4.7 Article

The design of dihalogenated TPE monoboronate complexes as mechanofluorochromic crystals

Journal

CRYSTENGCOMM
Volume 23, Issue 34, Pages 5908-5917

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ce00442e

Keywords

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Funding

  1. PAPIIT [IN209119]
  2. CONACYT [957838, A1-S-32820]
  3. DOE Office of Science User Facility [DE-AC02-05CH11231]
  4. UNAM

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Six mechanofluorochromic crystals have been reported, showing emission changes upon grinding in the 500-750 nm range. Replacing different moieties affects their quantum yields, with halogen substitution causing a decrease in φf. Analysis suggests that conformational changes upon grinding and reversible changes upon exposure to dichloromethane vapors are key characteristics of these crystals.
We report here six mechanofluorochromic crystals: three tetraphenylethylene difluoroboronates (-BF2, 3a-c) and three diphenylboronate derivatives (-B(Ph)(2), 4a-c) that change emission upon grinding. The corresponding photophysical studies allowed us to identify that most of them show emission in the 500-750 nm range, with the exchange of the -BF2 moiety for the -B(Ph)(2) moiety causing an improvement in their quantum yields (phi(f)). Halogen substitution in their structures caused a decrease of the phi(f) going from -Cl to -Br to -I. Combining single crystal and powder X-ray analyses, we determined that they are highly crystalline but prone to amorphization via mechanical stress, with a noticeable bathochromic shift of their emission upon grinding. Density functional theory computations indicate that conformational changes upon grinding could cause the observed changes. They undergo reversible changes upon exposure to vapors of dichloromethane, setting the path to develop bistable switches in the future.

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