Issue 8, 2024

Tuning the charge stabilization and transport in naphthalimide-based semiconductors via a fused-ring and core-engineering strategy

Abstract

The synthesis and characterization of a family of rationally designed compounds based on naphthalimide units attached, through conjugated nitrogenated linkers (i.e. pyrazine and imidazoline units), to fused thiophene-based moieties is shown. This combination of different donor–acceptor moieties allows fine tuning of the HOMO and LUMO energy levels, and thus the modulation of their electronic properties. A comprehensive physical chemistry study is carried out, in which the nature of the neutral and charged species are analyzed and their electrical performance is understood in terms of molecular and supramolecular characteristics.

Graphical abstract: Tuning the charge stabilization and transport in naphthalimide-based semiconductors via a fused-ring and core-engineering strategy

Supplementary files

Article information

Article type
Research Article
Submitted
09 Jan 2024
Accepted
06 Mar 2024
First published
11 Mar 2024
This article is Open Access
Creative Commons BY-NC license

Mater. Chem. Front., 2024,8, 1981-1992

Tuning the charge stabilization and transport in naphthalimide-based semiconductors via a fused-ring and core-engineering strategy

R. González-Núñez, M. J. Alonso-Navarro, F. Suárez-Blas, E. Gala, M. M. Ramos, J. L. Segura and R. Ponce Ortiz, Mater. Chem. Front., 2024, 8, 1981 DOI: 10.1039/D4QM00029C

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