Amplified Dimensionality Effect from 2D to 3D Covalent Organic Frameworks for Enhanced Fluorescent Sensing of Nitroaromatic Explosives

Jia-Long Song; Jun-Xia Ren; Bo Miao; Zheng-Hao Huang; Xiao Lv; Lei Cheng; Run-Lin Huang; Yu-Xuan Huang; Tian Zhong; Yao-Zu Liu; Jing An; Qian-Rong Fang

doi:10.1007/s10118-025-3531-3

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Amplified Dimensionality Effect from 2D to 3D Covalent Organic Frameworks for Enhanced Fluorescent Sensing of Nitroaromatic Explosives

RESEARCH ARTICLE | Updated：2026-04-01

- Amplified Dimensionality Effect from 2D to 3D Covalent Organic Frameworks for Enhanced Fluorescent Sensing of Nitroaromatic Explosives
- Chinese Journal of Polymer Science Vol. 44, Pages: 1-8(2026)
- Affiliations：
  
  a.School of Life Sciences, Zhuhai College of Science and Technology, Zhuhai 519040, China
  b.State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin University, Changchun 130012, China
  c.Macau University of Science and Technology, Macau 999078, China
- Author bio：
  
  yaozuliu@jlu.edu.cn (Y.Z.L.)
  anjing@jluzh.edu.cn (J.A.)
- Funds：
- DOI：10.1007/s10118-025-3531-3
  CLC：
- Received：28 October 2025，
  
  Accepted：10 January 2026，
  
  Online First：01 April 2026，
  
  Published：05 May 2026
- Accepted：
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Song, J. L.; Ren, J. X.; Miao, B.; Huang, Z. H.; Lv, X.; Cheng, L.; Huang, R. L.; Huang, Y. X.; Zhong, T.; Liu, Y. Z.; An, J.; Fang, Q. R. Amplified dimensionality effect from 2D to 3D covalent organic frameworks for enhanced fluorescent sensing of nitroaromatic explosives. Chinese J. Polym. Sci. https://doi.org/10.1007/s10118-025-3531-3

Jia-Long Song, Jun-Xia Ren, Bo Miao, et al. Amplified Dimensionality Effect from 2D to 3D Covalent Organic Frameworks for Enhanced Fluorescent Sensing of Nitroaromatic Explosives[J/OL]. Chinese Journal of Polymer Science, 2026, 441-8.
Song, J. L.; Ren, J. X.; Miao, B.; Huang, Z. H.; Lv, X.; Cheng, L.; Huang, R. L.; Huang, Y. X.; Zhong, T.; Liu, Y. Z.; An, J.; Fang, Q. R. Amplified dimensionality effect from 2D to 3D covalent organic frameworks for enhanced fluorescent sensing of nitroaromatic explosives. Chinese J. Polym. Sci. https://doi.org/10.1007/s10118-025-3531-3 DOI：

Jia-Long Song, Jun-Xia Ren, Bo Miao, et al. Amplified Dimensionality Effect from 2D to 3D Covalent Organic Frameworks for Enhanced Fluorescent Sensing of Nitroaromatic Explosives[J/OL]. Chinese Journal of Polymer Science, 2026, 441-8. DOI： 10.1007/s10118-025-3531-3.

摘要

Abstract

Efficient detection of nitroaromatic explosives remains a great challenge

and covalent organic frameworks (COFs) incorporating aggregation-induced emission (AIE) units provide a promising platform for high-performance fluorescent sensing. Herein

we designed and synthesized both

two-dimensional (2D) and three-dimensional (3D) AIE-active COFs to systematically investigate how dimensional differences (pore architecture

charge transfer efficiency

and AIE behavior) regulate sensing performance. Through a “4+4” imine condensation strategy

a 2D sql topological COF (TPPDA-TPTPE) was obtained from a planar tetraamine (TPPDA)

whereas a 3D

pts

topological COF (JUC-646) was constructed from a twisted tetraamine (BMTA) with

geometry—using the same TPTPE linker. Both COFs exhibit high crystallinity

stability

and strong AIE-derived luminescence

but show strikingly different sensing performances. In particular

JUC-646 achieves a quenching constant of 6.99×10

L/mol toward 2

6-trinitrophenol (TNP)

nearly five times higher than that of TPPDA-TPTPE. This superior performance originates from the 3D open-channel structure (facilitating analyte diffusion)

enhanced host-guest interactions

and energetically favorable photoinduced electron transfer—all of which are derived from dimensional differences. This comparative study explicitly establishes a structure-function relationship between framework dimensionality and sensing performance

offering direct guidance for the rational design of AIE-active COFs with tailored dimensionality for efficient explosive detection.

关键词

Keywords

references

Zhu, M. W.; Xu, S. Q.; Wang, X. Z.; Chen, Y.; Dai, L.; Zhao, X. The construction of fluorescent heteropore covalent organic frameworks and thei r applications in spectroscopic and visual detection of trinitrophenol with high selectivity and sensitivity. Chem. Commun. 2018 , 54 , 2308−2311..

