Journal of Catalysis, Journal Year: 2024, Volume and Issue: 434, P. 115519 - 115519
Published: April 26, 2024
Language: Английский
Journal of Catalysis, Journal Year: 2024, Volume and Issue: 434, P. 115519 - 115519
Published: April 26, 2024
Language: Английский
Angewandte Chemie International Edition, Journal Year: 2023, Volume and Issue: 63(8)
Published: Oct. 30, 2023
Within the sphere of traditional Pd
Language: Английский
Citations
26Chem Catalysis, Journal Year: 2025, Volume and Issue: unknown, P. 101257 - 101257
Published: Feb. 1, 2025
Language: Английский
Citations
2Journal of the American Chemical Society, Journal Year: 2022, Volume and Issue: 144(34), P. 15468 - 15474
Published: Aug. 22, 2022
A Pd-catalyzed enantioselective three-component reaction of N-sulfonylhydrazones, aryl bromides, and silylboronic esters is developed, enabling the synthesis chiral gem-diarylmethine silanes in high enantioselectivity with use a newly identified Ming-Phos. Compared N-tosyl, more easily decomposed N-mesitylsulfonyl suitable as masking group electron-rich hydrazone to improve efficiency. The features broad scope concerning both coupling partners, enantioselectivity, mild conditions. ready access enantiomers utility this catalytic method are also presented.
Language: Английский
Citations
31Small, Journal Year: 2023, Volume and Issue: 20(17)
Published: Dec. 4, 2023
Abstract Lithium–sulfur batteries (LSBs) with ultra‐high energy density (2600 W h kg −1 ) and readily available raw materials are emerging as a potential alternative device low cost for lithium‐ion batteries. However, the insulation of sulfur unavoidable shuttle effect leads to slow reaction kinetics LSBs, which in turn cause various roadblocks including poor rate capability, inferior cycling stability, coulombic efficiency. The most effective way solve issues mentioned above is rationally design control synthesis cathode host LSBs. Transition metal phosphides (TMPs) good electrical conductivity dual adsorption‐conversion capabilities polysulfide (PS) regarded promising hosts new‐generation In this review, main obstacles commercializing LSBs development processes their first elaborated. Then, fixation principles, methods TMPs briefly summarized recent progress reviewed detail. Finally, perspective on future research directions provided.
Language: Английский
Citations
21Nano Research, Journal Year: 2023, Volume and Issue: 16(5), P. 6380 - 6401
Published: March 13, 2023
Language: Английский
Citations
18Angewandte Chemie International Edition, Journal Year: 2022, Volume and Issue: 62(1)
Published: Nov. 4, 2022
Abstract Double hydrosilylation of alkynes represents a straightforward method to synthesize bis(silane)s, yet it is challenging if α‐substituted vinylsilanes act as the intermediates. Here, cobalt‐catalyzed regiodivergent double arylacetylenes reported for first time involving this challenge, accessing both vicinal and geminal bis(silane)s with exclusive regioselectivity. Various novel containing Si−H bonds can be easily obtained. The gram‐scale reactions could performed smoothly. Preliminarily mechanistic studies demonstrated that were initiated by α‐hydrosilylation alkynes, followed β‐hydrosilylation α‐vinylsilanes deliver or hydride‐catalyzed give ones. Notably, these used synthesis high‐refractive‐index polymers ( n d up 1.83), demonstrating great potential utility in optical materials.
Language: Английский
Citations
26ACS Applied Materials & Interfaces, Journal Year: 2022, Volume and Issue: 15(1), P. 1410 - 1417
Published: Dec. 27, 2022
Metal–organic frameworks have developed into a formidable heterogeneous catalysis platform in recent years. It is well established that thermolysis of coordinated solvents from MOF nodes can render highly reactive, coordinatively unsaturated metal complexes which are stabilized via site isolation and serve as active sites catalysis. Such approaches limited to featuring solvated transition-metal must be stable toward the formation "permanent" open sites. Herein, we exploit hemilability metal–carboxylate bonds generate transient an In(III) MOF, pertinent In-centered The catalyze Strecker reaction over multiple cycles without loss activity or crystallinity. We employ computational spectroscopic methods confirm dissociation In(III)–carboxylate bonds. Furthermore, amount within material thus catalytic performance temperature-modulated.
Language: Английский
Citations
25Chemical Science, Journal Year: 2022, Volume and Issue: 13(25), P. 7626 - 7633
Published: Jan. 1, 2022
Ligand exchange reactions of [Rh(COD){η4-Ge9(Hyp)3}] with L-type nucleophiles such as PMe3, PPh3, IMe4 (IMe4 = 1,3,4,5-tetramethylimidazol-2-ylidene) or [W(Cp)2H2] result in the displacement COD ligand to afford clusters coordinatively unsaturated trigonal pyramidal rhodium(i) centers [Rh(L){η3-Ge9(Hyp)3}]. These species can be readily protonated allowing access cationic rhodium-hydride complexes, e.g. [RhH(PPh3){η3-Ge9(Hyp)3}]+. act catalysts H/D between H2 and D2 alkene isomerisation, thereby illustrating that metal-functionalized Zintl are active both H-H C-H bond activation processes. The mechanism was probed using parahydrogen induced polarization experiments.
Language: Английский
Citations
24Chemical Society Reviews, Journal Year: 2023, Volume and Issue: 53(1), P. 361 - 379
Published: Dec. 12, 2023
This review focuses on the low-valent heavy group 14 compounds stabilized by N-heterocyclic boryl ligands and their applications in activation of small molecules inert chemical bonds.
Language: Английский
Citations
15Journal of Catalysis, Journal Year: 2024, Volume and Issue: 433, P. 115494 - 115494
Published: April 10, 2024
Language: Английский
Citations
6