Visible Light-Induced Transition Metal Catalysis

Chemical Reviews, Journal Year: 2021, Volume and Issue: 122(2), P. 1543 - 1625

Published: Oct. 8, 2021

In recent years, visible light-induced transition metal catalysis has emerged as a new paradigm in organic photocatalysis, which led to the discovery of unprecedented transformations well improvement known reactions. this subfield complex serves double duty by harvesting photon energy and then enabling bond forming/breaking events mostly via single catalytic cycle, thus contrasting established dual photocatalysis an exogenous photosensitizer is employed. addition, approach often synergistically combines catalyst–substrate interaction with photoinduced process, feature that uncommon conventional photoredox chemistry. This Review describes early development advances emerging field.

Language: Английский

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Visible‐Light‐Induced Homolysis of Earth‐Abundant Metal‐Substrate Complexes: A Complementary Activation Strategy in Photoredox Catalysis

Angewandte Chemie International Edition, Journal Year: 2021, Volume and Issue: 60(39), P. 21100 - 21115

Published: Feb. 18, 2021

Abstract The mainstream applications of visible‐light photoredox catalysis predominately involve outer‐sphere single‐electron transfer (SET) or energy (EnT) processes precious metal Ru II Ir III complexes organic dyes with low photostability. Earth‐abundant metal‐based M n L ‐type (M=metal, =polydentate ligands) are rapidly evolving as alternative photocatalysts they offer not only economic and ecological advantages but also access to the complementary inner‐sphere mechanistic modes, thereby transcending their inherent limitations ultrashort excited‐state lifetimes for use effective photocatalysts. generic process, termed visible‐light‐induced homolysis (VLIH), entails formation suitable light‐absorbing ligated metal–substrate (M ‐Z; Z=substrate) that can undergo homolytic cleavage generate n−1 Z . further transformations.

Language: Английский

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Ligand‐to‐Metal Charge Transfer (LMCT) Photochemistry at 3d‐Metal Complexes: An Emerging Tool for Sustainable Organic Synthesis

ChemCatChem, Journal Year: 2022, Volume and Issue: 14(19)

Published: Aug. 11, 2022

Abstract Despite the rich photochemistry of 3d‐metal complexes, utilization excited‐state reactivity these compounds in organic synthesis has been historically overlooked. The advent photoredox catalysis changed perception synthetic chemists towards photochemistry, and nowadays potential photoinduced, outer‐sphere single‐electron transfer events is widely recognized. More recently, an emerging new mode photoactivation taken spotlight, based on inner‐sphere triggered by population ligand‐to‐metal charge‐transfer (LMCT) excited states. Contrarily to photoredox, LMCT‐activation does not rely matching redox potentials, offers unique profiles particularly well suited Earth‐abundant metal complexes. Those appealing features are propelling development methods using this blueprint generate highly reactive open‐shell species under mild conditions. aim contribution provide a didactical tool for comprehension concept facilitate methodologies achieve sustainable chemical transformations.

Language: Английский

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Direct decarboxylative Giese reactions

Chemical Society Reviews, Journal Year: 2022, Volume and Issue: 51(4), P. 1415 - 1453

Published: Jan. 1, 2022

This review summarizes recent progress on using carboxylic acids directly as convenient precursors for the 1,4-radical conjugate addition (Giese) reaction.

Language: Английский

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Recent developments in the difunctionalization of alkenes with C–N bond formation

Organic Chemistry Frontiers, Journal Year: 2021, Volume and Issue: 8(18), P. 5206 - 5228

Published: Jan. 1, 2021

Various alkene difunctionalization reactions involving nitridization, diamination, azidation, oxyamination, carboamination, aminohalogenation, and nitration are introduced in this review.

