-Formylation of amines with CO as a cheap and non-toxic C1-feedstock and hydrosilane reducing agent is a practical and environment friendly method to synthesize formamides. This study describes an efficient and chemoselective mono--formylation of amines using CO and phenylsilane under mild conditions using a porous metal-organic framework (MOF)-supported single-site cobalt catalyst (pyrim-UiO-Co). The pyrim-UiO-Co MOF has a UiO-topology, and its organic linkers bear a pyridylimine ligated Co catalytic moiety. A wide range of aliphatic and aromatic amines are transformed into desired -formamides in moderate to excellent yields under 1-5 bar CO. Pyrim-UiO-Co is tolerant to various functional groups and could be recycled and reused at least 10 times. Mechanistic investigation using kinetic, spectroscopic and density functional theory studies suggests that the formylation of benzylamine proceeds sequentially oxidative addition of PhSiH and CO insertion, followed by a turn-over limiting reaction with an amine. Our work highlights the importance of MOF-based Earth-abundant metal catalysts for the practical and eco-friendly synthesis of fine chemicals using cheap feedstocks.
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http://dx.doi.org/10.1039/d3dt00058c | DOI Listing |
Chem Commun (Camb)
January 2025
Hunan Provincial Key Laboratory of Micro & Nano Materials Interface Science, College of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083, China.
A heterogeneous salen-based conjugated microporous polymer catalyst (CMP@Cu-salen) is prepared by a one-pot method for -formylation of amines with CO. The uniformly dispersed Cu-salen site and porous structure facilitates the enrichment of CO and transfer of substrates and the transformation. Our CMP@Cu-salen shows excellent catalytic performance (conversion: 99%, selectivity: 90%) for formylation of -methylaniline under mild conditions (0.
View Article and Find Full Text PDFNat Commun
January 2025
Zhejiang Key Laboratory of Advanced Fuel Cells and Electrolyzers Technology, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo, Zhejiang, PR China.
Amine-assisted two-step CO hydrogenation is an efficient route for methanol production. To maximize the overall catalytic performance, both the N-formylation of amine with CO (i.e.
View Article and Find Full Text PDFJ Phys Chem Lett
January 2025
School of Chemistry, Dalian University of Technology, Dalian 116024, Liaoning, China.
Using CO as the C1 source for N-formylation of amine is a crucial energy-storage pathway to address the greenhouse effect while generating high-value-added chemicals but is limited by the activation of inert molecules. Herein, a dual active site catalyst with high CO activation and dihydrogen dissociation capacity was fabricated by incorporating a Schiff base and Au nanoparticles (NPs) on silicon dioxide (SiO). The modification of the Schiff base not only provides an alkaline environment for CO absorption but also stabilizes Au NPs in a small and highly dispersed state, which regulates the electronic density of the metal for excellent H cleavage.
View Article and Find Full Text PDFJ Inorg Biochem
March 2025
Department of Molecular and Analytical Chemistry, Interdisciplinary Excellence Centre, University of Szeged, Dóm tér 7-8, H-6720 Szeged, Hungary. Electronic address:
Schiff bases derived from aminoguanidine are extensively investigated for their structural versatility. The tridentate 2-formylpyridine guanylhydrazones act as analogues of 2-formyl or 2-acetylpyridine thiosemicarbazones, where the thioamide unit is replaced by the guanidyl group. Six derivatives of 2-formylpyridine guanylhydrazone were synthesized and their proton dissociation and complex formation processes with Cu(II), Fe(II) and Fe(III) ions were studied using pH-potentiometry, UV-visible, NMR and electron paramagnetic resonance spectroscopic methods.
View Article and Find Full Text PDFOrg Biomol Chem
December 2024
Department of Chemistry, IIT Bombay, Powai-400076, Mumbai, India.
We report the synthesis, characterization, and studies of novel 3-pyrrolyl BODIPY-based Schiff base products 3-6 and 3-pyrrolyl BODIPY-based benzo[]thiazol-2-yl derivatives 7-8. The Schiff base compounds 3-6 were synthesized condensation of α-formyl 3-pyrrolyl BODIPY with various amine derivatives, while the Knoevenagel condensation products 7-8 were obtained by reacting α-formyl 3-pyrrolyl BODIPY with 2-(benzo[]thiazol-2-yl) acetonitrile and bis(benzo[]thiazol-2-yl) methane, respectively. The compounds were thoroughly characterized by using HR-MS, 1D and 2D NMR spectroscopy, and X-ray crystallography for two compounds.
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