1. Modification of Poly(maleic anhydride)-Based Polymers with H2N–R Nucleophiles: Addition or Substitution Reaction?
- Author
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Liang Du, Chengqi Zhang, Wentao Wang, Yuya Sugiyama, Hedi Mattoussi, Zhicheng Jin, Goutam Palui, and Sisi Wang
- Subjects
Pharmacology ,chemistry.chemical_classification ,Substitution reaction ,Addition reaction ,010405 organic chemistry ,Organic Chemistry ,Biomedical Engineering ,Pharmaceutical Science ,Maleic anhydride ,Bioengineering ,02 engineering and technology ,Polymer ,021001 nanoscience & nanotechnology ,01 natural sciences ,0104 chemical sciences ,chemistry.chemical_compound ,Thionyl chloride ,chemistry ,Nucleophile ,Polymer chemistry ,Copolymer ,0210 nano-technology ,Imide ,Biotechnology - Abstract
Reacting poly(maleic anhydride)-based polymers with H2N–R nucleophiles is a flexible and highly effective approach for preparing a variety of multifunctional, multicoordinating, and multireactive polymers. The exact transformation of the anhydride ring during this addition reaction is still an open question. In this report, we characterize the transformation of a representative block copolymer, poly(isobutylene-alt-maleic anhydride), with a few H2N–R nucleophiles. In particular, we test the effects of varying a few reaction parameters/conditions (e.g., temperature, solvent, reaction time, and addition of thionyl chloride) on the nature of the anhydride transformation and bond formed between the polymer and the lateral R groups. The resulting polymers are characterized using a combination of analytical techniques including FT-IR, one- and two-dimensional NMR, and gel electrophoresis. We find that the ring opening transformation occurs under mild conditions. Conversely, cyclic imide transformation can take ...
- Published
- 2019