Matches in SemOpenAlex for { <https://semopenalex.org/work/W2027831326> ?p ?o ?g. }
Showing items 1 to 48 of
48
with 100 items per page.
- W2027831326 abstract "Die Porphyrine 3a- k mit Alkylseitenketten in den Positionen 5,10,15 und 20 mit ω-standigen ionisierbaren funktionellen Gruppen wurden dargestellt und charakterisiert. 3i und das π-Radikalkation von 3 k bilden in wasriger Losung Aggregate, die bei Zugabe von Natriumlaurylsulfat vollstandig dissoziieren. Die Redoxeigenschaften entsprechen denen naturlicher Porphyrine. Die mogliche Eignung der neu dargestellten Porphyrine im Verbund mit Micellen und in molekularen Doppelschichten zur Sauerstoffaktivierung und zur Umwandlung von Licht- in Redoxenergie werden kurz diskutiert.Porphyrins in Polymeric Matrix and Micelles, I. - Preparation and Properties of ω-Carboxylic Acids, ω-Sulfonic Acids, and ω-Ammonium Salts of 5,10,15,20-Tetraalkyl- and Tetra-w-alkenylporphyrinsThe porphyrins 3a- k& containing alkyl side chains in the positions 5, 10, 15 and 20 with ionizable endgroups have been prepared and characterized. 3 i and the x-radical cation of 3k form aggregates in aqueous solutions which completely dissociate upon addition of sodium lauryl sulfate. The redox properties of the newly synthesized porphyrins correspond to those of natural porphyrins. The possible application of porphyrins in bimolecular layers or in micelles to activate oxygen or to convert light into redox energy is briefly discussed." @default.
- W2027831326 created "2016-06-24" @default.
- W2027831326 creator A5063246616 @default.
- W2027831326 creator A5078710808 @default.
- W2027831326 date "1976-12-06" @default.
- W2027831326 modified "2023-10-07" @default.
- W2027831326 title "Porphyrine in polymerer Matrix und in Micellen, I. Darstellung und Eigenschaften von ω-Carbonsäuren, ω-Sulfonsäuren und ω-Ammoniumsalzen der 5,10,15,20-Tetraalkyl- und Tetra-ω-alkenylporphyrine" @default.
- W2027831326 cites W1965549418 @default.
- W2027831326 cites W1969528942 @default.
- W2027831326 cites W1979637196 @default.
- W2027831326 cites W1992049179 @default.
- W2027831326 cites W1996843077 @default.
- W2027831326 cites W2051370418 @default.
- W2027831326 cites W2077260754 @default.
- W2027831326 cites W2107130448 @default.
- W2027831326 cites W2141554959 @default.
- W2027831326 cites W2146113971 @default.
- W2027831326 cites W2337629445 @default.
- W2027831326 cites W425109168 @default.
- W2027831326 doi "https://doi.org/10.1002/jlac.197619761113" @default.
- W2027831326 hasPublicationYear "1976" @default.
- W2027831326 type Work @default.
- W2027831326 sameAs 2027831326 @default.
- W2027831326 citedByCount "8" @default.
- W2027831326 crossrefType "journal-article" @default.
- W2027831326 hasAuthorship W2027831326A5063246616 @default.
- W2027831326 hasAuthorship W2027831326A5078710808 @default.
- W2027831326 hasConcept C11268172 @default.
- W2027831326 hasConcept C178790620 @default.
- W2027831326 hasConcept C184651966 @default.
- W2027831326 hasConcept C185592680 @default.
- W2027831326 hasConcept C188027245 @default.
- W2027831326 hasConcept C2780263894 @default.
- W2027831326 hasConcept C55904794 @default.
- W2027831326 hasConceptScore W2027831326C11268172 @default.
- W2027831326 hasConceptScore W2027831326C178790620 @default.
- W2027831326 hasConceptScore W2027831326C184651966 @default.
- W2027831326 hasConceptScore W2027831326C185592680 @default.
- W2027831326 hasConceptScore W2027831326C188027245 @default.
- W2027831326 hasConceptScore W2027831326C2780263894 @default.
- W2027831326 hasConceptScore W2027831326C55904794 @default.
- W2027831326 hasLocation W20278313261 @default.
- W2027831326 hasOpenAccess W2027831326 @default.
- W2027831326 hasPrimaryLocation W20278313261 @default.
- W2027831326 isParatext "false" @default.
- W2027831326 isRetracted "false" @default.
- W2027831326 magId "2027831326" @default.
- W2027831326 workType "article" @default.