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


ABSTRACT: A large 1,3-phenylene-bridged hexameric naphthalene wheel N6 and a heptameric wheel N7 were synthesized simply by Suzuki-Miyaura coupling via one-pot reaction from monomers. We could control the distribution of N6 and N7via the reaction conditions. The hexameric wheel structure was revealed by X-ray diffraction analysis. The wheel N6 exhibited C60 encapsulation ability in the solid state, which was also confirmed by single crystal X-ray analysis.

SUBMITTER: Mei P 

PROVIDER: S-EPMC9080899 | biostudies-literature | 2018 Jun

REPOSITORIES: biostudies-literature

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1,3-Phenylene-bridged naphthalene wheels synthesized by one-pot Suzuki-Miyaura coupling and the complex of the hexamer with C<sub>60</sub>.

Mei Peifeng P   Matsumoto Akinobu A   Hayashi Hironobu H   Suzuki Mitsuharu M   Aratani Naoki N   Yamada Hiroko H  

RSC advances 20180607 37


A large 1,3-phenylene-bridged hexameric naphthalene wheel N6 and a heptameric wheel N7 were synthesized simply by Suzuki-Miyaura coupling <i>via</i> one-pot reaction from monomers. We could control the distribution of N6 and N7<i>via</i> the reaction conditions. The hexameric wheel structure was revealed by X-ray diffraction analysis. The wheel N6 exhibited C<sub>60</sub> encapsulation ability in the solid state, which was also confirmed by single crystal X-ray analysis. ...[more]

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