Journal
MACROMOLECULES
Volume 53, Issue 13, Pages 5096-5104Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.macromol.0c00253
Keywords
-
Categories
Funding
- National Natural Science Foundation of the People's Republic of China [21674037]
- National Key Research and Development Program [2016YFC1100703]
- Natural Science Foundation of Shanghai [18ZR1410200]
- Science and Technology Commission of Shanghai Municipality [18JC1410802]
Ask authors/readers for more resources
gamma-Amide-e-caprolactones including 7-oxo-N-propyloxepane-4-carboxamide (NNCL), N-isopropyl-7-oxooxepane-4-carboxamide (NICL), N,N-diethyl-7-oxooxepane-4-carboxamide (DECL), and 5-(pyrrolidine-1-carbonyl)oxepan-2-one (VPyCL) were initially designed and synthesized to achieve biodegradable and thermosensitive materials. Ring-opening polymerization (ROP) of these newly developed caprolactones was thoroughly investigated by both theoretical calculation and experimental verification. Density functional theory revealed that the ring-opening enthalpy of gamma-amide-epsilon-caprolactones was more negative than that of gamma-estere-caprolactone (EMCL). Experimental results showed that ROP of NICL, DECL, and VPyCL catalyzed by 1,5,7-triazabicyclo[4.4.0]dec-5-ene with benzyl alcohol (BnOH) as an initiator underwent in a living and controlled manner, while that of NNCL and EMCL did not. Computational calculation consistently proved that a variety of substitutions greatly affected the ROP process. PNICL, PDECL, and PVPyCL exhibited reversible lower critical solution temperature-type phase transitions tuned by manipulating the feed ratio and hydrophilicity of comonomers. Furthermore, poly(gamma-amide-epsilon-caprolactone)s with excellent biodegradability and biocompatibility were demonstrated as an enzyme activity regulator, holding great promise for smart biomaterial application.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available