Positional Isomerism and Short Hydrogen Bonds Govern Photochromic Behaviour in dipyridyl-NDI…Formic Acid Co-crystals

Abstract

Positional isomerism in pyridyl naphthalene diimide formic acid co-crystals controls crystal symmetry, yielding centrosymmetric (I2/a) and polar (Pc) structures from 4- and 2-pyridyl isomers respectively. Both materials function as reversible photochromic switches upon UV irradiation via a proton-coupled electron transfer type mechanism, generating NDI radical anions, as confirmed by UV-Vis and ATR-FTIR spectroscopy.

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Article information

Article type
Paper
Submitted
02 Apr 2026
Accepted
28 May 2026
First published
29 May 2026
This article is Open Access
Creative Commons BY license

CrystEngComm, 2026, Accepted Manuscript

Positional Isomerism and Short Hydrogen Bonds Govern Photochromic Behaviour in dipyridyl-NDI…Formic Acid Co-crystals

A. Ishaq, L. Male and N. R. Champness, CrystEngComm, 2026, Accepted Manuscript , DOI: 10.1039/D6CE00262E

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