<?xml version="1.0" encoding="utf-8"?>
<XML>
<ISCJOURNAL>
<YEAR>2026</YEAR>
<VOL>6</VOL>
<NO>2</NO>
<PAGE_NO>17</PAGE_NO>
<ARTICLES>
			<ARTICLE>
				<TitleF></TitleF>
				<TitleE>Crystallinity control in covalent triazine frameworks: Synthetic approaches and mechanistic insights</TitleE>
				<TitleLang_ID>en</TitleLang_ID>
				<ABSTRACTS>
					<ABSTRACT>
						<Language_ID>en</Language_ID>
						<CONTENT>An important class of emerging porous organic materials is covalent triazine frameworks (CTFs), which have attracted much attention in wastewater treatment, energy conversion, and gas absorption due to their chemical and thermal properties and high nitrogen content. The synthesis of CTFs faces several challenges, including the reversibility of the reactions, which leads to structural defects and poor crystallinity. As a result, achieving high crystallinity is a major goal in the research and development of CTFs. This brief review focuses on the latest advances in the synthesis and control of crystallinity of these nitrogen-rich materials. The paper proceeds in order to review the principles governing crystal formation, the synthesis methods and factors affecting the reactions, and the final operations to prepare the product to enhance crystallinity. In addition, common crystallinity assessment techniques, including powder X-ray diffraction, Fourier transform infrared spectroscopy and advanced analysis, are reviewed. The effect of framework crystal structure on performance optimization is also discussed. Finally, challenges and future prospects in the development of synthesis techniques for the technological advancement of CTFs are presented.</CONTENT>
					</ABSTRACT>
				</ABSTRACTS>
				<PAGES>
					<PAGE>
						<FPAGE>127</FPAGE>
						<TPAGE>143</TPAGE>
					</PAGE>
				</PAGES>
				<AUTHORS>
					<AUTHOR>
						<NameE>Asieh</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Akhoondi</FamilyE>
						<Organizations>
							<Organization>Department of Chemical Engineering, Arak Branch</Organization>
						</Organizations>
						<Universities>
							<University>Islamic Azad University, Arak</University>
						</Universities>
						<Countries>
							<Country>Iran</Country>
						</Countries>
						<EMAILS>
							<Email>asieh.akhoondi@gmail.com</Email>			
						</EMAILS>
					</AUTHOR>
					<AUTHOR>
						<NameE>Bhaskar</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Bethi</FamilyE>
						<Organizations>
							<Organization>Department of Chemical Engineering, B V Raju Institute of Technology, Narsapur, Medak Dist. 502313, Telangana</Organization>
						</Organizations>
						<Universities>
							<University></University>
						</Universities>
						<Countries>
							<Country>India</Country>
						</Countries>
						<EMAILS>
							<Email></Email>			
						</EMAILS>
					</AUTHOR>
					<AUTHOR>
						<NameE>Mohammed Muzibur</NameE>
						<MidNameE></MidNameE>		
						<FamilyE>Rahman</FamilyE>
						<Organizations>
							<Organization>Center of Excellence for Advanced Materials Research and Chemistry Department</Organization>
						</Organizations>
						<Universities>
							<University>King Abdulaziz University, Jeddah 21589, P.O. Box 80203</University>
						</Universities>
						<Countries>
							<Country>Saudi Arabia</Country>
						</Countries>
						<EMAILS>
							<Email>mmrahman@kau.edu.sa</Email>			
						</EMAILS>
					</AUTHOR>
				</AUTHORS>
				<KEYWORDS>
					<KEYWORD>
						<KeyText>Covalent triazine frameworks</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>Crystallinity</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>Synthesis</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>Defect density</KeyText>
					</KEYWORD>
					<KEYWORD>
						<KeyText>Structure–property correlations</KeyText>
					</KEYWORD>
				</KEYWORDS>
				<PDFFileName>Vol 6 No 2 Paper 5.pdf</PDFFileName>
				<REFRENCES>
				<REFRENCE>
					<REF>[1]	M.G. Mohamed, A.F.M. EL-Mahdy, M.G. Kotp, S.-W. Kuo, Advances in porous organic polymers: syntheses, structures, and diverse applications, Mater. Adv. 3 (2022) 707–733. https://doi.org/10.1039/D1MA00771H.