Kayser, E.; Burlinson, N. Migration of explosives in soil: analysis of rdx, tnt, and tetryl from a 14c lysimeter study. J. Energet. Mater. 1988 , 6 , 45−71..

Shen, J.; Zhang, J.; Zuo, Y.; Wang, L.; Sun, X.; Li, J.; Han, W.; He, R. Biodegradation of 2,4,6-trinitrophenol by Rhodococcus sp. isolated from a picric acid-contaminated soil. J. Hazard. Mater. 2009 , 163 , 1199−1206..

Wyman, J.; Serve, M.; Hobson, D.; Lee, L.; Uddin, J. Safety data sheet for picric acid, resource of National Institute of Health. Toxicol Environ Health Part A 1992 , 37 , 313..

Junqueira, J. R.; de Araujo, W. R.; Salles, M. O.; Paixão, T. R. Flow injection analysis of picric acid explosive using a copper electrode as electrochemical detector. Talanta 2013 , 104 , 162−168..

Wang, C.; Li, Z. Molecular conformation and packing: their critical roles in the emission performan ce of mechanochromic fluorescence materials. Mater. Chem. Front. 2017 , 1 , 2174−2194..

Chen, Y.; Lam, J. W.; Kwok, R. T.; Liu, B.; Tang, B. Z. Aggregation-induced emission: fundamental understanding and future developments. Mater. Horiz. 2019 , 6 , 428−433..

Herwig, L.; Rice, A. J.; Bedbrook, C. N.; Zhang, R. K.; Lignell, A.; Cahn, J. K.; Renata, H.; Dodani, S. C.; Cho, I.; Cai, L. Directed evolution of a bright near-infrared fluorescent rhodopsin using a synthetic chromophore. Cell Chem. Biol. 2017 , 24 , 415−425..

Luo, J.; Xie, Z.; Lam, J. W.; Cheng, L.; Chen, H.; Qiu, C.; Kwok, H. S.; Zhan, X.; Liu, Y.; Zhu, D. Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole. Chem. Commun . 2001 , 1740−1741..

Liu, J.; Li, C.; Liu, Y.; Wang, Y.; Fang, Q. Highly-stable two-dimensional bicarbazole-based sp 2 -carbon-conjugated covalent organic framework for efficient electrocatalytic oxygen reduction. Acta Chim. Sin. (in Chinese) 2023 , 81 , 884..

Côté, A. P .; Benin, A. I.; Ockwig, N. W.; O'Keeffe, M.; Matzger, A. J.; Yaghi, O. M. Porous, crystalline, covalent organic frameworks. science 2005 , 310 , 1166−1170..

Liu, Y.; Ren, J.; Wang, Y.; Zhu, X.; Guan, X.; Wang, Z.; Zhou, Y.; Zhu, L.; Qiu, S.; Xiao, S.; Fang, Q. A stable luminescent covalent organic framework nanosheet for sensitive molecular recognition. CCS Chem. 2022 , 5 , 2033−2045..

Diercks, C. S.; Yaghi, O. M. The atom, the molecule, and the covalent organic framework. Science 2017 , 355 , eaal1585..

Huang, N.; Wang, P.; Jiang, D. Covalent organic frameworks: a materials platform for structural and functional designs. Nat. Rev. Mater. 2016 , 1 , 1−19..

Huang, N.; Zhai, L.; Coupry, D. E.; Addicoat, M. A.; Okushita, K.; Nishimura, K.; Heine, T.; Jiang, D. Multiple-component covalent organic frameworks. Nat. Commun. 2016 , 7 , 12325..

Song, J.; Wang, Z.; Liu, Y.; Tuo, C.; Wang, Y.; Fang, Q.; Qiu, S. A three-dimensional covalent organic frameworks for CO 2 uptake and d yes adsorption. Chem. Res. Chin. Univ. 2022 , 38 , 834−837..

[Fang, Q.; Gu, S.; Zheng, J.; Zhuang, Z.; Qiu, S.; Yan, Y. 3D microporous base-functionalized covalent organic frameworks for size-selective catalysis. Anal. Chem . 2014, 126 , 2922-2926..

Li, Z.; Zhang, Y.; Xia, H.; Mu, Y.; Liu, X. A robust and luminescent covalent organic framework as a highly sensitive and selective sensor for the detection of Cu 2+ ions. Chem. Commun. 2016 , 52 , 6613−6616..

Dalapati, S.; Jin, E.; Addicoat, M.; Heine, T.; Jiang, D. Highly emissive covalent organic frameworks. J. Am. Chem. Soc. 2016 , 138 , 5797−5800..

