The guanidine 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD) and the substituted derivatives [TBD-SiR ] and TBD-BR reacted with SO to give different FLP-SO adducts. Molecular structures, elucidated by X-ray diffraction, showed some structural similarities with the analogous CO adducts. Thermodynamic stabilities were both experimentally evidenced and computed through DFT calculations. The underlying parameters governing the relative stabilities of the different SO and CO adducts were discussed from a theoretical standpoint, with a focus on the influence of the Lewis acidic moiety.
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http://dx.doi.org/10.1002/chem.201901088 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
College of Chemistry, Chemical Engineering and Environment, Minnan Normal University, Zhangzhou 363000, China.
Chem Asian J
November 2024
Key Laboratory of Photochemical Conversion and Optoelectronic Materials, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Coupling hydrogen evolution reaction (HER) with biomass valorization using a photoelectrochemical (PEC) system presents a promising approach for effectively converting solar energy to chemical energy. A crucial biomass valorization reaction is the production of value-added 2,5-furandicarboxylic acid (FDCA) via 5-Hydroxymethylfurfural (HMF) oxidation reaction (HMFOR). To achieve efficient FDCA production, we demonstrate an effective photoanode strategy that combines metal silicidation, dopant segregation, and surface reconstruction to create a bimetallic silicide NiPtSi/n-Si photoanode.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
October 2024
Sorbonne Université, CNRS, Institut Parisien de Chimie Moléculaire, 4 Place Jussieu, 75005, Paris, France.
The metal-halogen exchange reaction constitutes one of the most important preparative routes towards polar organometallic reagents such as aryllithium or Grignard reagents. However, despite extensive developments over the past eight decades, this fundamental organometallic elementary step has only been exploited stoichiometrically. Against this background, we demonstrate that the sodium-bromine exchange reaction can be implemented in a catalytic setting as a mean to activate C(sp)-Br bonds in a transition metal-free manner en route to the regioselective and general preparation of (hetero)aryl silanes.
View Article and Find Full Text PDFLangmuir
August 2024
Department of Chemistry and Biochemistry, Montclair State University, Montclair, New Jersey 07043, United States.
ChemSusChem
November 2024
Institute of Chemical Technology, Universität Leipzig, Linnéstr. 3, 04103, Leipzig, Germany.
Commercial SSZ-13 zeolite with different n(Si)/n(Al) ratios and from different suppliers were subjected to a post-synthetic treatment in order to create mesopores of up to 15 nm. Furthermore, the materials were modified with copper ions and thoroughly physico-chemically characterized. The modified textural properties varied the nature of copper species, and thus, activity in the selective catalytic reduction of NO with ammonia (NH-SCR-DeNO).
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