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Updated: Aug 11, 2025

Ultrafast Time-resolved Near-IR Stimulated Raman Measurements of Functional π-conjugate Systems
Published on: February 10, 2020
Near-Infrared Piezochromism from an o-Carborane Dyad: Boron Clusters Facilitating a Wide-Range Redshift and High
Chunyan Lv1, Yunxia Shen2, Feng Cao1
1Department of Materials Chemistry, Huzhou University, East 2nd Ring Rd. No. 759, Huzhou, 313000, P. R. China.
Abstract:
Piezochromic materials, which exhibit a fluorescence response with large emission spectral shifts and high sensitivity, may be useful in important applications, but there have been few reports of such organic luminophores. Herein, we report a new high-sensitivity piezochromic material based on the incorporation of an o-carborane unit, which exhibits aggregation-induced emission properties. In a high-pressure experiment, compared to carborane-free MTY, which exhibits an emission spectral shift of 75 nm and a sensitivity of 19.1 nm ⋅ GPa-1 , the o-carborane dyad MTCb shows a larger emission wavelength difference of 131 nm and a higher sensitivity of 32.8 nm ⋅ GPa-1 , demonstrating a performance that ranks among the best of organic piezochromic materials reported thus far. MTCb molecules adopt a J-aggregated pattern and have relatively loose molecular packing in the crystalline state. Interestingly, nonconjugated spherical carborane can disrupt the π-π interactions between adjacent molecules during compression, which results in excellent piezochromic performance.
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