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Supramolecular Polymer Polymorphism: Spontaneous Helix-Helicoid Transition through Dislocation of Hydrogen-Bonded π-Rosettes.
Otsuka, Chie; Takahashi, Sho; Isobe, Atsushi; Saito, Takuho; Aizawa, Takumi; Tsuchida, Ryoma; Yamashita, Shuhei; Harano, Koji; Hanayama, Hiroki; Shimizu, Nobutaka; Takagi, Hideaki; Haruki, Rie; Liu, Luzhi; Hollamby, Martin J; Ohkubo, Takahiro; Yagai, Shiki.
Afiliação
  • Otsuka C; Division of Advanced Science and Engineering, Graduate School of Science and Engineering, Chiba University, Chiba 263-8522, Japan.
  • Takahashi S; Division of Advanced Science and Engineering, Graduate School of Science and Engineering, Chiba University, Chiba 263-8522, Japan.
  • Isobe A; Division of Advanced Science and Engineering, Graduate School of Science and Engineering, Chiba University, Chiba 263-8522, Japan.
  • Saito T; Division of Advanced Science and Engineering, Graduate School of Science and Engineering, Chiba University, Chiba 263-8522, Japan.
  • Aizawa T; Division of Advanced Science and Engineering, Graduate School of Science and Engineering, Chiba University, Chiba 263-8522, Japan.
  • Tsuchida R; Division of Advanced Science and Engineering, Graduate School of Science and Engineering, Chiba University, Chiba 263-8522, Japan.
  • Yamashita S; Division of Advanced Science and Engineering, Graduate School of Science and Engineering, Chiba University, Chiba 263-8522, Japan.
  • Harano K; Center for Basic Research on Materials, National Institute for Materials Science, Tsukuba 305-0044, Japan.
  • Hanayama H; Department of Applied Chemistry and Biotechnology, Graduate School of Engineering, Chiba University, Chiba 263-8522, Japan.
  • Shimizu N; Photon Factory, Institute of Materials Structure Science, High Energy Accelerator Research Organization, Tsukuba 305-0801, Japan.
  • Takagi H; Photon Factory, Institute of Materials Structure Science, High Energy Accelerator Research Organization, Tsukuba 305-0801, Japan.
  • Haruki R; Photon Factory, Institute of Materials Structure Science, High Energy Accelerator Research Organization, Tsukuba 305-0801, Japan.
  • Liu L; School of Chemistry and Chemical Engineering, Guangxi University, Nanning, Guangxi 530004, China.
  • Hollamby MJ; Department of Chemistry, School of Chemical and Physical Sciences, Keele University, Keele, Staffordshire ST55BG, U.K.
  • Ohkubo T; Department of Applied Chemistry and Biotechnology, Graduate School of Engineering, Chiba University, Chiba 263-8522, Japan.
  • Yagai S; Department of Applied Chemistry and Biotechnology, Graduate School of Engineering, Chiba University, Chiba 263-8522, Japan.
J Am Chem Soc ; 145(41): 22563-22576, 2023 Oct 18.
Article em En | MEDLINE | ID: mdl-37796243
ABSTRACT
Polymorphism, a phenomenon whereby disparate self-assembled products can be formed from identical molecules, has incited interest in the field of supramolecular polymers. Conventionally, the monomers that constitute supramolecular polymers are engineered to facilitate one-dimensional aggregation and, consequently, their polymorphism surfaces primarily when the states of assembly differ significantly. This engenders polymorphs of divergent dimensionalities such as one- and two-dimensional aggregates. Notwithstanding, realizing supramolecular polymer polymorphism, wherein polymorphs maintain one-dimensional aggregation, persists as a daunting challenge. In this work, we expound upon the manifestation of two supramolecular polymer polymorphs formed from a large discotic supramolecular monomer (rosette), which consists of six hydrogen-bonded molecules with an extended π-conjugated core. These polymorphs are generated in mixtures of chloroform and methylcyclohexane, attributable to distinctly different disc stacking arrangements. The face-to-face (minimal displacement) and offset (large displacement) stacking arrangements can be predicated on their distinctive photophysical properties. The face-to-face stacking results in a twisted helix structure. Conversely, the offset stacking induces inherent curvature in the supramolecular fiber, thereby culminating in a hollow helical coil (helicoid). While both polymorphs exhibit bistability in nonpolar solvent compositions, the face-to-face stacking attains stability purely in a kinetic sense within a polar solvent composition and undergoes conversion into offset stacking through a dislocation of stacked rosettes. This occurs without the dissociation and nucleation of monomers, leading to unprecedented helicoidal folding of supramolecular polymers. Our findings augment our understanding of supramolecular polymer polymorphism, but they also highlight a distinctive method for achieving helicoidal folding in supramolecular polymers.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Am Chem Soc Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Am Chem Soc Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Japão