scholarly journals ACS Catalysis and the Scope of Papers Sought in Three Catalysis Subdisciplines: Biocatalysis and Enzymology, Molecular Catalysis for Organic Synthesis, and Heterogeneous Photocatalysis

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. 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.


2011 ◽  
Vol 84 (3) ◽  
pp. 581-602 ◽  
Author(s):  
An-Hua Liu ◽  
Yu-Nong Li ◽  
Liang-Nian He

CO2 is very attractive as a typical renewable feedstock for manufacturing commodity chemicals, fuel, and materials since it is an abundant, nontoxic, nonflammable, and easily available C1 resource. The development of greener chemical methodologies for replacing the utility of hazardous and environmentally undesirable phosgene largely relies on ingenious activation and incorporation of CO2 into valuable compounds, which is of paramount importance from a standpoint of green chemistry and sustainable development. Great efforts have been devoted to constructing C–C, C–O, and C–N bond on the basis of CO2 activation through molecular catalysis owing to its kinetic and thermodynamic stability. The aim of this article is to demonstrate the versatile use of CO2 in organic synthesis as the alternative carbonyl source of phosgene, with the main focus on utilization of CO2 as phosgene replacement for the synthesis of value-added compounds such as cyclic carbonates, oxa-zolidinones, ureas, isocyanates, and polymers, affording greener pathways for future chemical processes.


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

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

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