##[2]	M. Liu, L. Guo, S. Jin, B. Tan, Covalent triazine frameworks: synthesis and applications, J. Mater. Chem. A. 7 (2019) 5153–5172. https://doi.org/10.1039/C8TA12442F.
##[3]	P. Xiong, S. Zhang, R. Wang, L. Zhang, Q. Ma, et al., Covalent triazine frameworks for advanced energy storage: challenges and new opportunities, Energy Environ. Sci. 16 (2023) 3181–3213. https://doi.org/10.1039/D3EE01360J.
##[4]	Y. Ren, S. Yang, Y. Xu, Crystalline Covalent Triazine Frameworks and 2D Triazine Polymers: Synthesis and Applications, Acc. Chem. Res. 58 (2025) 474–487. https://doi.org/10.1021/acs.accounts.4c00729.
##[5]	P. Kuhn, M. Antonietti, A. Thomas, Porous, Covalent Triazine-Based Frameworks Prepared by Ionothermal Synthesis, Angew. Chem. Int. Ed. 47 (2008) 3450–3453. https://doi.org/10.1002/anie.200705710. 
##[6]	Y. Zhang, S. Jin, Recent Advancements in the Synthesis of Covalent Triazine Frameworks for Energy and Environmental Applications, Polymers. 11 (2019) 31. https://doi.org/10.3390/polym11010031. 
##[7]	Y. Zheng, N.A. Khan, X. Ni, K.A.I. Zhang, Y. Shen, et al., Emerging covalent triazine framework-based nanomaterials for electrochemical energy storage and conversion, Chem. Commun. 59 (2023) 6314–6334. https://doi.org/10.1039/D3CC00712J. 
##[8]	Y. Ren, Y. Xu, Recent advances in two-dimensional polymers: synthesis, assembly and energy-related applications, Chem. Soc. Rev. 53 (2024) 1823–1869. https://doi.org/10.1039/D3CS00782K. 
##[9]	R. Sun, B. Tan, Covalent Triazine Frameworks (CTFs): Synthesis, Crystallization, and Photocatalytic Water Splitting, Chem. A. Eur. J. 29 (2023) e202203077. https://doi.org/10.1002/chem.202203077. 
##[10]	M. Liu, K. Jiang, X. Ding, S. Wang, C. Zhang, et al., Controlling Monomer Feeding Rate to Achieve Highly Crystalline Covalent Triazine Frameworks, Adv. Mater. 31 (2019) 1807865. https://doi.org/10.1002/adma.201807865.
##[11]	H. Wang, Z. Wang, M. Li, W. Hou, Q. Wen, et al., Recent Advances in Synthesis of Covalent Triazine Frameworks: Methods, Mechanism, and Crystallization Effects, Adv. Synth. Catal. 367 (2025) e70123. https://doi.org/10.1002/adsc.70123.
##[12]	L. Guo, X. Wang, Z. Zhan, Y. Zhao, L. Chen, et al., Crystallization of Covalent Triazine Frameworks via a Heterogeneous Nucleation Approach for Efficient Photocatalytic Applications, Chem. Mater. 33 (2021) 1994–2003. https://doi.org/10.1021/acs.chemmater.0c03716.
##[13]	C. Yang, X. Ci, X. Li, Z. Wei, Y. Lang, et al., Crystallinity Improvement of Covalent Triazine Frameworks Boosting Room Temperature Hydrogenation of Carbon Dioxide into Formic Acid, ACS Sustain. Chem. Eng. 13 (2025) 14903–14913. https://doi.org/10.1021/acssuschemeng.5c04653.
##[14]	S. Daliran, M. Blanco, A. Dhakshinamoorthy, A.R. Oveisi, J. Alemán, H. García, Defects and Disorder in Covalent Organic Frameworks for Advanced Applications, Adv. Funct. Mater. 34 (2024) 2312912. https://doi.org/10.1002/adfm.202312912. 
