Controlled Ring-Opening Polymerization: Polymers with designed Macromolecular Architecture
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- 15 February 2002
- book chapter
- Published by Springer Nature
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This publication has 114 references indexed in Scilit:
- Ring strain and polymerizability of cyclic estersPolymer, 1998
- End-functionalized poly(ϵ-caprolactone) oligomers through heterogeneous catalysis in protic conditions: a mechanistic approachPolymer, 1997
- Polylactones. 35. Macrocyclic and Stereoselective Polymerization of .beta.-D,L-Butyrolactone with Cyclic Dibutyltin InitiatorsMacromolecules, 1995
- (Co)polymers of L‐lactide, 1. Synthesis, thermal properties and hydrolytic degradationMacromolecular Chemistry and Physics, 1994
- Syndiospecific ring-opening polymerization of .beta.-butyrolactone to form predominantly syndiotactic poly(.beta.-hydroxybutyrate) using tin(IV) catalystsMacromolecules, 1993
- Synthesis and some properties of isomorphic copolymers of ϵ‐caprolactone and 1,5‐dioxepan‐2‐oneJournal of Polymer Science Part A: Polymer Chemistry, 1989
- Polymerization of Cyclic Esters, Urethans, Ureas and ImidesJournal of the American Chemical Society, 1958
- STUDIES OF POLYMERIZATION AND RING FORMATION. X. THE REVERSIBLE POLYMERIZATION OF SIX-MEMBERED CYCLIC ESTERSJournal of the American Chemical Society, 1932
- STUDIES ON POLYMERIZATION AND RING FORMATION. VI. ADIPIC ANHYDRIDEJournal of the American Chemical Society, 1930
- STUDIES ON POLYMERIZATION AND RING FORMATION. III. GLYCOL ESTERS OF CARBONIC ACIDJournal of the American Chemical Society, 1930