One-step, green synthesis of a supramolecular organogelator based on mellitic triimide for the recognition of aromatic compounds

Masashi Mamada, Tsuyoshi Minami, Hiroshi Katagiri, Takafumi Omiya, Shizuo Tokito

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Mellitic triimide derivatives with N-benzyl groups form conformations with concave cavities, that are capable of including aromatic molecules such as benzene, nitrobenzene, etc. In addition, they act as supramolecular gelators, which enable the detection of aromatic molecules as a gel-sol phase transition.

Original languageEnglish
Pages (from-to)8834-8837
Number of pages4
JournalChemical Communications
Volume53
Issue number63
DOIs
Publication statusPublished - Jan 1 2017

Fingerprint

Aromatic compounds
Molecules
Nitrobenzene
Polymethyl Methacrylate
Sols
Benzene
Conformations
Gels
Phase transitions
Derivatives
nitrobenzene

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Electronic, Optical and Magnetic Materials
  • Ceramics and Composites
  • Chemistry(all)
  • Surfaces, Coatings and Films
  • Metals and Alloys
  • Materials Chemistry

Cite this

One-step, green synthesis of a supramolecular organogelator based on mellitic triimide for the recognition of aromatic compounds. / Mamada, Masashi; Minami, Tsuyoshi; Katagiri, Hiroshi; Omiya, Takafumi; Tokito, Shizuo.

In: Chemical Communications, Vol. 53, No. 63, 01.01.2017, p. 8834-8837.

Research output: Contribution to journalArticle

Mamada, Masashi ; Minami, Tsuyoshi ; Katagiri, Hiroshi ; Omiya, Takafumi ; Tokito, Shizuo. / One-step, green synthesis of a supramolecular organogelator based on mellitic triimide for the recognition of aromatic compounds. In: Chemical Communications. 2017 ; Vol. 53, No. 63. pp. 8834-8837.
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