Journal Article FZJ-2016-04495

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png
The Initiation Mechanism of Butadiene Polymerization in Aliphatic Hydrocarbons: A Full Mechanistic Approach

 ;  ;  ;  ;  ;  ;  ;  ;  ;  ;

2016
Soc. Washington, DC

Macromolecules 49(15), 5397 - 5406 () [10.1021/acs.macromol.6b01115]

This record in other databases:    

Please use a persistent id in citations: doi:

Abstract: An in situ 1H NMR study has been carried out to examine the anionic initiation mechanism of 1,3-butadiene and tert-butyllithium (t-BuLi) using n-heptane as solvent. Additionally, mixtures of model compounds have been investigated ex situ to simulate very early stages of polymerization. The analysis of the NMR spectra in combination with density functional theory (DFT) calculations proves the coexistence of cross-aggregates of t-BuLi and initiated chains and their crucial role for the initiation mechanism. From the low concentrations of these species showing a characteristic maximum at t ≈ 50 min and the increase of the overall initiation rate constant with ongoing initiation, we propose a double-stage autocatalytic mechanism for this process. We first assume a fairly small reactivity of butadiene and t-BuLi, which exists under these reaction conditions as a tetrameric aggregate. However, after the reaction of the first t-BuLi unit with a monomer molecule, the reactivity of the remaining three t-BuLi units in the aggregate is increased considerably. The crucial second step of the autocatalytic mechanism is based on the unimer exchange between partially or fully initiated t-BuLi aggregates and the residual unreacted t-BuLi tetramers. As a result, the initiation rate constantly increases and leads to a sigmoidal consumption of initiator molecules during the polymerization. In addition, the time-dependent cross-aggregate concentrations are used as a benchmark for a full mechanistic approach compiling all literature assumptions. Numerical modeling allows a semiquantitative description of the data.

Classification:

Contributing Institute(s):
  1. Neutronenstreuung (ICS-1)
  2. Neutronenstreuung (Neutronenstreuung ; JCNS-1)
  3. Analytik (ZEA-3)
  4. Strukturbiochemie (ICS-6)
Research Program(s):
  1. 551 - Functional Macromolecules and Complexes (POF3-551) (POF3-551)
  2. 6G4 - Jülich Centre for Neutron Research (JCNS) (POF3-623) (POF3-623)
  3. 6215 - Soft Matter, Health and Life Sciences (POF3-621) (POF3-621)

Appears in the scientific report 2016
Database coverage:
Medline ; Current Contents - Physical, Chemical and Earth Sciences ; Ebsco Academic Search ; IF >= 5 ; JCR ; NCBI Molecular Biology Database ; NationallizenzNationallizenz ; No Authors Fulltext ; SCOPUS ; Science Citation Index ; Science Citation Index Expanded ; Thomson Reuters Master Journal List ; Web of Science Core Collection
Click to display QR Code for this record

The record appears in these collections:
Document types > Articles > Journal Article
Institute Collections > JCNS > JCNS-1
Institute Collections > IBI > IBI-8
Institute Collections > IBI > IBI-7
Institute Collections > ZEA > ZEA-3
Workflow collections > Public records
ICS > ICS-1
ICS > ICS-6
Publications database

 Record created 2016-08-26, last modified 2024-06-19


Restricted:
Download fulltext PDF Download fulltext PDF (PDFA)
Rate this document:

Rate this document:
1
2
3
 
(Not yet reviewed)