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Journal articles on the topic 'Halogenated Nitrobenzenes'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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1

Tian, Meng, Xueliang Cui, Man Yuan, Jin Yang, Jiantai Ma та Zhengping Dong. "Efficient chemoselective hydrogenation of halogenated nitrobenzenes over an easily prepared γ-Fe2O3-modified mesoporous carbon catalyst". Green Chemistry 19, № 6 (2017): 1548–54. http://dx.doi.org/10.1039/c6gc03386e.

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An easily prepared cost-effective γ-Fe<sub>2</sub>O<sub>3</sub>/MC catalyst was used for the hydrogenation of halogenated nitrobenzenes with 100% selectivity for the corresponding halogenated anilines.
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2

Zhao, Hong, Guiqin Yu, Man Yuan, Jin Yang, Dan Xu, and Zhengping Dong. "Ultrafine and highly dispersed platinum nanoparticles confined in a triazinyl-containing porous organic polymer for catalytic applications." Nanoscale 10, no. 45 (2018): 21466–74. http://dx.doi.org/10.1039/c8nr05756g.

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Highly dispersed ultrafine Pt nanoparticles were confined in a triazinyl-containing porous organic polymer for the catalytic hydrolysis of ammonia borane and the selective hydrogenation of halogenated nitrobenzenes with excellent catalytic activity.
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3

Zhao, Ming, Baoming Feng, Xiaofei Qiao, Ning Zhong, Xuemei Ge, and Yuan Ji. "Electronic Modulation of Palladium in Metal Phosphide Nanoparticles for Chemoselective Reduction of Halogenated Nitrobenzenes." Chemistry – An Asian Journal 14, no. 3 (2019): 407–10. http://dx.doi.org/10.1002/asia.201801620.

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4

Lyu, Jing-Hui, Xiao-Bo He, Chun-Shan Lu, et al. "The promoting role of minor amount of water in solvent-free hydrogenation of halogenated nitrobenzenes." Chinese Chemical Letters 25, no. 2 (2014): 205–8. http://dx.doi.org/10.1016/j.cclet.2013.10.024.

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5

Lv, Jing, Yunfeng Zheng, Yangyang Zhu, Man Yuan, Yanlong Chang, and Zhengping Dong. "Renewable Soybean Pulp Derived N‐Doped Carbon Materials for Efficient Chemoselective Hydrogenation of Halogenated Nitrobenzenes." ChemistrySelect 4, no. 14 (2019): 4083–91. http://dx.doi.org/10.1002/slct.201900733.

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6

Zhang, Xianwen, Ping Li, Bin Xu, et al. "In Situ Hydrogen Activation Inspiring Efficient One-Pot Hydrogenation of Halogenated Nitrobenzenes over Ni–Co-Based Composites." Industrial & Engineering Chemistry Research 60, no. 23 (2021): 8312–23. http://dx.doi.org/10.1021/acs.iecr.1c00330.

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7

Wu, Wei, Wei Zhang, Yu Long, Jiaheng Qin, and Jiantai Ma. "Different transfer hydrogenation pathways of halogenated nitrobenzenes catalyzed by Fe-, Co- or Ni-based species confined in nitrogen doped carbon." Molecular Catalysis 497 (December 2020): 111226. http://dx.doi.org/10.1016/j.mcat.2020.111226.

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8

Zhang, Wei, Wei Wu, Yu Long, Fushan Wang, and Jiantai Ma. "Co-Ag alloy protected by nitrogen doped carbon as highly efficient and chemoselective catalysts for the hydrogenation of halogenated nitrobenzenes." Journal of Colloid and Interface Science 522 (July 2018): 217–27. http://dx.doi.org/10.1016/j.jcis.2018.03.059.

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9

Dong, Liqi, Zilong Liu, Yingna Wang, Yuanpei Lan, Chaoyi Chen, and Wei Zhang. "Ni-based nanocatalyst protected by ultrathin mesoporous nitrogen-doped carbon layer with hollow structure for the efficient transfer hydrogenation of halogenated nitrobenzenes." Molecular Catalysis 547 (August 2023): 113339. http://dx.doi.org/10.1016/j.mcat.2023.113339.

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10

Cao, Yueling, Kangkai Liu, Chen Wu, Hepeng Zhang, and Qiuyu Zhang. "In situ-formed cobalt embedded into N-doped carbon as highly efficient and selective catalysts for the hydrogenation of halogenated nitrobenzenes under mild conditions." Applied Catalysis A: General 592 (February 2020): 117434. http://dx.doi.org/10.1016/j.apcata.2020.117434.

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11

Pinto, Sara M. A., Carolina S. Vinagreiro, Vanessa A. Tomé, Giusi Piccirillo, Liliana Damas, and Mariette M. Pereira. "Nitrobenzene method: A keystone in meso-substituted halogenated porphyrin synthesis and applications." Journal of Porphyrins and Phthalocyanines 23, no. 04n05 (2019): 329–46. http://dx.doi.org/10.1142/s1088424619300039.

