Photoinduced synthesis of oligoesters

Volkan Kumbaraci, Naciye Talinli*, Yusuf Yagci

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

39 Citations (Scopus)

Abstract

For the first time, a true step-growth polymerization, i.e, polyesterification, was achieved by a photochemical means. Thus, heterobifunctional monomers, namely benzodioxinone and naphthodioxinone compounds possessing both chromophoric and aliphatic hydroxyl groups in the structure (HDPD and HDNP, respectively), were synthesized by a ring closure and subsequent etherification processes and characterized. Photolysis of these compounds in CH2Cl2 at λiinc = 300 nm yielded oligoesters with narrow molecular weight distribution. In the case of HDNP, photolysis can be performed at higher wavelengths, e.g., at λinc = 350 nm, because of the extended absorption introduced by the naphthalene ring. The structure of the photochemically formed oligoester was confirmed by FT-IR and 1H NMR spectral measurements.

Original languageEnglish
Pages (from-to)6031-6035
Number of pages5
JournalMacromolecules
Volume39
Issue number18
DOIs
Publication statusPublished - 5 Sept 2006

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