##[15]	O. Oyegbeda, A.A. Ambushe, A critical review of covalent triazine framework-based materials: Bibliometric study, synthesis, enhancement strategies, emerging applications, and DFT insights, Chem. Eng. J. Adv. 24 (2025) 100939. https://doi.org/10.1016/j.ceja.2025.100939.
##[16]	Z. Lei, M. Liu, Y. Zhang, L. Li, S.-Q. Zang, et al., Covalent triazine frameworks: Fabrication for energy conversion, Coord. Chem. Rev. 537 (2025) 216703. https://doi.org/10.1016/j.ccr.2025.216703.
##[17]	A. Hayat, H. Ali, Z. Ajmal, A. Alshammari, M.M. Alghamdi, et al., Emerging breakthroughs in covalent triazine frameworks: From fundamentals towards photocatalytic water splitting and challenges, Prog. Mater. Sci. 147 (2025) 101352. https://doi.org/10.1016/j.pmatsci.2024.101352. 
##[18]	L. Liao. M. Li, Y. Yin, J. Chen, Q. Zhong, et al., Advances in the Synthesis of Covalent Triazine Frameworks, ACS Omega. 8 (2023) 4527–4542. https://doi.org/10.1021/acsomega.2c06961. 
##[19]	 H. Ali, B.A. Alwan, A.E. Jery, A.M. Alenad, A.M. Sadeq, M. Sohail, Covalent triazine frameworks: Synthesis strategies, physicochemical properties, and advanced sustainable energy applications, Desalination. 619 (2025) 119600. https://doi.org/10.1016/j.desal.2025.119600. 
##[20]	J. Liu, M. Liu, X. Wang, X. Wang, B. Tan, Crystalline Covalent Triazine Frameworks with Fibrous Morphology via a Low-Temperature Polycondensation of Planar Monomer, Nano. Micro. Small. 18 (2022) 2200984. https://doi.org/10.1002/smll.202200984. 
##[21]	M. Liu, Q. Huang, S. Wang, Z. Li, B. Li, et al., Crystalline Covalent Triazine Frameworks by In-Situ Oxidation of Alcohols to Aldehyde Monomers, Angew. Chem. Int. Ed. 57 (2018) 11968–11972. https://doi.org/10.1002/anie.201806664.
##[22]	I. Caivano, A. Guarnaccio, C. Grazioli, M. de Simone, V. Lanzilotto, Shaping covalent triazine frameworks into films and membranes: A review of bottom-up strategies, Mater. Today Chem. 55 (2026) 103797. https://doi.org/10.1016/j.mtchem.2026.103797. 
##[23]	V. Nguyen, M. Gruenwald, Microscopic origins of poor crystallinity in thesynthesis of covalent organic framework COF-5, J. Am. Chem. Soc. 140 (2018) 3306–3311. https://doi.org/10.1021/jacs.7b12529.
##[24]	L. Huang, Z. Luo, Y.-N. Zhou, Q. Zhang, H. Zhu, S. Zhu, Solvothermal synthesis of covalent triazine framework and its application in photodegradation of organic dyes, Mater. Today Chem. 20 (2021) 100475. https://doi.org/10.1016/j.mtchem.2021.100475.
##[25]	C. Qian, Q.-Y. Qi, G.-F. Jiang, F.-Z. Cui, Y. Tian, Z. Zhao, Toward Covalent Organic Frameworks Bearing Three Different Kinds of Pores: The Strategy for Construction and COF-to-COF Transformation via Heterogeneous Linker Exchange, J. Am. Chem. Soc. 139 (2017) 6736–6743. https://doi.org/10.1021/jacs.7b02303.
##[26]	Z.-A. Lan, M. Wu, Z. Fang, Y. Zhang, X. Chen, et al., Ionothermal Synthesis of Covalent Triazine Frameworks in a NaCl-KCl-ZnCl2 Eutectic Salt for the Hydrogen Evolution Reaction, Angew. Chem. Int. Ed. 61 (2022) e202201482. https://doi.org/10.1002/anie.202201482. 
