Please use this identifier to cite or link to this item:
|Title: ||Two-photon-absorption properties of pyrene-based dipolar D-π-A fluorophores|
|Authors: ||Wang, Chuan-Zeng|
Elsegood, Mark R.J.
Teat, Simon J.
|Issue Date: ||2018|
|Publisher: ||© Wiley-VCH|
|Citation: ||WANG, C-Z. ... et al., 2018. Two-photon-absorption properties of pyrene-based dipolar D-π-A fluorophores. ChemPhotoChem, 2, pp. 749-756.|
|Abstract: ||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‐π‐acceptor (D‐π‐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(CH3)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, δΦ), especially for 1348 GM, which indicated that these materials can be used as colorants for probe and bioimaging applications.|
|Description: ||This is the pre-peer reviewed version of the following article: WANG, C-Z. ... et al., 2018. Two-photon-absorption properties of pyrene-based dipolar D-π-A fluorophores. ChemPhotoChem, 2, pp. 749-756, which has been published in final form at https://doi.org/10.1002/cptc.201800053. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.|
|Sponsor: ||This present work was performed under the Cooperative Research Program of “Network Joint Research Center for Materials and
Devices (Institute for Materials Chemistry and Engineering, Kyushu University)"|
|Version: ||Accepted for publication|
|Publisher Link: ||https://doi.org/10.1002/cptc.201800053|
|Appears in Collections:||Published Articles (Chemistry)|
Files associated with this item:
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.