Language: Английский

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Iron Photoredox Catalysis–Past, Present, and Future

Journal of the American Chemical Society, Journal Year: 2023, Volume and Issue: 145(17), P. 9369 - 9388

Published: April 20, 2023

Photoredox catalysis of organic reactions driven by iron has attracted substantial attention throughout recent years, due to potential environmental and economic benefits. In this Perspective, three major strategies were identified that have been employed date achieve reactivities comparable the successful noble metal photoredox catalysis: (1) Direct replacement a center in archetypal polypyridyl complexes, resulting metal-centered photofunctional state. (2) situ generation photoactive complexes substrate coordination where are via intramolecular electron transfer involving charge-transfer states, for example, through visible-light-induced homolysis. (3) Improving excited-state lifetimes redox potentials states new ligand design. We seek give an overview evaluation developments rapidly growing field and, at same time, provide outlook on future iron-based catalysis.

Language: Английский

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Iron-Catalyzed C(Sp³)–H Borylation, Thiolation, and Sulfinylation Enabled by Photoinduced Ligand-to-Metal Charge Transfer

Journal of the American Chemical Society, Journal Year: 2023, Volume and Issue: 145(13), P. 7600 - 7611

Published: March 23, 2023

Catalytic C(sp3)-H functionalization has provided enormous opportunities to construct organic molecules, facilitating the derivatization of complex pharmaceutical compounds. Within this framework, direct hydrogen atom transfer (HAT) photocatalysis becomes an appealing approach goal. However, viable substrates utilized in these protocols are limited, and site selectivity shows preference activated thermodynamically favored bonds. Herein, we describe development undirected iron-catalyzed borylation, thiolation, sulfinylation reactions enabled by photoinduced ligand-to-metal charge (LMCT) process. These exhibit remarkably broad substrate scope (>150 examples total), most importantly, all three show unconventional regioselectivity, with occurrence preferentially at distal methyl position. The procedures operationally simple readily scalable provide access high-value products from hydrocarbons one step. Mechanistic studies control experiments indicate that afforded is not only relevant HAT species but also largely affected use boron- sulfone-based radical acceptors.

Language: Английский

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A Unified Approach to Decarboxylative Halogenation of (Hetero)aryl Carboxylic Acids

Journal of the American Chemical Society, Journal Year: 2022, Volume and Issue: 144(18), P. 8296 - 8305

Published: April 29, 2022

Aryl halides are a fundamental motif in synthetic chemistry, playing critical role metal-mediated cross-coupling reactions and serving as important scaffolds drug discovery. Although thermal decarboxylative functionalization of aryl carboxylic acids has been extensively explored, the scope existing halodecarboxylation methods remains limited, there currently exists no unified strategy that provides access to any type halide from an acid precursor. Herein, we report general catalytic method for direct halogenation (hetero)aryl via ligand-to-metal charge transfer. This accommodates exceptionally broad substrates. We leverage radical intermediate toward divergent pathways: (1) atom transfer bromo- or iodo(hetero)arenes (2) capture by copper subsequent reductive elimination generate chloro- fluoro(hetero)arenes. The proposed mechanism is supported through array spectroscopic studies.

Language: Английский

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Copper-photocatalyzed ATRA reactions: concepts, applications, and opportunities

Chemical Society Reviews, Journal Year: 2022, Volume and Issue: 51(13), P. 5287 - 5299

Published: Jan. 1, 2022

This review summarizes the different applications and underlying concepts that are applied for Cu( i )- or ii )-photocatalyzed difunctionalizations of alkenes.

Language: Английский

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Photoelectrochemical Asymmetric Catalysis Enables Direct and Enantioselective Decarboxylative Cyanation

Journal of the American Chemical Society, Journal Year: 2022, Volume and Issue: 144(44), P. 20201 - 20206

Published: Oct. 31, 2022

The development of efficient and sustainable methods for decarboxylative transformations is great importance due to the ease availability nontoxicity carboxylic acids. Despite tremendous efforts in this area, it remains challenging develop enantioselective direct from Herein we disclose a photoelectrocatalytic method cyanation. photoelectrochemical reactions convert acids enantioenriched nitriles by employing cerium/copper relay catalysis with cerium salt catalytic decarboxylation chiral copper complex stereoselective C-CN formation.

Language: Английский

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