Non-phosgene route: catalytic carbonylation of amines to form unsymmetrical ureas DOI Creative Commons
Shunji Xie, Ye Wang

National Science Review, Год журнала: 2024, Номер 12(1)

Опубликована: Дек. 6, 2024

Язык: Английский

Multifunctional Carbon‐Based Metal‐Free Catalysts for Cascade Electrochemical‐Chemical Coupling Catalyses DOI Open Access
Yan Li, Tom Lawson,

Yang Hou

и другие.

Advanced Functional Materials, Год журнала: 2025, Номер unknown

Опубликована: Март 10, 2025

Abstract Cascade electrochemical‐chemical coupling (CECC) involves sequential electrochemical and chemical reactions, using intermediates from processes as reactants for subsequent transformations to enhance the efficiency selectivity sustainable syntheses of complex chemicals. Despite its economic environmental benefits, CECC still faces multiple challenges, including a low utilization intermediate reactants, competitive side difficulties in design scale‐up catalysts, leading yield. To ensure economically viable CECC, it is imperative rationally develop cost‐efficient high‐performance such carbon‐based metal‐free electrocatalysts (C‐MFECs) certain carbon‐supported transition metal with high activity atomic precision desirable products. In this review, an overview recent advancements doping C‐MFECs provided enhancing their catalytic toward CECC. Three major systems based on are discussed; they hydrogen peroxide coupling, carbon dioxide upgrading, redox‐mediated systems. Current challenges future perspectives emerging field also addressed.

Язык: Английский

Процитировано

1

Organo-mediator enabled electrochemical transformations DOI
Wei-Mei Zeng, Yanwei Wang,

Chunhui Peng

и другие.

Chemical Society Reviews, Год журнала: 2025, Номер unknown

Опубликована: Янв. 1, 2025

This review highlights organo-mediators that enable electrochemical reactions via outer-sphere electron transfer (ET), offering advantages such as availability, tunability, and simplified post-processing compared to direct electrolysis.

Язык: Английский

Процитировано

1

Synthesis of Unsymmetrical Urea via Oxidative Carbonylation Reaction Based on the Strategy of Synchronous Amine Recognition DOI
Yujie Zhao, Lin‐Yu Jiao

Chinese Journal of Organic Chemistry, Год журнала: 2025, Номер 45(3), С. 1040 - 1040

Опубликована: Янв. 1, 2025

Язык: Английский

Процитировано

1

CO/CO₂ as C1 building blocks: Unveiling new horizons in coumarin synthesis DOI
Zechao Wang, Jiajia Mou, Hao Jia

и другие.

Molecular Catalysis, Год журнала: 2025, Номер 574, С. 114887 - 114887

Опубликована: Янв. 30, 2025

Язык: Английский

Процитировано

0

Revolutionizing Unsymmetrical Urea Synthesis: A Bimetallic Catalytic Approach with Synchronous Recognition Mechanism DOI Creative Commons
Zechao Wang

Green Carbon, Год журнала: 2025, Номер unknown

Опубликована: Фев. 1, 2025

Язык: Английский

Процитировано

0

Synthesis of organophosphorus (III) compounds from white phosphorus enabled by a tandem electro-thermal process DOI Creative Commons
Feng Kong, Hua Zhang

National Science Review, Год журнала: 2025, Номер 12(5)

Опубликована: Март 27, 2025

Язык: Английский

Процитировано

0

Online Coupling High‐Temperature Electrolysis with Carbonylation Reactions: A Powerful Method for Continuous Carbon Dioxide Utilization DOI Creative Commons
Kristóf Stágel, Kirsten Rath,

Prasad Kathe

и другие.

Angewandte Chemie, Год журнала: 2025, Номер unknown

Опубликована: Апрель 7, 2025

Abstract Despite being widely available, the broad utilization of CO 2 for chemical production remains in its infancy. The difficulty using as an important resource industry lies high stability molecule and associated inertia. In this work, we demonstrate how to overcome these limitations by utilizing a solid oxide electrolysis cell (SOEC) with optimized cathode produce dry through high‐temperature . We further integrate process synthesis setup continuous‐flow coil reactor boost reactivity various carbonylation processes, including amino‐, alkoxy‐, phenoxycarbonylation, carbonylative Sonogashira couplings, or redox‐active esters. Ultimately, our approach offers platform strategy rapid, scalable, continuous carbonyl compounds directly from while eliminating requirement storing large quantities.

Язык: Английский

Процитировано

0

Online Coupling High‐Temperature Electrolysis with Carbonylation Reactions: A Powerful Method for Continuous Carbon Dioxide Utilization DOI Creative Commons
Kristóf Stágel, Kirsten Rath,

Prasad Kathe

и другие.

Angewandte Chemie International Edition, Год журнала: 2025, Номер unknown

Опубликована: Апрель 7, 2025

Abstract Despite being widely available, the broad utilization of CO 2 for chemical production remains in its infancy. The difficulty using as an important resource industry lies high stability molecule and associated inertia. In this work, we demonstrate how to overcome these limitations by utilizing a solid oxide electrolysis cell (SOEC) with optimized cathode produce dry through high‐temperature . We further integrate process synthesis setup continuous‐flow coil reactor boost reactivity various carbonylation processes, including amino‐, alkoxy‐, phenoxycarbonylation, carbonylative Sonogashira couplings, or redox‐active esters. Ultimately, our approach offers platform strategy rapid, scalable, continuous carbonyl compounds directly from while eliminating requirement storing large quantities.

Язык: Английский

Процитировано

0

Emerging trends in CO carbonylation DOI
Chang‐Sheng Kuai, Yang Yuan, Xiao‐Feng Wu

и другие.

Chem, Год журнала: 2025, Номер unknown, С. 102503 - 102503

Опубликована: Апрель 1, 2025

Язык: Английский

Процитировано

0

Electrifying Redox-Neutral Palladium-Catalyzed Carbonylations: Multielectron Transfer as a Catalyst Driving Force DOI
Pierre‐Louis Lagueux‐Tremblay, Kwok‐Cheong Tam,

Meijing Jiang

и другие.

Journal of the American Chemical Society, Год журнала: 2025, Номер unknown

Опубликована: Апрель 22, 2025

Palladium-catalyzed bond-forming reactions such as carbonylations offer an efficient and versatile avenue to access products from often feedstock reagents. However, the use of catalysts also comes with a cost, their need be regenerated after each product-forming cycle requires balancing thermal operations. The latter can lead high barriers even well restrict application many products. We introduce herein alternative approach palladium catalyst design, where instead electrochemical potential drive catalysis by continual two-electron cycling metal oxidation state. power behind these redox steps offers route carry out carbonylation reactions, including catalytic synthesis high-energy aroyl halide electrophiles, at unprecedentedly mild ambient temperature pressure. More generally, analysis suggests this functions distinct multi-electron exchange pathway, reduction enables oxidative addition drives product elimination. combination creates unique platform both reverse operations are favored in same system energy only added source.

Язык: Английский

Процитировано

0