ChemInform Abstract: Efficient Photocatalytic Suzuki Cross-Coupling Reactions on Au-Pd Alloy Nanoparticles under Visible Light Irradiation.

ChemInform ◽  
2015 ◽  
Vol 46 (8) ◽  
pp. no-no
Author(s):  
Qi Xiao ◽  
Sarina Sarina ◽  
Esa Jaatinen ◽  
Jianfeng Jia ◽  
Dennis P. Arnold ◽  
...  
2014 ◽  
Vol 16 (9) ◽  
pp. 4272 ◽  
Author(s):  
Qi Xiao ◽  
Sarina Sarina ◽  
Esa Jaatinen ◽  
Jianfeng Jia ◽  
Dennis P. Arnold ◽  
...  

2020 ◽  
Vol 44 (27) ◽  
pp. 11513-11526 ◽  
Author(s):  
Roya Jahanshahi ◽  
Asma Khazaee ◽  
Sara Sobhani ◽  
José Miguel Sansano

g-C3N4/γ-Fe2O3/TiO2/Pd is developed as a new magnetically separable photocatalyst for efficient fluoride-free Hiyama and Suzuki–Miyaura cross-coupling reactions at room temperature under visible light irradiation.


ACS Catalysis ◽  
2014 ◽  
Vol 4 (6) ◽  
pp. 1725-1734 ◽  
Author(s):  
Qi Xiao ◽  
Sarina Sarina ◽  
Arixin Bo ◽  
Jianfeng Jia ◽  
Hongwei Liu ◽  
...  

Science ◽  
2019 ◽  
Vol 364 (6439) ◽  
pp. eaav9713 ◽  
Author(s):  
Asik Hossain ◽  
Aditya Bhattacharyya ◽  
Oliver Reiser

Visible-light photoredox catalysis offers a distinct activation mode complementary to thermal transition metal catalyzed reactions. The vast majority of photoredox processes capitalizes on precious metal ruthenium(II) or iridium(III) complexes that serve as single-electron reductants or oxidants in their photoexcited states. As a low-cost alternative, organic dyes are also frequently used but in general suffer from lower photostability. Copper-based photocatalysts are rapidly emerging, offering not only economic and ecological advantages but also otherwise inaccessible inner-sphere mechanisms, which have been successfully applied to challenging transformations. Moreover, the combination of conventional photocatalysts with copper(I) or copper(II) salts has emerged as an efficient dual catalytic system for cross-coupling reactions.


Catalysts ◽  
2018 ◽  
Vol 8 (9) ◽  
pp. 355 ◽  
Author(s):  
Yi Wang ◽  
Anan Liu ◽  
Dongge Ma ◽  
Shuhong Li ◽  
Chichong Lu ◽  
...  

Fulfilling the direct inert C–H bond functionalization of raw materials that are earth-abundant and commercially available for the synthesis of diverse targeted organic compounds is very desirable and its implementation would mean a great reduction of the synthetic steps required for substrate prefunctionalization such as halogenation, borylation, and metalation. Successful C–H bond functionalization mainly resorts to homogeneous transition-metal catalysis, albeit sometimes suffering from poor catalyst reusability, nontrivial separation, and severe biotoxicity. TiO2 photocatalysis displays multifaceted advantages, such as strong oxidizing ability, high chemical stability and photostability, excellent reusability, and low biotoxicity. The chemical reactions started and delivered by TiO2 photocatalysts are well known to be widely used in photocatalytic water-splitting, organic pollutant degradation, and dye-sensitized solar cells. Recently, TiO2 photocatalysis has been demonstrated to possess the unanticipated ability to trigger the transformation of inert C–H bonds for C–C, C–N, C–O, and C–X bond formation under ultraviolet light, sunlight, and even visible-light irradiation at room temperature. A few important organic products, traditionally synthesized in harsh reaction conditions and with specially functionalized group substrates, are continuously reported to be realized by TiO2 photocatalysis with simple starting materials under very mild conditions. This prominent advantage—the capability of utilizing cheap and readily available compounds for highly selective synthesis without prefunctionalized reactants such as organic halides, boronates, silanes, etc.—is attributed to the overwhelmingly powerful photo-induced hole reactivity of TiO2 photocatalysis, which does not require an elevated reaction temperature as in conventional transition-metal catalysis. Such a reaction mechanism, under typically mild conditions, is apparently different from traditional transition-metal catalysis and beyond our insights into the driving forces that transform the C–H bond for C–C bond coupling reactions. This review gives a summary of the recent progress of TiO2 photocatalytic C–H bond activation for C–C coupling reactions and discusses some model examples, especially under visible-light irradiation.


2020 ◽  
Vol 44 (9) ◽  
pp. 3794-3801
Author(s):  
Bo Liu ◽  
Tong Xu ◽  
Chunping Li ◽  
Jie Bai

A Pd1Cu4/CexOy catalyst can efficiently catalyze Suzuki reactions under both heating and visible light irradiation conditions.


2016 ◽  
Vol 6 (2) ◽  
pp. 320-338 ◽  
Author(s):  
Sunari Peiris ◽  
John McMurtrie ◽  
Huai-Yong Zhu

Metal nanoparticles (Au, Ag, Cu, Pd, Pt, Ir, Rh, Au–Pd alloyetc.) supported on inert support (ZrO2, zeolite) can be direct photocatalysts to series of organic synthesis with visible light irradiation.


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