Literature DB >> 26918910

Macrocyclic 2,7-Anthrylene Oligomers.

Yuta Yamamoto1, Kan Wakamatsu1, Tetsuo Iwanaga1, Hiroyasu Sato2, Shinji Toyota3.   

Abstract

A macrocyclic compound consisting of six 2,7-anthrylene units was successfully synthesized by Ni-mediated coupling of the corresponding dibromo precursor as a novel π-conjugated compound. This compound was sufficiently stable and soluble in organic solvents due to the presence of mesityl groups. X-ray analysis showed that the molecule had a nonplanar and hexagonal wheel-shaped framework of approximately S6 symmetry. The dynamic process between two S6 structures was observed by using the dynamic NMR technique, the barrier being 58 kJ mol(-1) . The spectroscopic properties of the hexamer were compared with those of analogous linear oligomers.
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  NMR spectroscopy; arenes; conformation analysis; macrocycles; oligomerization

Year:  2016        PMID: 26918910     DOI: 10.1002/asia.201600230

Source DB:  PubMed          Journal:  Chem Asian J        ISSN: 1861-471X


  1 in total

1.  1,3-Phenylene-bridged naphthalene wheels synthesized by one-pot Suzuki-Miyaura coupling and the complex of the hexamer with C60.

Authors:  Peifeng Mei; Akinobu Matsumoto; Hironobu Hayashi; Mitsuharu Suzuki; Naoki Aratani; Hiroko Yamada
Journal:  RSC Adv       Date:  2018-06-07       Impact factor: 3.361

  1 in total

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