13C NMR spectra of linear trimers of buta‐1,3‐diene obtained from the Ziegler–Natta process

A. V. Lubnin, I. S. Podkorytov, L. S. Bresler

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Titanium‐based Ziegler–Natta catalysts for the polymerization of buta‐1,3‐diene give linear trimers of butadiene among other by‐products. A combination of 1H and 13C NMR, DEPT and 2D‐INADEQUATE gives exhaustive assignments of their 13C NMR spectra and affords their structures. All these trimers are dodeca‐2,4,6,10‐tetraenes which have an isolated cis double bond. The internal double bond of the conjugated triad has a trans configuration in each isomer, and the trimers differ only in the outer double bonds. The 13C NMR spectra of the timers reveal that the signal position of the carbon involved in the conjugated double bond series is mainly controlled by the configuration of the adjacent double bond and, to a lesser extent, by the geometry of its own double bond. The oligomers studied serve as models for polyacetylene. Some reassignments in the spectra of oligomers of terminal acetylenes are proposed.

Original languageEnglish
Pages (from-to)847-849
Number of pages3
JournalMagnetic Resonance in Chemistry
Volume30
Issue number9
DOIs
StatePublished - Sep 1992

Scopus subject areas

  • Chemistry(all)
  • Materials Science(all)

Keywords

  • C NMR spectroscopy
  • 2D‐INADEQUATE
  • Buta‐1,3‐diene
  • Oligomers
  • Polyacetylene
  • Ziegler–Natta catalysis

Fingerprint

Dive into the research topics of '<sup>13</sup>C NMR spectra of linear trimers of buta‐1,3‐diene obtained from the Ziegler–Natta process'. Together they form a unique fingerprint.

Cite this