Synthetic Molecular Photoelectrochemistry: New Frontiers in Synthetic Applications, Mechanistic Insights and Scalability DOI Creative Commons
Shangze Wu, Jaspreet Kaur, Tobias A. Karl

et al.

Angewandte Chemie International Edition, Journal Year: 2021, Volume and Issue: 61(12)

Published: Sept. 3, 2021

Synthetic photoelectrochemistry (PEC) is receiving increasing attention as a new frontier for the generation and handling of reactive intermediates. PEC permits selective single-electron transfer (SET) reactions in much greener way broadens redox window possible transformations. Herein, most recent contributions are reviewed, demonstrating exciting opportunities, namely, combination with other reactivity paradigms (hydrogen-atom transfer, radical polar crossover, energy sensitization), scalability up to multigram scale, novel selectivities SET super-oxidations/reductions importance precomplexation temporally enable excited ion catalysis.

Language: Английский

Electrocatalysis as an enabling technology for organic synthesis DOI
Luiz F. T. Novaes, Jinjian Liu, Yifan Shen

et al.

Chemical Society Reviews, Journal Year: 2021, Volume and Issue: 50(14), P. 7941 - 8002

Published: Jan. 1, 2021

Electrochemistry has recently gained increased attention as a versatile strategy for achieving challenging transformations at the forefront of synthetic organic chemistry. Electrochemistry's unique ability to generate highly reactive radical and ion intermediates in controlled fashion under mild conditions inspired development number new electrochemical methodologies preparation valuable chemical motifs. Particularly, recent developments electrosynthesis have featured an use redox-active electrocatalysts further enhance control over selective formation downstream reactivity these intermediates. Furthermore, electrocatalytic mediators enable proceed manner that is mechanistically distinct from purely methods, allowing subversion kinetic thermodynamic obstacles encountered conventional synthesis. This review highlights key innovations within past decade area electrocatalysis, with emphasis on mechanisms catalyst design principles underpinning advancements. A host oxidative reductive are discussed grouped according classification transformation nature electrocatalyst.

Language: Английский

Citations

875

Organic Electrochemistry: Molecular Syntheses with Potential DOI Creative Commons
Cuiju Zhu, Nate W. J. Ang, Tjark H. Meyer

et al.

ACS Central Science, Journal Year: 2021, Volume and Issue: 7(3), P. 415 - 431

Published: March 9, 2021

Efficient and selective molecular syntheses are paramount to

Language: Английский

Citations

587

Technological Innovations in Photochemistry for Organic Synthesis: Flow Chemistry, High-Throughput Experimentation, Scale-up, and Photoelectrochemistry DOI
Laura Buglioni, Fabian Raymenants, Aidan Slattery

et al.

Chemical Reviews, Journal Year: 2021, Volume and Issue: 122(2), P. 2752 - 2906

Published: Aug. 10, 2021

Photoinduced chemical transformations have received in recent years a tremendous amount of attention, providing plethora opportunities to synthetic organic chemists. However, performing photochemical transformation can be quite challenge because various issues related the delivery photons. These challenges barred widespread adoption steps industry. past decade, several technological innovations led more reproducible, selective, and scalable photoinduced reactions. Herein, we provide comprehensive overview these exciting advances, including flow chemistry, high-throughput experimentation, reactor design scale-up, combination photo- electro-chemistry.

Language: Английский

Citations

540

Electrode Materials in Modern Organic Electrochemistry DOI Creative Commons
David M. Heard, Alastair J. J. Lennox

Angewandte Chemie International Edition, Journal Year: 2020, Volume and Issue: 59(43), P. 18866 - 18884

Published: July 7, 2020

The choice of electrode material is critical for achieving optimal yields and selectivity in synthetic organic electrochemistry. imparts significant influence on the kinetics thermodynamics electron transfer, frequently defines success or failure a transformation. Electrode processes are complex so often empirical underlying mechanisms rationale unknown. In this review, we aim to highlight recent instances where offered, which should aid future reaction development.

Language: Английский

Citations

386

New Redox Strategies in Organic Synthesis by Means of Electrochemistry and Photochemistry DOI Creative Commons
Jinjian Liu, Lingxiang Lu, Devin Wood

et al.

