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Journal articles on the topic 'Hydrogen-bonded organic framework'

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Author: Grafiati
Published: 10 December 2022
Last updated: 28 January 2023

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1

Cullen, Duncan A., Michael G. Gardiner, and Nicholas G. White. "A three dimensional hydrogen bonded organic framework assembled through antielectrostatic hydrogen bonds." Chemical Communications 55, no. 80 (2019): 12020–23. http://dx.doi.org/10.1039/c9cc06707h.

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2

Lin, Rui-Biao, Yabing He, Peng Li, Hailong Wang, Wei Zhou, and Banglin Chen. "Multifunctional porous hydrogen-bonded organic framework materials." Chemical Society Reviews 48, no. 5 (2019): 1362–89. http://dx.doi.org/10.1039/c8cs00155c.

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3

Yang, Wei, Wei Zhou, and Banglin Chen. "A Flexible Microporous Hydrogen-Bonded Organic Framework." Crystal Growth & Design 19, no. 9 (August 8, 2019): 5184–88. http://dx.doi.org/10.1021/acs.cgd.9b00582.

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4

Feng, Ji‐fei, Tian‐Fu Liu, and Rong Cao. "An Electrochromic Hydrogen‐Bonded Organic Framework Film." Angewandte Chemie International Edition 59, no. 50 (October 7, 2020): 22392–96. http://dx.doi.org/10.1002/anie.202006926.

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5

Feng, Ji‐fei, Tian‐Fu Liu, and Rong Cao. "An Electrochromic Hydrogen‐Bonded Organic Framework Film." Angewandte Chemie 132, no. 50 (October 7, 2020): 22578–82. http://dx.doi.org/10.1002/ange.202006926.

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6

Castells-Gil, Javier, Natalia M. Padial, and Carlos Martí-Gastaldo. "Structural reorganization in a hydrogen-bonded organic framework." New Journal of Chemistry 42, no. 19 (2018): 16138–43. http://dx.doi.org/10.1039/c8nj02738b.

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Self-recognition of 3,3′,5,5′-azobenzenetetracarboxylic acid yields a grid-like anionic hydrogen-bonded framework capable of undergoing structural reorganization by recrystallization in the presence of guanidinium cations.
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7

Ji, Qin, Kiyonori Takahashi, Shin-ichiro Noro, Yusuke Ishigaki, Kenta Kokado, Takayoshi Nakamura, and Ichiro Hisaki. "A Hydrogen-Bonded Organic Framework Based on Pyrazinopyrazine." Crystal Growth & Design 21, no. 8 (July 9, 2021): 4656–64. http://dx.doi.org/10.1021/acs.cgd.1c00506.

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8

Kirlikovali, Kent O., Subhadip Goswami, Mohammad Rasel Mian, Matthew D. Krzyaniak, Michael R. Wasielewski, Joseph T. Hupp, Peng Li, and Omar K. Farha. "An Electrically Conductive Tetrathiafulvalene-Based Hydrogen-Bonded Organic Framework." ACS Materials Letters 4, no. 1 (December 7, 2021): 128–35. http://dx.doi.org/10.1021/acsmaterialslett.1c00628.

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9

Liang, Weibin, Francesco Carraro, Marcello B. Solomon, Stephen G. Bell, Heinz Amenitsch, Christopher J. Sumby, Nicholas G. White, Paolo Falcaro, and Christian J. Doonan. "Enzyme Encapsulation in a Porous Hydrogen-Bonded Organic Framework." Journal of the American Chemical Society 141, no. 36 (August 19, 2019): 14298–305. http://dx.doi.org/10.1021/jacs.9b06589.

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10

Dong, Yanhong, Ning-Ning Wei, Liguo Gao, Juanyuan Hao, Dan Vasilescu, and Ce Hao. "Theoretical Study on the Sensing Mechanism of Luminescent Metal-Organic Framework [Zn(3-tzba)(2,2′-bipy)(H2O)] · 3H2O for Formaldehyde Detection." Journal of Computational and Theoretical Nanoscience 17, no. 7 (July 1, 2020): 2890–96. http://dx.doi.org/10.1166/jctn.2020.8971.

