Photoluminescent materials that exhibit tunable emission properties when subjected to mechanical stimuli have numerous potential applications. Although many organic/inorganic and organometallic compounds display this property, called mechanochromic luminescence, most of these materials undergo a crystalline-to-amorphous (C → A) phase transition; examples of crystalline-to-crystalline (C 1 → C 2 ) transformation are rare. Single-crystal X-ray diffraction may allow direct analysis of the molecular packing of mechanochromic luminescence materials before and after C 1 → C 2 transformation, which may help to understand the underlying mechanism of this transformation. Reported herein is a mechanochromic luminescence material that displays an unprecedented type of C 1 → C 2 transformation mediated by a transient amorphous phase (C 1 → [A] → C 2 ). This mechanochromic luminescence material was developed by introducing soft triethylene glycol side chains in a crystalline gold(I) complex that exhibits mechanochromic luminescence based on a C → A phase transition. When this new gold(I) complex bearing triethylene glycol chains was subjected to a mechanical or thermal stimulus, dynamic phase changes were observed with irreversible luminescence color changes from blue to yellow to green in both the cases. The crystallinity of the mechanically generated C 2 phase was lower than that of the thermally generated C 2 phase. This is because the mechanically induced C 1 → [A] → C 2 process was finished within seconds, whereas the thermal C 1 → [A] → C 2 process occurred over a few minutes. To control the C 1 → [A] → C 2 transformation, we doped the complex with an inactive soft component. This successfully made the transformation reversible (from green to blue) upon thermal annealing of the mechanically obtained C 2 phase. This approach allowed the development of an imaging process involving invisible information storage even under UV illumination.
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Yagai et al. (2015) studied this question.
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