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Effect of Alkyl Chain Length of N-Alkyl-N'-(2-benzylphenyl)ureas on Gelation.
Komiyama, Tomoki; Harada, Yoko; Hase, Takayuki; Mori, Sota; Kimura, Shinya; Yokoya, Masashi; Yamanaka, Masamichi.
Afiliação
  • Komiyama T; Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo, 204-8588, Japan.
  • Harada Y; Department of Chemistry, Shizuoka University, 836 Ohya, Suruga-ku, Shizuoka, 422-8529, Japan.
  • Hase T; Department of Chemistry, Shizuoka University, 836 Ohya, Suruga-ku, Shizuoka, 422-8529, Japan.
  • Mori S; Department of Chemistry, Shizuoka University, 836 Ohya, Suruga-ku, Shizuoka, 422-8529, Japan.
  • Kimura S; Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo, 204-8588, Japan.
  • Yokoya M; Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo, 204-8588, Japan.
  • Yamanaka M; Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo, 204-8588, Japan.
Chem Asian J ; 16(13): 1750-1755, 2021 Jul 05.
Article em En | MEDLINE | ID: mdl-34008323
ABSTRACT
Urea derivatives that were substituted with a 2-benzylphenyl group and an alkyl group functioned as low molecular weight gelators for various organic solvents and ionic liquids. Urea derivatives with long alkyl chains were effective for the gelation of polar solvents. However, they were not suitable for the gelation of non-polar solvents, whereas urea derivatives with short alkyl chains were effective. Ionic liquids were similar to polar solvents in that urea derivatives with long alkyl chains were the most effective gelators. The physical properties of the formed supramolecular gels were analyzed by dynamic viscoelasticity measurements using a rheometer.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article