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This review article briefly describes the available synthetic approaches for meso-arylporphyrins giving particular emphasis for one-pot nitrobenzene and nitrobenzene/NaY methods regarding the synthesis of meso-halogenated arylporphyrins. The review also describes the relevant applications of these halogenated porphyrins and their metalloporphyrin counterparts, prepared via nitrobenzene method, as photosensitizers for therapy (PDT and PDI), diagnostic (molecular contrast agents) and also for catalytic oxidation and CO2 cycloaddition reactions to epoxides.
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12

Leung, M. F., K. Geoghegan-Barek, G. B. Zamansky, and I. N. Chou. "Microtubule disassembly induced by sensitizing halogenated nitrobenzene derivatives." Toxicology in Vitro 4, no. 4-5 (1990): 252–63. http://dx.doi.org/10.1016/0887-2333(90)90059-3.

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13

Lyu, Jinghui, Jianguo Wang, Chunshan Lu, et al. "Size-Dependent Halogenated Nitrobenzene Hydrogenation Selectivity of Pd Nanoparticles." Journal of Physical Chemistry C 118, no. 5 (2014): 2594–601. http://dx.doi.org/10.1021/jp411442f.

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14

Ma, Lei, Jianguo Wang, Hanbing Wang, et al. "High halogenated nitrobenzene hydrogenation selectivity over nano Ir particles." Chinese Journal of Chemical Engineering 25, no. 3 (2017): 306–12. http://dx.doi.org/10.1016/j.cjche.2016.08.005.

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15

Xie, Ruigang, Xueqin Cao, Yue Pan, and Hongwei Gu. "Synthesis of Pt nanocatalysts for selective hydrogenation of ortho-halogenated nitrobenzene." Science China Chemistry 58, no. 6 (2015): 1051–55. http://dx.doi.org/10.1007/s11426-015-5322-0.

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16

McManus, Iain J., Helen Daly, Haresh G. Manyar, S. F. Rebecca Taylor, Jillian M. Thompson, and Christopher Hardacre. "Selective hydrogenation of halogenated arenes using porous manganese oxide (OMS-2) and platinum supported OMS-2 catalysts." Faraday Discussions 188 (2016): 451–66. http://dx.doi.org/10.1039/c5fd00227c.

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Porous manganese oxide (OMS-2) and platinum supported on OMS-2 catalysts have been shown to facilitate the hydrogenation of the nitro group in chloronitrobenzene to give chloroaniline with no dehalogenation. Complete conversion was obtained within 2 h at 25 °C and, although the rate of reaction increased with increasing temperature up to 100 °C, the selectivity to chloroaniline remained at 99.0%. Use of Pd/OMS-2 or Pt/Al<sub>2</sub>O<sub>3</sub> resulted in significant dechlorination even at 25 °C and 2 bar hydrogen pressure giving a selectivity to chloroaniline of 34.5% and 77.8%, respectivel
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17

Chen, Ruo-nan, Zhi-qiang Cai, Wei Zhang, et al. "An Amphiphilic Star-Shaped Polymer (Star-PEG-PCL2) used as a Stationary Phase for GC." Acta Chimica Slovenica 70, no. 1 (2023): 1–11. http://dx.doi.org/10.17344/acsi.2022.7390.

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A star-shaped polymer (Star-PEG-PCL2) was synthesized to with PCL and PEG, and used as a stationary phase for gas chromatography. The statically coated Star-PEG-PCL2 column exhibited an efficiency of 2260 plates/m determined by naphthalene at 120 °C and moderate polarity. The Star-PEG-PCL2 column showed high resolution performance for isomers of a wide ranging polarity, including methylnaphthalenes, halogenated benzenes, nitrobenzene, phenols, and anilines, and displayed dual-nature selectivity for a mixture of 17 analytes. Also, the Star-PEG-PCL2 column exhibited good separation performance a
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18

Zhou, Li, Huizi Gu, and Xinhuan Yan. "A Novel Transfer Hydrogenation with High Hydrogen Utilization for the Hydrogenation of Halogenated Nitrobenzene without Hydrodehalogenation." Catalysis Letters 132, no. 1-2 (2009): 16–21. http://dx.doi.org/10.1007/s10562-009-0036-6.

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19

Gulaboski, Rubin, Kai Riedl, and Fritz Scholz. "Standard Gibbs energies of transfer of halogenate and pseudohalogenate ions, halogen substituted acetates, and cycloalkyl carboxylate anions at the water|nitrobenzene interface." Physical Chemistry Chemical Physics 5, no. 6 (2003): 1284–89. http://dx.doi.org/10.1039/b210356g.

