Visible-light-induced controllable transformations of cumulative aryldienes through an energy transfer process

被引:0
|
作者
Ling Qian [1 ]
Ziqi Yu [1 ]
Jiaxin Liu [2 ]
Yin Wei [3 ]
Min Shi [1 ,3 ]
机构
[1] Key Laboratory for Advanced Materials and Institute of Fine Chemicals,Key Laboratory for Advanced Materials and Feringa Nobel Prize Scientist Joint Research Center,School of Chemistry & Molecular Engineering,East China University of Science and Technology
[2] Key Laboratory of Fluorine and Nitrogen Chemistry and Advanced Materials,Shanghai Institute of Organic Chemistry,University of Chinese Academy of Sciences,Chinese Academy of Sciences
[3] State Key Laboratory of Organometallic Chemistry,Center for Excellence in Molecular Synthesis,University of Chinese Academy of Sciences,Shanghai Institute of Organic Chemistry,Chinese Academy of
关键词
D O I
暂无
中图分类号
O643.36 [催化剂]; O644.1 [光化学]; O625.12 [不饱和侧链烃];
学科分类号
摘要
In this work,we report a visible light-induced energy transfer process related photochemical protocol of cumulative diene containing compounds for the construction of benzocyclohexene skeletons or the corresponding aromatized structures through an energy transfer process,1,5-hydrogen atom transfer and a 6π electrocyclization or demethoxylation in the presence of different photocatalysts such as [Ir(dF(Me)ppy)2(dtbbpy)]PF6 or thioxanthone.This newly developed photochemical strategy is characterized by mild conditions,broad substrate applicability,good functional group tolerance and good yields.The mechanistic paradigm was clarified by deuterium labeling,kinetic,photophysical and electrochemical analyses,control experiments and density functional theory(DFT) calculations.The transformation of the obtained product to the drug-like molecules such as Sertraline and the luminescent conjugated aromatic compounds has also been disclosed.
引用
收藏
页码:987 / 1001
页数:15
相关论文
共 50 条
  • [1] Visible-light-induced controllable transformations of cumulative aryldienes through an energy transfer process
    Qian, Ling
    Yu, Ziqi
    Liu, Jiaxin
    Wei, Yin
    Shi, Min
    SCIENCE CHINA-CHEMISTRY, 2025, 68 (03) : 987 - 1001
  • [2] Visible-Light-Induced Organic Photochemical Reactions through Energy-Transfer Pathways
    Zhou, Quan-Quan
    Zou, You-Quan
    Lu, Liang-Qiu
    Xiao, Wen-Jing
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2019, 58 (06) : 1586 - 1604
  • [3] Visible-light-induced synthesis of bibenzofuranones via a cerium-mediated energy transfer process
    Lv, Jiaoyue
    Lang, Yatao
    Li, Chao-Jun
    Zeng, Huiying
    CHEMICAL COMMUNICATIONS, 2025, 61 (20) : 4054 - 4057
  • [4] Visible-Light-Induced Photocatalytic Reductive Transformations of Organohalides
    Kim, Hyejin
    Lee, Chulbom
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2012, 51 (49) : 12303 - 12306
  • [5] Nickel-Catalyzed Etherification of Phenols and Aryl Halides through Visible-Light-Induced Energy Transfer
    Zhu, Da-Liang
    Jiang, Shan
    Wu, Qi
    Wang, Hao
    Li, Hai-Yan
    Li, Hong-Xi
    ORGANIC LETTERS, 2021, 23 (21) : 8327 - 8332
  • [6] Energy transfer in covalent organic frameworks for visible-light-induced hydrogen evolution
    Ding, San-Yuan
    Wang, Peng-Lai
    Yin, Guan-Lin
    Zhang, Xuqiang
    Lu, Gongxuan
    INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2019, 44 (23) : 11872 - 11876
  • [7] Metal Sulfide Photocatalysis: Visible-Light-Induced Organic Transformations
    Hao, Huimin
    Lang, Xianjun
    CHEMCATCHEM, 2019, 11 (05) : 1378 - 1393
  • [8] Visible-light-induced controllable ?-chlorination of nafimidone derivatives through LMCT excitation of CuCl2
    Shen, Jiabin
    Wang, Zhihao
    Shen, Chao
    Zhang, Pengfei
    MOLECULAR CATALYSIS, 2023, 537
  • [9] Visible-Light-Induced Dearomatizations
    Okumura, Mikiko
    Sarlah, David
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2020, 2020 (10) : 1259 - 1273
  • [10] Visible-light-induced dehydrogenation of dihydroquinolinones via the combination of energy transfer and hydrogen atom transfers
    Feng, Jin
    Tang, Hanguang
    Guo, Hao
    Ding, Aishun
    ORGANIC CHEMISTRY FRONTIERS, 2025, 12 (04): : 1183 - 1188