##[27]	X. Suo, F. Zhang, Z. Yang, H. Chen, T. Wang, et al., Highly Perfluorinated Covalent Triazine Frameworks Derived from a Low-Temperature Ionothermal Approach Towards Enhanced CO2 Electroreduction, Angew. Chem. Int. Ed. 60 (2021) 25688–25694. https://doi.org/10.1002/anie.202109342.
##[28]	T. Wang, J.A. Gaugler , M. Li, B.P. Thapaliya, J. Fan, et al., Construction of Fluorine- and Piperazine-Engineered Covalent Triazine Frameworks Towards Enhanced Dual-Ion Positive Electrode Performance, ChemSusChem. 16 (2023) e202201219. https://doi.org/10.1002/cssc.202201219.
##[29]	T. Zeng, S. Jin, S. Li, J. Bao, Z. Jin, et al., Covalent Triazine Frameworks with Defective Accumulation Sites: Exceptionally Modulated Electronic Structure for Solar-Driven Oxidative Activation of Peroxymonosulfate, Environ. Sci. Technol. 56 (2022) 9474–9485. https://doi.org/10.1021/acs.est.2c00126.
##[30]	S. Abednatanzi, P. Gohari Derakhshandeh, S. Dalapati, S.K.P. Veerapandian, A.-C. Froissart, et al., Metal-Free Chemoselective Reduction of Nitroarenes Catalyzed by Covalent Triazine Frameworks: The Role of Embedded Heteroatoms, ACS Appl. Mater. Interfaces. 14 (2022) 15287–15297. https://doi.org/10.1021/acsami.2c01091.
##[31]	 C. Mollart, E. Sherrett; P. Heasman, M.J.G. Peach, A. Rowling, et al., Diversity-oriented route to functional covalent triazine frameworks, Polym. Chem. 17 (2026) 325–331. https://doi.org/10.1039/d5py00872g.
##[32]	C. Mollart, S. Holcroft, M.J.G. Peach, A. Rowling, A. Trewin, Artificial synthesis of covalent triazine frameworks for local structure and property determination, Phys. Chem. Chem. Phys. 24 (2022) 20025–20029. https://doi.org/10.1039/D2CP02430F. 
##[33]	P. Gao, Q. Han, A Functionalized Covalent Organic Frameworks with Triazine and Triazole Motifs, Stud. Health Technol. Inform. 308 (2023) 743–748. https://doi.org/10.3233/SHTI230907.
##[34]	R. Sun, X. Wang, X. Wang, B. Tan, Three-Dimensional Crystalline Covalent Triazine Frameworks via a Polycondensation Approach, Angew. Chem. Int. Ed. 61 (2022) e202117668. https://doi.org/10.1002/anie.202117668.
##[35]	L. Guan, Z. Guo, Q. Zhou, J. Zhang, C. Cheng, et al., A highly proton conductive perfluorinated covalent triazine framework via low-temperature synthesis, Nat. Commun. 14 (2023) 8114. https://doi.org/10.1038/s41467-023-43829-4.
##[36]	Y. Zou, S. Abednatanzi, P. Gohari Derakhshandeh, S. Mazzanti, C.M. Schüßlbauer, et al., Red edge effect and chromoselective photocatalysis with amorphous covalent triazine-based frameworks, Nat. Commun. 13 (2022) 2171. https://doi.org/10.1038/s41467-022-29781-9.
##[37]	T. Zhou, Y. Zhao, J.W. Choi, A. Coskun, Lithium-Salt Mediated Synthesis of a Covalent Triazine Framework for Highly Stable Lithium Metal Batteries, Angew. Chem. Int. Ed. 58 (2019) 16795–16799. https://doi.org/10.1002/anie.201908513.
##[38]	V.M. Rangaraj, K.S.K. Reddy, G.N. Karanikolos, Ionothermal synthesis of phosphonitrilic-core covalent triazine frameworks for carbon dioxide capture, Chem. Eng. J. 429 (2022) 132160. https://doi.org/10.1016/j.cej.2021.132160. 
