Parallel Light Reaction Instrument
Parallel Light Reaction Instrument
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  • Parallel Light Reaction Instrument
  • Parallel Light Reaction Instrument

Parallel Light Reaction Instrument

The "Parallel Light Reaction Instrument" boasts a powerful light source, reaching up to 11 W/cm², with six independently adjustable reaction slots and built-in rubidium-magnet for strong magnetic stirring. It features efficient heat dissipation, stable parameters, and high repeatability. This instrument is primarily used for scientific research in photocatalytic reactions across multiple fields, including drug synthesis and screening, material modification, and biological modification.

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  • Product Description
  • Product Features

    Integrated Temperature Control and Mixing: Features intelligent fan-based temperature control, combined with strong rubidium-iron stirring for effective irradiation in both homogeneous and heterogeneous reactions.

    Versatile Vial/Tube Holder: Compatible with Schlenk tubes, reaction vials, and cuvettes. The instrument's compact size allows for easy mobility.

    Standardized Light Source Module: Offers replaceable wavelengths, ranges from 365 nm-980 nm, with optical power reaching up to 10.4W/cm². Its modular design and three-pin connector allow for efficient and easy replacement.

    Dual Control with Touch Screen and Knob: Enables easy adjustment of power, speed, and reaction time through a combination of touch screen and knob controls.

     

    Product Specifications

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    Stirring speed:200-100rpm

    Light source band:365-980 NM

    Product size:266*192*125 mm

    Operating temperature:0-50 degrees Celsius

    Power range:0-18w

    Product weight:2kg

     

     

     

    Product practical operation

     

