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Co-Authored-By: Claude Sonnet 5.5 <noreply@anthropic.com>
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| 19 | ref-19 | verificata | 10.1016/j.dyepig.2008.12.001 | https://doi.org/10.1016/j.dyepig.2008.12.001 | 2009 | Dyes and Pigments | 82 | 102-108 | Elsevier BV | journal-article |
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[19] Luňák (2009) - The synthesis, absorption and fluorescence of polar diketo-pyrrolo-pyrroles
Come è scritta nella tesi
Luňák, S., Vyňuchal, J., Vala, M., Havel, L. & Hrdina, R. The synthesis, absorption and fluorescence of polar diketo-pyrrolo-pyrroles. Dyes Pigments 82, 102–108 (2009).
Scheda bibliografica
Citazione completa: Luňák, S.; Vyňuchal, J.; Vala, M.; Havel, L.; Hrdina, R. The synthesis, absorption and fluorescence of polar diketo-pyrrolo-pyrroles. Dyes and Pigments 2009, 82 (2), 102-108. https://doi.org/10.1016/j.dyepig.2008.12.001
- Pubblicato in: Dyes and Pigments, vol. 82, n. 2, pp. 102-108 (2009)
- Editore: Elsevier BV · tipo: journal-article
- ISSN: 0143-7208
- Data di pubblicazione: 2008-12-12
- Lingua: en
- Finanziamenti: Ministerstvo Školství, Mládeže a Tělovýchovy; Ministerstvo Průmyslu a Obchodu
Autori e affiliazioni
- Stanislav Luňák (ORCID) - University of Pardubice
- Jan Vyňuchal - University of Pardubice; Research Institute of Organic Syntheses (Czechia)
- Martin Vala (ORCID) - Brno University of Technology
- Lukáš Havel - University of Pardubice
- Radim Hrdina (ORCID) - University of Pardubice
Stato della verifica
Verificata (Crossref/OpenAlex) - fonte dati: Crossref + OpenAlex
Dove trovarla
- DOI: https://doi.org/10.1016/j.dyepig.2008.12.001
- OpenAlex: https://openalex.org/W2074639148
- Accesso: closed - il testo completo richiede un abbonamento dell'editore o l'acquisto
Abstract
Non disponibile da fonti aperte.
Argomenti e parole chiave
- Argomenti (OpenAlex): Photochemistry and Electron Transfer Studies (Physical and Theoretical Chemistry); Synthesis and Characterization of Pyrroles (Organic Chemistry); Porphyrin and Phthalocyanine Chemistry (Materials Chemistry)
- Parole chiave: push-pull dyes, cyano substituents, bathochromic shift, hyperchromic shift, vibronic structure, dipole-dipole interaction, solvent polarity, fluorescence, Stokes shift, absorption spectra
- Concetti: Bathochromic shift, Chemistry, Substituent, Stokes shift, Polar, Excited state, Fluorescence, Photochemistry, Dipole, Absorption (acoustics)
Contenuto in sintesi
Il testo completo non è ad accesso aperto e non è stato consultato: sono disponibili solo i metadati e l'abstract riportati sopra. Per approfondire, aprire la fonte dal DOI (o tramite biblioteca/abbonamento).
Come è citata nella tesi
- Sez. 1.1.2 Struttura e reattività (
tesi.mdr. 215): Ad esempio, la funzionalizzazione del core dichetopirrolopirrolico con gruppi aventi caratteristiche elettroniche differenti (presenza simultanea di gruppi elettron-donatori ed elettron-attrattori) promuove un marcato effetto batocromico, ovvero una transizione dell'assorbimento verso lunghezze d'onda maggiori, insieme ad un aumento dell'intensità di assorbimento e a un allargamento della differenza tra i picchi di assorbimento e di emissione (Stokes shift)[19].