##[39]	T. Sun, Y. Liang, W. Luo, L. Zhang, X. Cao, Y. Xu, A General Strategy for Kilogram-Scale Preparation of Highly Crystalline Covalent Triazine Frameworks, Angew. Chem. Int. Ed. 61 (2022) e202203327. https://doi.org/10.1002/anie.202203327. 
##[40]	G. Li, Y. Liu, Z. He, K. Shi, F. Liu, Retrievable ultrafast covalent triazine framework membranes for organic solvent nanofiltration, Chem. Eng. J. 484 (2024) 149488. https://doi.org/10.1016/j.cej.2024.149488. 
##[41]	X. Hu, Z. Zhan, J. Zhang, I. Hussain, B. Tan, Immobilized covalent triazine frameworks films as effective photocatalysts for hydrogen evolution reaction, Nat. Commun. 12 (2021) 6596. https://doi.org/10.1038/s41467-021-26817-4.
##[42]	J. Fan, X. Suo, T .Wang, Z. Wang, C.-L. Do-Thanh, et al., Mechanochemistry-driven phase transformation of crystalline covalent triazine frameworks assisted by alkaline molten salts, J. Mater. Chem. A. 10 (2022) 14310–14315. https://doi.org/10.1039/d2ta02117j.
##[43]	L.S. Häser, S. Moos, F. Egger, K. Birkelbach, M. Zobel, et al., Accessing photocatalytically active covalent triazine-based frameworks by ball milling: a fast and facile synthesis method, Green Chem. 28 (2026) 4292–4301. https://doi.org/10.1039/d5gc06349c.
##[44]	I.D. Wessely, A.M. Schade, S. Dey, A. Bhunia, A. Nuhnen, et al., Covalent Triazine Frameworks Based on the First Pseudo-Octahedral Hexanitrile Monomer via Nitrile Trimerization: Synthesis, Porosity, and CO2 Gas Sorption Properties, Materials. 14 (2021) 3214. https://doi.org/10.3390/ma14123214.
##[45]	M. Liu, Z. Lei, P. Ma, L. Feng, Y. Wang, et al., Water-mediated kinetic engineering of CTF QDs for emerging solar cells, Chem. Sci. 17 (2026) 3516–3524. https://doi.org/10.1039/d5sc08329j.
##[46]	S.E. Peter, P. Thomas, P. Vairavel, N.V. Anil Kumar, Cyanuric chloride as a linker towards the synthesis of covalent triazine polymers: a review, Mater. Adv. 5 (2024) 9175–9209. https://doi.org/10.1039/d4ma00739e. 
##[47]	M. Bagheri, S. Nasrian, Porous Covalent Triazine-Based Frameworks: Synthesis and Applications in Adsorption and Catalysis, Commun. Catal. 2 (2025) 22–43. https://doi.org/10.22049/CIC.2024.29487.1036. 
##[48]	S.-Y. Yu, J. Mahmood, H.-J. Noh, J.-M. Seo, S.-M. Jung, et al., Direct Synthesis of a Covalent Triazine-Based Framework from Aromatic Amides, Angew. Chem. Int. Ed. 57 (2018) 8438–8442. https://doi.org/10.1002/anie.201801128. 
##[49]	W. Huang, Z.J. Wang, B.C. Ma, S. Ghasimi, D. Gehrig, et al., Hollow nanoporous covalent triazine frameworks via acid vapor-assisted solid phase synthesis for enhanced visible light photoactivity, J. Mater. Chem. A. 4 (2016) 7555–7559. https://doi.org/10.1039/c6ta01828a.
##[50]	S. Hutsch, A. Leonard, S. Grätz, M.V. Höfler, T. Gutmann, L. Borchardt, Mechanochemical Cyclotrimerization: A Versatile Tool to Covalent Organic Frameworks with Tunable Stacking Mode, Angew. Chem. Int. Ed. 63 (2024) e202403649. https://doi.org/10.1002/anie.202403649.
##[51]	Z. Wang, X. Zou, M. Lv, B. Zhang, Covalent triazine frameworks (CTFs) drive innovative advances in rechargeable metal-ion batteries: a review, Energy Mater. 4 (2024) 400072. https://doi.org/10.20517/energymater.2024.39.
