Matches in SemOpenAlex for { <https://semopenalex.org/work/W1964100375> ?p ?o ?g. }
- W1964100375 endingPage "10506" @default.
- W1964100375 startingPage "10500" @default.
- W1964100375 abstract "A derivative of phenazine, dibenzo[a,c]phenazine (DBPZ), can be used as a very good hydrogen-bonding probe unlike its parent phenazine molecule. Steady-state absorption and fluorescence studies reveal that DBPZ is completely insensitive to polarity of the medium. However, DBPZ can form a hydrogen bond very efficiently in its first excited singlet state. The extent of this excited-state hydrogen-bond formation depends both on size and on hydrogen-bond donor ability of the solvents. Time-resolved fluorescence studies and theoretical calculations also suggest that this hydrogen-bond formation is much more favorable in the excited state as compared to the ground state. In the excited state, the electron density is pushed toward the nitrogen atoms from the benzene rings, thereby increasing the dipole moment of the DBPZ molecule. Although the dipole moment of DBPZ increases upon photoexcitation, like other polarity probes, the molecule remains fully insensitive to the polarity of the interacting solvent. This unusual behavior of DBPZ as compared to simple phenazine and other polarity probes is due to the structure of the molecule. Hydrogen atoms at the 1 and 8 positions of DBPZ are sterically interacting with a lone pair of electrons on the proximate nitrogen atoms and make both of the nitrogen atoms inaccessible to solvent molecules. For this reason, DBPZ cannot sense the polarity of the medium. However, DBPZ can only sense solvents, those that have hydrogen with some electropositive nature, that is, the hydrogen-bond donating solvents. Hydrogen being the smallest among all elements can only interact with the lone pair of electrons of nitrogen atoms. Thus, DBPZ can act as a sensor for the hydrogen-bond donating solvents irrespective of their dielectrics." @default.
- W1964100375 created "2016-06-24" @default.
- W1964100375 creator A5048932792 @default.
- W1964100375 creator A5051389777 @default.
- W1964100375 creator A5062797674 @default.
- W1964100375 creator A5070568880 @default.
- W1964100375 creator A5081623542 @default.
- W1964100375 creator A5090301487 @default.
- W1964100375 date "2007-09-25" @default.
- W1964100375 modified "2023-10-05" @default.
- W1964100375 title "Dibenzo[<i>a</i>,<i>c</i>]phenazine: A Polarity-Insensitive Hydrogen-Bonding Probe" @default.
- W1964100375 cites W1966867774 @default.
- W1964100375 cites W1984373289 @default.
- W1964100375 cites W1987357613 @default.
- W1964100375 cites W2008318184 @default.
- W1964100375 cites W2022950330 @default.
- W1964100375 cites W2041931011 @default.
- W1964100375 cites W2046943018 @default.
- W1964100375 cites W2047429347 @default.
- W1964100375 cites W2055442639 @default.
- W1964100375 cites W2057003691 @default.
- W1964100375 cites W2057049368 @default.
- W1964100375 cites W2066189187 @default.
- W1964100375 cites W2079473982 @default.
- W1964100375 cites W2080685263 @default.
- W1964100375 cites W2082222403 @default.
- W1964100375 cites W2082759718 @default.
- W1964100375 cites W2100456799 @default.
- W1964100375 cites W2136201011 @default.
- W1964100375 cites W2200102932 @default.
- W1964100375 cites W4244914404 @default.
- W1964100375 doi "https://doi.org/10.1021/jp0731811" @default.
- W1964100375 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/17892276" @default.
- W1964100375 hasPublicationYear "2007" @default.
- W1964100375 type Work @default.
- W1964100375 sameAs 1964100375 @default.
- W1964100375 citedByCount "15" @default.
- W1964100375 countsByYear W19641003752013 @default.
- W1964100375 countsByYear W19641003752014 @default.
- W1964100375 countsByYear W19641003752016 @default.
- W1964100375 countsByYear W19641003752017 @default.
- W1964100375 countsByYear W19641003752022 @default.
- W1964100375 crossrefType "journal-article" @default.
- W1964100375 hasAuthorship W1964100375A5048932792 @default.
- W1964100375 hasAuthorship W1964100375A5051389777 @default.
- W1964100375 hasAuthorship W1964100375A5062797674 @default.
- W1964100375 hasAuthorship W1964100375A5070568880 @default.
- W1964100375 hasAuthorship W1964100375A5081623542 @default.
- W1964100375 hasAuthorship W1964100375A5090301487 @default.
- W1964100375 hasConcept C112887158 @default.
- W1964100375 hasConcept C121332964 @default.
- W1964100375 hasConcept C139286075 @default.
- W1964100375 hasConcept C159467904 @default.
- W1964100375 hasConcept C173523689 @default.
- W1964100375 hasConcept C178790620 @default.
- W1964100375 hasConcept C181500209 @default.
- W1964100375 hasConcept C184779094 @default.
- W1964100375 hasConcept C185592680 @default.
- W1964100375 hasConcept C201194858 @default.
- W1964100375 hasConcept C2778370995 @default.
- W1964100375 hasConcept C32909587 @default.
- W1964100375 hasConcept C46000676 @default.
- W1964100375 hasConcept C69523127 @default.
- W1964100375 hasConcept C71240020 @default.
- W1964100375 hasConcept C75473681 @default.
- W1964100375 hasConcept C8010536 @default.
- W1964100375 hasConceptScore W1964100375C112887158 @default.
- W1964100375 hasConceptScore W1964100375C121332964 @default.
- W1964100375 hasConceptScore W1964100375C139286075 @default.
- W1964100375 hasConceptScore W1964100375C159467904 @default.
- W1964100375 hasConceptScore W1964100375C173523689 @default.
- W1964100375 hasConceptScore W1964100375C178790620 @default.
- W1964100375 hasConceptScore W1964100375C181500209 @default.
- W1964100375 hasConceptScore W1964100375C184779094 @default.
- W1964100375 hasConceptScore W1964100375C185592680 @default.
- W1964100375 hasConceptScore W1964100375C201194858 @default.
- W1964100375 hasConceptScore W1964100375C2778370995 @default.
- W1964100375 hasConceptScore W1964100375C32909587 @default.
- W1964100375 hasConceptScore W1964100375C46000676 @default.
- W1964100375 hasConceptScore W1964100375C69523127 @default.
- W1964100375 hasConceptScore W1964100375C71240020 @default.
- W1964100375 hasConceptScore W1964100375C75473681 @default.
- W1964100375 hasConceptScore W1964100375C8010536 @default.
- W1964100375 hasIssue "42" @default.
- W1964100375 hasLocation W19641003751 @default.
- W1964100375 hasLocation W19641003752 @default.
- W1964100375 hasOpenAccess W1964100375 @default.
- W1964100375 hasPrimaryLocation W19641003751 @default.
- W1964100375 hasRelatedWork W1982248343 @default.
- W1964100375 hasRelatedWork W2029714001 @default.
- W1964100375 hasRelatedWork W2048277732 @default.
- W1964100375 hasRelatedWork W2079346183 @default.
- W1964100375 hasRelatedWork W2084891561 @default.
- W1964100375 hasRelatedWork W2500179633 @default.
- W1964100375 hasRelatedWork W2788975530 @default.
- W1964100375 hasRelatedWork W2893189752 @default.
- W1964100375 hasRelatedWork W2941448768 @default.
- W1964100375 hasRelatedWork W4284896012 @default.