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The sensing mechanism of luminescent metal-organic framework [Zn(3-tzba)(2,2′-bipy)(H2O)] -3H2O for formaldehyde detection was explored by using density functional theory and time-dependent density functional theory methods. Our investigation found that luminescent metal-organic framework [Zn(3-tzba)(2,2′-bipy)(H2O)] • 3H2O is able to interact with formaldehyde through hydrogen bonding to the framework. The luminescent mechanism of the hydrogen-bonded complex is photo-induced electron transfer; while the luminescent mechanism of luminescent metal-organic framework [Zn(3-tzba)(2,2′-bipy)(H2O)]-3H2O is ligand-to-ligand charge transfer. The intermolecu-lar hydrogen bond was found to be stronger in the excited state than that in the ground state by analyzing the geometry nuclear magnetic resonance, binding energy and infrared spectrum in different electronic states. Calculated fluorescence radiative rate coefficient and internal conversion rate coefficient qualitatively indicated a reduced radiative process and an enhanced internal conversion process of the hydrogen-bonded complex. The hydrogen-bonded complex exhibits luminescence weakening or even quenching due to the enhancement of the intermolecular hydrogen bond in the excited state compare with luminescent metal-organic framework [Zn(3-tzba)(2,2′-bipy)(H2O)]-3H2O. The variable luminescence demonstrated the potential of luminescent metal-organic framework [Zn(3-tzba)(2,2′-bipy)(H2O)]-3H2O as luminescent sensor for formaldehyde detection.
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11

Jiang, Xiao-Tian, Qi Yin, Bai-Tong Liu, Jun-Yu Chen, Rui Wang, and Tian-Fu Liu. "Porous hydrogen-bonded organic framework membranes for high-performance molecular separation." Nanoscale Advances 3, no. 12 (2021): 3441–46. http://dx.doi.org/10.1039/d1na00199j.

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12

Suzuki, Yuto, Norimitsu Tohnai, Akinori Saeki, and Ichiro Hisaki. "Hydrogen-bonded organic frameworks of twisted polycyclic aromatic hydrocarbon." Chemical Communications 56, no. 87 (2020): 13369–72. http://dx.doi.org/10.1039/d0cc06081j.

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13

Liu, Ting, Bin Wang, Ru He, Hadi Arman, Kirk S. Schanze, Shengchang Xiang, Dan Li, and Banglin Chen. "A novel hydrogen-bonded organic framework for the sensing of two representative organic arsenics." Canadian Journal of Chemistry 98, no. 7 (July 2020): 352–57. http://dx.doi.org/10.1139/cjc-2019-0417.

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A novel fluorescent hydrogen-bonded organic framework with a double fold interpenetrated structure, HOF-22, has been successfully constructed and structurally characterized. HOF-22 is capable of sensitive detection of two representative organic arsenics from aqueous solution.
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14

Aitchison, Catherine M., Christopher M. Kane, David P. McMahon, Peter R. Spackman, Angeles Pulido, Xiaoyan Wang, Liam Wilbraham, et al. "Photocatalytic proton reduction by a computationally identified, molecular hydrogen-bonded framework." Journal of Materials Chemistry A 8, no. 15 (2020): 7158–70. http://dx.doi.org/10.1039/d0ta00219d.

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A hydrogen-bonded organic framework is an effective photocatalyst for producing hydrogen from water. Its crystal structure is key to its activity; a chemically identical, amorphous version is almost inactive, as rationalized by crystal structure prediction.
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15

Xie, Feng, Hao Wang, and Jing Li. "Flexible hydrogen-bonded organic framework to split ethane and ethylene." Matter 5, no. 8 (August 2022): 2516–18. http://dx.doi.org/10.1016/j.matt.2022.06.043.

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16

Chen, Tong, Hui-Bo Jiang, Kai-Bin Jiang, De-Lin Hu, Li-Zhen Cai, Ming-Sheng Wang, and Guo-Cong Guo. "Photochromic Semiconductive Hydrogen-Bonded Organic Framework (HOF) with Broadband Absorption." ACS Applied Materials & Interfaces 14, no. 9 (February 24, 2022): 11619–25. http://dx.doi.org/10.1021/acsami.1c23328.

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17

Sun, Zhiyong, Yangxue Li, Li Chen, Xiabin Jing, and Zhigang Xie. "Fluorescent Hydrogen-Bonded Organic Framework for Sensing of Aromatic Compounds." Crystal Growth & Design 15, no. 2 (January 14, 2015): 542–45. http://dx.doi.org/10.1021/cg501652r.

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18

Wang, Bin, Xiu-Liang Lv, Jie Lv, Li Ma, Rui-Biao Lin, Hui Cui, Jian Zhang, Zhangjing Zhang, Shengchang Xiang, and Banglin Chen. "A novel mesoporous hydrogen-bonded organic framework with high porosity and stability." Chemical Communications 56, no. 1 (2020): 66–69. http://dx.doi.org/10.1039/c9cc07802a.

