Issue 23, 2022

Highly efficient dual-state emission and two-photon absorption of novel naphthalimide functionalized cyanostilbene derivatives with finely tuned terminal alkoxyl groups

Abstract

Organic luminogens (OLs) that are capable of yielding strong fluorescence in both solution and the aggregated state are referred to as dual-state emission luminogens (DSEgens). They are able to achieve multiple functions within onefold materials owing to their applicability in both states, and are highly desirable though less explored compared to conventional and aggregation-induced-emission (AIE) OLs. In this work, cyanostilbene (CS) and naphthalimide (NI) were incorporated to construct novel DSEgens, which were functionalized by various alkoxyl chains at the CS unit (NICS-X, X = M, E, P, and B, respectively) by balancing the design principles for conventional and AIE OLs. The photophysical properties of NICS-Xs were investigated by steady-state and transient spectroscopies, which showed strong emission with quantum yields of luminescence (φ) above 0.70 in both solution and solids. In particular, the attachment of different terminal alkoxyl chains finely tuned the emission wavelength of NICS-Xs with a difference of up to ∼59 nm. Single-crystal structure analysis and theoretical calculations of these materials suggested that simply changing the length of the terminal alkoxyl chains could effectively adjust the molecular conformation and packing structure, thus inducing large shifts of the photoluminescence (PL) spectra. In addition, NICS-Xs show two-photon absorption behaviors in the dual states with a cross section of up to 238 Goeppert-Mayer. On the one hand, our study reported a new family of DESgens and a straightforward strategy to finely tune their photophysical properties. On the other hand, the correlations between the photophysical properties and the molecular/solid-state structures were revealed, which suggested new design ideas for developing novel high-performance DSEgens.

Graphical abstract: Highly efficient dual-state emission and two-photon absorption of novel naphthalimide functionalized cyanostilbene derivatives with finely tuned terminal alkoxyl groups

Associated articles

Supplementary files

Article information

Article type
Research Article
Submitted
23 set 2022
Accepted
14 out 2022
First published
31 out 2022

Mater. Chem. Front., 2022,6, 3522-3530

Highly efficient dual-state emission and two-photon absorption of novel naphthalimide functionalized cyanostilbene derivatives with finely tuned terminal alkoxyl groups

Y. Ni, L. Yang, L. Kong, C. Wang, Q. Zhang and J. Yang, Mater. Chem. Front., 2022, 6, 3522 DOI: 10.1039/D2QM00937D

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements