Dual-ionic imidazolium salts to promote synthesis of cyclic carbonates at atmospheric pressure DOI Creative Commons
Tengfei Wang, Danning Zheng,

Beibei An

и другие.

Green Energy & Environment, Год журнала: 2021, Номер 7(6), С. 1327 - 1339

Опубликована: Фев. 25, 2021

Novel dual-ionic imidazolium salts are shown to display excellent catalytic activity for cycloaddition of carbon dioxide and epoxides under room temperature atmospheric pressure (0.1 MPa) without any solvent co-catalyst leading 96.1% product yield. It can be reused five times keep the yield over 90%. These intriguing results attributed a new reaction mechanism, which is supported by theoretical calculations along with measurements 13C NMR spectrum Fourier transform infrared spectroscopy (FT-IR). The traced CO2-philic group an electrophilic hydrogen atom. Our work shows that incorporation feasible pathway develop efficient ionic liquids.

Язык: Английский

Catalytic Hydrogenation of Cyclic Carbonates using Manganese Complexes DOI Creative Commons
Akash Kaithal, Markus Hölscher, Walter Leitner

и другие.

Angewandte Chemie International Edition, Год журнала: 2018, Номер 57(41), С. 13449 - 13453

Опубликована: Авг. 22, 2018

Catalytic hydrogenation of cyclic carbonates to diols and methanol was achieved using a molecular catalyst based on earth-abundant manganese. The complex [Mn(CO)

Язык: Английский

Процитировано

125

Manganese-catalyzed hydroboration of carbon dioxide and other challenging carbonyl groups DOI Creative Commons
Christina Erken, Akash Kaithal, Suman Sen

и другие.

Nature Communications, Год журнала: 2018, Номер 9(1)

Опубликована: Окт. 24, 2018

Reductive functionalization of the C=O unit in carboxylic acids, carbonic acid derivatives, and ultimately carbon dioxide itself is a challenging task key importance for synthesis value-added chemicals. In particular, it can open novel pathways valorization non-fossil feedstocks. Catalysts based on earth-abundant, cheap, benign metals would greatly contribute to development sustainable synthetic processes derived from this concept. Herein, manganese pincer complex [Mn(Ph2PCH2SiMe2)2NH(CO)2Br] (1) reported enable reduction broad range carbonates, even CO2 using pinacolborane as reducing agent. The shown operate under mild reaction conditions (80-120 °C), low catalyst loadings (0.1-0.2 mol%) runs solvent-less conditions. Mechanistic studies including crystallographic characterisation borane adduct imply that metal-ligand cooperation facilitates substrate activation.

Язык: Английский

Процитировано

123

Catalytic C1 Alkylation with Methanol and Isotope‐Labeled Methanol DOI

Jan Sklyaruk,

Jannik C. Borghs,

O. El-Sepelgy

и другие.

Angewandte Chemie International Edition, Год журнала: 2018, Номер 58(3), С. 775 - 779

Опубликована: Ноя. 20, 2018

Abstract A metal‐catalyzed methylation process has been developed. By employing an air‐ and moisture‐stable manganese catalyst together with isotopically labeled methanol, a series of D‐, CD 3 ‐, 13 C‐labeled products were obtained in good yields under mild reaction conditions water as the only byproduct.

Язык: Английский

Процитировано

115

Manganese Catalyzed Hydrogenation of Carbamates and Urea Derivatives DOI
Uttam Kumar Das, Amit Kumar,

Yehoshoa Ben‐David

и другие.

Journal of the American Chemical Society, Год журнала: 2019, Номер 141(33), С. 12962 - 12966

Опубликована: Июль 31, 2019

We report the hydrogenation of carbamates and urea derivatives, two most challenging carbonyl compounds to be hydrogenated, catalyzed for first time by a complex an earth-abundant metal. The reaction these CO2-derived compounds, manganese pincer complex, yields methanol in addition amine alcohol, which makes this methodology sustainable alternative route conversion CO2 methanol, involving base-metal catalyst. Moreover, proceeds under mild pressure (20 bar). Our observations support mechanism Mn–H complex. A plausible catalytic cycle is proposed based on informative mechanistic experiments.

Язык: Английский

Процитировано

113

Manganese(I)‐Catalyzed β‐Methylation of Alcohols Using Methanol as C1 Source DOI Creative Commons
Akash Kaithal, Pit van Bonn, Markus Hölscher

и другие.

Angewandte Chemie International Edition, Год журнала: 2019, Номер 59(1), С. 215 - 220

Опубликована: Окт. 25, 2019

Highly selective β-methylation of alcohols was achieved using an earth-abundant first row transition metal in the air stable molecular manganese complex [Mn(CO)

Язык: Английский

Процитировано

111

Efficient catalytic conversion of terminal/internal epoxides to cyclic carbonates by porous Co(ii) MOF under ambient conditions: structure–property correlation and computational studies DOI
Bhavesh Parmar, Parth Patel, Renjith S. Pillai

и другие.

Journal of Materials Chemistry A, Год журнала: 2019, Номер 7(6), С. 2884 - 2894

Опубликована: Янв. 1, 2019

Efficient CO2 capture/utilization by Co(ii) MOF as a heterogeneous catalyst in CO2–epoxide cycloaddition at ambient condition has been investigated and correlated with computational studies.

Язык: Английский

Процитировано

109

Recent Progress with Pincer Transition Metal Catalysts for Sustainability DOI Open Access
Luca Piccirilli, Danielle L. J. Pinheiro, Martin Nielsen

и другие.

Catalysts, Год журнала: 2020, Номер 10(7), С. 773 - 773

Опубликована: Июль 11, 2020

Our planet urgently needs sustainable solutions to alleviate the anthropogenic global warming and climate change. Homogeneous catalysis has potential play a fundamental role in this process, providing novel, efficient, at same time eco-friendly routes for both chemicals energy production. In particular, pincer-type ligation shows promising properties terms of long-term stability selectivity, as well allowing mild reaction conditions low catalyst loading. Indeed, pincer complexes have been applied plethora chemical processes, such hydrogen release, CO2 capture conversion, N2 fixation, biomass valorization synthesis high-value fuels. work, we show main advances last five years use transition metal key catalytic processes aiming more

Язык: Английский

Процитировано

97

Reversible interconversion between methanol-diamine and diamide for hydrogen storage based on manganese catalyzed (de)hydrogenation DOI Creative Commons
Zhihui Shao, Yang Li, Chenguang Liu

и другие.

Nature Communications, Год журнала: 2020, Номер 11(1)

Опубликована: Янв. 30, 2020

Abstract The development of cost-effective, sustainable, and efficient catalysts for liquid organic hydrogen carrier systems is a significant goal. However, all the reported relied on use precious metal catalysts. Herein, system based non-noble catalysis was established. Mn-catalyzed dehydrogenative coupling methanol N , ’-dimethylethylenediamine to form ’-(ethane-1,2-diyl)bis( -methylformamide), reverse hydrogenation reaction constitute storage with theoretical capacity 5.3 wt%. A rechargeable could be achieved by subsequent resulting dehydrogenation mixture regenerate H 2 -rich compound. maximum selectivity amide formation 97%.

Язык: Английский

Процитировано

87

Metal-catalyzed hydrogenation and dehydrogenation reactions for efficient hydrogen storage DOI
Takuya Shimbayashi, Ken‐ichi Fujita

Tetrahedron, Год журнала: 2020, Номер 76(11), С. 130946 - 130946

Опубликована: Янв. 18, 2020

Язык: Английский

Процитировано

83

Sustainable Alkylation of Nitriles with Alcohols by Manganese Catalysis DOI

Jannik C. Borghs,

Mai Anh Tran,

Jan Sklyaruk

и другие.

The Journal of Organic Chemistry, Год журнала: 2019, Номер 84(12), С. 7927 - 7935

Опубликована: Май 22, 2019

A general and chemoselective catalytic alkylation of nitriles using a homogeneous nonprecious manganese catalyst is presented. This reaction uses naturally abundant alcohols readily available as coupling partners. The tolerates wide range functional groups heterocyclic moieties, efficiently providing useful cyanoalkylated products with water the only side product. Importantly, methanol can be used C1 source C-methylation achieved. mechanistic investigations support multiple role metal-ligand catalyst, dehydrogenative activation alcohol, α-C-H nitrile, hydrogenation in-situ-formed unsaturated intermediate.

Язык: Английский

Процитировано

81