ACS Central Science, Journal Year: 2020, Volume and Issue: 6(8), P. 1317 - 1340

Published: July 16, 2020

As the breadth of radical chemistry grows, new means to promote and regulate single-electron redox activities play increasingly important roles in driving modern synthetic innovation. In this regard, photochemistry electrochemistry-both considered as niche fields for decades-have seen an explosive renewal interest recent years gradually have become a cornerstone organic chemistry. Outlook article, we examine current state-of-the-art areas electrochemistry photochemistry, well nascent area electrophotochemistry. These techniques employ external stimuli activate molecules imbue privileged control reaction progress selectivity that is challenging traditional chemical methods. Thus, they provide alternative entries known reactive intermediates enable distinct strategies were previously unimaginable. Of many hallmarks, electro- are often classified "green" technologies, promoting reactions under mild conditions without necessity potent wasteful oxidants reductants. This reviews most growth these with special emphasis on conceptual advances given rise enhanced accessibility tools trade.

Language: Английский

Citations

377

Powering the Future: How Can Electrochemistry Make a Difference in Organic Synthesis? DOI Creative Commons
Tjark H. Meyer, Isaac Choi, Cong Tian

et al.

Chem, Journal Year: 2020, Volume and Issue: 6(10), P. 2484 - 2496

Published: Sept. 24, 2020

Language: Английский

Citations

377

Photons or Electrons? A Critical Comparison of Electrochemistry and Photoredox Catalysis for Organic Synthesis DOI
Nicholas E. S. Tay, Dan Lehnherr, Tomislav Rovis

et al.

Chemical Reviews, Journal Year: 2021, Volume and Issue: 122(2), P. 2487 - 2649

Published: Nov. 9, 2021

Redox processes are at the heart of synthetic methods that rely on either electrochemistry or photoredox catalysis, but how do and catalysis compare? Both approaches provide access to high energy intermediates (e.g., radicals) enable bond formations not constrained by rules ionic 2 electron (e) mechanisms. Instead, they 1e mechanisms capable bypassing electronic steric limitations protecting group requirements, thus enabling chemists disconnect molecules in new different ways. However, while providing similar intermediates, differ several physical chemistry principles. Understanding those differences can be key designing transformations forging disconnections. This review aims highlight these similarities between comparing their underlying principles describing impact electrochemical photochemical methods.

Language: Английский

Citations

360

Synthetic Photoelectrochemistry DOI Creative Commons
Joshua P. Barham,

Burkhard König

Angewandte Chemie International Edition, Journal Year: 2019, Volume and Issue: 59(29), P. 11732 - 11747

Published: Dec. 5, 2019

Photoredox catalysis (PRC) and synthetic organic electrochemistry (SOE) are often considered competing technologies in synthesis. Their fusion has been largely overlooked. We review state-of-the-art photoelectrochemistry, grouping examples into three categories: 1) electrochemically mediated photoredox (e-PRC), 2) decoupled photoelectrochemistry (dPEC), 3) interfacial (iPEC). Such synergies prove beneficial not only for "greenness" chemical selectivity, but also the accumulation of energy accessing super-oxidizing or -reducing single electron transfer (SET) agents. Opportunities challenges this emerging exciting field discussed.

Language: Английский

Citations

353

Electrochemical Oxidation Induced Selective C–C Bond Cleavage DOI
Shi‐Hui Shi, Yujie Liang, Ning Jiao

et al.

Chemical Reviews, Journal Year: 2020, Volume and Issue: 121(1), P. 485 - 505

Published: Oct. 5, 2020

Selective C–C bond cleavage under mild conditions can serve as a valuable tool for organic syntheses and macromolecular degradation. However, the conventional chemical methods have largely involved use of noble transition-metal catalysts well stoichiometric perhaps environmentally unfriendly oxidants, compromising overall sustainable nature transformation chemistry. In this regard, electrochemical has been identified scalable strategy that employs electricity to replace byproduct-generating reagents. To date, progress made in area mainly relied on Kolbe electrolysis related processes. Encouragingly, more examples bonds via other maneuvers recently developed. This review provides an overview most recent significant developments electrochemically oxidative selective cleavage, with emphasis both synthetic outcomes reaction mechanisms, it showcases innate advantages exciting potentials synthesis.

Language: Английский

Citations

352

Recent advances in visible light-activated radical coupling reactions triggered by (i) ruthenium, (ii) iridium and (iii) organic photoredox agents DOI Creative Commons
Jonathan D. Bell, John A. Murphy

Chemical Society Reviews, Journal Year: 2021, Volume and Issue: 50(17), P. 9540 - 9685

Published: Jan. 1, 2021

Visible light-activated reactions continue to expand and diversify. The example shown here is a Birch reduction achieved by organophotoredox reagents.

Language: Английский

Citations

343