Matches in SemOpenAlex for { <https://semopenalex.org/work/W1964486567> ?p ?o ?g. }
Showing items 1 to 56 of
56
with 100 items per page.
- W1964486567 endingPage "628" @default.
- W1964486567 startingPage "623" @default.
- W1964486567 abstract "Die seit langem bekannten Pyrazolidon-Azomethinimine 1 sind als carbonylstabilisierte 1,3-Dipole aufzufassen und lassen sich relativ leicht synthetisieren [1, 2]. Später wurde erkannt, daß diese Verbindungen beim Belichten aus der 1,3-Dipolform 1 in die bicyclische Diaziridinform 2 übergehen und daß diese Reaktion thermisch reversibel ist [3]. Uns interessierte die Frage, ob die Diaziridine 2 auch photochemisch wieder in die Dipolform überführbar sind. Azomethine-Imines. I. To the Photoreversibility of the System Azomethine-Imine/Diaziridine,Investigated on Pyrazolidone-Azomethine-Imines Pyrazolidone-azomethine-Imines of the type 1 with polycyclic aromatic substituents R undergo a photoreversible reaction to diaziridines 2. In the u.v./VIS-spectra of the two forms 1 and 2 the difference of the λmax-values is about 100 nm. Therefore this system is suitable as a new reversible photochromic system. The influence of substituents R′ to the u.v./VIS-spectra of the 1.3-dipolar form 1 is discussed." @default.
- W1964486567 created "2016-06-24" @default.
- W1964486567 creator A5033615112 @default.
- W1964486567 creator A5052339783 @default.
- W1964486567 creator A5063464084 @default.
- W1964486567 date "1980-01-01" @default.
- W1964486567 modified "2023-09-26" @default.
- W1964486567 title "Azomethinimine. I. Zur Photoreversibilität des Systems Azomethinimin/Diaziridin, untersucht an Pyrazolidon-Azomethiniminen" @default.
- W1964486567 cites W2002570909 @default.
- W1964486567 cites W2014070915 @default.
- W1964486567 cites W2041690862 @default.
- W1964486567 cites W2092153271 @default.
- W1964486567 cites W1966589860 @default.
- W1964486567 doi "https://doi.org/10.1002/prac.19803220413" @default.
- W1964486567 hasPublicationYear "1980" @default.
- W1964486567 type Work @default.
- W1964486567 sameAs 1964486567 @default.
- W1964486567 citedByCount "18" @default.
- W1964486567 countsByYear W19644865672013 @default.
- W1964486567 crossrefType "journal-article" @default.
- W1964486567 hasAuthorship W1964486567A5033615112 @default.
- W1964486567 hasAuthorship W1964486567A5052339783 @default.
- W1964486567 hasAuthorship W1964486567A5063464084 @default.
- W1964486567 hasConcept C155647269 @default.
- W1964486567 hasConcept C161790260 @default.
- W1964486567 hasConcept C178790620 @default.
- W1964486567 hasConcept C185592680 @default.
- W1964486567 hasConcept C2776573223 @default.
- W1964486567 hasConcept C71240020 @default.
- W1964486567 hasConceptScore W1964486567C155647269 @default.
- W1964486567 hasConceptScore W1964486567C161790260 @default.
- W1964486567 hasConceptScore W1964486567C178790620 @default.
- W1964486567 hasConceptScore W1964486567C185592680 @default.
- W1964486567 hasConceptScore W1964486567C2776573223 @default.
- W1964486567 hasConceptScore W1964486567C71240020 @default.
- W1964486567 hasIssue "4" @default.
- W1964486567 hasLocation W19644865671 @default.
- W1964486567 hasOpenAccess W1964486567 @default.
- W1964486567 hasPrimaryLocation W19644865671 @default.
- W1964486567 hasRelatedWork W1970503549 @default.
- W1964486567 hasRelatedWork W2026575664 @default.
- W1964486567 hasRelatedWork W2112176562 @default.
- W1964486567 hasRelatedWork W2165132375 @default.
- W1964486567 hasRelatedWork W2358812085 @default.
- W1964486567 hasRelatedWork W2933716871 @default.
- W1964486567 hasRelatedWork W2949930653 @default.
- W1964486567 hasRelatedWork W2950541438 @default.
- W1964486567 hasRelatedWork W2951932282 @default.
- W1964486567 hasRelatedWork W2953125826 @default.
- W1964486567 hasVolume "322" @default.
- W1964486567 isParatext "false" @default.
- W1964486567 isRetracted "false" @default.
- W1964486567 magId "1964486567" @default.
- W1964486567 workType "article" @default.