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19

Kanetomo, Takuya, Zhen Ni, and Masaya Enomoto. "Hydrogen-bonded cobalt(ii)-organic framework: normal and reverse spin-crossover behaviours." Dalton Transactions 51, no. 13 (2022): 5034–40. http://dx.doi.org/10.1039/d2dt00453d.

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20

Qi, De-Qiang, Gui-Ge Hou, Jian-Ping Ma, Ru-Qi Huang, and Yu-Bin Dong. "A novel three-dimensional framework constructed by 2-[(1H-imidazol-1-yl)methyl]-1H-benzimidazole and infinite chains of hydrogen-bonded water molecules." Acta Crystallographica Section C Crystal Structure Communications 65, no. 3 (February 7, 2009): o85—o87. http://dx.doi.org/10.1107/s0108270109001814.

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A novel three-dimensional framework of 2-[(1H-imidazol-1-yl)methyl]-1H-benzimidazole dihydrate, C11H10N4·2H2O orL·2H2O, (I), in whichLacts as both hydrogen-bond acceptor and donor in the supramolecular construction with water, has been obtained by self-assembly reaction ofLwith H2O. The two independent water molecules are hydrogen bonded alternately with each other to form a one-dimensional infinite zigzag water chain. These water chains are linked by the benzimidazole molecules into a three-dimensional framework, in which each organic molecule is hydrogen bonded by three water molecules. This study shows that the diversity of hydrogen-bonded patterns plays a crucial role in the formation of the three-dimensional framework. More significantly, as water molecules are important in contributing to the conformation, stability, function and dynamics of biomacromolecules, the infinite chains of hydrogen-bonded water molecules seen in (I) may be a useful model for water in other chemical and biological processes.
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21

Jiang, Weiwei, Lingling Xia, Dan Li, Pengyan Wu, Tongtong Zou, Xingcheng Yuan, Wen Wei, and Jian Wang. "An Ultrasensitive Picric Acid Sensor Based on a Robust 3D Hydrogen-Bonded Organic Framework." Biosensors 12, no. 9 (August 25, 2022): 682. http://dx.doi.org/10.3390/bios12090682.

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Hydrogen-bonded organic frameworks (HOFs), as a newly developed porous material, have been widely used in various fields. To date, several organic building units (OBUs) with tri-, tetra-, and hexa-carboxylic acid synthons have been applied to synthesize HOFs. To our knowledge, di-carboxylic acids have rarely been reported for the construction of HOFs, in particular, di-carboxylic acid-based HOFs with fluorescence sensing properties have not been reported. In this study, a rare example of a di-carboxylic acid-based, luminescent three-dimensional hydrogen-bonded organic framework has been successfully constructed and structurally characterized; it has a strong electron-rich property originated from its organic linker 9-phenylcarbazole-3,6-dicarboxylic acid. It represents the first example of HOF-based sensors for the highly selective and sensitive detection of PA (Picric acid) with reusability; the LOD is less than 60 nM. This work thus provides a new avenue for the fabrication of fluorescent HOFs sensing towards explosives.
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22

Yoon, Tae-Ung, Seung Bin Baek, Dongwook Kim, Eun-Jung Kim, Wang-Geun Lee, Bhupendra Kumar Singh, Myoung Soo Lah, Youn-Sang Bae, and Kwang S. Kim. "Efficient separation of C2 hydrocarbons in a permanently porous hydrogen-bonded organic framework." Chemical Communications 54, no. 67 (2018): 9360–63. http://dx.doi.org/10.1039/c8cc04139c.

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23

Lee, Wang-Geun, Tae-Ung Yoon, Youn-Sang Bae, Kwang S. Kim, and Seung Bin Baek. "Selective separation of Xe/Kr and adsorption of water in a microporous hydrogen-bonded organic framework." RSC Advances 9, no. 63 (2019): 36808–14. http://dx.doi.org/10.1039/c9ra08184d.

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24

Hisaki, Ichiro, Shoichi Nakagawa, Hiroyasu Sato, and Norimitsu Tohnai. "Alignment of paired molecules of C60 within a hexagonal platform networked through hydrogen-bonds." Chemical Communications 52, no. 63 (2016): 9781–84. http://dx.doi.org/10.1039/c6cc04310k.

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25

Banerjee, Rahul. "Intra-molecular Interactions in Porous Covalent Organic Frameworks." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C530. http://dx.doi.org/10.1107/s2053273314094698.

