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The utilization of CO as a C building block remains a key challenge in sustainable organic synthesis. We now report a recyclable metal ion modified titanium oxide (M/TiO, where M represents Mg, Rh, Cr, Mn, Fe, Ni, Cu, Zn, and Al) photocatalytic system used with a tetrabutylammonium halide (TBAX, X = I, Br, Cl) as a co-catalyst, which enables the cycloaddition of CO with various epoxides under visible light irradiation at room temperature. This catalyst system exhibits a broad range of responsiveness to visible light and is compatible with simulated solar light, and operates solvent-free conditions without the need for high pressure. Excellent yields and selectivities were achieved by the Mg/TiO photocatalyst, and the method was successfully scaled to gram-scale synthesis without any loss of efficiency. Simulated post-combustion exhaust gas (CO: 7.5%, N: 92.5%, relative humidity: 90%) was concentrated to 97% and used for the reaction, yielding 88% styrene carbonate from styrene oxide by the catalysis of Mg/TiO. Furthermore, the Mg/TiO catalyst could be readily recovered and reused over multiple cycles. Mechanistic investigations supported by density functional theory (DFT) calculations indicated that the bromine radical (Br•), generated via photooxidation of bromide ion from TBABr, initiates the epoxide ring-opening.
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http://dx.doi.org/10.1002/chem.202501845 | DOI Listing |
Inorg Chem
September 2025
Department of Chemistry, Panskura Banamali College, Panskura RS, Purba Medinipur, WB 721152, India.
We report the synthesis and characterization of a new Schiff base ligand (HL), derived from 2-picolylamine and 2-hydroxy-3-methoxy-5-methylbenzaldehyde. Its reaction with Ni(NO)·6HO and Ln(NO)·HO (Ln = Gd, Tb, Dy) in the presence of triethylamine affords a carbonato-bridged family of heterobimetallic NiLn complexes: [NiLn(L)(L')(μ-CO)(NO)]·MeOH·HO (). During the complexation reaction, ligand HL undergoes an oxidation, followed by C-C coupling to generate a secondary ligand (HL').
View Article and Find Full Text PDFACS Macro Lett
September 2025
Department of Chemistry, Yonsei University, Seoul 03722, Republic of Korea.
Alkyne groups provide exceptional versatility for functionalization in macromolecular systems. However, the controlled anionic ring-opening polymerization (AROP) of epoxide monomers bearing terminal alkynes remains challenging due to the lability of alkynes under strongly basic conditions. Herein, we present a controlled AROP of glycidyl propargyl ether enabled by Lewis pair organocatalysis, employing a phosphazene base and triethylborane.
View Article and Find Full Text PDFACS Omega
August 2025
Institute of Chemistry, Universidade Federal do Rio Grande do Sul, Av. Bento Gonçalves, 9500, Porto Alegre, RS 91501-970, Brazil.
This review examines the role of ionic liquids (ILs) in the catalytic carbonation of epoxides for the synthesis of cyclic carbonates, focusing on the key factors that influence reaction efficiency. The nucleophilicity and basicity of the anions in IL catalysts are highlighted as critical components for promoting the cycloaddition reaction with CO. The solubility and ionicity of the ILs also significantly affect the reaction, with higher ionicity leading to better solubilization and catalytic performance.
View Article and Find Full Text PDFNanoscale
August 2025
Department of Chemistry, Malaviya National Institute of Technology Jaipur, Rajasthan-302017, India.
Developing efficient and sustainable catalytic systems for carbon dioxide utilization is crucial in tackling the challenges posed by increasing greenhouse gas emissions. This study investigates the co-catalyst- and solvent-free cycloaddition of CO with epoxides using a series of iron-based metal phosphonates, FePPA (iron phenylphosphonate), FeHEDP (iron hydroxyethylidene diphosphonate), and FeEDTMP (iron ethylenediamine tetramethylene phosphonate), with the aim of elucidating the role of acidic-basic sites in enhancing their catalytic performance. These catalysts, prepared using phosphonic acids with various functional groups, offer a platform for examining how structural modifications influence CO fixation efficiency.
View Article and Find Full Text PDFChem Mater
August 2025
Department of Chemistry, University of Warwick, Coventry CV4 7AL, U.K.
We describe the synthesis of a functional macroporous polymer material and its potential use as a scaffold to support the 3D culture of hematopoietic stem and progenitor cells (HSPCs). Glycidyl methacrylate (GMA)-based emulsion-templated porous polymers (known as polyHIPEs) were prepared by photopolymerization and subsequently surface functionalized with hyaluronic acid (HA) using Huisgen azide-alkyne cycloaddition click reaction, inferring a high degree of functionalization based on the near-quantitative nature of the reactions. Quantitative azidation of GMA-based polyHIPEs is achieved by the ring opening reaction of epoxide rings with sodium azide.
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