• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

由碘代硼二吡咯和抗坏血酸钠促进的光催化全反式维甲酸反应。

Photocatalytic ATRA reaction promoted by iodo-Bodipy and sodium ascorbate.

作者信息

Magagnano G, Gualandi A, Marchini M, Mengozzi L, Ceroni P, Cozzi P G

机构信息

Dipartimento di Chimica "G. Ciamician" ALMA MATER STUDIORUM, Università di Bologna, Via Selmi 2, 40126 Bologna, Italy.

出版信息

Chem Commun (Camb). 2017 Feb 4;53(10):1591-1594. doi: 10.1039/c6cc09387f. Epub 2017 Jan 13.

DOI:10.1039/c6cc09387f
PMID:28085164
Abstract

Using ascorbate as a sacrificial reductant, iodo-Bodipy dye 1b is able to promote the ATRA reaction between bromoderivatives and alkenes. This finding expands the possibility of using Bodipy dyes to promote photocatalytic reactions in efficient ways.

摘要

使用抗坏血酸盐作为牺牲性还原剂，碘代硼二吡咯染料1b能够促进溴代衍生物与烯烃之间的全反式维甲酸（ATRA）反应。这一发现扩展了以有效方式使用硼二吡咯染料促进光催化反应的可能性。

相似文献

1
Photocatalytic ATRA reaction promoted by iodo-Bodipy and sodium ascorbate.由碘代硼二吡咯和抗坏血酸钠促进的光催化全反式维甲酸反应。
Chem Commun (Camb). 2017 Feb 4;53(10):1591-1594. doi: 10.1039/c6cc09387f. Epub 2017 Jan 13.
2
Visible light photocatalytic cross-coupling and addition reactions of arylalkynes with perfluoroalkyl iodides.可见光催化芳基炔烃与全氟烷基碘的交叉偶联及加成反应。
Org Biomol Chem. 2020 Nov 4;18(42):8686-8693. doi: 10.1039/d0ob01767a.
3
Photochemical Synthesis of Lactones, Cyclopropanes and ATRA Products: Revealing the Role of Sodium Ascorbate.内酯、环丙烷和全反式维甲酸产物的光化学合成：揭示抗坏血酸钠的作用
Chemistry. 2024 Apr 11;30(21):e202400253. doi: 10.1002/chem.202400253. Epub 2024 Feb 22.
4
Visible light-mediated atom transfer radical addition via oxidative and reductive quenching of photocatalysts.可见光促进原子转移自由基加成反应：通过光催化剂的氧化和还原猝灭。
J Am Chem Soc. 2012 May 30;134(21):8875-84. doi: 10.1021/ja300798k. Epub 2012 May 16.
5
Light-driven hydrogen evolution by BODIPY-sensitized cobaloxime catalysts.由BODIPY敏化的钴肟催化剂实现光驱动析氢
Inorg Chem. 2014 May 5;53(9):4527-34. doi: 10.1021/ic500218q. Epub 2014 Apr 11.
6
The relationship between the boron dipyrromethene (BODIPY) structure and the effectiveness of homogeneous and heterogeneous solar hydrogen-generating systems as well as DSSCs.硼二吡咯亚甲基（BODIPY）结构与均相和异相太阳能制氢系统以及染料敏化太阳能电池（DSSCs）效率之间的关系。
Phys Chem Chem Phys. 2015 Apr 21;17(15):9716-29. doi: 10.1039/c5cp00732a.
7
Electrochemistry and electrogenerated chemiluminescence of BODIPY dyes.BODIPY 染料的电化学与电致化学发光。
Acc Chem Res. 2012 Nov 20;45(11):1844-53. doi: 10.1021/ar200278b. Epub 2012 Apr 19.
8
Porous material-immobilized iodo-Bodipy as an efficient photocatalyst for photoredox catalytic organic reaction to prepare pyrrolo[2,1-a]isoquinoline.多孔材料固载碘代 BODIPY 作为一种高效光催化剂用于光氧化还原催化有机反应制备吡咯并[2,1-a]异喹啉。
Chem Commun (Camb). 2013 Oct 7;49(77):8689-91. doi: 10.1039/c3cc44486d.
9
The Structure-property Relationships of D-π-A BODIPY Dyes for Dye-sensitized Solar Cells.用于染料敏化太阳能电池的D-π-A型硼二吡咯染料的结构-性能关系
Chem Rec. 2016 Apr;16(2):719-33. doi: 10.1002/tcr.201500251. Epub 2016 Feb 5.
10
Structure-Property Relationship Study of Donor and Acceptor 2,6-Disubstituted BODIPY Derivatives for High Performance Dye-Sensitized Solar Cells.用于高性能染料敏化太阳能电池的供体和受体2,6-二取代BODIPY衍生物的结构-性能关系研究
Chemistry. 2017 Oct 20;23(59):14747-14759. doi: 10.1002/chem.201702285. Epub 2017 Sep 25.

