Home Journals Articles Updates About
CN
image
收藏切换
Nitrogen-containing linkage-bonds in covalent organic frameworks: Synthesis and applications
收藏切换
PDF
Liying Oua, Zhenluan Xuea, Bo Lia, *, Zhiwei Jina, Jiaochan Zhongb, Lixia Yangb, Penghui Shaob, *, Shenglian Luob
Chinese Chemical Letters | 2025, 36(6) : 110294
Less
收藏切换
Chinese Chemical Letters | 2025, 36(6): 110294
• Review •
Nitrogen-containing linkage-bonds in covalent organic frameworks: Synthesis and applications
Full
Liying Oua, Zhenluan Xuea, Bo Lia, *, Zhiwei Jina, Jiaochan Zhongb, Lixia Yangb, Penghui Shaob, *, Shenglian Luob
Affiliations
  • aSchool of Materials Science and Engineering, Nanchang Hangkong University, Nanchang 330063, China
  • bKey Laboratory of Jiangxi Province for Persistent Pollutants Prevention Control and Resource Reuse, Nanchang Hangkong University, Nanchang 330063, China
Published: 2025-06-15 doi: 10.1016/j.cclet.2024.110294
Outline
收藏切换

Covalent organic frameworks (COFs) are crystalline porous polymeric materials composed of organic monomers connected by strong covalent bonds and offer high stability, good crystallinity, a large specific surface area, and controllable structures. COFs are widely used in the fields of adsorption and separation, catalysis, photovoltaics, and drug-delivery. The structural regulation and performance optimization of COFs can be realized through the modification of ligands and the selection of linkage methods. In which, the types of linkage are closely related to the stability and performance of COFs. In this review, nitrogen-containing linkage-bonds (NCLBs) in COFs are divided into N-containing double bonds, N-containing conjugated rings and N-containing unconjugated rings. The association between structure and performance of COFs is elaborated and the synthesis methods of COFs are systematically summarized. Moreover, the structural design, theoretical prediction and machinable application of COFs are prospected

Covalent organic frameworks  /  Nitrogen-containing linkage-bonds  /  Structure and properties  /  Synthesis strategy and application  /  Porous materials
Liying Ou, Zhenluan Xue, Bo Li, Zhiwei Jin, Jiaochan Zhong, Lixia Yang, Penghui Shao, Shenglian Luo. Nitrogen-containing linkage-bonds in covalent organic frameworks: Synthesis and applications[J]. Chinese Chemical Letters, 2025 , 36 (6) : 110294 - . DOI: 10.1016/j.cclet.2024.110294
Full Text
Less
1 Introduction
Less
COFs are a class of organic, porous crystalline materials composed of light elements (e.g., C, O, N, and B) connected by covalent bonds. COFs have been in public view since Yaghi published his initial study in 2005 [1]. In less than two decades, COFs have emerged as highly desirable materials owing to its exceptional crystallization properties, low density, large specific surface area, and remarkable structural designability. Therefore, they possess great application potential in molecular adsorption and separation [2], catalysis [3], sensing [2,4], energy storage [5], drug-delivery [6], etc.
Generally, the synthesis of covalent bonds in COFs is reversible [7], which contributes to optimize the structure of COFs and repair defects, thus forming a highly ordered framework structure. COFs formed by combining monomers with different shapes can be categorized as two-dimensional (2D) and three-dimensional (3D) COFs. According to the shape of stacked units, 2D COFs are further divided into triangles, quadrilaterals, pentagons, and hexagons [8].
COFs belong to crystalline polymers, in which monomers are linked by specific dynamic covalent bonds to form a lattice structure. Among the many linkages in the COFs, nitrogen-containing linkage-bonds (NCLBs) develop rapidly because of its easy synthesis, excellent environment stability, great coordination and catalysis.
In this review, the common COFs with NCLBs are classified into three types, including carbon/nitrogen-nitrogen double bonds, N-containing conjugated rings and N-containing unconjugated rings. The corresponding synthesis methods (Tables S1-S8 in Supporting information) and applications are expounded. Additionally, the cultivation methods of single crystals COFs (scCOFs) are briefly summarized, and the CCDC numbers of common scCOFs are provided (Table S9 and Fig. S1 in Supporting information), and the development of COFs is prospected.
2 Classification of NCLBs in COFs
Less
With cross-disciplinary interaction and integration, various types of COFs structures and connection methods are developed to meet different application requirements. Currently, NCLBs in COFs primarily include C═N, N═N and imidazole. We categorize these bonds into three groups based on structural commonality (Fig. 1) and summarize the general equations of the COFs synthesis (Ar, Ar1 and Ar2 represent different aromatic ligands, R, R1, R2 represent different substituents).
2.1 COFs based on N-containing double bonds linkage units
2.1.1 Imine-linked units
An imine bond (C=N) is primarily formed through the Schiff base condensation reaction between aldehydes (or ketones) and amines (or ammonia), catalyzed by acid (Eq. 1). Most imine-linked COFs, such as JUC-641 [9], NI-COF-1 [10], and DAA-TFPT-COF [11], were synthesized using acetic acid as the catalyst under solvothermal conditions (Table S1). The synthetic methods of these COFs are similar and have a certain reference value. Moreover, the synthesis of aldehyde and amine monomers is relatively straightforward, which contributes to the rapid development of this kind COFs materials over the past two decades. Currently, COFs are mainly connected by imine bonds, and the imine-linked COFs account for more than 60% of the total COFs [12]. Imine-linked COFs with a variety of structures and exceptional crystallinity have been explored extensively in both 2D and 3D COFs. They are widely used in various fields, including organic catalysis, adsorption and separation, photocatalysis, and sensor.
