Direct synthesis of tetrazine functionalities on polymer backbones


Kara S. S. , Ates M. Y. , Deveci G., Cetinkaya A., Kahveci M. Ü.

JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, cilt.57, ss.673-680, 2019 (SCI İndekslerine Giren Dergi) identifier identifier

  • Cilt numarası: 57 Konu: 6
  • Basım Tarihi: 2019
  • Doi Numarası: 10.1002/pola.29308
  • Dergi Adı: JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
  • Sayfa Sayıları: ss.673-680

Özet

Tetrazine mediated inverse Electron Demand Diels-Alder Reaction (IEDDA) is an important modification technique due to its high selectivity and super-fast kinetics. Incorporation of tetrazine moieties on polymer chains requires multistep synthetic pathways and a post-polymerization step leading to functional polymeric materials. Such approaches involve separate syntheses of polymer and the molecule which will be employed in modification. Herein, we introduce a straightforward synthetic approach for direct synthesis of tetrazine groups on polymers as side chains. As model systems, tetrazine functional poly(N-isopropylacrylamide)-and poly(ethylene glycol)-based polymers from corresponding precursor polymers with nitrile moieties as pendant groups are prepared and IEDDA Click Reaction is achieved with trans-cyclooctene derivatives. The click reaction is monitored by both NMR and UV-vis spectroscopies. (c) 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019, 57, 673-680