4.7 Article

Synthesis and properties investigation of hydroxyl functionalized polyisoprene prepared by cobalt catalyzed co-polymerization of isoprene and hydroxylmyrcene

Journal

POLYMER CHEMISTRY
Volume 11, Issue 12, Pages 2034-2043

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9py01808e

Keywords

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Funding

  1. Natural Science Foundation of China [21304050, 21971130]
  2. Natural Science Foundation of Zhejiang Province [Y19B040010]
  3. Key Laboratory of Urban Environment and Health, Institute of Urban Environment, Chinese Academy of Sciences [NUEORS201807]
  4. Open Research Fund of State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences [2019-11]
  5. K. C. Wong Magna Fund of Ningbo University

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The intrinsic hydrophobicity of rubber matrices renders compatibility with polar fillers rather difficult in most cases. In this manuscript, a cobalt complex supported by a 2-oxazoline-pyridine ligand armed with a labile 6-(di-tert-butyl-phosphine oxide) moiety is prepared and characterized. In combination with excess AlEt2Cl, the precursor actively copolymerizes isoprene with the bio-sourced myrcene derivative 2-methyl-6-methyleneoct-7-en-3-ol with adjustable comonomer incorporation from 4.4 mol% to 31.5 mol%. The presence of hydroxyl functionalized polyisoprene was characterized by using Fourier transform infrared spectroscopy, H-1/C-13 NMR, and validated by the improved hydrophilicity, elevated glass transition temperature and microphase separation observed by AFM. Up to 30 wt% SiO2 loading can be individually dispersed in the 4.4 mol% hydroxyl functionalized polyisoprene copolymer with substantially reduced aggregation. The improved filler-polymer interfacial interactions via hydrogen bonds offer not only effective improvement of the tensile strength (9.6 +/- 0.2 MPa), but an unusual stretchability of over 885.3 +/- 2.0% and improved hysteresis loss with respect to pristine polyisoprene/SiO2 vulcanizates.

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