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A new strategy of intramolecular hydrogen bonding in 2D covalent organic framework as an extra stabilizing factor has been introduced, which helps to improve the crystallinity, porosity and chemical stability of the COF. Using this concept, highly stable porphyrin containing covalent organic frameworks have been synthesized using the Schiff base reaction. The stability of the COFs mainly arises due to the strong intramolecular O-H...N=C hydrogen bonding. Validation of this postulate was cross-checked by synthesizing methoxy (OCH3) substituted COF in which no hyrogen bonding exists. It was found that methoxy substituted COF have a low crystallinity, porosity and chemical stability as compared to hydrogen bonded COF.
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26

Zentner, Cassandra A., Holden W. H. Lai, Joshua T. Greenfield, Ren A. Wiscons, Matthias Zeller, Charles F. Campana, Orhan Talu, Stephen A. FitzGerald, and Jesse L. C. Rowsell. "High surface area and Z′ in a thermally stable 8-fold polycatenated hydrogen-bonded framework." Chemical Communications 51, no. 58 (2015): 11642–45. http://dx.doi.org/10.1039/c5cc04219d.

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27

Zhou, Hui, Qun Ye, Xiangyang Wu, Jing Song, Ching Mui Cho, Yun Zong, Ben Zhong Tang, T. S. Andy Hor, Edwin Kok Lee Yeow, and Jianwei Xu. "A thermally stable and reversible microporous hydrogen-bonded organic framework: aggregation induced emission and metal ion-sensing properties." Journal of Materials Chemistry C 3, no. 45 (2015): 11874–80. http://dx.doi.org/10.1039/c5tc02790j.

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28

Liu, Wen-Ju, Ya-Qiong Wen, Jia-Wei Wang, Di-Chang Zhong, Jing-Bo Tan, and Tong-Bu Lu. "Nitrogen- and iodine-doped microporous carbon derived from a hydrogen-bonded organic framework: an efficient metal-free electrocatalyst for the oxygen reduction reaction." Journal of Materials Chemistry A 7, no. 16 (2019): 9587–92. http://dx.doi.org/10.1039/c8ta07994c.

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29

Wang, Yijie, Jianbo Yin, Di Liu, Chengqi Gao, Zixi Kang, Rongming Wang, Daofeng Sun, and Jianzhuang Jiang. "Guest-tuned proton conductivity of a porphyrinylphosphonate-based hydrogen-bonded organic framework." Journal of Materials Chemistry A 9, no. 5 (2021): 2683–88. http://dx.doi.org/10.1039/d0ta07207a.

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A porous porphyrin-based hydrogen-bonded organic framework (HOF) was constructed, and its proton conductivity was improved through a two-step guest-tuned strategy. After regulation, the proton conductivity of the HOF reaches 1.59 × 10−1 S cm−1 at 80 °C and 99% RH.
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30

Huang, Qiuyi, Wenlang Li, Zhu Mao, Hao Zhang, Yang Li, Dongyu Ma, Huiyan Wu, et al. "Dynamic molecular weaving in a two-dimensional hydrogen-bonded organic framework." Chem 7, no. 5 (May 2021): 1321–32. http://dx.doi.org/10.1016/j.chempr.2021.02.017.

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31

Liu, Xiaolin, Xiya Yang, Hailong Wang, Ichiro Hisaki, Kang Wang, and Jianzhuang Jiang. "A robust redox-active hydrogen-bonded organic framework for rechargeable batteries." Journal of Materials Chemistry A 10, no. 4 (2022): 1808–14. http://dx.doi.org/10.1039/d1ta09194h.

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A robust HOF has been employed as cathode for LIBs. The decoration of rich redox-active moieties in HOFs introduces the surface-controlled capacitive mechanism in LIBs, accessing a high capacity, high rate capability and excellent cycling stability.
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32

Lv, Yuanchao, Delin Li, Ang Ren, Zhile Xiong, Yinan Yao, Kaicong Cai, Shengchang Xiang, Zhangjing Zhang, and Yong Sheng Zhao. "Hydrogen-Bonded Organic Framework Microlasers with Conformation-Induced Color-Tunable Output." ACS Applied Materials & Interfaces 13, no. 24 (June 11, 2021): 28662–67. http://dx.doi.org/10.1021/acsami.1c06312.

