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Showing 1–9 of 9 results
Advanced filters: Author: Michito Yoshizawa Clear advanced filters
  • Long hydrocarbon chains are important biomolecules, but their selective recognition within synthetic hosts can be problematic due to the lack of specific binding sites. Here, the authors present a polyaromatic molecular tube capable of selectively binding a range of long hydrocarbons.

    • Kohei Yazaki
    • Yoshihisa Sei
    • Michito Yoshizawa
    Research
    Nature Communications
    Volume: 5, P: 1-6
  • The complex, multicomponent structures often found in nature are difficult to mimic synthetically. Here, the authors assemble a molecular analogue of a peanut through coordinative and π-stacking interactions, in which a polyaromatic double capsule ‘pod’ held together by metal ions encapsulates fullerene ‘beans’.

    • Kohei Yazaki
    • Munetaka Akita
    • Michito Yoshizawa
    ResearchOpen Access
    Nature Communications
    Volume: 8, P: 1-8
  • Radical initiators are useful chemical reagents for synthesis, but rapidly decompose on exposure to light. Here, the authors report a supramolecular nanocapsule capable of encapsulating radical initiators and imparting excellent photochemical stability.

    • Masahiro Yamashina
    • Yoshihisa Sei
    • Michito Yoshizawa
    Research
    Nature Communications
    Volume: 5, P: 1-7
  • Short nucleotides with just one or two bases do not generally form stable hydrogen-bonded pairs in water. Now, however, it has been shown that the hydrophobic interior of water-soluble coordination cages offers a sheltered environment in which stable duplexes can be formed.

    • Tomohisa Sawada
    • Michito Yoshizawa
    • Makoto Fujita
    Research
    Nature Chemistry
    Volume: 1, P: 53-56
  • The structures of inorganic clusters are commonly characterized by mass spectrometry (MS), but neutral sulfur clusters heavily fragment under MS conditions, preventing their exact mass determination. Here, the authors successfully perform MS on labile cyclic sulfur clusters by stabilizing them within ionic supramolecular capsules.

    • Sho Matsuno
    • Masahiro Yamashina
    • Michito Yoshizawa
    ResearchOpen Access
    Nature Communications
    Volume: 8, P: 1-7
  • Typical micelles are molecular assemblies composed of amphiphiles bearing linear alkyl chains. Herein, the authors present an uncommon type of cycloalkane-based bent amphiphile and its micelle which encapsulates large metal- complexes with high uptake efficiency, selectivity, and emissivity in water.

    • Mamiko Hanafusa
    • Yamato Tsuchida
    • Michito Yoshizawa
    ResearchOpen Access
    Nature Communications
    Volume: 11, P: 1-8
  • Photoresponsive molecular capsules that can be used in water are rare. Here, the authors construct polyaromatic nanocapsules via self-assembly from photoswitch-bearing amphiphilic molecules in water. Light induces a structural change in the amphiphiles, triggering the capsule to disassemble into monomers and release encapsulated guests.

    • Lorenzo Catti
    • Natsuki Kishida
    • Michito Yoshizawa
    ResearchOpen Access
    Nature Communications
    Volume: 10, P: 1-8
  • Molecular capsules typically bind only guests with volumes smaller than their cavities. Here, the authors find that a polyaromatic capsule accommodates linear amphiphilic oligomers in a length-dependent manner, whereas short chains are fully crammed into the cavity, long chains can be incorporated into the capsule in a threaded fashion.

    • Masahiro Yamashina
    • Shunsuke Kusaba
    • Michito Yoshizawa
    ResearchOpen Access
    Nature Communications
    Volume: 9, P: 1-10
  • Nonvolatile luminescent liquids are solvent-free fluids with a range of flexible electronic applications. Here, the authors show that anthracenes enveloped in branched aliphatic compounds are stable emissive liquids, with emissive and thermoresponsive properties that may be tuned by addition of dopants.

    • Sukumaran Santhosh Babu
    • Martin J. Hollamby
    • Takashi Nakanishi
    ResearchOpen Access
    Nature Communications
    Volume: 4, P: 1-8