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Synthesis of ordered carbonaceous frameworks from organic crystals

Despite recent advances in the carbonization of organic crystalline solids like metal-organic frameworks or supramolecular frameworks, it has been challenging to convert crystalline organic solids into ordered carbonaceous frameworks. Herein, we report a route to attaining such ordered frameworks vi...

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Detalles Bibliográficos
Autores principales: Nishihara, Hirotomo, Hirota, Tetsuya, Matsuura, Kenta, Ohwada, Mao, Hoshino, Norihisa, Akutagawa, Tomoyuki, Higuchi, Takeshi, Jinnai, Hiroshi, Koseki, Yoshitaka, Kasai, Hitoshi, Matsuo, Yoshiaki, Maruyama, Jun, Hayasaka, Yuichiro, Konaka, Hisashi, Yamada, Yasuhiro, Yamaguchi, Shingi, Kamiya, Kazuhide, Kamimura, Takuya, Nobukuni, Hirofumi, Tani, Fumito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524644/
https://www.ncbi.nlm.nih.gov/pubmed/28740078
http://dx.doi.org/10.1038/s41467-017-00152-z
Descripción
Sumario:Despite recent advances in the carbonization of organic crystalline solids like metal-organic frameworks or supramolecular frameworks, it has been challenging to convert crystalline organic solids into ordered carbonaceous frameworks. Herein, we report a route to attaining such ordered frameworks via the carbonization of an organic crystal of a Ni-containing cyclic porphyrin dimer (Ni(2)-CPD(Py)). This dimer comprises two Ni–porphyrins linked by two butadiyne (diacetylene) moieties through phenyl groups. The Ni(2)-CPD(Py) crystal is thermally converted into a crystalline covalent-organic framework at 581 K and is further converted into ordered carbonaceous frameworks equipped with electrical conductivity by subsequent carbonization at 873–1073 K. In addition, the porphyrin’s Ni–N(4) unit is also well retained and embedded in the final framework. The resulting ordered carbonaceous frameworks exhibit an intermediate structure, between organic-based frameworks and carbon materials, with advantageous electrocatalysis. This principle enables the chemical molecular-level structural design of three-dimensional carbonaceous frameworks.