Most of imine-linked COFs focus on elucidating structure-function relationship, and excellent properties can be obtained by introducing different chemical groups into the structure. For example, pyridine groups can improve the adsorption and recovery abilities of Hg2+ in wastewater [13], and changing the orientation of imine bonds can significantly alter the photophysical and electrochemical properties of COFs [14]. At present, the study of imine-linked COFs has gradually focused on the regulation of ligand conformation, which extends from the original planar 2D network to the 3D framework. For example, drawing inspiration from the torsion phenomenon observed in 2D planar molecules, Cheng et al. synthesized a highly crystalline 3D-An-COF by incorporating anthracene units to form steric hindrance in the vertical direction [15]. Due to the absence of π···π interactions, anthracene units were exposed to the pore structure. 3D-An-COF exhibited distinct yellow fluorescent emission under ultraviolet (UV) light excitation, which can be utilized as a sensor to detect trace amounts of antibiotics in aqueous environments. Fang et al. synthesized 3D COFs (JUC-641 and JUC-642) with nia nets by using planar hexagonal and triangular prism nodes [9]. Both COFs had high crystallinity and can maintain abundant pores in strong acidic and alkaline environments. The separation factor of JUC-642 for benzene and cyclohexane was as high as 2.02, which exceeds the previously reported 3D COFs (Fig. 2a). It indicates that the COFs can be further optimized and developed by studying the structure and properties.
To date, a wide range of organic ligands with various functional groups have been designed (Fig. 2b) to satisfy the requirements for regulating the properties of materials. For example, molecules with donor-acceptor (D-A) properties, such as 4,7-diphenylbenzo[c][1,2,5] thiadiazole [16], 4,4′,4′′,4′′′-(benzo[c][1,2,5]thiadiazole-4,7-diylbis(9,9-dimethyl-9,10-dihydroacridine-10,2,7-triyl))tetrabenzaldehyde [17] and pyrene-based monomers [18], were used to construct photocatalytic hydrogen evolution monomers. And heterotriangulenes were used to enhance charge-carrier mobility [19]. It is worth noting that certain molecules can serve multiple roles as monomers. An et al. synthesized the COFs utilizing four (4-methylphenyl)vinyl units as monomers, which exhibited catalytic capabilities for 2e oxygen reduction reaction (ORR) [20]. You et al. demonstrated the great potential of COFs based on tetraphenylethylene in tumor cell imaging and therapy through its aggregation-induced emission properties [21]. Additionally, molecules with distorted conformations, such as tetra-phenylmethane [22] and saddle-shaped cyclooctatetrathiophene [23], and organic monomers with cage-like structures [24], were used to construct 3D COFs. However, currently, the structure of ligands cannot predict the folding and interlayer arrangement of COFs accurately [25], and the unique nonplanar spatial assembly further complicates synthesis procedures. Even though imine-linked COFs have surpassed other categories in terms of quantity, there is still ample room for exploration.
In addition, imine bond is an important chemical intermediate, which is widely used in organic materials synthesis and drug synthesis. Provided that the framework structure of the COFs remains stable, the imine bond can be transformed into other types of linkage bonds, such as amide bond [26], C—N bond [27], azo bond [28], quinolone [29,30], azoles [31,32] and other cyclic connecting units (Fig. 2c). In 2018, Li et al. demonstrated that imine-linked COF-1 can be transformed into quinoline-linked MF-1 by aza-Diels-Alder cycloaddition reaction. Cyclic quinoline improved the stability of the structure, and can effectively adjust the π electron delocalization, thus enhancing the photoelectric performance of the imine bonds [30]. In addition, these aromatic rings exposed to the pore can further meet the design requirements of some specific properties. Thus, many studies adopted "4 + 2 cycloaddition" reaction to further transform imine bonds. In 2024, Zhao et al. demonstrated that imine-linked Im-COF-TFPPy-PDA can be converted into azine-linked Py-azine COF by monomer exchange. The first fused BF-COFs linked with bicyclic-fused-ring was obtained by Criss-Cross [3 + 2] cycloaddition [33]. This strategy realized the transformation of the linking bond from linear to cyclic structure, which makes the structure of COFs on longer limited to direct synthesis or monomers conversion.
2.1.2 Azo-linked units
The methods of introducing azo bonds into COFs are few due to the low reversibility and difficulty of azo bond synthesis reaction [28]. Here, three methods of introducing azo bonds into COFs are summarized as follows:
Firstly, azo-linkage can be obtained by catalyzing the coupling reaction of amines group (Eq. 2). In 2021, Wu et al. prepared Azo-CTF by copper-catalyzed oxidative homocoupling reaction of 4,4ʹ,4ʹʹ-(1,3,5-triazine-2,4,6-triyl)trianiline monomers [34]. Triazine in this structure can be used as a nitrogen-rich center, and azo bond can be used as an active energy storage site in organic electrode materials for LIBs (Fig. 3a). In addition, the porous structures of Azo-CTF provided an open space for lithium ions transmission. The ions transport path is shortened, which is conducive to the redox reaction of the battery. Azo-CTF cathode showed a large and reversible capacity output of 205.6 mAh/g at a current density of 0.1 A/g. However, compared to other types of linkage bonds, the harsh conditions and cumbersome steps of azo bond synthesis may be one of the reasons for the slow development of azo bonded COFs.
Secondly, azo-linkage can be obtained by the conversion of imine linked-COFs. In 2022, Zhao et al. treated imine-linked Im-COF-1 with 1,4-dinitrosobenzene under solvothermal conditions, and successfully prepared azo-COF-1 based on azo bonds connection (Fig. 3b) [28]. This method realized the transformation of COFs from –C═N– to –N═N– by changing linking monomers. Moreover, it solved the problem that the azo bond cannot be constructed through conventional monomer condensation due to its low reversibility. The successful formation of an azo bond not only expanded the repertoire of methods and strategies to connect COFs, but also presented a novel approach for synthesizing COFs that were previously challenging to fabricate due to their limited solubility and propensity for fragmentation reactions. In addition, as a bridging functional group, the azo bond exhibits narrow band gap characteristics [35], which has the potential to be used in a variety of applications such as electron transport and redox. However, the number of azo-linked COFs is much less than other types, and more synthetic methods and strategies need to be developed.
