Photomechanochromic vs. mechanochromic fluorescence of a unichromophoric bimodal molecular solid: multicolour fluorescence patterning

Mechanofluorochromism (MFC) of molecular solids generally results from the variation of intermolecular interactions induced by external mechanical forces. However, the use of internal photomechanical forces to perturb intermolecular interactions for multicolour fluorescence responses has yet to be d...

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Published inChemical science (Cambridge) Vol. 9; no. 48; pp. 8990 - 9001
Main Authors Hsu, Li-Yun, Maity, Subhendu, Matsunaga, Yuki, Hsu, Ying-Feng, Liu, Yi-Hung, Peng, Shie-Ming, Shinmyozu, Teruo, Yang, Jye-Shane
Format Journal Article
LanguageEnglish
Published CAMBRIDGE Royal Soc Chemistry 28.12.2018
Royal Society of Chemistry
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Abstract Mechanofluorochromism (MFC) of molecular solids generally results from the variation of intermolecular interactions induced by external mechanical forces. However, the use of internal photomechanical forces to perturb intermolecular interactions for multicolour fluorescence responses has yet to be demonstrated. Herein we report a unichromophoric anthracene-pentiptycene derivative (1) that displays both MFC and photomechanofluorochromism (PMFC), which lead to various fluorescence colours including red-green-blue (RGB) and near-pure white-light emission. Compound 1 crystallizes in two polymorphs, the yellow (Y) and green (G) emissive forms, in which the pairwise stacked anthracene groups undergo [4 + 4] photodimerization to form the UV (black) emissive photodimer 2 and meanwhile exert photomechanical stresses on the neighbouring molecules. While the photomechanical stresses cause an excimer-to-monomer switching that results in a blue fluorescent state for the Y form, a red-emissive super dimer is photomechanically produced for the G form. The recovery of the Y form demands heating, but the G form could be restored by selective photoexcitation of the super dimer. X-ray crystal structures of the Y and G forms and the photodimer 2 generated through single-crystal-to-single-crystal transformation provide a clue to the origins of polymorph-dependent PMFC. The corresponding MFC and mechano-activated vapofluorochromism (VFC) of 1 also shed light on the structure-property relationship. The ability to spatially and temporally control the fluorochromicity of 1 is demonstrated by a series of multicolour fluorescence patterning of angelfishes.
AbstractList Mechanofluorochromism (MFC) of molecular solids generally results from the variation of intermolecular interactions induced by external mechanical forces. However, the use of internal photomechanical forces to perturb intermolecular interactions for multicolour fluorescence responses has yet to be demonstrated. Herein we report a unichromophoric anthracene-pentiptycene derivative ( ) that displays both MFC and photomechanofluorochromism (PMFC), which lead to various fluorescence colours including red-green-blue (RGB) and near-pure white-light emission. Compound crystallizes in two polymorphs, the yellow (Y) and green (G) emissive forms, in which the pairwise stacked anthracene groups undergo [4 + 4] photodimerization to form the UV (black) emissive photodimer and meanwhile exert photomechanical stresses on the neighbouring molecules. While the photomechanical stresses cause an excimer-to-monomer switching that results in a blue fluorescent state for the Y form, a red-emissive "super dimer" is photomechanically produced for the G form. The recovery of the Y form demands heating, but the G form could be restored by selective photoexcitation of the super dimer. X-ray crystal structures of the Y and G forms and the photodimer generated through single-crystal-to-single-crystal transformation provide a clue to the origins of polymorph-dependent PMFC. The corresponding MFC and mechano-activated vapofluorochromism (VFC) of also shed light on the structure-property relationship. The ability to spatially and temporally control the fluorochromicity of is demonstrated by a series of multicolour fluorescence patterning of "angelfishes".
