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 in | Chemical science (Cambridge) Vol. 9; no. 48; pp. 8990 - 9001 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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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. |
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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 |
Author_xml | – sequence: 1 givenname: Li-Yun surname: Hsu fullname: Hsu, Li-Yun organization: Natl Taiwan Univ, Dept Chem, Taipei 10617, Taiwan – sequence: 2 givenname: Subhendu orcidid: 0000-0002-6622-5806 surname: Maity fullname: Maity, Subhendu organization: Natl Taiwan Univ, Dept Chem, Taipei 10617, Taiwan – sequence: 3 givenname: Yuki surname: Matsunaga fullname: Matsunaga, Yuki organization: Natl Taiwan Univ, Dept Chem, Taipei 10617, Taiwan – sequence: 4 givenname: Ying-Feng surname: Hsu fullname: Hsu, Ying-Feng organization: Natl Taiwan Univ, Dept Chem, Taipei 10617, Taiwan – sequence: 5 givenname: Yi-Hung surname: Liu fullname: Liu, Yi-Hung organization: Natl Taiwan Univ, Dept Chem, Taipei 10617, Taiwan – sequence: 6 givenname: Shie-Ming surname: Peng fullname: Peng, Shie-Ming organization: Natl Taiwan Univ, Dept Chem, Taipei 10617, Taiwan – sequence: 7 givenname: Teruo surname: Shinmyozu fullname: Shinmyozu, Teruo organization: Natl Taiwan Univ, Dept Chem, Taipei 10617, Taiwan – sequence: 8 givenname: Jye-Shane orcidid: 0000-0003-4022-2989 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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Keywords | DELAYED FLUORESCENCE LUMINESCENCE TUNABLE EMISSION PHOTOISOMERIZATION DIARYLETHENE WHITE-LIGHT EMISSION PHOTOCHROMISM VAPOCHROMISM CRYSTAL POLYMER-FILMS |
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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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