##[52]	P. Kuhn, A. Thomas, M. Antonietti, Toward Tailorable Porous Organic Polymer Networks: A High-Temperature Dynamic Polymerization Scheme Based on Aromatic Nitriles, Macromolecules. 42 (2009) 319–326. https://doi.org/10.1021/ma802322j.
##[53]	S. Ren, M.J. Bojdys, R. Dawson, A. Laybourn, Y.Z. Khimyak, et al., Porous, Fluorescent, Covalent Triazine-Based Frameworks Via Room-Temperature and Microwave-Assisted Synthesis, Adv. Mater. 24 (2012) 2357–2361. https://doi.org/10.1002/adma.201200751. 
##[54]	M.J. Bojdys, J. Jeromenok, A. Thomasm, M. Antonietti, Rational Extension of the Family of Layered, Covalent, Triazine-Based Frameworks with Regular Porosity, Adv. Mater. 22 (2010) 2202–2205. https://doi.org/10.1002/adma.200903436. 
##[55]	W. Zhang, C. Li, Y.-P. Yuan, L.-G. Qiu, A.-J. Xie, et al., Highly energy- and time-efficient synthesis of porous triazine-based framework: Microwave-enhanced ionothermal polymerization and hydrogen uptake, J. Mater. Chem. 20 (2010) 6413−6415. https://doi.org/10.1039/C0JM01392G. 
##[56]	K. Wang, L.-M. Yang, X. Wang, L. Guo, G. Cheng, et al., Covalent Triazine Frameworks via a Low-Temperature Polycondensation Approach, Angew. Chem. Int. Ed. 56 (2017) 14149–14153. https://doi.org/10.1002/anie.201708548.
##[57]	O. Buyukcakir, S.H. Je, S.N. Talapaneni, D. Kim, A. Coskun, Charged Covalent Triazine Frameworks for CO2 Capture and Conversion, ACS Appl. Mater. Interfaces. 9 (2017) 7209–7216. https://doi.org/10.1021/acsami.6b16769.
##[58]	W. Huang, B.C. Ma, H. Lu, R. Li, L. Wang, et al., Visible-Light-Promoted Selective Oxidation of Alcohols Using a Covalent Triazine Framework, ACS Catal. 7 (2017) 5438–5442. https://doi.org/10.1021/acscatal.7b01719. 
##[59]	J. Yang, F. Kang, X. Wang, Q. Zhang, Design strategies for improving the crystallinity of covalent organic frameworks and conjugated polymers: a review, Mater. Horiz. 9 (2022) 121–146. https://doi.org/10.1039/d1mh00809a.
##[60]	G. Wang, Design of Covalent Triazine Frameworks for Selective Carbon Capture and Storage, PhD Thesis, Ghent University. (2018). 
##[61]	A. Iemhoff, M. Vennewald, R. Palkovits, Single-Atom Catalysts on Covalent Triazine Frameworks: at the Crossroad between Homogeneous and Heterogeneous Catalysis, Angew. Chem. Int. Ed. 62 (2022) e202212015. https://doi.org/10.1002/anie.202212015. 
##[62]	F. Haase, B.V. Lotsch, Solving the COF trilemma: towards crystalline, stable and functional covalent organic frameworks, Chem. Soc. Rev. 49 (2020) 8469–8500. https://doi.org/10.1039/d0cs01027h. 
##[63]	L. Bourda, C. Krishnaraj, P. Van Der Voort, K. Van Hecke, Conquering the crystallinity conundrum: efforts to increase quality of covalent organic frameworks, Mater. Adv. 2 (2021) 2811–2845. https://doi.org/10.1039/d1ma00008j.
##[64]	Z. Yang, H. Chen, S. Wang, W. Guo, T. Wang, et al., Transformation Strategy for Highly Crystalline Covalent Triazine Frameworks: From Staggered AB to Eclipsed AA Stacking, J. Am. Chem. Soc. 142 (2020) 6856–6860. https://doi.org/10.1021/jacs.0c00365. 
