1,3-Phenylene-bridged naphthalene wheels synthesized by one-pot Suzuki–Miyaura coupling and the complex of the hexamer with C(60)

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...

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Autores principales: Mei, Peifeng, Matsumoto, Akinobu, Hayashi, Hironobu, Suzuki, Mitsuharu, Aratani, Naoki, Yamada, Hiroko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080899/
https://www.ncbi.nlm.nih.gov/pubmed/35542343
http://dx.doi.org/10.1039/c8ra03601b
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author Mei, Peifeng
Matsumoto, Akinobu
Hayashi, Hironobu
Suzuki, Mitsuharu
Aratani, Naoki
Yamada, Hiroko
author_facet Mei, Peifeng
Matsumoto, Akinobu
Hayashi, Hironobu
Suzuki, Mitsuharu
Aratani, Naoki
Yamada, Hiroko
author_sort Mei, Peifeng
collection PubMed
description 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 C(60) encapsulation ability in the solid state, which was also confirmed by single crystal X-ray analysis.
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spelling pubmed-90808992022-05-09 1,3-Phenylene-bridged naphthalene wheels synthesized by one-pot Suzuki–Miyaura coupling and the complex of the hexamer with C(60) Mei, Peifeng Matsumoto, Akinobu Hayashi, Hironobu Suzuki, Mitsuharu Aratani, Naoki Yamada, Hiroko RSC Adv Chemistry 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 C(60) encapsulation ability in the solid state, which was also confirmed by single crystal X-ray analysis. The Royal Society of Chemistry 2018-06-07 /pmc/articles/PMC9080899/ /pubmed/35542343 http://dx.doi.org/10.1039/c8ra03601b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Mei, Peifeng
Matsumoto, Akinobu
Hayashi, Hironobu
Suzuki, Mitsuharu
Aratani, Naoki
Yamada, Hiroko
1,3-Phenylene-bridged naphthalene wheels synthesized by one-pot Suzuki–Miyaura coupling and the complex of the hexamer with C(60)
title 1,3-Phenylene-bridged naphthalene wheels synthesized by one-pot Suzuki–Miyaura coupling and the complex of the hexamer with C(60)
title_full 1,3-Phenylene-bridged naphthalene wheels synthesized by one-pot Suzuki–Miyaura coupling and the complex of the hexamer with C(60)
title_fullStr 1,3-Phenylene-bridged naphthalene wheels synthesized by one-pot Suzuki–Miyaura coupling and the complex of the hexamer with C(60)
title_full_unstemmed 1,3-Phenylene-bridged naphthalene wheels synthesized by one-pot Suzuki–Miyaura coupling and the complex of the hexamer with C(60)
title_short 1,3-Phenylene-bridged naphthalene wheels synthesized by one-pot Suzuki–Miyaura coupling and the complex of the hexamer with C(60)
title_sort 1,3-phenylene-bridged naphthalene wheels synthesized by one-pot suzuki–miyaura coupling and the complex of the hexamer with c(60)
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080899/
https://www.ncbi.nlm.nih.gov/pubmed/35542343
http://dx.doi.org/10.1039/c8ra03601b
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