Bibliografia della fonte
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- Iqbal The synthesis and properties of 1,4-diketo-pyrrolo[3,4-C]pyrroles Bulletin des Societes Chimiques Belges 1988 97 615 https://doi.org/10.1002/bscb.19880970804
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- Lorenz DPP dyes as ligands in transition-metal complexes Chemistry – A European Journal 2002 8 4047 https://doi.org/10.1002/1521-3765(20020902)8:17<4047::AID-CHEM4047>3.0.CO;2-M
- Beyerlein New photoluminescent conjugated polymers with 1,4-dioxo-3,6-diphenylpyrrolo[3,4-c]pyrrole (DPP) and 1,4-phenylene units in the main chain Macromolecular Rapid Communications 2000 21 182 https://doi.org/10.1002/(SICI)1521-3927(200003)21:4<182::AID-MARC182>3.0.CO;2-O
- Rabindranath Red emitting N-functionalized poly(1,4-diketo-3,6-diphenylpyrrolo[3,4-c]pyrrole) (poly-DPP): a deeply colored polymer with unusually large Stokes shift Macromolecules 2006 39 8250 https://doi.org/10.1021/ma061024e
- Mizuguchi Electronic-spectra of 1,4-diketo-3,6-diphenyl-pyrrolo-[3,4-c]-pyrrole in the solid-state Berichte der Bunsen-Gesellschaft – Physical Chemistry Chemical Physics 1992 96 597 https://doi.org/10.1002/bbpc.19920960414
- Mizuguchi Structures of 3,6-bis(3-chlorophenyl)pyrrolo[3,4-c]pyrrole-1,4-dione and 3,6-bis(4-chlorophenyl)pyrrolo[3,4-c]pyrrole-1,4-dione Acta Crystallographica Section B – Structural Science 1993 49 1056 https://doi.org/10.1107/S0108768193007645
- Wallquist 2002 159
- Jacquemin Substitution and chemical environment effects on the absorption spectrum of indigo Journal of Chemical Physics 2006 124 074104 https://doi.org/10.1063/1.2166018
- Dreuw Single-reference ab initio methods for the calculation of excited states of large molecules Chemical Reviews 2005 102 4009 https://doi.org/10.1021/cr0505627
- Luňák Excited-states of azo-compounds. 2. Vibrational structure of the electronic absorption-spectra of 4,4′-di-substituted azobenzene derivatives Chemical Physics 1994 184 255 https://doi.org/10.1016/0301-0104(94)00058-1
- Dähne Coupling principles in organic dyes Angewandte Chemie International Edition 1966 5 984 https://doi.org/10.1002/anie.196609841
- Edman Polarized-light spectroscopy of dihydropyrrolopyrroledione in liquids and liquid-crystals – molecular-conformation and influence by an anisotropic environment Journal of Physical Chemistry 1995 99 8504 https://doi.org/10.1021/j100021a009
- Potrawa Fluorescent dyes with large Stokes shifts – soluble dihydropyrrolopyrrolediones Chemische Berichte-Recueil 1987 120 1075 https://doi.org/10.1002/cber.19871200702
- Yamamoto H, Dan N. WO 005571 (Ciba Specialty Chemicals Holding); 2005.
- Strehmel The influence of sigma and pi acceptors on two-photon absorption and solvatochromism of dipolar and quadrupolar unsaturated organic compounds ChemPhysChem. 2003 4 249 https://doi.org/10.1002/cphc.200390041
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- Frisch 2004
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- Oxindigo: Color Deepening, Strong Fluorescence, and Large Stokes Shift by Donor‐Substitution (1996) - https://doi.org/10.1002/anie.199610161 - citato 6 volte
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Metriche
- Citata 65 volte (OpenAlex); riferimenti nella fonte: 28
- Citazioni per anno: 2026: 1, 2024: 2, 2023: 3, 2022: 2, 2021: 4, 2020: 5
Torna alla bibliografia della tesi · Generata dal catalogo bibliografia.json e da Crossref, OpenAlex, Europe PMC.