The synthesis of group IV metallocene precatalysts for the polymerization of propylene generally yields two different isomers: The racemic isomer that produces isotactic polypropylene (iPP) and the meso isomer that produces atactic polypropylene (aPP). Due to its poor physical properties, aPP has very limited applications. To avoid obtaining blends of both polymers and thus diminish the mechanical and thermal properties of iPP, the meso metallocene complexes need to be separated from the racemic ones tediously-rendering the metallocene-based polymerization of propylene industrially far less attractive than the Ziegler/Natta process. To overcome this issue, we established an isomerization protocol to convert meso metallocene complexes into their racemic counterparts. This protocol increased the yield of iPP by 400 % while maintaining the polymer's excellent physical properties and was applicable to both hafnocene and zirconocene complexes, as well as different precatalyst activation methods. Through targeted variation of the ligand frameworks, methoxy groups at the indenyl moieties were found to be the structural motifs responsible for an isomerization to take place-this experimental evidence was confirmed by density functional theory calculations. Liquid injection field desorption ionization mass spectrometry, as well as H and Si nuclear magnetic resonance studies, allowed the proposal of an isomerization mechanism.
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Angew Chem Int Ed Engl
September 2024
Wacker-Lehrstuhl für Makromolekulare Chemie Catalysis Research Center, Technische Universität München TUM School of Natural Sciences, Lichtenbergstraße 4, 85748, Garching Garching bei München, Germany.
The synthesis of group IV metallocene precatalysts for the polymerization of propylene generally yields two different isomers: The racemic isomer that produces isotactic polypropylene (iPP) and the meso isomer that produces atactic polypropylene (aPP). Due to its poor physical properties, aPP has very limited applications. To avoid obtaining blends of both polymers and thus diminish the mechanical and thermal properties of iPP, the meso metallocene complexes need to be separated from the racemic ones tediously-rendering the metallocene-based polymerization of propylene industrially far less attractive than the Ziegler/Natta process.
View Article and Find Full Text PDFBiosensors (Basel)
May 2024
School of Food and Biological Engineering, Jiangsu University, Zhenjiang 212013, China.
Metal-organic frameworks (MOFs) are frequently utilized as sensing materials. Unfortunately, the low conductivity of MOFs hinder their further application in electrochemical determination. To overcome this limitation, a novel modification strategy for MOFs was proposed, establishing an electrochemical determination method for cyanides in Baijiu.
View Article and Find Full Text PDFThe conversion of C1 feedstock molecules such as CO into commodity chemicals is a desirable, but challenging, endeavour. When the U(iii) complex, [(CMe)U(O-2,6- Bu-4-MeCH)], is exposed to 1 atm of CO, only coordination is observed by IR spectroscopy as well as X-ray crystallography, unveiling a rare structurally characterized f element carbonyl. However, using [(CMe)(MesO)U (THF)], Mes = 2,4,6-MeCH, reaction with CO forms the bridging ethynediolate species, [{(CMe)(MesO)U}(μ-OCCO)].
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2022
Wacker-Lehrstuhl für Makromolekulare Chemie, Catalysis Research Center, Technische Universität München, Lichtenbergstraße 4, 85748, Garching bei München, Germany.
For more than 40 years, the synthesis of C -symmetric indenyl-based racemic metallocenes for the isoselective polymerization of propylene relied on a tedious separation of the produced rac and meso isomers. Status quo, latter are considered wasteful as they produce atactic polypropylene (aPP) rather than isotactic polypropylene (iPP) if activated with methylaluminoxane (MAO). Unexpectedly, the in situ activation of meso hafnocene I yielded perfectly isotactic polypropylene.
View Article and Find Full Text PDFInorg Chem
August 2022
Department of Chemistry, University of the Free State, Bloemfontein 9300, South Africa.
Ferrocenylbutoxy-bearing dodecylated phthalocyanines, MPc(CH)(OCHFc) with M = 2H (compound series and ) or Zn (compound series , and ), ≤ 8 and ≤ 4, were synthesized through either metal-free statistical condensation between 3,6-bis(dodecyl)phthalonitrile, , and 4- (), or 3-(4'-ferrocenylbutoxy)phthalonitrile, , or a zinc template statistical condensation between 4,5-bis(dodecyl)phthalonitrile, , and in the presence of anhydrous zinc acetate, or by zinc insertion into metal-free phthalocyanines. Compounds were designed to have eight nonperipheral dodecyl substituents, six nonperipheral dodecyl, either one peripheral or one nonperipheral 4'-ferrocenylbutoxy substituent, four nonperipheral dodecyl and two peripheral 4'-ferrocenylbutoxy substituents, or four peripheral 4'-ferrocenylbutoxy substituents. The compound having six peripheral dodecyl and one peripheral 4'-ferrocenylbutoxy substituents was also synthesized.
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