Supramolecularly engineered perylene bisimide assemblies exhibiting thermal transition from columnar to multilamellar structures

Shiki Yagai, Mari Usui, Tomohiro Seki, Haruno Murayama, Yoshihiro Kikkawa, Shinobu Uemura, Takashi Karatsu, Akihide Kitamura, Atsushi Asano, Shu Seki

Research output: Contribution to journalArticle

91 Citations (Scopus)

Abstract

Perylene 3,4:9,10-tetracarboxylic acid bisimide (PBI) was functionalized with ditopic cyanuric acid to organize it into complex columnar architectures through the formation of hydrogen-bonded supermacrocycles (rosette) by complexing with ditopic melamines possessing solubilizing alkoxyphenyl substituents. The aggregation study in solution using UV-vis and NMR spectroscopies showed the formation of extended aggregates through hydrogen-bonding and π-π stacking interactions. The cylindrical fibrillar nanostructures were visualized by microscopic techniques (AFM, TEM), and the formation of lyotropic mesophase was confirmed by polarized optical microscopy and SEM. X-ray diffraction study revealed that a well-defined hexagonal columnar (Col h) structure was formed by solution-casting of fibrillar assemblies. All of these results are consistent with the formation of hydrogen-bonded PBI rosettes that spontaneously organize into the Col h structure. Upon heating the Col h structure in the bulk state, a structural transition to a highly ordered lamellar (Lam) structure was observed by variable-temperature X-ray diffraction, differential scanning calorimetry, and AFM studies. IR study showed that the rearrangement of the hydrogen-bonding motifs occurs during the structural transition. These results suggest that such a striking structural transition is aided by the reorganization in the lowest level of self-organization, i.e., the rearrangement of hydrogen-bonded motifs from rosette to linear tape. A remarkable increase in the transient photoconductivity was observed by the flash-photolysis time-resolved microwave conductivity (FP-TRMC) measurements upon converting the Col h structure to the Lam structure. Transient absorption spectroscopy revealed that electron transfer from electron-donating alkoxyphenyl groups of melamine components to electron-deficient PBI moieties takes place, resulting in a higher probability of charge carrier generation in the Lam structure compared to the Col h structure.

Original languageEnglish
Pages (from-to)7983-7994
Number of pages12
JournalJournal of the American Chemical Society
Volume134
Issue number18
DOIs
Publication statusPublished - May 9 2012
Externally publishedYes

Fingerprint

Lamellar structures
Hydrogen
Melamine
Hot Temperature
Electrons
Hydrogen Bonding
X-Ray Diffraction
Hydrogen bonds
X ray diffraction
Acids
Nanostructures
Photolysis
Differential Scanning Calorimetry
Photoconductivity
Microwaves
Ultraviolet spectroscopy
Charge carriers
Absorption spectroscopy
Heating
Tapes

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Chemistry(all)
  • Biochemistry
  • Colloid and Surface Chemistry

Cite this

Supramolecularly engineered perylene bisimide assemblies exhibiting thermal transition from columnar to multilamellar structures. / Yagai, Shiki; Usui, Mari; Seki, Tomohiro; Murayama, Haruno; Kikkawa, Yoshihiro; Uemura, Shinobu; Karatsu, Takashi; Kitamura, Akihide; Asano, Atsushi; Seki, Shu.

In: Journal of the American Chemical Society, Vol. 134, No. 18, 09.05.2012, p. 7983-7994.

Research output: Contribution to journalArticle

Yagai, Shiki ; Usui, Mari ; Seki, Tomohiro ; Murayama, Haruno ; Kikkawa, Yoshihiro ; Uemura, Shinobu ; Karatsu, Takashi ; Kitamura, Akihide ; Asano, Atsushi ; Seki, Shu. / Supramolecularly engineered perylene bisimide assemblies exhibiting thermal transition from columnar to multilamellar structures. In: Journal of the American Chemical Society. 2012 ; Vol. 134, No. 18. pp. 7983-7994.
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abstract = "Perylene 3,4:9,10-tetracarboxylic acid bisimide (PBI) was functionalized with ditopic cyanuric acid to organize it into complex columnar architectures through the formation of hydrogen-bonded supermacrocycles (rosette) by complexing with ditopic melamines possessing solubilizing alkoxyphenyl substituents. The aggregation study in solution using UV-vis and NMR spectroscopies showed the formation of extended aggregates through hydrogen-bonding and π-π stacking interactions. The cylindrical fibrillar nanostructures were visualized by microscopic techniques (AFM, TEM), and the formation of lyotropic mesophase was confirmed by polarized optical microscopy and SEM. X-ray diffraction study revealed that a well-defined hexagonal columnar (Col h) structure was formed by solution-casting of fibrillar assemblies. All of these results are consistent with the formation of hydrogen-bonded PBI rosettes that spontaneously organize into the Col h structure. Upon heating the Col h structure in the bulk state, a structural transition to a highly ordered lamellar (Lam) structure was observed by variable-temperature X-ray diffraction, differential scanning calorimetry, and AFM studies. IR study showed that the rearrangement of the hydrogen-bonding motifs occurs during the structural transition. These results suggest that such a striking structural transition is aided by the reorganization in the lowest level of self-organization, i.e., the rearrangement of hydrogen-bonded motifs from rosette to linear tape. A remarkable increase in the transient photoconductivity was observed by the flash-photolysis time-resolved microwave conductivity (FP-TRMC) measurements upon converting the Col h structure to the Lam structure. Transient absorption spectroscopy revealed that electron transfer from electron-donating alkoxyphenyl groups of melamine components to electron-deficient PBI moieties takes place, resulting in a higher probability of charge carrier generation in the Lam structure compared to the Col h structure.",
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