4.7 Article

Facile Synthesis of Clickable, Water-Soluble, and Degradable Polyphosphoesters

Journal

ACS MACRO LETTERS
Volume 1, Issue 2, Pages 328-333

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/mz200226m

Keywords

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Funding

  1. National Heart Lung and Blood Institute of the National Institutes of Health [HHSN268201000046C]
  2. National Science Foundation [DMR-0906815, DMR-1105304]
  3. Welch Foundation [A-0001]
  4. Division Of Materials Research
  5. Direct For Mathematical & Physical Scien [0906815] Funding Source: National Science Foundation

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Click chemistry is a library of efficient and reliable reactions, which have been used to functionalize various classes of bio- and synthetic macromolecular systems for the incorporation of designed properties and functions. In this report, azide-alkyne Huisgen cycloaddition and thiol-yne reactions, two classical click chemistries, were employed to functionalize biodegradable, clickable polyphosphoester homopolymers, and their water-soluble copolymers. A stable alkyne-functionalized phospholane monomer was synthesized, its organocatalyzed polymerization kinetics were evaluated, and the resulting (co)polymers were utilized to develop this facile method that provides the synthesis of clickable, water-soluble, and degradable polyphosphoesters, which can be adapted for various applications.

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