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Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta...
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The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the...
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Anionic Chain-Growth Polymerization: Overview01:20

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The polymerization process that involves carbanion as an intermediate is called anionic polymerization. It is also a type of addition or chain-growth polymerization. Anionic polymerization gets initiated by a strong nucleophile such as an organolithium or a Grignard reagent. The most commonly used initiator for anionic polymerization is butyl lithium. Monomers involved in anionic polymerization must possess a vinyl group bonded to one or two electron-withdrawing groups. For instance,...
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Catalysis

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The presence of a catalyst affects the rate of a chemical reaction. A catalyst is a substance that can increase the reaction rate without being consumed during the process. A basic comprehension of a catalysts’ role during chemical reactions can be understood from the concept of reaction mechanisms and energy diagrams.
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Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry.
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Acyclic diene metathesis polymerization or ADMET polymerization involves cross-metathesis of terminal dienes, such as 1,8-nonadiene, to give linear unsaturated polymer and ethylene. As ADMET is a reversible process, the formed ethylene gas must be removed from the reaction mixture to complete the polymerization process.
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Undiscovered Potential: Ge Catalysts for Lactide Polymerization.

Ruth D Rittinghaus1, Jakub Tremmel2, Ales Růžička2

  • 1Institute of Inorganic Chemistry, RWTH Aachen University, Landoltweg 1, 52074, Aachen, Germany.

Chemistry (Weinheim an Der Bergstrasse, Germany)
|October 7, 2019
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Summary
This summary is machine-generated.

Germanium catalysts show high activity in polylactide polymerization, offering a non-toxic alternative to tin. These novel germanium complexes enable the production of high molar mass bioplastics.

Keywords:
bioplasticsgermaniumlactidering-opening polymerizationzinc

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Area of Science:

  • Polymer Chemistry
  • Materials Science
  • Green Chemistry

Background:

  • Polylactide (PLA) is a promising bioplastic with potential to replace conventional oil-based plastics.
  • Current industrial-scale PLA production uses tin catalysts, which pose toxicity concerns.
  • There is a need for benign catalysts for sustainable PLA synthesis.

Purpose of the Study:

  • To develop and investigate novel germanium (Ge) complexes as catalysts for polylactide (PLA) polymerization.
  • To explore the potential of germanium as a non-toxic alternative to tin in industrial catalysis.
  • To establish structure-property relationships for Ge-based catalysts to optimize polymerization activity.

Main Methods:

  • Synthesis and characterization of germanium complexes, including those with zinc and copper co-catalysts.
  • Bulk polymerization of lactide at 150°C using the developed Ge catalysts.
  • Structural analysis using single-crystal X-ray diffraction (XRD).
  • Computational studies employing Density Functional Theory (DFT) calculations.

Main Results:

  • The synthesized Ge complexes exhibited high polymerization activities for lactide.
  • Catalyst activity was correlated with systematic variations in complex structure.
  • High molar mass polylactide polymers were successfully produced.
  • Germanium was identified as the active catalytic site, likely operating via a coordination-insertion mechanism.

Conclusions:

  • Novel germanium complexes, in conjunction with zinc and copper, are highly active catalysts for lactide polymerization.
  • These Ge-based systems represent a viable, non-toxic alternative to traditional tin catalysts for PLA production.
  • Understanding structure-activity relationships is key to optimizing these catalysts for industrial applications.