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Surfactant Media To Grow New Crystalline Cobalt 1,3,5-Benzenetricarboxylate Metal–Organic Frameworks

  • Hai-Sheng Lu
  • , Linlu Bai
  • , Wei-Wei Xiong
  • , Peizhou Li
  • , Junfeng Ding
  • , Guodong Zhang
  • , Tom Wu
  • , Yanli Zhao
  • , Jong-Min Lee
  • , Yanhui Yang*
  • , Baoyou Geng*
  • , Qichun Zhang*
  • *Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

Abstract

In this report, three new metal-organic frameworks (MOFs), [Co 3(μ3-OH)(HBTC)(BTC)2Co(HBTC)]·(HTEA)3·H2O (NTU-Z30), [Co(BTC)] ·HTEA·H2O (NTU-Z31), [Co3(BTC)4]·(HTEA)4 (NTU-Z32), where H3BTC = 1,3,5-benzenetricarboxylic acid, TEA = triethylamine, and NTU = Nanyang Technological University, have been successfully synthesized under surfactant media and have been carefully characterized by single-crystal X-ray diffraction, powder X-ray diffraction, thermogravimetric analysis, and IR spectromtry. NTU-Z30 has an unusual trimeric [Co3(μ3-OH)(COO)7] secondary building unit (SBU), which is different from the well-known trimeric [Co3O(COO)6] SBU. The topology studies indicate that NTU-Z30 and NTU-Z32 possess two new topologies, 3,3,6,7-c net and 2,8-c net, respectively, while NTU-Z31 has a known topology rtl type (3,6-c net). Magnetic analyses show that all three materials have weak antiferromagnetic behavior. Furthermore, NTU-Z30 has been selected as the heterogeneous catalyst for the aerobic epoxidation of alkene, and our results show that this material exhibits excellent catalytic activity as well as good stability. Our success in growing new crystalline cobalt 1,3,5- benzenetricarboxylate MOFs under surfactant media could pave a new road to preparing new diverse crystalline inorganic materials through a surfactant-thermal method. © 2014 American Chemical Society.
Original languageEnglish
Pages (from-to)8529-8537
JournalInorganic Chemistry
Volume53
Issue number16
Online published7 Aug 2014
DOIs
Publication statusPublished - 18 Aug 2014
Externally publishedYes

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