Thirdly, azo bonds can be introduced into monomers as functional groups through modification, and then COFs are constructed by other bridging methods. Most of high-performance COFs were obtained by this strategy, e.g., Tp-Azo [36] and NKCOF-47 [37]. It is worth noting that azobenzene is a commonly used photoswitching molecule, and its double bond structure can undergo reversible E-Z photoisomerization reaction. After UV irradiation, the structures and properties of the two isomers are quite different, leading to be applied in different fields. Previous studies have reported the synthesis of azobenzene-based photosensitive molecules [38] and its application [39] in the field of wastewater treatment. In 2023, Zhao et al. constructed Azo-COFs by condensation of (E)-2′-(phenyldiazenyl)-[1,1′:4′,1′′-terphenyl]-4,4′′-diamine with azobenzene structure and 4-[1,2,2-tris(4-formylphenyl)ethenyl]benzaldehyde (TPE) monomer [40]. The unique porous characteristics of the framework structure provided enough free space for the reversible trans-to-cis isomerization of azobenzene. After UV irradiation, the trans azobenzene exposed to pore space transformed into a cis configuration that extends out of the plane of the COFs layer, releasing more pore volume. Thus the diffusion of Light Green SF Yellowish (LGSF) into the pores was favorable and the adsorption capacity of Azo-COFs on LGSF was about 3.7-fold higher (74.78 mg/g) than that without UV irradiation (20.35 mg/g) (Fig. 3c). Luo et al. designed D-A (donor-acceptor) system with electron-rich benzene and electron-withdrawing triazine units, and introduced azobenzene in the form of branched chain to obtain ECUT-Azo-COF-1 [41]. After UV irradiation, the isomerization effect of azo bonds increased the absorption capacity of UO22+ by ECUT-Azo-1 from 220 mg/g to 1380 mg/g, and the yield of hydrogen peroxide in water increased from 62.8 µmol/l to 537.7 µmol/l.
2.1.3 Hydrazone-linked units
Hydrazone-linked COFs can be prepared by nucleophilic addition between carbonyl compounds (aldehydes/ketones) and hydrazine (Eq. 3). Compared with imine, hydrazone is more stable and can exist under normal conditions, and has garnered considerable attention in recent years. Wan et al. synthesized hydrazone-linked COF-DHz-APS with zwitterion groups under solvent thermal conditions. COF-DHz-APS was melted with Bro̷nsted acid (HA) and then processed into thin films by a simple hot-casting knife method. The porosity and density of these films leads to potential applications in fast ionic conduction and selective separation. Moreover, the structure and crystallinity of COFs were not destroyed, which solves the problem that COFs are powdery and difficult to process (Fig. 4a) [42].
Hydrazone-linked COFs possess multiple active sites and a regular π-conjugated system, thereby facilitating the contact with analytes and exhibiting advantageous signal amplification when utilized in sensing applications. Jiang et al. synthesized a Pythz-COF linked by hydrazone using pyrene-based monomer, which exhibited excellent crystallinity and thermal and chemical stability [43]. COFs doped with pyrene elements provided fluorescent channels, so Pythz-COF demonstrated the fluorescence quenching sensing effects toward p-nitrophenol, 2,4-dinitrophenol, and 2,4,6-trinitrophenol. In particular, the limit of detection for 2,4,6-trinitrophenol by Pythz-COF was only 0.76 µmol/l. Thus, it is an exceptional cyclic fluorescence sensor material for detecting nitrophenol explosives.
Hydrazone-linked COFs possess a receptor structure (carbonyl group) and have potential application in photocatalytic hydrogen evolution. Tang et al. introduced electron-rich conjugated benzotrithiophene (BTT) to prepare BTT-Hz-1 [44]. The hydrazone bond in this structure can be served as anchor site for Pt-species, which was conducive to the photogenerated electron reduction from Pt4+ to Pt0. Subsequently, the electron transfer process from Pt0 to H+ yielded final product (H2). The conjugated BTT structure can broaden the absorption range of visible light and improve the transfer efficiency of photocarriers. In addition, the electron-rich property of BBT contributes to improve the electron-hole separation efficiency. Therefore, BBT-Hz-1 had a high photocatalytic hydrogen evolution rate (17.27 mmol g-1h-1).
Modification of hydrazone-linked COFs is considered an effective strategy for optimizing stability, which can be achieved via monomer modification and post-treatment of COFs. Wang et al. introduced azobenzene groups into the conjugated framework, thereby enhancing the chemical stability of acylhydrazone-connected COFs by promoting π–π packing between adjacent layers [45]. The modified COF-NHU6 exhibited greatly stability in harsh environment, such as in strong acid, strong alkali, and boiling water (even after being exposed to air for one year). In addition, Yang et al. prepared a hydrazide-linked COF by oxidizing hydrazone-linked COFs under mild conditions [46]. Compared with before oxidation, the hydrazide-MTH-TFPB COF maintained high crystallinity and porosity even under severe conditions, such as boiling water, strong acids, and strong bases, demonstrating superior chemical stability (Fig. 4b). Furthermore, due to the favorable interactions between iodine molecules and hydrazide functional groups, the adsorption capacity of hydrazide-MTH-TFPB COF for iodine can be increased to 3050 mg/g.
2.2 COFs based on N-containing conjugated rings linkage units
2.2.1 Triazine-linked units
Generally, covalent triazine frameworks (CTFs) are synthesized through cyclic trimerization of aromatic nitriles (Eq. 4). In 2008, Thomas et al. synthesized the first triazine-linked CTF-1 using 1,4-dicyanobenzene as a raw material [47]. Most COFs of this type are catalyzed by ZnCl2 and reacted at 400 ℃. Although the structure of the triazine ring is very stable, some products will inevitably decompose at high temperature. Moreover, Zn2+ residue exists in the obtained material, which is not conducive to the application of CTFs. Some other synthetic methods also have been developed to construct triazine-linked COFs, such as superacid catalysis [48], amidine-based polycondensation at low temperature [49], P2O5 as a catalyst to promote aromatic amide transform into triazine rings [50], and nitrile trimerization routes optimized for polyphosphoric acid (H6P4O13) [51]. The development of these methods provides feasible mechanisms to synthesize CTFs with diverse structures. In 2023, a method of synthesizing CTFs by cyclotrimerization of aromatic aldehyde was proposed by Jin et al. The target products can be obtained under mild reaction condition (160 ℃, a small amount of catalyst), and perfluorinated CTF (CTF-TF) can be prepared by this method. The load of H3PO4 can be effectively locked upon the interaction of electronegative fluorine site and triazine unit. The proton conductivity of CTF-TF at 150 ℃ was 1.82 × 10−1 S/cm, which is the highest among the reported CTFs (Fig. 5a) [52]. Xu et al. confirmed that crystalline dual-porous pyridinyl CTF (Fe-CTF) with layered structure was successfully synthesized for the first time by using FeCl3-catalyzed polymerization of 2,6-pyridinitrile without solvent. More importantly, FeCl3 can coordinate with pyridine and triazine to form unique Fe-N3 single-atom active sites. During electrocatalysis, Fe-N3 can accelerate ORR reaction kinetics, thus improving battery performance [53].
