Stereochemical studies at the Herman F. Mark Polymer Research Institute

Mark M. Green

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Although stereochemistry plays a key role in the structure and function of biological polymers it was not until the discovery of isotactic polypropylene, now about 60 years ago, that the role of stereochemistry was seen to be of importance in synthetic polymers. Staudinger had predicted that although the nature of the bonding in small molecules and in macromolecules was identical, polymers would have special properties associated with the size of macromolecules. This article outlines how stereochemical studies demonstrate Staudinger's prescience in many ways. The story takes us from the tactic nature of vinyl polymers and their unrecognized and recognized chirality, to helicity, a characteristic shared by biological and certain synthetic polymers. There is an advantage to studying stereochemistry in synthetic polymers: their chiral characteristics can be manipulated in ways not possible in biological polymers, allowing discovery of new phenomena that cross boundaries outside of the polymer realm.

Original languageEnglish (US)
Title of host publicationHierarchical Macromolecular Structures
Subtitle of host publication60 Years After The Staudinger Nobel Prize I
PublisherSpringer New York LLC
Pages263-270
Number of pages8
ISBN (Print)9783319011363
DOIs
StatePublished - 2013

Publication series

NameAdvances in Polymer Science
Volume261
ISSN (Print)0065-3195

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Keywords

  • Chirality
  • Helix
  • Macromolecules
  • Mark
  • Polymers
  • Staudinger
  • Stereochemistry
  • Tactic polymers

ASJC Scopus subject areas

  • Chemical Engineering(all)
  • Organic Chemistry
  • Polymers and Plastics

Cite this

Green, M. M. (2013). Stereochemical studies at the Herman F. Mark Polymer Research Institute. In Hierarchical Macromolecular Structures: 60 Years After The Staudinger Nobel Prize I (pp. 263-270). (Advances in Polymer Science; Vol. 261). Springer New York LLC. https://doi.org/10.1007/12_2013_270