Photoinitiated free radical polymerization using benzoxazines as hydrogen donors

M. Atilla Tasdelen, Baris Kiskan, Yusuf Yagci*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

87 Citations (Scopus)

Abstract

Free radical polymerization of methyl methacrylate (MMA) is initiated upon irradiation at λ > 350 nm in CH2Cl2 that contains benzoxazine (P-a) and one of the following photosensitizers: benzophenone (BP), thioxanthone (TX), 2-chlorothioxanthone (CTX), 2-isopropyl thioxanthone (ITX), and camphorquinone (CQ). The postulated mechanism is based on the intermolecular reaction of the excited photosensitizer with the tertiary amino moiety of the ground state P-a and a subsequent hydrogen abstraction reaction. The resulting aminoalkyl radicals initiate the poly-merization. The incorporation of P-a groups into polymers is demonstrated by spectroscopic methods. The possibility of deep curing using the described photoinitiating system followed by the thermal ring opening of the incorporated P-a groups is also demonstrated.

Original languageEnglish
Pages (from-to)1539-1544
Number of pages6
JournalMacromolecular Rapid Communications
Volume27
Issue number18
DOIs
Publication statusPublished - 22 Sept 2006

Keywords

  • Benzoxazine
  • Hydrogen abstraction
  • Photopolymerization
  • Ring opening polymerization

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