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Pendant-Type Helicene Oligomers with p-Phenylene Ethynylene Main Chains: Synthesis, Reversible Formation of Ladderlike Bimolecular Aggregates, and Control of Intramolecular and Intermolecular Aggregation.
Saito, Nozomi; Kondo, Yutaro; Sawato, Tsukasa; Shigeno, Masanori; Amemiya, Ryo; Yamaguchi, Masahiko.
Afiliação
  • Saito N; Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University , Aoba, Sendai 980-8578, Japan.
  • Kondo Y; Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University , Aoba, Sendai 980-8578, Japan.
  • Sawato T; Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University , Aoba, Sendai 980-8578, Japan.
  • Shigeno M; Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University , Aoba, Sendai 980-8578, Japan.
  • Amemiya R; Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University , Aoba, Sendai 980-8578, Japan.
  • Yamaguchi M; Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University , Aoba, Sendai 980-8578, Japan.
J Org Chem ; 82(16): 8389-8406, 2017 08 18.
Article em En | MEDLINE | ID: mdl-28686027
ABSTRACT
Pendant-type (P)-helicene oligomers with p-phenylene ethynylene main chains up to a tetramer were synthesized by a building block method. The (P)-tetramer reversibly formed a ladderlike bimolecular aggregate upon cooling and disaggregated upon heating in (trifluoromethyl)benzene. Two bis(tetramer)s, in which two (P)-tetramers were connected by hexadecamethylene linkers, were also synthesized. The head-to-tail bis(tetramer) formed an intramolecular aggregate, and the head-to-head bis(tetramer) formed an intermolecular aggregate in toluene. The results suggest the antiparallel aggregation structure of the pendant-type (P)-tetramers. The structure of the linker was proven to be effective in controlling intramolecular and intermolecular aggregations.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article