Triazine ring has good conjugation, and its conjugation links with ethylene or benzene ring groups can exhibit great photoelectromagnetic properties. For example, the biphenyl unit in CTF-2 formed a layered micro-mesoporous structure [54], which can enhance the structural stability compared to CTF-1. And it provided a large number of lithium storage active sites. Thus, as an anode, CTF-2 had ultrahigh capacitance (1526 mAh/g at 0.1 A/g), and can be applied to lithium batteries due to the excellent electrochemical performance. Moreover, CTFs can also store K and Na with physical properties similar to Li. Thus, CTFs had great potential application in energy storage devices [55]. In addition, Liu et al. obtained a hyperconjugated structure of a TA-Por-sp2-COF by connecting the porphyrin unit with triazine [56]. The synergistic effect of the electron donor and electron absorbing groups in the hyperconjugated system realized a high photogenerated electron utilization rate. And it had sufficient porosity to provide the reactants for full diffusion; thus, TA-Por-sp2-COF had good photo-catalytic performance. Benzylamine can be completely reacted by TA-Por-sp2-COF (as a photocatalyst) within 2 h under white LED irradiation. The selectivity of this reaction was more than 99%, which showed excellent performance in other similar photocatalytic reactions.
Triazine ring is conjugated and nitrogen-rich, which can be utilized as an active site for gas storage or adsorption separation. Zhou et al. used 4-acetylbenzonitrile as a two-in-one monomer and trifluoromethanesulfonic acid-catalyzed trimerization to synthesize an aryl-triazine-linked 2D COF, which had good thermal stability and can be used for the adsorption of phenol, bisphenol A, 1-naphthol, and other organic pollutants [57].
2.2.2 Imidazole-linked units
Imidazole is one of the important structures in N-containing heterocycles. In the past decades, people have explored a variety of imidazole synthesis methods and tried to apply them to the synthesis of imidazole-linked COFs. The common synthetic pathway of imidazole-linked COFs is Debus-Radziszewski reaction. In this reaction process, diketone and ammonia are dehydrated and condensed into diimine, and then condensed with aldehyde to form imidazole ring (Eq. 5). Wang et al. synthesized imidazole-linked fully conjugated 3D BUCT-COF-7 through one-pot multicomponent Debus-Radziszewski reaction of the saddle-shaped aldehyde-substituted cyclooctatetrathiophene, pyrene-4,5,9,10-tetraone, and ammonium acetate [58]. BUCT-COF-7 can be used as a metal-free electrocatalyst because of its rich heteroatom and excellent ORR activity. BUCT-COF-7 as cathode catalyst was assembled into the electrolyzer, the electrochemical yield rate of H2O2 was as high as 326.9 mmol g-1h-1, indicating the potential application of BUCT-COF-7 in energy and environmental catalysis.
On the basis of Debus-Radziszewski synthesis method, Zhang et al. proposed an approach of constructing imidazole-linked COFs with multiple monomers (Fig. 5b). The structures of N-substituted imidazolyl COFs can be designed variously by using ammonium acetate, diketone, aldehyde and aromatic amine as raw materials [59]. The synthesized COFs exhibited ultrastability in strong acid and alkali, and the substituent groups can be replaced according to different applications. Under the guidance of this strategy, phosphate-functionalized LZU-530 was synthesized and showed good adsorption capacity for UO22+ in strong acid environment (95 mg/g, 2 mol/L HNO3).
2.2.3 Thiazole-linked units
Thiazole ring can be synthesized in two ways. The first is the reaction between imine bonds and sulphur monomers. The electrophilicity of sp2-C and the nucleophilicity of S8 in imines can be used in cascade cycloaddition to obtain thiazoles. The second is that the amino group condenses with aldehyde group and then oxidizes with the adjacent sulfhydryl group to form a ring. The above two methods to obtain thiazole are essentially post-modified cyclization by imine bonds (Eq. 6). In 2018, imide-linked TTT-COF was converted into thiazole-linked TTI-COF by Bettina's team through sulfur-assisted imine bond [60]. The linkage-change from imine to thiazole improved the acid resistance, which provided enlightenment for the synthesis of thiazole-linked COFs. In 2023, Lang et al. applied TTT-COF to the photocatalytic oxidation of organic sulfides based on the research result of Bettina [61]. Under blue LED irradiation, methyl phenyl sulfide can be converted into sulfoxide under the action of TTT-COF and TTI-COF, respectively. The conversion rate of methyl phenyl sulfide in TTT-COF was about 8 times that in TTI-COF. Wang et al. synthesized three kinds of azoles-linked COFs based on imine-linked ILCOF-1, including thiazole-linked TZ-COF, oxazole-linked OZ-COF and imidazole-linked IZ-COF (Fig. 5c) [62]. D-π-A structure was formed by combining pyrene group with linkage units. This structural feature can effectively promote charge transfer and separation of H+ from the carrier, thus inhibiting photoexcited charge recombination. Among these three azole structures, thiazole linkage possessed wider visible light absorption, narrower band gap, and more effective electron-hole separation. In the process of photocatalytic production of H2O2, the yield of TZ-COF (268 µmol h-1g-1) was higher than that of OZ-COF (220 µmol h-1g-1) and IZ-COF (120 µmol h-1g-1).
