4.7 Article

Thermochromism of rapid responses to temperature changes versus mechanochromism in a Ni-dithiolene complex salt

Journal

DALTON TRANSACTIONS
Volume 52, Issue 26, Pages 8918-8926

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d3dt01401k

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A thermochromic or mechanochromic material that can switch between stable states in response to temperature or pressure changes was investigated in this study. The material was found to form a uniform mixed stack through alternating stacking of its cations and anions, and a molecular solid through Coulomb and van der Waals interactions. The material exhibited reversible thermochromism, irreversible mechanochromism, intense near-IR absorbance, and a dielectric anomaly, all of which were attributed to the structural phase transition and alteration of p-orbital overlap between the anion and cation within the mixed stack.
A thermochromic or mechanochromic material can switch between at least two stable states in response to changes in temperature or static pressure/strain. In this study, we investigated a Ni-dithiolene dianion salt, 1,1'-diheptyl-4,4'-bipyridinium bis(maleonitriledithiolato)nickelate (1), and found that its cations and anions stack alternately to form a uniform mixed stack. These mixed stacks then combine to form a molecular solid through Coulomb and van der Waals interactions. Upon heating, 1 undergoes a reversible phase transition at around 340/320 K during the first heating/cooling cycle, resulting in rapid thermochromism with a color change from green (stable state) to red (metastable state) within a few seconds. This is the first report of a crystal of bis(maleonitriledithiolato)nickelate(II) salt with green color. Additionally, 1 exhibits irreversible mechanochromism, intense near-IR absorbance, and a dielectric anomaly. The structural phase transition is responsible for these properties, as it induces alterations in the p-orbital overlap between the anion and cation within a mixed stack. The intense near-IR absorbance arises from the ionpair charge transfer transition from [Ni(mnt)2]2- to 4,4'-bipyridinium.

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