Tailoring Colors by O Annulation of Polycyclic Aromatic Hydrocarbons

Abstract: The synthesis of O‐doped polyaromatic hydro‐ carbons in which two polycyclic aromatic hydrocarbon sub units are bridged through one or two O atoms has been achieved. This includes high‐yield ring‐closure key steps that, depending on the reaction conditions, result in the formation of furanyl or pyranopyranyl linkages through intramolecular C−O bond formation. Comprehensive photophysical measurements in solution showed that these compounds have exceptionally high emission yields and tunable absorption properties throughout the UV/Vis spectral region. Electrochemical investigations showed that in all cases O annulation increases the electron‐donor capabilities by raising the HOMO energy level, whereas the LUMO energy level is less affected. Moreover, third‐order nonlinear optical (NLO) measurements on solutions or thin films containing the dyes showed very good values of the second hyperpolarizability. Importantly, poly (methyl methacrylate) films containing the pyranopyranyl derivatives exhibited weak linear absorption and NLO absorption compared to the nonlinearity and NLO refraction, respectively, and thus revealed them to be exceptional organic materials for photonic devices.

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
Tailoring Colors by O Annulation of Polycyclic Aromatic Hydrocarbons ; volume:23 ; number:10 ; year:2017 ; pages:2363-2378 ; extent:16
Chemistry - a European journal ; 23, Heft 10 (2017), 2363-2378 (gesamt 16)

Creator
Miletić, Tanja
Fermi, Andrea
Orfanos, Ioannis
Avramopoulos, Aggelos
De Leo, Federica
Demitri, Nicola
Bergamini, Giacomo
Ceroni, Paola
Papadopoulos, Manthos G.
Couris, Stelios
Bonifazi, Davide

DOI
10.1002/chem.201604866
URN
urn:nbn:de:101:1-2022092506283544599605
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
15.08.2025, 7:22 AM CEST

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