The development of functionalized, luminescent, pyrene-based monomers has been and continues to be an area of great interest in terms of the design and fabrication of optical and electronic devices. Herein, a facile strategy to tune the emission color of pyrene-based chromophores has been established by simple functional group modification at the para position to the diphenylamino on the donor building block. Intriguing photophysical properties were obtained and are described both in different solutions and in the solid state. The results obtained could be explained by the Hammett method and by density functional theory (DFT) calculations. A good correlation was observed between the Hammett σpara constants of the functional groups para to the phenyl and the wavenumber (cm–1) of the emission profile. This positive correlation, namely between the σ constants of the functional groups and the emission properties of the monomers, can be used to develop a predictive method for these types of systems.
Two-photon absorption (TPA) properties of pyrene-based derivatives are rare as a result of the limited number of controllable synthetic methods to prepare them. However, these materials are in great demand given their potential practical application in photics and biological imaging. Herein, we present a set of pyrene-based dipolar donor-p-acceptor (D-p-A) fluorophores with a wide-range of color tuning and large TPA cross-sections (up to 2200 GM at 780 nm) by regioselective substitution at the 1,3-and 6,8-positions under the perspective of theoretical analysis. The linear and nonlinear optical properties of these compounds have been studied. The near-identical emission wavelengths between the two-photon-excited fluorescence (TPEF) and one-photon excited fluorescence (OPEF) indicated that they are generated from the same fluorescent excited state by either one-or two-photon excitation. With the exception of the strong donor [N(CH 3 ) 2 ] appended fluorophore, the TPEF exhibited a large red-shift compared with the OPEF spectra as a result of the complicated working mechanisms in operation, including intramolecular charge transfer (ICT) and twisted intramolecular charge transfer (TICT). All fluorophores exhibit high two-photon cross-sections (or two-photon brightness, dF), especially for 1348 GM, which indicated that these materials can be used as colorants for probe and bioimaging applications.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.