Issue 47, 2019

Donor–acceptor substituted 1,8-naphthalimides: design, synthesis, and structure–property relationship

Abstract

Research on developing new donor–acceptor (D–A) substituted 1,8-naphthalimide (NI) based molecular systems is a rapidly growing research area, which has resulted in several technological applications including fluorescent dyes, laser dyes, brightening agents, metal sensors, pH sensors, bioimaging, organic photovoltaics (OPVs), organic light-emitting diodes (OLEDs), and many more. The functionalization of the NI unit at the N-imide site and aromatic core is easy and cost-effective, which allows one not only to produce a vast array of NI derivatives but also tune its photophysical and electronic properties. The photophysical and electrochemical properties of D–A based NIs are dependent on the substitution pattern and the nature of the donor unit, which makes them prime derivatives for application in organic photonics and electronics as well as in biological studies. In this review, we have discussed the recent developments in the design, synthesis, and applications of D–A based NIs. The photonic and electronic properties of D–A based NIs are also discussed. This review will be helpful in generating potential strategies for tuning the photophysical and electronic properties of D–A based NIs for optoelectronic applications.

Graphical abstract: Donor–acceptor substituted 1,8-naphthalimides: design, synthesis, and structure–property relationship

Article information

Article type
Review Article
Submitted
18 May 2019
Accepted
04 Nov 2019
First published
12 Nov 2019

J. Mater. Chem. C, 2019,7, 14798-14815

Donor–acceptor substituted 1,8-naphthalimides: design, synthesis, and structure–property relationship

M. Poddar, G. Sivakumar and R. Misra, J. Mater. Chem. C, 2019, 7, 14798 DOI: 10.1039/C9TC02634G

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