Three-Dimensional Covalent Organic Frameworks with hea Topology

被引:54
|
作者
Li, Zonglong [1 ]
Sheng, Li [1 ]
Hsueh, Chouhung [1 ]
Wang, Xiaolin [1 ]
Cui, Hao [1 ]
Gao, Hongqiang [1 ]
Wu, Yanzhou [1 ]
Wang, Jianlong [1 ]
Tang, Yaping [1 ]
Xu, Hong [1 ]
He, Xiangming [1 ]
机构
[1] Tsinghua Univ, Inst Nucl & New Energy Technol, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
TARGETED SYNTHESIS; SURFACE-AREA; CRYSTALLINE; DESIGN; POLYMERS; CONDUCTION; HYDROGEN; CEQ;
D O I
10.1021/acs.chemmater.1c03156
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Three-dimensional (3D) covalent organic frameworks (COFs) are a new type of crystalline organic porous material, which have great application potential in various fields due to their complex pore structures and fully exposed active sites. The synthesis of 3D COFs with novel topologies is still challenging on account of limited secondary building units. Herein, we report a 3D COF with hea topology, which has never been reported before, utilizing a D-3h-symmetric precursor [2,3,6,7,14,15-hexakis(4-formylphenyl)triptycene (HFPTP)] and [tetrakis(4-amino biphenyl)methane (TABPM)]. 3D-hea-COFs display permanent porosity and a Brunauer-Emmett-Teller surface area of 1804.0 m(2) g(-1). Owing to the huge internal free volume of triptycene, 3D-hea-COFs show good adsorption performance for H-2, CO2, and CH4. Moreover, theoretical calculation reveals that both triptycene and tetraphenylmethane units contribute to enhance hydrogen storage capacity. The novel topology in this work expands the family of 3D COFs and provides new possibilities for designing efficient gas storage materials.
引用
收藏
页码:9618 / 9623
页数:6
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