2.3 COFs based on N-containing unconjugated rings linkage units
2.3.1 Imide-linked units
Imide-linked COFs (PI-COF) can be obtained by the reaction of aromatic dianhydride and triamine (Eq. 7). In 2014, Yan et al. employed the solvothermal method to prepare the first imide-connected PI-COF-1 with a pore size of 33 Å. PI-COF-3 with a pore size of 53 Å was prepared by increasing the length of the monomer molecule [63]. Since then, most PI-COFs of this type have been synthesized using solvothermal method. However, the invertibility of the imide bond in the synthesis process is poor, which leads to the difficulty of product crystallization and long reaction time. To solve this problem, Johannes et al. proposed the ionothermal synthesis of PI-COFs, where porous PI-COFs were synthesized in the mixture of zinc chloride and eutectic salts at high temperature [64]. Compared with the traditional solvothermal method, the reaction time of the ion thermal method was reduced considerably; however, the reaction process was performed at high temperature. In view of this, in 2022, they also proposed an alcohol-assisted hydrothermal polymerization approach for PI-COFs, which converted imine bonds into imide bonds through ion exchange and realized the conversion between COFs in an environmentally friendly manner [65].
Pyromellitic dianhydride, naphthalene-1,4,5,8-tetracarboxylic acid, and perylene-3,4,9,10-tetracarboxylic dianhydride are the commonly used PI-COF monomers. The combination of monomers with different conjugated structures has a significant influence on the energy storage performance of PI-COFs. Gu et al. precisely regulated the size of conjugated units in COFs at the atomic level [66]. They found that the spin density isosurfaces of the imine radical intermediates around single atoms decreased with the increase of conjugated group size. Therefore, the radical electrons can delocalize effectively within the molecule, which enhanced the thermodynamic stability of the imine radical intermediates. Correspondingly, at a current density of 50 mA/g, the capacitance retention of the COF-modified cathode increased from 56% to 96% after 100 cycles. Additionally, Huang et al. synthesized imide-linked HAHATN-PMDA-COF using hexa(p-anilinyl) hexaazatrinaphthalene and pyromellitic dianhydride. There are two kinds of pores in the structure of HAHATN-PMDA-COF, and their sizes were 1.58 nm and 0.95 nm, respectively. Carbonyl and phenazine units were distributed in these uniform one-dimensional channels, which contributed to the homogeneous deposition of lithium ions, thus improving lithium utilization and stability in battery applications (Fig. 6) [67]. In addition to planar adjustments, 3D spatial adjustments can also change the performance of COFs. Besides, the performance of COFs can be modulated by adjusting 3D spatial structure. In addition, the performance of COFs can be adjusted by adjusting the three-dimensional spatial structure. Wang et al. introduced a modulator to adjust the interlayer stacking mode of NKCOF-11 from overlapping (AA) to stagger stacking (ABC) [68]. The absorption capacity of ABC-stacked COFs for ethylene (C2H4) or carbon dioxide (CO2) was increased by 60%. These synthetic strategies provide some inspiration and guidance for COFs structural adjustments.
2.3.2 Other nitrogen-containing rings
o-Difluoro can form non-conjugated heterocycles (Eq. 8) by nucleophilic substitution with the amino group on aromatic ring and its neighbouring groups (amine, mercapto, etc.). Zeng et al. prepared CoPc-DNDS-COF by using 2,5-diaminobenzene-1,4-dithiol monomer [69]. Huang et al. synthesized a new piperazine-linked M1Pc-NH2−M2PcF8 via nucleophilic substitution reaction between octaminophthalocyanines and hexadecafluorophthalocyanines [70]. Piperazine linkage can be readily oxidized to cationic radicals, leading to the formation of doped COFs with high electrical conductivity. The film sample of M1Pc-NH2−M2PcF8 had high conductivity (12.7 S/m) (Fig. 7).
3 Synthesis of scCOFs
Less
It is of importance to accurately analyze the chemical structure of COFs. It is well known that scCOFs can be characterized by single crystal X-ray diffraction. According to the measured data, we can not only accurately analyze the structure of COFs, but also infer the reasons for its performance. However, for polycrystalline COFs, more characterization methods are needed to indirectly infer the structural characteristics. Therefore, the preparation of scCOFs is beneficial to obtain more accurate structural information and reasonable utilization. At present, preparation of scCOFs mainly includes three methods as follows:
(1) Adding a specific substance as a modulator into the reaction system. The competitive reaction between modulating agent and monomer can reduce the polymerization rate, which contributes to improve crystal defects and obtains high-quality single crystals. In 2016, Bein et al. verified that the crystallinity of COF-5-X (X being the functionalized group) can be improved by introducing a modulating agent [71], which provides guidance for the synthesis of scCOFs. In 2018, Yaghi et al. developed a method to grow high-quality 3D porous scCOFs using aniline as a modulator [72]. Aniline can decrease the reaction rate of monomer and increase the process of imine exchange, which offered sufficient time for the growth of scCOFs (Fig. 8a). In 2020, Wang et al. also used aniline as a modulator to successfully obtain the first non-interpenetrate scCOF (3D LZU-306) [73]. In 2024, acetic acid/aniline was replaced by 2,2,2-trifluoroacetic acid (CF3COOH)/2,2,2-trifluoroethylamine (CF3CH2NH2) in the growth process of single crystal by Wang's team, and the growth of scCOFs can be completed within 1–2 days [74].
(2) Controlling the growth condition and rate of crystal nucleus by adjusting the solvent conditions. In 2019, Dichtel et al. revealed that the boronate ester-linked COFs can be transformed into single crystals structure by adding nitrile-containing cosolvents [75]. Wei et al. controlled the crystallization kinetics by adding supercritical CO2 (sc-CO2), which effectively accelerated the synthesis process (Fig. 8b) [76]. Borate-linked COF-5 can be prepared within 2–5 min by this way. In 2023, Zheng et al. used amphiphilic amino-acid derivatives with long hydrophobic chains to self-assemble into micelles. Hydrophobic compartments were formed inside the micelles, which were able to separate different monomers according to the solubility differences of substances. This strategy avoids the precipitation phenomenon caused by irregular binding between monomers and thus regulating the orderly crystallization process of molecules [77].