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    Frontline tracking

Total Synthesis of (−)-Calycanthine via Iron-Catalyzed Stereoselective Oxidative Dimerization. Leiyang Bai, Yinhao Ma, and Xuefeng Jiang*. J. Am. Chem. Soc. 2021, 143, 49, 20609 - 20615. DOI: 10.1021/jacs.1c10498.
From symmetrical tetrasulfides to trisulfide dioxides via photocatalysis. Kai Gong, Yilin Zhou and Xuefeng Jiang*. Green Chem., 2021, 23, 9865. DOI: 10.1039/d1gc03242a.
Electrophotocatalytic Decoupled Radical Relay Enables Highly Efficient and Enantioselective Benzylic C–H Functionalization. Wenzheng Fan, Xueyao Zhao, Yunshun Deng, Pinhong Chen, Fei Wang*, and Guosheng Liu* J. Am. Chem. Soc. 2022, 144, 47, 21674–21682. doi.org/10.1021/jacs.2c09366
Stepwise benzylic oxygenation via uranyl-photocatalysis. Deqing Hua and Xuefeng Jiang*. Green Chem., 2022. 24.124. Doi: 10.1039/d1gc04042a
From aniline to phenol: carbon-nitrogen bond activation via uranyl photoredox catalysis. Deqing Hu, Yilin Zhou, Xuefeng Jiang*. Natl Sci Rev. 2022. Doi: 10.1093/nsr/nwab156
Hydroxylation of organoborons via uranyl photocatalysis. Catalysis science & technology, 2023, 13(11):2688-2694. Doi: 10.1039/d3qo00468f
Parallel photoreactor development with enhanced photon efficiency and reproducibility based on laws of optics. Rizvi Syed Aal E Ali, Yilin Zhou, Kai Gong, Xuefeng Jiang. Green Synthesis & Catalysis, 2023, 4(2). Doi: 10.1016/j.gresc.2022.10.007
Diaryl Dihydrophenazine-Based Porous Organic Polymers Enhance Synergistic Catalysis in Visible-Light-Driven Organic Transformations. Yan Cheng, Yan-Xiang Li, Chun-Hua Liu, Yuan-Yuan Zhu, Wenbin Lin. Angewandte Chemie, 2023, 135(41). Doi: 10.1002/anie.202310470
Visible-Light-Mediated Activation of Remote C(sp3)−H Bonds by Carbon-Centered Biradical via Intramolecular 1,5- or 1,6-Hydrogen Atom Transfer. Xintao Gu, Jiahao Shen, Ziyu Xu, Jiaxin Liu, Min Shi, Yin Wei. Angewandte Chemie, 2024. Doi: 10.1002/anie.202409463
Catalytic Asymmetric Cascade Dearomatization of Indoles via a Photoinduced Pd-Catalyzed 1,2-Bisfunctionalization of Butadienes. Xiaohang Zhan, Dr. Zhiwen Nie, Na Li, Ao Zhou, Haotian Lv, Mingrong Liang, Keqin Wu, Gui-Juan Cheng, Qin Yin. Angewandte Chemie, 2024, 136(26). Doi: 10.1002/ange.202404388
Integration of N-Aryl Phenoxazine Photosensitizers and Nickel Catalysts in Polymer Supports Enhances Photocatalytic Organic Transformations. Chen Zhu, Yan-Xiang Li, Chun-Hua Liu, Huai-Ping Cong, Yuan-Yuan Zhu*, Wenbin Lin. ACS Catal. 2024, 14, 23, 17609–17621. Doi: 10.1021/acscatal.4c04920
Direct construction of aryl amide N-glycosides from glycosyl oxamic acids via photoredox palladium-catalyzed aminocarbonylations. Xinyue Xie, Shiyin Zhao, Yang Han, Anrong Chen, Bo Yang, Bo Zhu, Yingzi Li, Jun Zhou, Feng Zhu. Chem Catalysis, 2024, (10):4. Doi: 10.1016/j.checat.2024.101109
From aryl chlorides to phenols: Photouranium-catalyzed hydroxylation via water splitting. Mengjing Sun, Leiyang Bai, Chengliang Li, Xuefeng Jiang.Chem Catalysis, 2024(7):4. Doi: 10.1016/j.checat.2024.101027
2,2′-Bipyridine-Enabled Photocatalytic Radical [4+2] Cyclization of N-Aryl-α-amino Acids for Synthesizing Polysubstituted Tetrahydroquinolines. Ren-Xu Xiao, Ting Tian, Ting-You Yang, Ming-Xing Lan, Shuo Lv, Xue-Qing Mou, Yong-Zheng Chen, and Bao-Dong Cui*.Org. Lett., 2024, 26, 15, 3195–3201. Doi: 10.1021/acs.orglett.4c00794
Visible-light-mediated site-selective C(sp2)–H alkylation of tropones facilitates semi-synthesis of cephafortunoids A and B. Qi-Xiang Zeng, Cheng-Yu Zheng, Zhan-Peng Ge,  Jin-Xin Zhao  and  Jian-Min Yue. Chem. Sci., 2025, 16, 8836-8844. Doi: 10.1039/D5SC01006C
N-Heterocyclic Selone-Catalyzed [2σ + 2π] Cycloaddition of Bicyclo[1.1.0]butanes via Photoredox Radical Buffer. Kejun Lin, Chen-Rui Luo-Wei, Yuan Gao, Jianyong Lan, and Tingshun Zhu*. J. Am. Chem. Soc. 2025. DOI: 10.1021/jacs.5c05306.
Photocatalytic unactivated aliphatic C–H bonds azidation: A versatile platform for functionalization of commodity polymers. Guanwen Huang, Zhongming Wang, Binbin Xu, Xinghao Du, Jianbo Tan*, Chun Feng*. Eur. Polym. J. 2025, 228, 113834. DOI: 10.1016/j.eurpolymj.2025.113834.
Visible-Light-Induced Difunctionalization of Styrenes with Aryl Hydrazines and tert-Butyl Nitrite: One-Pot Access to α-Arylethanone Oximes. Ping Jiang, Meifang Wang, Akbar Sohail, Farah Firdous, and Keyume Ablajan*. Org. Lett. 2025. DOI: 10.1021/acs.orglett.5c03229.
N-Heterocyclic Selone-Catalyzed [2σ+2π] Cycloaddition of Bicyclo[1.1.0]butanes via Photoredox Radical Buffer. Kejun Lin, Chen-Rui Luo-Wei, Yuan Gao, Jianyong Lan, Tingshun Zhu*. J. Am. Chem. Soc. 2025, 147, 35, 31521–31529. DOI: 10.1021/jacs.5c05306

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