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Sigmoidally hydrochromic molecular porous crystal with rotatable dendrons

Vapochromic behaviour of porous crystals is beneficial for facile and rapid detection of gaseous molecules without electricity. Toward this end, tailored molecular designs have been established for metal–organic, covalent-bonded and hydrogen-bonded frameworks. Here, we explore the hydrochromic chemi...

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Detalles Bibliográficos
Autores principales: Yamagishi, Hiroshi, Nakajima, Sae, Yoo, Jooyoung, Okazaki, Masato, Takeda, Youhei, Minakata, Satoshi, Albrecht, Ken, Yamamoto, Kimihisa, Badía-Domínguez, Irene, Oliva, Maria Moreno, Delgado, M. Carmen Ruiz, Ikemoto, Yuka, Sato, Hiroyasu, Imoto, Kenta, Nakagawa, Kosuke, Tokoro, Hiroko, Ohkoshi, Shin-ichi, Yamamoto, Yohei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9814496/
https://www.ncbi.nlm.nih.gov/pubmed/36703455
http://dx.doi.org/10.1038/s42004-020-00364-3
Descripción
Sumario:Vapochromic behaviour of porous crystals is beneficial for facile and rapid detection of gaseous molecules without electricity. Toward this end, tailored molecular designs have been established for metal–organic, covalent-bonded and hydrogen-bonded frameworks. Here, we explore the hydrochromic chemistry of a van der Waals (VDW) porous crystal. The VDW porous crystal VPC-1 is formed from a novel aromatic dendrimer having a dibenzophenazine core and multibranched carbazole dendrons. Although the constituent molecules are connected via VDW forces, VPC-1 maintains its structural integrity even after desolvation. VPC-1 exhibits reversible colour changes upon uptake/release of water molecules due to the charge transfer character of the constituent dendrimer. Detailed structural analyses reveal that the outermost carbazole units alone are mobile in the crystal and twist simultaneously in response to water vapour. Thermodynamic analysis suggests that the sigmoidal water sorption is induced by the affinity alternation of the pore surface from hydrophobic to hydrophilic.