Mechanofluorochromism (MFC) of molecular solids generally results from the variation of intermolecular interactions induced by external mechanical forces. However, the use of internal photomechanical forces to perturb intermolecular interactions for multicolour fluorescence responses has yet to be demonstrated. Herein we report a unichromophoric anthracene-pentiptycene derivative (1) that displays both MFC and photomechanofluorochromism (PMFC), which lead to various fluorescence colours including red-green-blue (RGB) and near-pure white-light emission. Compound 1 crystallizes in two polymorphs, the yellow (Y) and green (G) emissive forms, in which the pairwise stacked anthracene groups undergo [4 + 4] photodimerization to form the UV (black) emissive photodimer 2 and meanwhile exert photomechanical stresses on the neighbouring molecules. While the photomechanical stresses cause an excimer-to-monomer switching that results in a blue fluorescent state for the Y form, a red-emissive super dimer is photomechanically produced for the G form. The recovery of the Y form demands heating, but the G form could be restored by selective photoexcitation of the super dimer. X-ray crystal structures of the Y and G forms and the photodimer 2 generated through single-crystal-to-single-crystal transformation provide a clue to the origins of polymorph-dependent PMFC. The corresponding MFC and mechano-activated vapofluorochromism (VFC) of 1 also shed light on the structure-property relationship. The ability to spatially and temporally control the fluorochromicity of 1 is demonstrated by a series of multicolour fluorescence patterning of angelfishes.
Mechanofluorochromism (MFC) of molecular solids generally results from the variation of intermolecular interactions induced by external mechanical forces. However, the use of internal photomechanical forces to perturb intermolecular interactions for multicolour fluorescence responses has yet to be demonstrated. Herein we report a unichromophoric anthracene–pentiptycene derivative ( 1 ) that displays both MFC and photomechanofluorochromism (PMFC), which lead to various fluorescence colours including red-green-blue (RGB) and near-pure white-light emission. Compound 1 crystallizes in two polymorphs, the yellow (Y) and green (G) emissive forms, in which the pairwise stacked anthracene groups undergo [4 + 4] photodimerization to form the UV (black) emissive photodimer 2 and meanwhile exert photomechanical stresses on the neighbouring molecules. While the photomechanical stresses cause an excimer-to-monomer switching that results in a blue fluorescent state for the Y form, a red-emissive “super dimer” is photomechanically produced for the G form. The recovery of the Y form demands heating, but the G form could be restored by selective photoexcitation of the super dimer. X-ray crystal structures of the Y and G forms and the photodimer 2 generated through single-crystal-to-single-crystal transformation provide a clue to the origins of polymorph-dependent PMFC. The corresponding MFC and mechano-activated vapofluorochromism (VFC) of 1 also shed light on the structure–property relationship. The ability to spatially and temporally control the fluorochromicity of 1 is demonstrated by a series of multicolour fluorescence patterning of “angelfishes”.
Author Liu, Yi-Hung
Hsu, Ying-Feng
Matsunaga, Yuki
Maity, Subhendu
Peng, Shie-Ming
Shinmyozu, Teruo
Yang, Jye-Shane
Hsu, Li-Yun
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  surname: Yang
  fullname: Yang, Jye-Shane
  email: jsyang@ntu.edu.tw
  organization: Natl Taiwan Univ, Dept Chem, Taipei 10617, Taiwan
BackLink https://www.ncbi.nlm.nih.gov/pubmed/30647891$$D View this record in MEDLINE/PubMed
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Issue 48
Keywords DELAYED FLUORESCENCE
LUMINESCENCE
TUNABLE EMISSION
PHOTOISOMERIZATION
DIARYLETHENE
WHITE-LIGHT EMISSION
PHOTOCHROMISM
VAPOCHROMISM
CRYSTAL
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Snippet Mechanofluorochromism (MFC) of molecular solids generally results from the variation of intermolecular interactions induced by external mechanical forces....
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SubjectTerms Anthracene
Chemistry
Chemistry, Multidisciplinary
Crystal structure
Crystallography
Dimers
Emissivity
Excimers
Fluorescence
Light emission
Mechanoluminescence
NMR
Nuclear magnetic resonance
Photoexcitation
Physical Sciences
Science & Technology
Single crystals
Stability
Stresses
White light
Title Photomechanochromic vs. mechanochromic fluorescence of a unichromophoric bimodal molecular solid: multicolour fluorescence patterning
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https://www.ncbi.nlm.nih.gov/pubmed/30647891
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