039/d2py01345b
Autor:
Karin Ratzenböck, Mir Mehraj Ud Din, Susanne M. Fischer, Ema Žagar, David Pahovnik, A. Daniel Boese, Daniel Rettenwander, Christian Slugovc
Publikováno v:
Chemical Science
Using water as a monomer in polymerization reactions presents a unique and exquisite strategy towards more sustainable chemistry. Herein, the feasibility thereof is demonstrated by the introduction of the oxa-Michael polyaddition of water and divinyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::090d56a497ef5ae996f2f6039d74bf6e
https://doi.org/10.1039/d2sc02124b
https://doi.org/10.1039/d2sc02124b
Publikováno v:
Catalysis Science & Technology. 12:6204-6212
The performance of the strong Lewis base tris(2,4,6-trimethoxyphenyl)phosphine (TTMPP) in catalysing oxa-Michael reactions is assessed and compared with other electron-rich tertiary arylphosphines and, as the benchmark, with the Brønsted base 1-tert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44b130ea627d048cd8151f28630a646b
https://doi.org/10.1039/d2cy01335e
https://doi.org/10.1039/d2cy01335e
Herein we propose the preparation of crosslinked polymers from off-stoichiometric oxa-Michael formulations proceeding via a self-limiting base catalyzed reaction between difunctional Michael acceptors and substoichiometric amounts of diols followed b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b11a3be221c3083e0614ff365b3ba48a
https://doi.org/10.26434/chemrxiv-2022-9dpd6
https://doi.org/10.26434/chemrxiv-2022-9dpd6
Autor:
Karin Ratzenböck, Mir Mehraj Ud Din, Susanne M. Fischer, Ema Žagar, David Pahovnik, A. Daniel Boese, Daniel Rettenwander, Christian Slugovc
Using water as monomer in polymerization reactions presents a unique and exquisite strategy towards more sustainable chemistry. Herein, the feasibility thereof is demonstrated by the introduction of the oxa-Michael polyaddition of water and divinyl s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61489f5bf53415d953bd5c86b3674d8a
https://doi.org/10.26434/chemrxiv-2022-gqqg6
https://doi.org/10.26434/chemrxiv-2022-gqqg6
Autor:
Maes, Stephan, Habets, Thomas, Fischer, Susanne M., Grignard, Bruno, Detrembleur, Christophe, Du Prez, Filip E.
Publikováno v:
Polymer Chemistry; 6/14/2024, Vol. 15 Issue 22, p2296-2307, 12p
Publikováno v:
Chemical Monthly / Monatshefte für Chemie; May2023, Vol. 154 Issue 5, p443-458, 16p
Publikováno v:
Polymer Chemistry; 3/14/2023, Vol. 14 Issue 10, p1081-1084, 4p