(3) Transformation from single crystal to single crystal (SCSC). In 2023, Jiang et al. constructed USTB-5 single crystal by using tetraphenylmethane monomer. The imine linkage bond in the structure was reduced to amine through degassing of USTB-5 single crystal, and a new USTB-5r single crystal was obtained. In addition, the imine bond in USTB-5 can also be oxidized into an amide bond by sodium chlorite to obtain a new USTB-5o single crystal (Fig. 8c) [78].
4 Potential application of COFs in environmental field
Less
Nitrogen plays an important role in wastewater treatment. Activated carbon, zeolite and other water purification materials often need to be modified to introduce some active sites such as N, S and O to improve the purification capacity. NCLB-COFs contains nitrogen and other heteroatoms, which can provide abundant active sites. Combined with the porous characteristics, NCLB-COFs can detect, adsorb or degrade pollutants. Therefore, NCLB-COFs has advantages in wastewater treatment [79].
Coordination mechanism is a common strategy to adsorb heavy metal ions or organic pollutants. The rich porous structure of NCLB-COFs ensures that pollutants in water can fully diffuse into the material. And then the pollutants can be coordinated, captured and locked by nitrogen and other heteroatom [80]. Adsorbents with coordination mechanism were highly favored, because the coordination process is reversible. Therefore, the adsorbed pollutants can be released from NCLB-COFs without changing the structure, thus realizing the absorption/desorption cycle. Additionally, COFs with photocatalytic properties can be obtained by introducing specific activity or reasonably designing D-A (donor-acceptor) structure, which can photodegrade harmful pollutants and transform them into harmless substances [81,82]. Moreover, the specified organic pollutants can be quantitatively detected by introducing photothermal reactive groups into the COFs structure [83-85]. Therefore, NCLB-COFs has a significant application prospect in environmental treatment.
5 Conclusions and prospects
Less
The geometry and spatial arrangement of the COFs is largely determined by the connection methods of nodes and the symmetry of the molecular structure. The skeleton and structural properties of COFs are closely related to the composition and classes of chemical bonds. The majority of COFs were constructed following the bottom-up strategy, that is, starting from monomer molecules and then building rings by bridging functional groups. The development of COFs linked by common nodes is often limited by some objective factors (such as the solubility of ligand molecules or the specificity of reaction products). Therefore, some new synthetic methods (such as the synthesis of COF-B by exchanging the "parts" of the COF-A skeleton) have been developed. At present, the chemical bonds of the reported COFs are mostly reversible, which can make the molecules constantly self-repair (formation-fracture-regeneration) during ring formation, and finally form a highly crystalline structure. Additionally, there are also a few COFs constructed by irreversible covalent bonds, which use the rigidity of the structural units and the orientation of the chemical bonds in linkage nodes to promote the crystallization of the molecules. In a word, the diversified synthesis strategies can provide significant references for the development of new COFs.
Despite the remarkable progress in the research of COFs, some challenges still need to be overcome for future applications. (1) Exploring new molecular modules and developing novel linked-bonds to meet different application requirements are still the center driver for the development of COFs. Based on the reported synthesis methods (such as click chemistry), we should further explore the economic, simple preparation methods of COFs. (2) The combination of theoretical calculation and artificial intelligence for COFs research is still at early stage. It is necessary to establish more systematic theoretical algorithms, rich databases and appropriate evaluation methods to strengthen the theoretical research of COFs and optimize the synthesis of COFs. (3) The poor machinability of powdered COFs hinders its development of industrial and commercial applications. It is still necessary to explore the material forming process suitable for mass production to improve the practicability of COFs.
To sum up, we summarize the research progress of NCLB-COFs in recent years. We hope that this review can provide beneficial guidance for studying the synthesis and properties of COFs. We believe that the research of COFs will achieve more outstanding progress in the near future through the continuous efforts of researchers.
Declaration of competing interest
Less
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
CRediT authorship contribution statement
Less
Liying Ou: Writing – original draft, Validation, Software, Resources, Investigation, Formal analysis, Data curation. Zhenluan Xue: Writing – review & editing, Supervision, Investigation, Funding acquisition. Bo Li: Writing – review & editing, Visualization, Funding acquisition, Conceptualization. Zhiwei Jin: Validation, Software, Formal analysis. Jiaochan Zhong: Validation, Software. Lixia Yang: Validation, Software, Formal analysis. Penghui Shao: Writing – review & editing, Resources, Funding acquisition, Conceptualization. Shenglian Luo: Supervision, Funding acquisition, Conceptualization.
Acknowledgments
Less
This study was financially supported by the National Key Research and Development Program of China (Nos. 2022YFD1700800 and 2023YFC3905903), the Science and Technology Project of Education Department of Jiangxi Province (No. GJJ2201103), the Fund of Nanchang Hangkong University (Nos. EA202201110 and EA202201065) and National Undergraduate Innovation and Entrepreneurship Training Program (No. 202310406023) the National Natural Science Foundation of China (No. 52470149).
Supplementary materials
Less
Supplementary material associated with this article can be found, in the online version, at doi:10.1016/j.cclet.2024.110294.
References
Less
[1]
A.P. Côté, A.I. Benin, N.W. Ockwig, et al., Science 310 (2005) 1166–1170.
[2]
D.S. Zhen, C.L. Liu, Q.H. Deng, et al., Chin. Chem. Lett. 35 (2024) 109249.
[3]
T. Wang, X. Yu, Y.Q. Xie, Chin. Chem. Lett. 35 (2024) 109320.
[4]
G.R. Li, Y.J. Wu, C. Zhong, et al., Chin. Chem. Lett. 35 (2024) 108904.
[5]
Y.Y. Zhao, C.T. Yang, Y.J. Yu, Chin. Chem. Lett. 35 (2024) 108865.
[6]
M.X. Wu, Y.W. Yang, Chin. Chem. Lett. 28 (2017) 1135–1143.
[7]
N. Huang, P. Wang, D.L. Jiang, Nat. Rev. Mater. 1 (2016) 16068.
[8]
D.L. Cui, D.F. Perepichka, J.M. MacLeod, et al., Chem. Soc. Rev. 49 (2020) 2020–2038.
