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An Ultrastable and Easily Regenerated Hydrogen-Bonded Organic Molecular Framework with Permanent Porosity.
Hu, Falu; Liu, Caiping; Wu, Mingyan; Pang, Jiandong; Jiang, Feilong; Yuan, Daqiang; Hong, Maochun.
Afiliação
  • Hu F; State Key Lab of Structure Chemistry, Fujian Institute of Research on the Structure of Matter, CAS Institution, Fuzhou, 350002, China.
  • Liu C; University of Chinese Academy of Sciences, Beijing, 100049, China.
  • Wu M; State Key Lab of Structure Chemistry, Fujian Institute of Research on the Structure of Matter, CAS Institution, Fuzhou, 350002, China.
  • Pang J; State Key Lab of Structure Chemistry, Fujian Institute of Research on the Structure of Matter, CAS Institution, Fuzhou, 350002, China.
  • Jiang F; State Key Lab of Structure Chemistry, Fujian Institute of Research on the Structure of Matter, CAS Institution, Fuzhou, 350002, China.
  • Yuan D; University of Chinese Academy of Sciences, Beijing, 100049, China.
  • Hong M; State Key Lab of Structure Chemistry, Fujian Institute of Research on the Structure of Matter, CAS Institution, Fuzhou, 350002, China.
Angew Chem Int Ed Engl ; 56(8): 2101-2104, 2017 02 13.
Article em En | MEDLINE | ID: mdl-28090721
ABSTRACT
A robust hydrogen-bonded organic framework HOF-TCBP (H4 TCBP=3,3',5,5'-tetrakis-(4-carboxyphenyl)-1,1'-biphenyl) has been successfully constructed and structurally characterized. It possesses a permanent 3D porous structure with a 5-fold interpenetrated dia topological network. This activated HOF-TCBP has a high BET surface area of 2066 m2 g-1 and is capable of highly selective adsorption and separation of light hydrocarbons under ambient conditions. It shows excellent thermal stability, as demonstrated by PXRD experiments and N2 adsorption tests. Practical use of HOF-TCBP is facilitated by the ease of its preparation and renewal through rotary evaporation.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article