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Fluoride‐Triggered Self‐Degradation of Poly(2,4‐disubstitued 4‐hydroxybutyric acid) Derivatives
Author(s) -
Kan XiaoWei,
Zhang LiJing,
Li ZhaoYue,
Du FuSheng,
Li ZiChen
Publication year - 2021
Publication title -
macromolecular rapid communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 154
eISSN - 1521-3927
pISSN - 1022-1336
DOI - 10.1002/marc.202100169
Subject(s) - depolymerization , polymer chemistry , chemistry , ethylene glycol , aldehyde , polymer , ether , fluoride , dimer , isocyanide , silyl ether , polyester , polymerization , end group , acetal , organic chemistry , silylation , inorganic chemistry , catalysis
Self‐immolative polymers are a special kind of degradable polymers that depolymerize into small molecules through a cascade of reactions upon stimuli‐triggered cleavage of the polymer chain ends. This work reports the design and synthesis of a fluoride‐triggered self‐immolative polyester. A 2,4‐disubstitued 4‐hydroxy butyrate is first confirmed to quickly cyclize in solution to form a γ −butyrolactone derivative. Then, the Passerini three component reaction (P‐3CR) of an AB dimer (A: aldehyde, B: carboxylic acid) with tert ‐butyl isocyanide or oligo(ethylene glycol) isocyanide affords two poly(2,4‐disubstitued 4‐hydroxybutyrate) derivatives ( P2 and P3 ). Two silyl ether end‐capped polymers ( P4 and P5 ) are abtained from P2 and P3 , and their degradation in solution is examined by NMR spectrum and size exclusion chromatography. Polymers P4 and P5 are stable in the absence of tetrabutylammonium fluoride (TBAF), while in the presence of TBAF, the molar masses of P4 and P5 gradually decrease with time together with the increase of the amount of formed 2,4‐disubstitued γ ‐butyrolactone. The depolymerization mechanism is proposed. The first step is the fast removal of the silyl ether by fluoride. Then, the released hydroxyl group initiates the quick head‐to‐tail depolymerization of the polyester via intramolecular cyclization.