Coupling Strategy for CO2 Valorization Integrated with Organic Synthesis by Heterogeneous Photocatalysis

Author(s):  
Yi-Jun Xu
ChemPhotoChem ◽  
2020 ◽  
Vol 4 (7) ◽  
pp. 451-451
Author(s):  
Sebastian Gisbertz ◽  
Bartholomäus Pieber

2003 ◽  
Vol 5 (3) ◽  
pp. 175-182 ◽  
Author(s):  
Siniša Marinković ◽  
Norbert Hoffmann

Using heterogeneous photocatalysis, the radical addition of tertiary amines with electron deficient alkenes can be performed in high yields (up to 98%) and high facial diastereoselectivity. The photochemical induced electron transfer process initiates the radical chain reaction and inorganic semiconductors likeTiO2and ZnS were used. According to the proposed mechanism, the reaction takes place at the surface of the semiconductor and the termination step results from an interfacial electron transfer from the conduction band to the oxoallyl radical intermediate. Frequently, semiconductors are used for the mineralisation of organic compounds in wastewater. However, in this case, they are used in organic synthesis. The process can be performed in a convenient way and is particularly interesting from the ecological and economical point of view. No previous functionalization of the tertiary amines is necessary for C − C bond formation. Further on, the amines are used both as reactant and as solvent. The excess is recycled by distillation and the inexpensive sensitiser can be easily removed by filtration. In this way, products of high interest for organic synthesis are obtained by a diastereoselective radical reaction.


2007 ◽  
Vol 79 (11) ◽  
pp. 1949-1958 ◽  
Author(s):  
Norbert Hoffmann

Photochemically induced electron transfer considerably enriches the redox chemistry of organic molecules. This primary step has been used to produce α-amino alkyl radicals that can be added to various double bonds. The addition to olefinic and carbonyl bonds is discussed. Homogeneous and heterogeneous photocatalysis methods with various electron-transfer sensitizers are described.


2020 ◽  
Vol 16 ◽  
pp. 1495-1549 ◽  
Author(s):  
Christopher G Thomson ◽  
Ai-Lan Lee ◽  
Filipe Vilela

The synergy between photocatalysis and continuous flow chemical reactors has shifted the paradigms of photochemistry, opening new avenues of research with safer and scalable processes that can be readily implemented in academia and industry. Current state-of-the-art photocatalysts are homogeneous transition metal complexes that have favourable photophysical properties, wide electrochemical redox potentials, and photostability. However, these photocatalysts present serious drawbacks, such as toxicity, limited availability, and the overall cost of rare transition metal elements. This reduces their long-term viability, especially at an industrial scale. Heterogeneous photocatalysts (HPCats) are an attractive alternative, as the requirement for the separation and purification is largely removed, but typically at the cost of efficiency. Flow chemical reactors can, to a large extent, mitigate the loss in efficiency through reactor designs that enhance mass transport and irradiation. Herein, we review some important developments of heterogeneous photocatalytic materials and their application in flow reactors for sustainable organic synthesis. Further, the application of continuous flow heterogeneous photocatalysis in environmental remediation is briefly discussed to present some interesting reactor designs that could be implemented to enhance organic synthesis.


ChemPhotoChem ◽  
2020 ◽  
Vol 4 (7) ◽  
pp. 456-475 ◽  
Author(s):  
Sebastian Gisbertz ◽  
Bartholomäus Pieber

ACS Catalysis ◽  
2016 ◽  
Vol 6 (7) ◽  
pp. 4782-4785 ◽  
Author(s):  
Sukbok Chang ◽  
Paolo Fornasiero ◽  
T. Brent Gunnoe ◽  
Christopher W. Jones ◽  
Suljo Linic ◽  
...  

ChemPhotoChem ◽  
2020 ◽  
Vol 4 (7) ◽  
pp. 454-454 ◽  
Author(s):  
Sebastian Gisbertz ◽  
Bartholomäus Pieber

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