Matches in SemOpenAlex for { <https://semopenalex.org/work/W2053897983> ?p ?o ?g. }
- W2053897983 endingPage "620" @default.
- W2053897983 startingPage "611" @default.
- W2053897983 abstract "Photoinduced charge separation and thermal charge recombination reactions in a series of structurally related donor−acceptor molecules based on the 4-(N-pyrrolidinyl)naphthalene-1,8-dicarboximide (5ANI) and 4-(N-piperidinyl)naphthalene-1,8-dicarboximide (6ANI) chromophores were studied in the nematic liquid crystals 4-cyano-4‘-(n-pentyl)biphenyl (5CB) and N-(4‘-methoxybenzylidene)-4-(n-butyl)aniline (MBBA) as well as in the isotropic solvents pyridine, 2-methyltetrahydrofuran, and pentyl propionate over a temperature range of 293−353 K. The photoexcited 5ANI and 6ANI chromophores donate an electron to pyromellitimide (PI), which is attached to the donors via a N−N single bond between their imide groups to give 5ANI−PI and 6ANI−PI, respectively. The photoexcited 6ANI chromophore also accepts electrons from p-methoxyaniline, which is attached to the 4-position of the naphthalene-1,8-dicarboximide as a N‘-(4‘-methoxyphenyl)piperazinyl substituent to give MeOAn−6ANI. Attachment of a secondary PI acceptor to M..." @default.
- W2053897983 created "2016-06-24" @default.
- W2053897983 creator A5072522213 @default.
- W2053897983 creator A5090580435 @default.
- W2053897983 date "2003-01-07" @default.
- W2053897983 modified "2023-09-27" @default.
- W2053897983 title "Effects of Solvent and Structural Dynamics on Electron Transfer Reactions of 4-Aminonaphthalene-1,8-dicarboximide Donor−Acceptor Molecules in Nematic Liquid Crystals and Isotropic Solvents" @default.
- W2053897983 cites W1630368370 @default.
- W2053897983 cites W1967845583 @default.
- W2053897983 cites W1971092996 @default.
- W2053897983 cites W1981554467 @default.
- W2053897983 cites W1981910650 @default.
- W2053897983 cites W1984750191 @default.
- W2053897983 cites W1984874582 @default.
- W2053897983 cites W1991417868 @default.
- W2053897983 cites W1992507268 @default.
- W2053897983 cites W1999449827 @default.
- W2053897983 cites W2002164208 @default.
- W2053897983 cites W2010450284 @default.
- W2053897983 cites W2015387163 @default.
- W2053897983 cites W2015874704 @default.
- W2053897983 cites W2017980221 @default.
- W2053897983 cites W2024685126 @default.
- W2053897983 cites W2024793089 @default.
- W2053897983 cites W2025785781 @default.
- W2053897983 cites W2028772401 @default.
- W2053897983 cites W2030369590 @default.
- W2053897983 cites W2034478630 @default.
- W2053897983 cites W2035361319 @default.
- W2053897983 cites W2041931011 @default.
- W2053897983 cites W2046218188 @default.
- W2053897983 cites W2054947925 @default.
- W2053897983 cites W2061720126 @default.
- W2053897983 cites W2063699768 @default.
- W2053897983 cites W2067171751 @default.
- W2053897983 cites W2071946219 @default.
- W2053897983 cites W2072366124 @default.
- W2053897983 cites W2077966858 @default.
- W2053897983 cites W2081201968 @default.
- W2053897983 cites W2081728674 @default.
- W2053897983 cites W2085130723 @default.
- W2053897983 cites W2163542599 @default.
- W2053897983 cites W327427082 @default.
- W2053897983 cites W4250808650 @default.
- W2053897983 doi "https://doi.org/10.1021/jp021833+" @default.
- W2053897983 hasPublicationYear "2003" @default.
- W2053897983 type Work @default.
- W2053897983 sameAs 2053897983 @default.
- W2053897983 citedByCount "35" @default.
- W2053897983 countsByYear W20538979832013 @default.
- W2053897983 countsByYear W20538979832016 @default.
- W2053897983 countsByYear W20538979832020 @default.
- W2053897983 countsByYear W20538979832021 @default.
- W2053897983 countsByYear W20538979832023 @default.
- W2053897983 crossrefType "journal-article" @default.
- W2053897983 hasAuthorship W2053897983A5072522213 @default.
- W2053897983 hasAuthorship W2053897983A5090580435 @default.
- W2053897983 hasConcept C120665830 @default.
- W2053897983 hasConcept C121332964 @default.
- W2053897983 hasConcept C123669783 @default.
- W2053897983 hasConcept C13274807 @default.
- W2053897983 hasConcept C147120987 @default.
- W2053897983 hasConcept C147597530 @default.
- W2053897983 hasConcept C147789679 @default.
- W2053897983 hasConcept C159467904 @default.
- W2053897983 hasConcept C178790620 @default.
- W2053897983 hasConcept C184050105 @default.
- W2053897983 hasConcept C185592680 @default.
- W2053897983 hasConcept C26873012 @default.
- W2053897983 hasConcept C2779892579 @default.
- W2053897983 hasConcept C2780471494 @default.
- W2053897983 hasConcept C2900893 @default.
- W2053897983 hasConcept C32909587 @default.
- W2053897983 hasConcept C41999313 @default.
- W2053897983 hasConcept C59593255 @default.
- W2053897983 hasConcept C62520636 @default.
- W2053897983 hasConcept C75473681 @default.
- W2053897983 hasConceptScore W2053897983C120665830 @default.
- W2053897983 hasConceptScore W2053897983C121332964 @default.
- W2053897983 hasConceptScore W2053897983C123669783 @default.
- W2053897983 hasConceptScore W2053897983C13274807 @default.
- W2053897983 hasConceptScore W2053897983C147120987 @default.
- W2053897983 hasConceptScore W2053897983C147597530 @default.
- W2053897983 hasConceptScore W2053897983C147789679 @default.
- W2053897983 hasConceptScore W2053897983C159467904 @default.
- W2053897983 hasConceptScore W2053897983C178790620 @default.
- W2053897983 hasConceptScore W2053897983C184050105 @default.
- W2053897983 hasConceptScore W2053897983C185592680 @default.
- W2053897983 hasConceptScore W2053897983C26873012 @default.
- W2053897983 hasConceptScore W2053897983C2779892579 @default.
- W2053897983 hasConceptScore W2053897983C2780471494 @default.
- W2053897983 hasConceptScore W2053897983C2900893 @default.
- W2053897983 hasConceptScore W2053897983C32909587 @default.
- W2053897983 hasConceptScore W2053897983C41999313 @default.
- W2053897983 hasConceptScore W2053897983C59593255 @default.
- W2053897983 hasConceptScore W2053897983C62520636 @default.
- W2053897983 hasConceptScore W2053897983C75473681 @default.
- W2053897983 hasIssue "5" @default.