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33

Mouchaham, Georges, Nans Roques, Abdellah Kaiba, Philippe Guionneau, and Jean-Pascal Sutter. "Tubular crystals growth for a nanoporous hydrogen-bonded metal–organic framework." CrystEngComm 12, no. 11 (2010): 3496. http://dx.doi.org/10.1039/c0ce00256a.

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34

Yang, Wei, Bin Li, Hailong Wang, Osamah Alduhaish, Khalid Alfooty, Mohie Aldin Zayed, Peng Li, Hadi D. Arman, and Banglin Chen. "A Microporous Porphyrin-Based Hydrogen-Bonded Organic Framework for Gas Separation." Crystal Growth & Design 15, no. 4 (February 27, 2015): 2000–2004. http://dx.doi.org/10.1021/acs.cgd.5b00147.

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35

Yang, Wei, Jiawei Wang, Hailong Wang, Zongbi Bao, John Cong-Gui Zhao, and Banglin Chen. "Highly Interpenetrated Robust Microporous Hydrogen-Bonded Organic Framework for Gas Separation." Crystal Growth & Design 17, no. 11 (October 23, 2017): 6132–37. http://dx.doi.org/10.1021/acs.cgd.7b01322.

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36

Li, Bo, Lei Wang, Yang Li, Dongqi Wang, Rui Wen, Xinghua Guo, Shoujian Li, Lijian Ma, and Yin Tian. "Conversion of supramolecular organic framework to uranyl-organic coordination complex: a new “matrix-free” strategy for highly efficient capture of uranium." RSC Advances 7, no. 15 (2017): 8985–93. http://dx.doi.org/10.1039/c6ra28356j.

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Conversion of hydrogen-bonded supramolecular organic frameworks (HSOF) to a uranyl-organic coordination complex (UOCC) by uranyl-induced disassembly and reassembly: innovative “matrix-free” strategy for highly efficient uranium capture.
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37

Lv, Yuanchao, Zhile Xiong, Yunbin Li, Delin Li, Jiashuai Liang, Yisi Yang, Fahui Xiang, Shengchang Xiang, Yong Sheng Zhao, and Zhangjing Zhang. "Framework-Shrinkage-Induced Wavelength-Switchable Lasing from a Single Hydrogen-Bonded Organic Framework Microcrystal." Journal of Physical Chemistry Letters 13, no. 1 (December 28, 2021): 130–35. http://dx.doi.org/10.1021/acs.jpclett.1c03855.

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38

Liang, Jun, Shanghua Xing, Philipp Brandt, Alexander Nuhnen, Carsten Schlüsener, Yangyang Sun, and Christoph Janiak. "A chemically stable cucurbit[6]uril-based hydrogen-bonded organic framework for potential SO2/CO2 separation." Journal of Materials Chemistry A 8, no. 38 (2020): 19799–804. http://dx.doi.org/10.1039/d0ta07457h.

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Both high SO2 uptake and excellent SO2/CO2 selectivity are achieved by an organic cage-based hydrogen-bonded organic framework (HOF) material based on experimental and theoretical studies.
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39

Nandi, Shyamapada, Debanjan Chakraborty, and Ramanathan Vaidhyanathan. "A permanently porous single molecule H-bonded organic framework for selective CO2 capture." Chemical Communications 52, no. 45 (2016): 7249–52. http://dx.doi.org/10.1039/c6cc02964g.

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40

Li, Tao, Bai-Tong Liu, Zhi-Bin Fang, Qi Yin, Rui Wang, and Tian-Fu Liu. "Integrating active C3N4 moieties in hydrogen-bonded organic frameworks for efficient photocatalysis." Journal of Materials Chemistry A 9, no. 8 (2021): 4687–91. http://dx.doi.org/10.1039/d1ta00100k.

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This study reports a photocatalyst based on a hydrogen-bonded organic framework exhibiting a high H2 evolution rate and easy recyclability. The ordered arrangement of photosensitizers is proved to play a vital role in the photocatalytic activity.
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41

Yan, Wenqing, Xiaopeng Yu, Tao Yan, Doufeng Wu, Erlong Ning, Yi Qi, Ying-Feng Han, and Qiaowei Li. "A triptycene-based porous hydrogen-bonded organic framework for guest incorporation with tailored fitting." Chemical Communications 53, no. 26 (2017): 3677–80. http://dx.doi.org/10.1039/c7cc00557a.