DeBlase, C. R.; Silberstein, K. E.; Truong, T.-T.; Abruña, H. D.; Dichtel, W. R. β-Ketoenamine-linked covalent organic frameworks capable of pseudocapacitive energy storage. J. Am. Chem. Soc . 2013 , 135 , 16821-16824..

Ding, X.; Guo, J.; Feng, X.; Honsho, Y.; Guo, J.; Seki, S.; Maitarad, P.; Saeki, A.; Nagase, S.; Jiang, D. Synthesis of metallophthalocyanine covalent organic frameworks that exhibit high carrier mobility and photoconductivity. Angew. Chem. Int. Ed. 2011 , 50 , 1289−1293..

Huynh, T. P.; Sosnowska, M.; Sobczak, J. W.; Kc, C. B.; Nesterov, V. N.; D’Souza, F.; Kutner, W. Simultaneous chronoamperometry and piezoelectric microgravimetry determination of nitroaromatic explosives using molecularly imprinted thiophene polymers. Anal. chem. 2013 , 85 , 8361−8368..

Zhang, C.; Zhang, S.; Yan, Y.; Xia, F.; Huang, A.; Xian, Y. Highly fluorescent polyimide covalent organic nanosheets as sensing probes for the detection of 2, 4, 6-trinitrophenol. ACS Appl. Mater. Interfaces 2017 , 9 , 13415−13421..

Das, G.; Biswal, B. P.; Kandambeth, S.; Venkatesh, V.; Kaur, G.; Addicoat, M.; Heine, T.; Verma, S.; Banerjee, R. Chemical sensing in two dimensional porous covalent organic nanosheets. Chem. Sci. 2015 , 6 , 3931−3939..

Ma, L.; Feng, X.; Wang, S.; Wang, B. Recent advances in AIEgen-based luminescent metal–organic frameworks and covalent organic frameworks. Mater. Chem. Front. 2017 , 1 , 2474−2486..

Niu, Q.; Gao, K.; Lin, Z.; Wu, W. Amine-capped carbon dots as a nanosensor for sensitive and selective detection of picric acid in aqueous solution via electrostatic interaction. Anal. Methods 2013 , 5 , 6228−6233..

Roy, B.; Bar, A. K.; Gole, B.; Mukherjee, P. S. Fluorescent tris-imidazolium sensors for picric acid explosive. J. Org. Chem. 2013 , 78 , 1306−1310..

Wan, S.; Guo, J.; Kim, J.; Ihee, H.; Jiang, D. A photoconductive covalent organic framework: self-condensed arene cubes composed of eclipsed 2D polypyrene sheets for photocurrent generation. Angew. Chem. Int. Ed. 2009 , 48 , 5439−5442..

Meng, Y.; Luo, Y.; Shi, J.; Ding, H.; Lang, X.; Chen, W.; Zheng, A.; Sun, J.; Wang, C. 2D and 3D porphyrinic covalent organic frameworks: the influence of dimensionality on functionality. Angew. Chem. Int. Ed . 2020 , 59 , 3624–3629..

Wang, K.; Kang, X.; Yuan, C.; Han, X.; Liu, Y.; Cui, Y. Porous 2D and 3D covalent organic frameworks with dimensionality-dependent photocatalytic activity in promoting radical ring-opening polymerization. Angew. Chem. Int. Ed . 2021 , 60 , 19466–19476..

Gong, C.; Yan, C.; Liu, J.; Li, H.; Zhang, H.; Chen, Y.; Zhang, S.; Ding, X.; Liu, Y. Insights into sensing applications of fluorescent covalent organic frameworks. TrAC Trends Anal. Chem. 2024 , 173 , 117625..

Gao, Q.; Li, X.; Ning, G.-H.; Leng, K.; Tian, B.; Liu, C.; Tang, W.; Xu, H.-S.; Loh, K. P. Highly photoluminescent two-dimensional imine-based covalent organic frameworks for chemical sensing. Chem. Commun. 2018 , 54 , 2349−2352..

Venkatramaiah, N.; Kumar, S.; Patil, S. Fluoranthene based fluorescent chemosensors for detection of explosive nitroaromatics. Chem. Commun. 2012 , 48 , 5007−5009..

Chang, J.; Zhang, Z.; Zheng, H.; Li, H.; Suo, J.; Ji, C.; Chen, F.; Zhang, S.; Wang, Z.; Valtchev, V.; Qiu, S.; Sun, J.; Fang, Q. Synthesis of three-dimensional covalent organic frameworks through a symmetry reduction strategy. Nat. Chem. 2025 , 17 , 571−581..

El-Mahdy, A. F.; Mohamed, M. G.; Mansoure, T. H.; Yu, H.-H.; Chen, T.; Kuo, S. W. Ultrastable tetraphenyl-p-phenylenediamine-based covalent organic frameworks as platforms for high-performance electrochemical supercapacitors. Chem. Commun. 2019 , 55 , 14890−14893..

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