[9]
J.H. Chang, F.Q. Chen, H. Li, et al., Nat. Commun. 15 (2024) 813.
[10]
Z.T. Wang, Y.J. Huang, New J. Chem. 47 (2023) 3668–3671.
[11]
Q. Ma, X.Y. Liu, J. Qian, et al., Sep. Purif. Technol. 323 (2023) 124368.
[12]
C. Qian, L.L. Feng, W.L. Teo, et al., Nat. Rev. Chem. 6 (2022) 881–898.
[13]
Q.B. Fu, T.T. Zhang, X. Sun, et al., Chem. Eng. J. 454 (2023) 140154.
[14]
W.B. Dong, Z.Y. Qin, K.X. Wang, et al., Angew. Chem. Int. Ed. 62 (2022) e202216073.
[15]
Y.P. Cheng, J.J. Xin, L.B. Xiao, et al., J. Am. Chem. Soc. 145 (2023) 18737–18741.
[16]
L. Hao, K.H. Huang, N.X. Wang, et al., Dalton Trans. 51 (2022) 14952–14959.
[17]
G.B. Wang, H.P. Xu, K.H. Xie, et al., J. Mater. Chem. A 11 (2023) 4007–4012.
[18]
X.L. Fu, Z. Lu, H.J. Yang, et al., J. Polym. Sci. 59 (2021) 2036–2044.
[19]
D.W. Burke, R.R. Dasari, V.K. Sangwan, et al., J. Am. Chem. Soc. 145 (2023) 11969–11977.
[20]
S.H. An, X.W. Li, S.S. Shang, et al., Angew. Chem. Int. Ed. 62 (2023) e202218742.
[21]
J. You, F. Yuan, S.S. Cheng, et al., Chem. Mater. 34 (2022) 7078–7089.
[22]
C.J. Kang, Z.Q. Zhang, S. Kusaka, et al., Nat. Mater. 22 (2023) 636–643.
[23]
R. Bao, Z.H. Xiang, Z.L. Qiao, et al., Angew. Chem. Int. Ed. 62 (2023) e202216751.
[24]
J.H. Ding, X.Y. Guan, J. Lv, et al., J. Am. Chem. Soc. 145 (2023) 3248–3254.
[25]
R.Y. Liu, K.T. Tan, Y.F. Gong, et al., Chem. Soc. Rev. 50 (2021) 120–242.
[26]
W.Q. Wang, D.K. Huang, W.L. Zheng, et al., Chem. Mater. 35 (2023) 7154–7163.
[27]
Z.W. Lu, C.Y. Yang, L. He, et al., J. Am. Chem. Soc. 144 (2022) 9624–9633.
[28]
Z.B. Zhou, P.J. Tian, J. Yao, et al., Nat. Commun. 13 (2022) 2180.
[29]
Y.L. Yang, L. Yu, T.C. Chu, et al., Nat. Commun. 13 (2022) 2615.
[30]
X.L. Li, C.L. Zhang, S.L. Cai, et al., Nat. Commun. 9 (2018) 2998.
[31]
L. Cusin, H. Peng, A. Ciesielski, et al., Angew. Chem. Int. Ed. 60 (2021) 14236–14250.
[32]
Y.Q. Zhu, D.K. Huang, W.Q. Wang, et al., Angew. Chem. Int. Ed. 63 (2024) e202319909.
[33]
Z.B. Zhou, H.H. Sun, Q.Y. Qi, et al., CCS Chem. 6 (2024) 2230–2240.
[34]
C.G. Wu, M.J. Hu, X.R. Yan, et al., Energy Storage Mater. 36 (2021) 347–354.
[35]
H. Fliegl, A. Köhn, C. Hättig, et al., J. Am. Chem. Soc. 125 (2003) 9821–9827.
[36]
M.K. Hota, S. Chandra, Y.J. Lei, et al., Adv. Funct. Mater. 32 (2022) 22011.
[37]
S.P. Jia, L.Q. Hao, Y.J. Liu, et al., ACS Mater. Lett. 5 (2023) 458–465.
[38]
D. Fang, Z.Y. Zhang, Z.C. Shangguan, et al., J. Am. Chem. Soc. 143 (2021) 14502–14510.
[39]
J. Gemen, J.R. Church, T.-P. Ruoko, et al., Science 381 (2023) 1357–1363.
[40]
Y.L. Zhao, X.F. Tao, J.P. Lin, et al., Adv. Funct. Mater 33 (2023) 2302225.
[41]
L.C. Guo, Y.T. Yang, L.L. Gong, et al., Adv. Funct. Mater. 36 (2024) 2674–2684.
[42]
X.L. Gu, L.Y. Zhao, J. Sun, et al., Chem. Mater. 36 (2024) 2674–2684.
[43]
S. Jiang, L.C. Meng, M.X. Lv, et al., Microporous Mesoporous Mater. 348 (2023) 112405.
[44]
Q.Q. Tang, Y.Y. Gu, J. Ning, et al., Chem. Eng. J. 470 (2023) 144106.
[45]
Y.L. Zhao, Y. Zhao, C.L. Wu, et al., Chem. Eur. J. 27 (2021) 9391–9397.
[46]
Y.X. Yang, X.H. Tang, J.L. Wu, et al., ACS Appl. Polymer. Mater. 4 (2022) 4624–4631.
[47]
P. Kuhn, M. Antonietti, A. Thomas, Angew. Chem. Int. Ed. 47 (2008) 3450–3453.
[48]
S.J. Ren, M.J. Bojdys, R. Dawson, et al., Adv. Mater. 24 (2012) 2357–2361.
[49]
K.W. Wang, L.M. Yang, X. Wang, et al., Angew. Chem. Int. Ed. 56 (2017) 14149–14153.
[50]
S.-Y. Yu, J. Mahmood, H.-J. Noh, et al., Angew. Chem. Int. Ed. 57 (2018) 8438–8442.
[51]
T. Sun, Y. Liang, W.J. Luo, et al., Angew. Chem. Int. Ed. 61 (2022) e202203327.
[52]
L.J. Guan, Z.Q. Guo, Q. Zhou, et al., Nat. Commun. 14 (2023) 8114.