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By employing a robust and non-coplanar building block strategy, a triptycene-based hydrogen-bonded organic framework was constructed with almost no sacrifice of molecular surfaces, and it was capable of incorporating C60 molecules in high concentration in the channels with tailored fitting.
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42

Su, Jian, Shuai Yuan, Yi-Xun Cheng, Zhi-Mei Yang, and Jing-Lin Zuo. "Coordination-bond-directed synthesis of hydrogen-bonded organic frameworks from metal–organic frameworks as templates." Chemical Science 12, no. 42 (2021): 14254–59. http://dx.doi.org/10.1039/d1sc03962h.

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The MOF-to-HOF transformation was realized in a single-crystal-to-single-crystal manner by the oxidation and hydration of the CuI center in CuI-TTFTB. The corbelled S⋯S and π⋯π interactions ensured the framework stability during transformation.
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43

Yang, Chaoqing, Flavia Artizzu, Karel Folens, Gijs Du Laing, and Rik Van Deun. "Excitation dependent multicolour luminescence and colour blue-shifted afterglow at room-temperature of europium incorporated hydrogen-bonded multicomponent frameworks." Journal of Materials Chemistry C 9, no. 22 (2021): 7154–62. http://dx.doi.org/10.1039/d1tc01627j.

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Multicoloured luminescence and long-lived blue-shifted afterglow have been obtained in a europium-doped hydrogen-bonded organic framework (HOF). The material displays multi-stimuli responsive emission with anticounterfeiting application potential.
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44

Goswami, Subhadip, Kaikai Ma, Jiaxin Duan, Kent O. Kirlikovali, Jiaquan Bai, Joseph T. Hupp, Peng Li, and Omar K. Farha. "Understanding Diffusional Charge Transport within a Pyrene-Based Hydrogen-Bonded Organic Framework." Langmuir 38, no. 4 (January 20, 2022): 1533–39. http://dx.doi.org/10.1021/acs.langmuir.1c02915.

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45

Wang, Hailong, Bin Li, Hui Wu, Tong-Liang Hu, Zizhu Yao, Wei Zhou, Shengchang Xiang, and Banglin Chen. "A Flexible Microporous Hydrogen-Bonded Organic Framework for Gas Sorption and Separation." Journal of the American Chemical Society 137, no. 31 (August 3, 2015): 9963–70. http://dx.doi.org/10.1021/jacs.5b05644.

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46

Zhang, Xu, Libo Li, Jia-Xin Wang, Hui-Min Wen, Rajamani Krishna, Hui Wu, Wei Zhou, et al. "Selective Ethane/Ethylene Separation in a Robust Microporous Hydrogen-Bonded Organic Framework." Journal of the American Chemical Society 142, no. 1 (December 14, 2019): 633–40. http://dx.doi.org/10.1021/jacs.9b12428.

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47

Cui, Peng, Erik Svensson Grape, Peter R. Spackman, Yue Wu, Rob Clowes, Graeme M. Day, A. Ken Inge, Marc A. Little, and Andrew I. Cooper. "An Expandable Hydrogen-Bonded Organic Framework Characterized by Three-Dimensional Electron Diffraction." Journal of the American Chemical Society 142, no. 29 (June 27, 2020): 12743–50. http://dx.doi.org/10.1021/jacs.0c04885.

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48

Stackhouse, Chavis, Junyu Ren, Chuan Shan, Ayman Nafady, Abdullah M. Al-Enizi, Mohd Ubaidullah, Zheng Niu, and Shengqian Ma. "Microporous Cyclen-Based Octacarboxylate Hydrogen-Bonded Organic Framework Exhibiting Selective Gas Adsorption." Crystal Growth & Design 19, no. 11 (September 13, 2019): 6377–80. http://dx.doi.org/10.1021/acs.cgd.9b00851.

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49

Veselovsky, Vladimir V., Antonina V. Lozanova, Vera I. Isaeva, Vera D. Nissenbaum, Nikolai A. Davshan, Anna A. Lobova, and Vladimir V. Chernyshev. "New Chiral Hydrogen-Bonded Organic Framework Based on Substituted Diarylacetylene Dicarboxylic Acid." Crystal Growth & Design 20, no. 6 (April 21, 2020): 3713–21. http://dx.doi.org/10.1021/acs.cgd.9b01713.

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50

Han, Bin, Hailong Wang, Chiming Wang, Hui Wu, Wei Zhou, Banglin Chen, and Jianzhuang Jiang. "Postsynthetic Metalation of a Robust Hydrogen-Bonded Organic Framework for Heterogeneous Catalysis." Journal of the American Chemical Society 141, no. 22 (May 22, 2019): 8737–40. http://dx.doi.org/10.1021/jacs.9b03766.

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