Syntheses of 2-phenyl-3-vinyloxirane derivatives that undergo radical ring-opening polymerization
Abstract
Abstract 2‐Phenyl‐3‐vinyloxirane derivatives that undergo radical ring‐opening polymerization were prepared from allyl bromide and corresponding aldehydes. The difunctional monomers containing vinyloxirane structure were also synthesized from dialdehydes such as isophthalaldehyde and terephthalaldehyde. The obtained monomers undertook the radical isomeric polymerization to obtain the corresponding polymers.
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Vinyl oxiranes yield polyethers via ROP.
“Vinyl oxiranes yield polyethers via ROP [12 -14] (see Figure 3).”
From Ring-Opening Polymerization—An Introductory Review (2013) · cites this paper as [14]
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References 8 · Cited by 34
- Authors
- Endo, T., & Kanda, N.
- Affiliations
- Tokyo Institute of Technology (JP)
- Venue
- Journal of Polymer Science: Polymer Chemistry Edition
- Publisher
- Wiley
- Published
- 1985-07
- Volume
- 23
- Issue
- 7
- Pages
- 1931-1938
- ISSN
- 0360-6376 (ISSN-L)
- 1542-9369
- OpenAlex
- W2025447447
- Cited by
- 34
- References
- 8
- Citations by year
- 2026: 2 · 2018: 1 · 2017: 2 · 2016: 2 · 2015: 1 · 2014: 1 · 2013: 1 · 2012: 1
- FWCI
- 1.14
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Polymer Science Polymer Chemistry Edition (publishedVersion)
- Topics
- Physical Sciences › Chemistry › Organic Chemistry › Advanced Polymer Synthesis and Characterization
- Physical Sciences › Materials Science › Polymers and Plastics › Polymer Synthesis and Characterization
- Physical Sciences › Chemistry › Organic Chemistry › Photopolymerization techniques and applications
- Keywords
- radical ring-opening polymerization, allyl bromide, aldehydes, dialdehydes, isophthalaldehyde, terephthalaldehyde, difunctional monomers, polymer synthesis
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