[53]
K. Cui, X.L. Tang, X.P. Xu, et al., Angew. Chem. Int. Ed. 63 (2024) e202317664.
[54]
F. Jiang, Y.J. Wang, T.P. Qiu, et al., J. Power Sources 523 (2022) 231041.
[55]
P. Xiong, S.L. Zhang, R. Wang, et al., Energy Environ. Sci. 16 (2023) 3181–3213.
[56]
X.X. Liu, R.L. Qi, S.M. Li, et al., J. Am. Chem. Soc. 144 (2022) 23396–23404.
[57]
C.D. Zhou, H.Y. Zhou, S.Y. Tang, et al., Mater. Lett. 332 (2023) 133493.
[58]
Y.T. Zhang, Z.L. Qiao, R. Zhang, et al., Angew. Chem. Int. Ed. 62 (2023) e202314539.
[59]
Z.C. Zhang, P.L. Wang, Y.F. Sun, et al., J. Am. Chem. Soc. 146 (2024) 4822–4829.
[60]
F. Haase, E. Troschke, G. Savasci, et al., Nat. Commun. 9 (2018) 2600.
[61]
Y.X. Wang, F.W. Huang, W.L. Sheng, et al., Appl. Catal. B 338 (2023) 123070.
[62]
Y. Mou, X.D. Wu, C.C. Qin, et al., Angew. Chem. Int. Ed. 62 (2023) e202309480.
[63]
Q.R. Fang, Z.B. Zhuang, S. Gu, et al., Nat. Commun. 5 (2014) 4503.
[64]
J. Maschita, T. Banerjee, G. Savasci, et al., Angew. Chem. Int. Ed. 59 (2020) 15750–15758.
[65]
J. Maschita, T. Banerjee, B.V. Lotsch, Chem. Mater. 34 (2022) 2249–2258.
[66]
S. Gu, X.X. Ma, J.J. Chen, et al., J. Energy Chem. 69 (2022) 428–433.
[67]
X.Y. Wu, S.Q. Zhang, X.Y. Xu, et al., Angew. Chem. Int. Ed. 63 (2024) e202319355.
[68]
Z.F. Wang, Y.S. Zhang, T. Wang, et al., Small 19 (2023) 2303684.
[69]
X.B. Yang, X.W. Li, M.H. Liu, et al., ACS Mater. Lett. 5 (2023) 1611–1618.
[70]
Y. Yue, H.Y. Li, H.Z. Chen, et al., J. Am. Chem. Soc. 144 (2022) 2873–2878.
[71]
M. Calik, T. Sick, M. Dogru, et al., J. Am. Chem. Soc. 138 (2016) 1234–1239.
[72]
T. Ma, E.A. Kapustin, S.X. Yin, et al., Science 361 (2018) 48–52.
[73]
L. Liang, Y. Qiu, W.D. Wang, et al., Angew. Chem. Int. Ed. 59 (2020) 17991–17995.
[74]
J. Han, J. Feng, J. Kang, et al., Science 383 (2024) 1014–1019.
[75]
A.M. Evans, I. Castano, A. Brumberg, et al., J. Am. Chem. Soc. 141 (2019) 19728–19735.
[76]
L. Peng, Q.Y. Guo, C.Y. Song, et al., Nat. Commun. 12 (2021) 5077.
[77]
Z.P. Zhou, L. Zhang, Y.H. Yang, et al., Nat. Chem. 15 (2023) 841–847.
[78]
B.Q. Yu, R.B. Lin, G. Xu, et al., Nat. Chem. 16 (2024) 114–121.
[79]
Z.L. Zhou, Y.T. Xiao, J. Tian, et al., J. Mater. Chem. A 11 (2023) 3245–3261.
[80]
D.C. Mei, L.J. Liu, B. Yan, Coord. Chem. Rev. 475 (2023) 214917.
[81]
H.R. Zhang, L. Zhang, S.S. Dong, et al., J. Hazard. Mater. 446 (2023) 130756.
[82]
S.P. Qi, R.T. Guo, Z.X. Bi, et al., Small 19 (2023) 2303632.
[83]
W.Z. She, C.H. Li, R.S. Li, et al., Sep. Purif. Technol. 330 (2024) 125294.
[84]
Y.X. Yu, Q.Q. Jin, Y.B. Ren, et al., Chem. Eng. J. 465 (2023) 142819.
[85]
Z.C. Xiao, X.Y. Nie, Y. Li, et al., ACS Appl. Mater. Interfaces 15 (2023) 9524–9532.
Appendix
Less
Year 2025 volume 36 Issue 6
PDF
3896
1964
Cite this Article
BibTeX
Article Info
doi: 10.1016/j.cclet.2024.110294
  • Receive Date：2024-02-27
  • Online Date：2025-10-29
  • Published：2025-06-15
Article Data
Affiliations
History
  • Received：2024-02-27
  • Revised：2024-06-25
  • Accepted：2024-07-24
Affiliations
    aSchool of Materials Science and Engineering, Nanchang Hangkong University, Nanchang 330063, China
    bKey Laboratory of Jiangxi Province for Persistent Pollutants Prevention Control and Resource Reuse, Nanchang Hangkong University, Nanchang 330063, China
References
Share
https://castjournals.cast.org.cn/joweb/ccl/EN/10.1016/j.cclet.2024.110294
Share to
QR

Scan QR to access full text

Cite this article
BibTeX
Citations
表12种不同金属材料的力学参数
科
Family		 属数
Number of
genus		 种数
Number of
species		 占总种数比例
Percentage of
total species (%)		 属
Genus		 种数
Number of
species		 占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
关闭全屏
  • BibTeX
  • EndNote
  • RefWorks
  • TxT
Links
Articles
Latest Articles
Most Read
Collections
Updates
Events
News
Multimedia
About
About Us
Contact
No. 86 Xueyuan South Road, Haidian District, Beijing
100081
010-62199257
qkjq@cast.org.cn

Copyright © 2025 China Association for Science and Technology. All rights reserved. For all open access content, the relevant licensing terms apply.
Sponsored by the Office of the Leading Group for Cybersecurity and Informatization of CAST, and supported by Science and Technology Review Publishing House