引用本文的文献

1
Application of Lead-Free Metal Halide Perovskite Heterojunctions for the Carbohalogenation of C-C Multiple Bonds.无铅金属卤化物钙钛矿异质结在碳-碳多重键碳卤化反应中的应用。
Org Lett. 2025 Apr 11;27(14):3667-3672. doi: 10.1021/acs.orglett.5c00780. Epub 2025 Apr 1.
2
Singlets-Driven Photoredox Catalysts: Transforming Noncatalytic Red Fluorophores to Efficient Catalysts.单线态驱动的光氧化还原催化剂：将非催化红色荧光团转化为高效催化剂。
JACS Au. 2024 Nov 18;4(12):4892-4898. doi: 10.1021/jacsau.4c00877. eCollection 2024 Dec 23.
3
Solvent and alkyl substitution effects on charge-transfer mediated triplet state generation in BODIPY dyads: a combined computational and experimental study.
溶剂和烷基取代对BODIPY二元体系中电荷转移介导的三重态产生的影响：一项计算与实验相结合的研究
Photochem Photobiol Sci. 2024 Mar;23(3):451-462. doi: 10.1007/s43630-023-00530-1. Epub 2024 Feb 7.
4
Isoacridone dyes with parallel reactivity from both singlet and triplet excited states for biphotonic catalysis and upconversion.用于双光子催化和上转换的具有来自单重态和三重态激发态的平行反应性的异吖啶酮染料。
Chem Sci. 2023 Oct 2;14(40):11180-11191. doi: 10.1039/d3sc02768f. eCollection 2023 Oct 18.
5
Photoredox catalysis harvesting multiple photon or electrochemical energies.光氧化还原催化可收集多个光子或电化学能量。
Beilstein J Org Chem. 2023 Jul 28;19:1055-1145. doi: 10.3762/bjoc.19.81. eCollection 2023.
6
Pyrene-based metal-organic framework NU-1000 photocatalysed atom-transfer radical addition for iodoperfluoroalkylation and ()-selective perfluoroalkylation of olefins by visible-light irradiation.基于芘的金属有机框架材料NU-1000通过可见光照射光催化碘全氟烷基化以及烯烃的（）-选择性全氟烷基化原子转移自由基加成反应。 （注：括号内内容原文缺失）
RSC Adv. 2018 Sep 24;8(57):32610-32620. doi: 10.1039/c8ra06181e. eCollection 2018 Sep 18.
7
Effect of the iodine atom position on the phosphorescence of BODIPY derivatives: a combined computational and experimental study.碘原子位置对 BODIPY 衍生物磷光的影响：计算与实验的综合研究。
Photochem Photobiol Sci. 2022 May;21(5):777-786. doi: 10.1007/s43630-021-00152-5. Epub 2022 Jan 13.
8
-Antracenyl-BODIPY Dyad as a New Photocatalyst in Atom-Transfer Radical Addition Reactions.-蒽基-硼二吡咯二元化合物作为原子转移自由基加成反应中的新型光催化剂
ACS Omega. 2021 Nov 19;6(48):32809-32817. doi: 10.1021/acsomega.1c04724. eCollection 2021 Dec 7.
9
The serendipitous effect of KF in Ritter reaction: Photo-induced amino-alkylation of alkenes.KF在 Ritter 反应中的意外效应：光诱导烯烃的氨基烷基化反应
iScience. 2021 Aug 11;24(9):102969. doi: 10.1016/j.isci.2021.102969. eCollection 2021 Sep 24.
10
Design of BODIPY dyes as triplet photosensitizers: electronic properties tailored for solar energy conversion, photoredox catalysis and photodynamic therapy.作为三线态光敏剂的BODIPY染料设计：为太阳能转换、光氧化还原催化和光动力疗法量身定制的电子性质
Chem Sci. 2021 Apr 14;12(19):6607-6628. doi: 10.1039/d1sc00732g.