##[65]	K. Geng, T. He, R. Liu, S. Dalapati, K.T. Tan, et al., Covalent Organic Frameworks: Design, Synthesis, and Functions, Chem. Rev. 120 (2020) 8814–8933. https://doi.org/10.1021/acs.chemrev.9b00550. 
##[66]	H.M. Rietveld, A profile refinement method for nuclear and magnetic structures, J. Appl. Crystallogr. 2 (1969) 65–71. https://doi.org/10.1107/S0021889869006558.
##[67]	P. Scherrer, Bestimmung der Größe und der inneren Struktur von Kolloidteilchen mittels Röntgenstrahlen. Nachrichten von der Gesellschaft der Wissenschaften zu Göttingen, Math. Phys. Klass. 2 (1918) 98–100. 
##[68]	B.D. Cullity, S.R. Stock, Elements of X-Ray Diffraction, 3rd ed, Pearson, Upper Saddle River, NJ : Prentice Hall. (2001). 
##[69]	T. Egami, S.J.L. Billinge, Total Scattering Experiments, Pergamon Mater. Ser. 16 (2012) 113–158. https://doi.org/10.1016/B978-0-08-097133-9.00004-6.
##[70]	X. Luo, R.J. Wei, G.H. Ning, D. Li, Covalent Metal-Organic Frameworks, Handbook of Metal-Organic Frameworks. Springer, Singapore. (2025) 1–43. https://doi.org/10.1007/978-981-99-8242-4_12-1.
##[71]	W. Clegg, A.J. Blake, J.M. Cole, J.S.O. Evans, P. Main, et al., Crystal Structure Analysis: Principles and Practice (2nd edn), International Union of Crystallography Texts on Crystallography, Oxford. (2009). https://doi.org/10.1093/acprof:oso/9780199219469.001.0001. 
##[72]	G. Socrates, Infrared and Raman Characteristic Group Frequencies:  Tables and Charts, J. Am. Chem. Soc. 124 (2002) 1830. https://doi.org/10.1021/ja0153520.
##[73]	S. Zhang, G. Cheng, L. Guo, N. Wang, B. Tan, S. Jin, Strong-Base-Assisted Synthesis of a Crystalline Covalent Triazine Framework with High Hydrophilicity via Benzylamine Monomer for Photocatalytic Water Splitting, Angew. Chem. Int. Ed. 59 (2020) 6007–6014. https://doi.org/10.1002/anie.201914424.
##[74]	C. Banwell, E. McCash, Fundamentals for Molecular Spectroscopy, McGraw Hill / Europe, Middle East and Africa. (1994). 
##[75]	J.E. Castle, Practical surface analysis by Auger and X-ray photoelectron spectroscopy. D. Briggs and M. P. Seah (Editors). John Wiley and Sons Ltd, Chichester. (1983) 533. https://doi.org/10.1002/sia.740060611. 
##[76]	S. Bi, C. Yang, W. Zhang, J. Xu, L. Liu, et al., Two-dimensional semiconducting covalent organic frameworks via condensation at arylmethyl carbon atoms, Nat. Commun. 10 (2019) 2467. https://doi.org/10.1038/s41467-019-10504-6.
##[77]	W.-L. Jin, S.-C. Li, H.-Z. Zhou, S.-H. Ma, W. Li, et al., A Key to Crystallinity and Reusability of Covalent Organic Frameworks: Adsorption-Induced Deformation, ACS Materials Lett. 6 (2024) 1474–1483. https://doi.org/10.1021/acsmaterialslett.4c00059. 
##[78]	S. Qiu, T. Ben, Porous Polymers: Design, Synthesis and Applications, Monographs in supramolecular chemistry, CPI Group (UK) Ltd, Croydon, UK. (2015). https://doi.org/10.1039/9781782622260. 
##[79]	Y. Shen, C. Zhu, S. Song, T. Zeng, L. Li, Z. Cai, Defect-Abundant Covalent Triazine Frameworks as Sunlight-Driven Self-Cleaning Adsorbents for Volatile Aromatic Pollutants in Water, Environ. Sci. Technol. 53 (2019) 9091–9101. https://doi.org/10.1021/acs.est.9b02222.
