TY - JOUR
T1 - Coordination-Supported Imidazolate Networks
T2 - Water- and Heat-Stable Mesoporous Polymers for Catalysis
AU - Zhang, Pengfei
AU - Yang, Shize
AU - Chisholm, Matthew F.
AU - Jiang, Xueguang
AU - Huang, Caili
AU - Dai, Sheng
N1 - Publisher Copyright:
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2017/7/26
Y1 - 2017/7/26
N2 - The poor water stability of most porous coordination polymers (PCPs) or metal-organic frameworks (MOFs) is widely recognized as a barrier hampering their practical applications. Here, a facile and scalable route to prepare metal-containing polymers with a good stability in boiling water (100 °C, 24 h) and air (up to 390 °C) is presented. The bifunctional 1-vinylimidazole (VIm) with a coordinating site and a polymerizable organic group is introduced as the building block. This core strategy includes the synthesis of a rigid monomer with four VIm branches through a coordination process at room temperature, followed by a radical polymerization. We refer to this material as coordination-supported imidazolate networks (CINs). Interestingly, CINs are composed of rich mesopores from 2–15 nm, as characterized by low-energy (60 kV) STEM-HAADF images. In particular, the stable CINs illustrate a high turnover frequency (TOF) of 779 h−1 in the catalytic oxidation of phenol with H2O as the green solvent.
AB - The poor water stability of most porous coordination polymers (PCPs) or metal-organic frameworks (MOFs) is widely recognized as a barrier hampering their practical applications. Here, a facile and scalable route to prepare metal-containing polymers with a good stability in boiling water (100 °C, 24 h) and air (up to 390 °C) is presented. The bifunctional 1-vinylimidazole (VIm) with a coordinating site and a polymerizable organic group is introduced as the building block. This core strategy includes the synthesis of a rigid monomer with four VIm branches through a coordination process at room temperature, followed by a radical polymerization. We refer to this material as coordination-supported imidazolate networks (CINs). Interestingly, CINs are composed of rich mesopores from 2–15 nm, as characterized by low-energy (60 kV) STEM-HAADF images. In particular, the stable CINs illustrate a high turnover frequency (TOF) of 779 h−1 in the catalytic oxidation of phenol with H2O as the green solvent.
KW - coordination polymers
KW - mesoporous materials
KW - phenol oxidation
KW - polymers
KW - porous ionic liquids
UR - http://www.scopus.com/inward/record.url?scp=85021668223&partnerID=8YFLogxK
U2 - 10.1002/chem.201702430
DO - 10.1002/chem.201702430
M3 - Article
C2 - 28557146
AN - SCOPUS:85021668223
SN - 0947-6539
VL - 23
SP - 10038
EP - 10042
JO - Chemistry - A European Journal
JF - Chemistry - A European Journal
IS - 42
ER -