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Synthesis and Evaluation of a 1,3a,6a-Triazapentalene (TAP)-Bonded System.
Ito, Masami; Mera, Akane; Mashimo, Takaki; Seki, Tomohiro; Karanjit, Sangita; Ohashi, Eisaku; Nakayama, Atsushi; Kitamura, Kei; Hamura, Toshiyuki; Ito, Hajime; Namba, Kosuke.
Afiliación
  • Ito M; Department of Pharmaceutical Science, Tokushima University, 1-78-1 Shomachi, Tokushima, 770-8505, Japan.
  • Mera A; Department of Pharmaceutical Science, Tokushima University, 1-78-1 Shomachi, Tokushima, 770-8505, Japan.
  • Mashimo T; Division of Applied Chemistry & Frontier Chemistry Center, Faculty of Engineering, Hokkaido University, Sapporo, Hokkaido, 060-8628, Japan.
  • Seki T; Division of Applied Chemistry & Frontier Chemistry Center, Faculty of Engineering, Hokkaido University, Sapporo, Hokkaido, 060-8628, Japan.
  • Karanjit S; Department of Pharmaceutical Science, Tokushima University, 1-78-1 Shomachi, Tokushima, 770-8505, Japan.
  • Ohashi E; Department of Pharmaceutical Science, Tokushima University, 1-78-1 Shomachi, Tokushima, 770-8505, Japan.
  • Nakayama A; Department of Pharmaceutical Science, Tokushima University, 1-78-1 Shomachi, Tokushima, 770-8505, Japan.
  • Kitamura K; Department of Applied Chemistry for Environment, School of Science and Technology, Kwansei Gakuin University, 2-1 Gakuen, Sanda, Hyogo, 669-1337, Japan.
  • Hamura T; Department of Applied Chemistry for Environment, School of Science and Technology, Kwansei Gakuin University, 2-1 Gakuen, Sanda, Hyogo, 669-1337, Japan.
  • Ito H; Division of Applied Chemistry & Frontier Chemistry Center, Faculty of Engineering, Hokkaido University, Sapporo, Hokkaido, 060-8628, Japan.
  • Namba K; Department of Pharmaceutical Science, Tokushima University, 1-78-1 Shomachi, Tokushima, 770-8505, Japan.
Chemistry ; 24(67): 17727-17733, 2018 Dec 03.
Article en En | MEDLINE | ID: mdl-30298702
A method of synthesizing a directly connected 1,3a,6a-triazapentalene (TAP) ring system as a linearly bonded aromatic system with a planar form was established. Various TAP-dimers and a 2-alkyl-TAP-trimer were synthesized and their fluorescence properties were evaluated. Although the direct connection of the TAP ring with other TAP rings did not affect the fluorescence properties in diluted solvent, TAP-dimers showed unique fluorescence properties derived from the aggregation state under highly concentrated conditions. In particular, TAP-dimer 5 f showed aggregation-induced emission in highly concentrated solution, and 5 b showed typical mechanochromic fluorescence in the solid state despite their compact molecular size.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2018 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2018 Tipo del documento: Article País de afiliación: Japón