The dominant nature of Herzberg–Teller terms in the photophysical description of naphthalene compared to anthracene and tetracene
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2045-2322
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
The dominant nature of Herzberg–Teller terms in the photophysical description of naphthalene compared to anthracene and tetracene ; volume:12 ; number:1 ; day:12 ; month:12 ; year:2022 ; pages:1-12 ; date:12.2022
Scientific reports ; 12, Heft 1 (12.12.2022), 1-12, 12.2022
- Urheber
-
Manian, Anjay
Russo, Salvy P.
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1038/s41598-022-24081-0
- URN
-
urn:nbn:de:101:1-2023022121093112496539
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:52 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Manian, Anjay
- Russo, Salvy P.
- SpringerLink (Online service)
Ähnliche Objekte (12)
Thermally Induced Synthesis of Anthracene‐, Pyrene‐ and Naphthalene‐Fused Porphyrins
Synthesis and characterization of 1,2,3,4-naphthalene and anthracene diimides
Ring Rearrangement Reactions of 4‐Alkenylisocoumarins and Photophysical Evaluation of Multi‐Substituted Anthracene Products
Correlating the Structural and Photophysical Properties of Ortho, Meta, and Para ‐Carboranyl–Anthracene Dyads
Cooperative supramolecular polymerization of an amine-substituted naphthalene-diimide and its impact on excited state photophysical properties
Anthracene‐Porphyrin Nanoribbons
Anthracene‐Porphyrin Nanoribbons
Über Synthesen methylierter Anthracene
High-pressure studies of naphthalene, anthracene, pyrene, and benzo[a]pyrene using single-crystal X-ray diffraction in a diamond anvil cell
Naphthalene based conjugated materials
Gold-catalyzed naphthalene functionalization
Zur Synthese peri-anellierter Anthracene
Thermally Induced Synthesis of Anthracene‐, Pyrene‐ and Naphthalene‐Fused Porphyrins
Synthesis and characterization of 1,2,3,4-naphthalene and anthracene diimides
Ring Rearrangement Reactions of 4‐Alkenylisocoumarins and Photophysical Evaluation of Multi‐Substituted Anthracene Products
Correlating the Structural and Photophysical Properties of Ortho, Meta, and Para ‐Carboranyl–Anthracene Dyads
Cooperative supramolecular polymerization of an amine-substituted naphthalene-diimide and its impact on excited state photophysical properties
Anthracene‐Porphyrin Nanoribbons
Anthracene‐Porphyrin Nanoribbons
Über Synthesen methylierter Anthracene
High-pressure studies of naphthalene, anthracene, pyrene, and benzo[a]pyrene using single-crystal X-ray diffraction in a diamond anvil cell
Naphthalene based conjugated materials
Gold-catalyzed naphthalene functionalization
Zur Synthese peri-anellierter Anthracene
Thermally Induced Synthesis of Anthracene‐, Pyrene‐ and Naphthalene‐Fused Porphyrins
Synthesis and characterization of 1,2,3,4-naphthalene and anthracene diimides
Ring Rearrangement Reactions of 4‐Alkenylisocoumarins and Photophysical Evaluation of Multi‐Substituted Anthracene Products
Correlating the Structural and Photophysical Properties of Ortho, Meta, and Para ‐Carboranyl–Anthracene Dyads
Cooperative supramolecular polymerization of an amine-substituted naphthalene-diimide and its impact on excited state photophysical properties
Anthracene‐Porphyrin Nanoribbons
Anthracene‐Porphyrin Nanoribbons
Über Synthesen methylierter Anthracene
High-pressure studies of naphthalene, anthracene, pyrene, and benzo[a]pyrene using single-crystal X-ray diffraction in a diamond anvil cell
Naphthalene based conjugated materials
Gold-catalyzed naphthalene functionalization