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In this study, a series of partially chain-straightened propylene oligomers and functional propylene−methyl acrylate (P-MA) co-oligomers were synthesized with 8-alkyl-iminopyridyl Pd(II) catalysts. The molecular weight and polar monomer incorporation ratio could be tuned by using Pd(II) catalysts with various 8-alkyl-naphthyl substituents (8-alkyl: H, Me, and n-Bu). In propylene oligomerization, all the 8-alkyl-iminopyridyl Pd(II) catalysts convert propylene to partially chain-straightened (119−136/1000 C) oligomers with low molecular weights (0.3−1.5 kg/mol). Among the catalysts, Pd1 with non-substituent (H) on the ligand showed the highest activity of 5.4 × 104 g/((mol of Pd) h), generating oligomers with the lowest molecular weight (Mn: 0.3 kg/mol). Moreover, polar-functionalized propylene-MA co-oligomers with very high incorporation ratios (22.8−36.5 mol %) could be obtained in the copolymerization using these 8-alkyl-iminopyridyl Pd(II) catalysts. Additionally, Pd1 exhibited the best performance in propylene-MA copolymerization as it displayed the highest MA incorporation ratio of up to 36.5 mol%. All the three catalysts are capable of generating partially chain-straightened P-MA co-oligomers and the activities decrease gradually while the molecular weight increases with the increasing steric hindrance of the alkyl substituent (H < Me < n-Bu). Compared to Pd4 with the rigid 8-aryl substituent, the flexible 8-alkyl-iminopyridyl Pd(II) catalysts (Pd1-3) not only showed much higher activities in the propylene oligomerization, but also yielded P-MA co-oligomers with significantly higher incorporation ratios in the propylene co-oligomerization.
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http://dx.doi.org/10.3390/polym15010111 | DOI Listing |
Chem Commun (Camb)
September 2025
Anhui Laboratory of Molecule-Based Materials, Key Laboratory of Functional Molecular Solids, Ministry of Education, School of Chemistry and Materials Science, Anhui Normal University, Wuhu 241002, China.
Gas-phase polymerization is typically employed for the synthesis of high-molecular-weight crystalline polyolefin materials, yet the production of low-molecular-weight hyperbranched ethylene oligomers this method is seldom reported. In this study, we utilized flexible bulky iminopyridyl Pd(II) catalysts to catalyze the gas-phase oligomerization of ethylene, resulting in the preparation of hyperbranched ethylene oligomers. These catalysts demonstrated higher activity and stability comparable to those observed in solution polymerization, yielding hyperbranched ethylene oligomers with lower branching density and higher molecular weights.
View Article and Find Full Text PDFJ Am Chem Soc
August 2025
Roger Adams Laboratory, Department of Chemistry, University of Illinois Urbana-Champaign, Urbana, Illinois 61801, United States.
-alkyl arylamines are important structural motifs in pharmaceuticals, yet traditional alkylating methods rely on the nucleophilicity of the amine and make access to such compounds with valuable bioproperties challenging. While metal-mediated reactions may alleviate these limitations, they often encounter amine-metal interactions that can hinder catalysis or lead to deleterious pathways. Herein, we report a palladium(II) [Pd(II)]/sulfoxide-oxazoline(SOX)/phosphoric acid-mediated C(sp)H/N(sp) cross-coupling of 53 arylamine nucleophiles and 39 terminal olefins to furnish >80 diverse tertiary (3°) arylamines in excellent yields (average 82%) and selectivities (>20:1 /, >20:1 linear/branched).
View Article and Find Full Text PDFRSC Adv
August 2025
Laboratory Physical-Chemistry of the Solid State, Department of Chemistry, Faculty of Sciences of Sfax, University of Sfax BP 1171 3000 Sfax Tunisia
A new one-dimensional (1D) palladium-based hybrid perovskite, (CHN)[PdCl(HO)], has been synthesized and structurally characterized, revealing a distinctive asymmetric architecture with two non-equivalent formula units (' = 2). The compound exhibits a see-saw coordination geometry around Pd(ii), stabilized through a network of hydrogen bonds, π-π stacking, and halogen-halogen interactions, which collectively enhance its structural robustness and functional properties. Beyond its architectural novelty, the material demonstrated excellent catalytic activity as a cathodic modifier in a Boron-Doped Diamond (BDD)-assisted electro-Fenton system for paraquat degradation.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Department of Chemistry, The Scripps Research Institute, La Jolla, California 92037, United States.
For over half a century, -halogenated arenes, widely used in cross-coupling reactions, are mainly synthesized and manufactured by stoichiometric-directed -lithiation/halogenation technology. While catalytic C-H halogenation has emerged as a potentially environmentally friendly method, the need for stoichiometric bases, expensive oxidants, and installation of directing groups prevented its adoption in scalable synthesis. In addition, the ligandless Pd(II)-catalyzed C-H halogenation is incompatible with heterocyclic substrates, thus limiting its use in medicinal chemistry substantially.
View Article and Find Full Text PDFAcc Chem Res
September 2025
Department of Chemistry, University of Houston, Houston, Texas 77204-5003, United States.
ConspectusPolyolefins are by far the most ubiquitous industrially produced polymers and are primarily produced by early transition metal catalysts. These catalysts are not functional group tolerant, and copolymerization of ethylene and polar vinyl monomers is quite challenging. Furthermore, early metal catalysts convert ethylene to linear polyethylene, and introduction of branches requires addition of comonomers.
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