Polyimide covalent organic frameworks bearing star-shaped electron-deficient polycyclic aromatic hydrocarbon building blocks: molecular innovations for energy conversion and storage
Literature Information
Bin Yao, Guowang Li, Xianying Wu, Hongfei Sun, Xingyan Liu, Fei Li, Tingwang Guo
Polyimide covalent organic frameworks (PI-COFs) are outstanding functional materials for electrochemical energy conversion and storage owing to their integrated advantages of the high electroactive feature of polyimides and the periodic porous structure of COFs. Nevertheless, only anhydride monomers with C2 symmetry are generally used, and limited selectivity of electron-deficient monomers has become a major obstacle in the development of materials. The introduction of polycyclic aromatic hydrocarbons (PAHs) is a very effective method to regulate the structure–activity relationship of PI-COFs due to their excellent stability and electrical properties. Over the past two years, various star-shaped electron-deficient PAH building blocks possessing different compositions and topologies have been successfully fabricated, greatly improving the monomer selectivity and electrochemical performances of PI-COFs. This paper systematically summarizes the recent highlights in PI-COFs based on these building blocks. Firstly, the preparation of anhydride (or phthalic acid) monomers and PI-COFs related to different star-shaped PAHs is presented. Secondly, the applications of these PI-COFs in energy conversion and storage and the corresponding factors influencing their performance are discussed in detail. Finally, the future development of this meaningful field is briefly proposed.
Recommended Journals

Polycyclic Aromatic Compounds

Main Group Chemistry

Journal of the Indian Institute of Science

Medicinal Chemistry Research

Chinese Journal of Chemistry

Critical Reviews in Solid State and Materials Sciences

Bioorganic & Medicinal Chemistry Letters

Bioorganic & Medicinal Chemistry

Cellulose

Journal of Asian Natural Products Research
Related Literature
TiO2 doping by hydroxyurea at the nucleation stage: towards a new photocatalyst in the visible spectral range
R. Azouani, S. Tieng, K. Chhor, J.-F. Bocquet, P. Eloy, E. M. Gaigneaux, K. Klementiev, A. V. Kanaev
DOI: 10.1039/B923548E
Nitrogen oxide reaction with six-atom silver clusters supported on LTA zeolite
Amgalanbaatar Baldansuren, Rüdiger-A. Eichel, Emil Roduner
DOI: 10.1039/B903870A
A spiro-configured ambipolar host material for impressively efficient single-layer green electrophosphorescent devices
Wen-Yi Hung, Ting-Chih Wang, Hao-Chih Chiu, Hsiao-Fan Chen, Ken-Tsung Wong
DOI: 10.1039/C0CP00490A
Refractive indices for molecular crystals from the response of X-ray constrained Hartree–Fock wavefunctions
Dylan Jayatilaka, Parthapratim Munshi, Michael J. Turner, Judith A. K. Howard, Mark A. Spackman
DOI: 10.1039/B906072C
PELDOR study of conformations of double-spin-labeled single- and double-stranded DNA with non-nucleotide inserts
Nikita A. Kuznetsov, Alexandr D. Milov, Vladimir V. Koval, Rimma I. Samoilova, Yuri A. Grishin, Dmitry G. Knorre, Yuri D. Tsvetkov, Olga S. Fedorova, Sergei A. Dzuba
DOI: 10.1039/B904873A
Methaneactivation by V3PO10˙+ and V4O10˙+clusters: A comparative study
Xun-Lei Ding, Sheng-Gui He
DOI: 10.1039/C0CP00360C
Double layer in room temperature ionic liquids: influence of temperature and ionic size on the differential capacitance and electrocapillary curves
Renata Costa, Carlos M. Pereira, Fernando Silva
DOI: 10.1039/C003920A
Intermolecular vibrations of (CH2)2O–HF and –DF hydrogen bonded complexes investigated by Fourier transform infrared spectroscopy and ab initio calculations
DOI: 10.1039/C004100A
Temperature effects on COadsorption/desorption at Pt film electrodes: an electrochemical in situ infrared spectroscopic study
Bin Geng, Jun Cai, Sangzi Liang, Shao Xiong Liu, Ming Fang Li, Yan-Xia Chen
DOI: 10.1039/C002665D
A new cyanoaromatic photosensitizer vs.9,10-dicyanoanthracene: systematic comparison of the photophysical properties
Sylvie Blanc, Thierry Pigot, Cyril Cugnet, Ross Brown, Sylvie Lacombe
DOI: 10.1039/C002705G
You might also like
What precautions should be taken when handling 2-Chloro-1,2-bis(4-methylphenyl)ethanone (CAS: 71193-32-3)?
When handling 2-Chloro-1,2-bis(4-methylphenyl)ethanone (CAS: 71193-32-3), it is ...
What industries use 4-Ethoxy-3-(5-methyl-4-oxo-7-propyl-1,4-dihydroimidazo[5,1-f][1,2,4]triazin-2-yl)benzenesulfonyl chloride (CAS: 224789-26-8)?
4-Ethoxy-3-(5-methyl-4-oxo-7-propyl-1,4-dihydroimidazo[5,1-f][1,2,4]triazin-2-yl...
How should Methyl 3-Oxo-4-Androsten-17-Carboxylate (CAS: 2681-55-2) be stored?
Methyl 3-Oxo-4-Androsten-17-Carboxylate (CAS: 2681-55-2) should be stored in a c...
What are the main uses of (R)-3-Amino-4-(3-hexylphenylamino)-4-oxobutylphosphonic acid (CAS: 909725-61-7)?
(R)-3-Amino-4-(3-hexylphenylamino)-4-oxobutylphosphonic acid is primarily used i...
What regulatory guidelines apply to 2-Methyl-2-propanyl 3-amino-3-carbamoyl-1-azetidinecarboxylate (CAS: 1254120-14-3)?
2-Methyl-2-propanyl 3-amino-3-carbamoyl-1-azetidinecarboxylate (CAS: 1254120-14-...
Are there alternatives to (E)-4-(tert-Butoxy)-4-oxobut-2-enoic acid (CAS: 135355-96-3) in synthesis?
There are alternative reagents that can be used in synthesis instead of (E)-4-(t...
What are the physical and chemical properties of [2-(3-Chlorophenyl)-1,3-thiazol-4-yl]methanol (CAS: 121202-20-8)?
[2-(3-Chlorophenyl)-1,3-thiazol-4-yl]methanol (CAS: 121202-20-8) is a crystallin...
What is the market or research trend for Methyl (2S)-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]{[(4-methylphenyl)sulfonyl]oxy}acetate (CAS: 166249-17-8)?
The market and research trends for Methyl (2S)-[(4S)-2,2-dimethyl-1,3-dioxolan-4...
What is the market or research trend for 1-Bromo-2-isocyanatoethane (CAS: 42865-19-0)?
The market for 1-Bromo-2-isocyanatoethane (CAS: 42865-19-0) is driven by its use...
What are the main uses of 4-Nitro-D-phenylalanine hydrochloride (CAS: 147065-06-3)?
4-Nitro-D-phenylalanine hydrochloride (CAS: 147065-06-3) is primarily used in re...
Source Journal
Chemical Communications

ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry




