scholarly journals Synthetic applications of eosin Y in photoredox catalysis

2014 ◽  
Vol 50 (51) ◽  
pp. 6688-6699 ◽  
Author(s):  
Durga Prasad Hari ◽  
Burkhard König
Keyword(s):  
Organic Synthesis ◽  
Eosin Y ◽  
Photoredox Catalysis ◽  
Dye Molecule

Eosin Y, a long known dye molecule, has recently been widely applied as a photoredox catalyst in organic synthesis.

Rhodamines as Photocatalyst in Organic Synthesis

2020 ◽  
Vol 07 ◽  
Author(s):  
Avik K. Bagdi ◽  
Papiya Sikdar
Keyword(s):  
Visible Light ◽  
Organic Synthesis ◽  
Organic Dyes ◽  
Transition Metal Catalysts ◽  
Visible Light Photocatalysis ◽  
Eosin Y ◽  
Organic Transformations ◽  
The Sustainable Development ◽  
Mechanistic Pathway ◽  
Green Model

Abstract:: Organic synthesis under environment friendly conditions has great impact in the sustainable development. In this context, visible light photocatalysis has emerged as a green model as this offers an energy-efficient pathway towards the organic transformation. Different transition-metal catalysts (Ir-, Ru-, Cu- etc) and organic dyes (eosin Y, rose bengal, methylene blue etc) are well-known photocatalysts in organic synthesis. Apart from the well-known organophotoredox catalysts, rhodamines (Rhodamine B and Rhodamine 6G) have been also employed as efficient photocatalysts for different organic transformations. In this review, we will focus on the photocatalysis by rhodamines in organic synthesis. Mechanistic pathway of the methodologies will also be discussed. We believe this review will stimulate the employment of rhodamines in the visible light photocatalysis for efficient organic transformations in the future.

Visible light photocatalysis in synthesis of pharmaceutically relevant heterocyclic scaffolds

2022 ◽  
Author(s):  
Vishal Srivastava ◽  
Pravin Kumar Singh ◽  
Shraddha Tivari ◽  
Praveen Pratap Singh
Keyword(s):  
Natural Products ◽  
Visible Light ◽  
Chemical Bond ◽  
Organic Synthesis ◽  
Bond Formation ◽  
Visible Light Photocatalysis ◽  
Photoredox Catalysis ◽  
Chemical Bond Formation

Visible light and photoredox catalysis have emerged as a powerful and long-lasting tool for organic synthesis, demonstrating the importance of a variety of chemical bond formation methods. Natural products, physiologically...

The remarkable activity and stability of a dye-sensitized single molecular layer MoS2ensemble for photocatalytic hydrogen production

2015 ◽  
Vol 51 (70) ◽  
pp. 13496-13499 ◽  
Author(s):  
Tiantian Jia ◽  
Molly M. J. Li ◽  
Lin Ye ◽  
Sam Wiseman ◽  
Guoliang Liu ◽  
...  
Keyword(s):  
Hydrogen Production ◽  
Binding Affinity ◽  
Molecular Layer ◽  
Single Layer ◽  
Eosin Y ◽  
Photocatalytic Hydrogen Production ◽  
Dye Sensitized ◽  
Strong Binding ◽  
Single Molecular Layer ◽  
Dye Molecule

Single layer MoS2synthesized by exfoliation with Li is demonstrated to take up the dye molecule, Eosin Y, with strong binding affinityviasulfur vacancies.

Organic Photoredox Catalysis for Pschorr Reaction: A Metal-Free and Mild Approach to 6H-Benzo[c]chromenes

Synlett ◽  
2018 ◽  
Vol 29 (17) ◽  
pp. 2311-2315 ◽  
Author(s):  
Gaofeng Feng ◽  
Jing-Yao He ◽  
Qi-Fan Bai ◽  
Chengan Jin
Keyword(s):  
Diazonium Salts ◽  
Eosin Y ◽  
Photoredox Catalysis ◽  
Synthetic Route ◽  
Metal Free ◽  
Mild Conditions ◽  
Pschorr Reaction