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20

Sharf, V. Z., V. F. Dovganyuk, V. I. Isaeva, and B. I. Maksimov. "Study of the catalytic activity of metal complexes attached to a solid support. 6. Reduction of nitrobenzene and its halogenated derivatives by chemically bound hydrogen in the presence of immobilized Rh complexes." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 38, no. 3 (1989): 468–72. http://dx.doi.org/10.1007/bf00958034.

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21

Gao, Mengmeng, Jinfang Kou, Manhua Xu, Kun Yuan, Mengyang Li, and Zhengping Dong. "Electron-rich Pt anchored on covalent triazine frameworks for the selective hydrogenation of halogenated nitrobenzenes." Green Chemistry, 2024. http://dx.doi.org/10.1039/d3gc04671k.

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Halogenated nitroarenes hydrogenation on metal-based catalysts without dehalogenation to synthesize halogenated amines is a research challenge. Herein, using a covalent organic framework (COF) as support and benefiting from strong metal-support...
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22

Bai, Jia-qi, Jiahui Xu, Mei Ma, et al. "Photo-thermal Catalytic Hydrogenation of Halogenated Nitrobenzenes over Ni/P25 Catalyst." Langmuir, May 29, 2024. http://dx.doi.org/10.1021/acs.langmuir.4c01132.

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23

"N,P co-Doped Carbon Materials Derived from Yeast for Selective Reduction of Halogenated Nitrobenzenes." Synfacts 20, no. 10 (2024): 1075. http://dx.doi.org/10.1055/s-0043-1775065.

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24

Lin, Yuemin, Yuanyuan Zhang, Renfeng Nie, et al. "Room-temperature hydrogenation of halogenated nitrobenzenes over metal—organic-framework-derived ultra-dispersed Ni stabilized by N-doped carbon nanoneedles." Frontiers of Chemical Science and Engineering, November 5, 2022. http://dx.doi.org/10.1007/s11705-022-2220-9.

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25

Zhang, Wei, Wei Wu, Fei Guo, and Xinwei Dong. "Fe3C nanoclusters integrated with Fe single-atom planted in nitrogen doped carbon derived from truncated hexahedron zeolitic imidazolate framework for the efficient transfer hydrogenation of halogenated nitrobenzenes." Journal of Colloid and Interface Science, March 2023. http://dx.doi.org/10.1016/j.jcis.2023.03.006.

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26

Xu, Jiahui, Jia-qi Bai, Wenjie Si, et al. "N,S-Co-doping Significantly Improves the Co–Nx Content of the Co-NSPC Catalyst and Enhances the Catalytic Performance for Selective Hydrogenation of Halogenated Nitrobenzenes." Industrial & Engineering Chemistry Research, February 22, 2023. http://dx.doi.org/10.1021/acs.iecr.2c04127.

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27

Carlsson, Josefine, Tim Åström, Conny Östman, and Ulrika Nilsson. "Solvent-free automated thermal desorption-gas chromatography/mass spectrometry for direct screening of hazardous compounds in consumer textiles." Analytical and Bioanalytical Chemistry, June 20, 2023. http://dx.doi.org/10.1007/s00216-023-04780-x.

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AbstractThe global production of textiles utilizes numerous large-volume chemicals that may remain to some extent in the finished garments. Arylamines, quinolines, and halogenated nitrobenzene compounds are possible mutagens, carcinogens and/or skin sensitizers. For prevention, control of clothing and other textiles must be improved, especially those imported from countries without regulations of textile chemicals. An automated analytical methodology with on-line extraction, separation, and detection would largely simplify screening surveys of hazardous chemicals in textiles. Automated thermal
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28

Ma, Chaofan, Yebin Zhou, Wei Yan, et al. "Predominant Catalytic Performance of Nickel Nanoparticles Embedded into Nitrogen-Doped Carbon Quantum Dot-Based Nanosheets for the Nitroreduction of Halogenated Nitrobenzene." ACS Sustainable Chemistry & Engineering, June 15, 2022. http://dx.doi.org/10.1021/acssuschemeng.2c01345.

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29

Rubab, Anosha, Muhammad Sharif, Rauf Razzaq, et al. "Highly active iron oxide@NC catalyst derived from the iron acetate/polyacrylonitrile threads: Driving nitroarene conversion to value‐added amines." Journal of Applied Polymer Science, August 7, 2024. http://dx.doi.org/10.1002/app.56062.

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AbstractChemoselective reduction of nitroarenes to corresponding arylamines is a significant reaction in the chemical industry. However, in the presence of other reducible groups, including halogenated nitrobenzene, nitrobiphenyl, and nitroquinoline in the same molecule of nitroaromatics, the control of chemoselectivity remains challenging. Here, a facile fabrication of a heterogeneous iron‐based catalyst is reported as a potential alternative to precious metal catalysts for the chemoselective reduction of nitroarenes. The pyrolysis of iron acetate/polyacrylonitrile (PAN) template under an ine
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