##[80]	C. Lin, P. Feng, P. Geng, S. Zhang, Y. Chen, et al., Engineering covalent triazine frameworks for high-performance lithium–sulfur batteries, Chem. Commun. 61 (2025) 16354–16371. https://doi.org/10.1039/d5cc03560k.
##[81]	P. Puthiaraj; Y.-R. Lee; S. Zhang; W.-S. Ahn, Triazine-based covalent organic polymers: design, synthesis and applications in heterogeneous catalysis, J. Mater. Chem. A. 4 (2016) 16288–16311. https://doi.org/10.1039/c6ta06089g.
##[82]	Z. Li, J. Tao, C. Li, Y. Jin, J.-P. Jeon, et al., Triazine Vertex-Directed Engineering of Interlayer Interactions in Vinyl-Linked Covalent Organic Frameworks for Enhanced Charge-Carrier Transport and Photocatalytic Activity, Nano Lett. 25 (2025) 17739–17746. https://doi.org/10.1021/acs.nanolett.5c04802.
##[83]	J. Yu, L. Cheng, X. Zhang, X. Shi, H.-g. Wang, Integrating p-type phenazine into covalent triazine framework to achieve co-storage of cations and anions for quasi-solid-state dual-ion batteries, Chem. Eng. J. 489 (2024) 151320. https://doi.org/10.1016/j.cej.2024.151320.
##[84]	P. Wu, J. Lu, F. Xi, X. Li, W. Ma, et al., Phase engineering of covalent triazine frameworks to enhance photocatalytic hydrogen evolution performance, Chem. Sci. 16 (2025) 4127–4135. https://doi.org/10.1039/d4sc06496h.
##[85]	C. Bi, P. Wang, Z. Yao, H. Yu, Y. Xie, et al., Covalent triazine frameworks as photocatalysts for CO2 reduction: mechanistic insights, structural tailoring, and heterojunction design, Coord. Chem. Rev. 567 (2026) 218268. https://doi.org/10.1016/j.ccr.2026.218268. 
##[86]	K. Kamiya, Selective single-atom electrocatalysts: a review with a focus on metal-doped covalent triazine frameworks, Chem. Sci. 11 (2020) 8339–8349. https://doi.org/10.1039/d0sc03328f. 
##[87]	G. Liu, S. Liu, C. Lai, L. Qin, M. Zhang, et al., Strategies for Enhancing the Photocatalytic and Electrocatalytic Efficiency of Covalent Triazine Frameworks for CO2 Reduction, Small. 20 (2024) 2307853. https://doi.org/10.1002/smll.202307853. 
##[88]	K. Cui, X. Tang, X. Xu, M. Kou, P. Lyu, Y. Xu, Crystalline Dual-Porous Covalent Triazine Frameworks as a New Platform for Efficient Electrocatalysis, Angew. Chem. Int. Ed. 63 (2024) e202317664. https://doi.org/10.1002/anie.202317664. 
##[89]	S. Dalapati, S. Jin, J. Gao,Y. Xu, A. Nagai, D. Jiang, An Azine-Linked Covalent Organic Framework, J. Am. Chem. Soc. 135 (2013) 17310–17313. https://doi.org/10.1021/ja4103293.
##[90]	Y. Wang, J. Li, Q. Yang, C. Zhong, Two-Dimensional Covalent Triazine Framework Membrane for Helium Separation and Hydrogen Purification, ACS Appl. Mater. Interfaces. 8 (2016) 8694–8701. https://doi.org/10.1021/acsami.6b00657.
##[91]	X. Chen, M. Addicoat, S. Irle, A. Nagai, D. Jiang, Control of Crystallinity and Porosity of Covalent Organic Frameworks by Managing Interlayer Interactions Based on Self-Complementary π‑Electronic Force, J. Am. Chem. Soc. 135 (2013) 546–549. https://doi.org/10.1021/ja3100319. 
##[92]	T. Zhang, G. Zhang, L. Chen, 2D Conjugated Covalent Organic Frameworks: Defined Synthesis and Tailor-Made Functions, Acc. Chem. Res. 55 (2022) 795–808. https://doi.org/10.1021/acs.accounts.1c00693.  
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