An expedient organic photoredox Pschorr reaction has been developed that opens up a synthetic route to 6H-benzo[c]chromenes. The process can be performed under mild conditions by using eosin Y as a photoredox catalyst and acetonitrile as the solvent. The diazonium salts can be either preformed or generated in situ from the corresponding amines with t-BuONO. The process is amenable to gram-sale synthesis of 6H-benzo[c]chromenes, which can be further transformed into both 6H-benzo[c]chromen-6-ones through oxidation or to 6H-benzo[c]chromen-6-amine through sp3 C–H bond amination. The protocol provides an attractive route for the synthesis of a library of 6H-benzo[c]chromes.

Metal-Free Regioselective Alkylation of Imidazo[1,2-a]pyridines with N-Hydroxyphthalimide Esters under Organic Photoredox Catalysis

Synlett ◽  
2020 ◽  
Vol 31 (04) ◽  
pp. 363-368 ◽  
Author(s):  
Can Jin ◽  
Bin Sun ◽  
Tengwei Xu ◽  
Liang Zhang ◽  
Rui Zhu ◽  
...  
Keyword(s):  
Visible Light ◽  
Carboxylic Acids ◽  
Room Temperature ◽  
Eosin Y ◽  
Photoredox Catalysis ◽  
Mechanistic Studies ◽  
Metal Free ◽  
Regioselective Alkylation ◽  
Decarboxylative Coupling ◽  
Aliphatic Carboxylic Acids

A visible-light-induced direct C–H alkylation of imidazo[1,2-a]pyridines has been developed. It proceeds at room temperature by employing inexpensive Eosin Y as a photocatalyst and alkyl N-hydroxyphthalimide (NHP) esters as alkylation reagents. A variety of NHP esters derived from aliphatic carboxylic acids (primary, secondary, and tertiary) were tolerated in this protocol, giving the corresponding C-5-alkylated products in moderate to excellent yields. Mechanistic studies indicate that a radical decarboxylative coupling pathway was involved in this process.

Excited radical anions and excited anions in visible light photoredox catalysis

2019 ◽  
Vol 4 (12) ◽  
Author(s):  
Indrajit Ghosh
Keyword(s):  
Visible Light ◽  
Organic Synthesis ◽  
Transition Metal Complexes ◽  
Organic Dyes ◽  
Visible Light Photocatalysis ◽  
Radical Anions ◽  
Photoredox Catalysis ◽  
Inorganic Semiconductors ◽  
Redox Active ◽  
Excited Radical

Abstract Over the last decade, visible light photocatalysis has dramatically increased the arsenal of methods for organic synthesis and changed the way we activate molecules for chemical reactions. Polypyridyl transition metal complexes, redox-active organic dyes, and inorganic semiconductors are typically used as photocatalysts for such transformations. This chapter reviews the applications of radical anions and anions as photosensitizers in visible light photoredox catalysis.

scholarly journals Investigations of alkynylbenziodoxole derivatives for radical alkynylations in photoredox catalysis

2018 ◽  
Vol 14 ◽  
pp. 1215-1221 ◽  
Author(s):  
Yue Pan ◽  
Kunfang Jia ◽  
Yali Chen ◽  
Yiyun Chen
Keyword(s):  
Organic Synthesis ◽  
Photoredox Catalysis ◽  
Radical Acceptor ◽  
First Time

The alkynylbenziodoxole derivatives are recently developed alkynylation reagents in organic synthesis, which demonstrate excellent radical alkynylation reactivity in photoredox catalysis reactions. Herein we report the synthesis of alkynylbenziodoxole derivatives with difluoro, monofluoro, monomethoxy, and dimethoxy substitution on the benziodoxole moiety, and investigated their radical alkynylation reactivity for the first time. A series of mechanistic experiments were conducted to study the radical acceptor and oxidative quencher reactivity of alkynylbenziodoxoles, in which unsubstituted alkynylbenziodoxoles played balancing roles in both processes, while electron-rich benziodoxole derivatives demonstrate synthetic advantages in some cases.

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