Self-assembly and macromolecular design

David B. Amabilino, J. Fraser Stoddart

Research output: Contribution to journalArticlepeer-review

56 Scopus citations

Abstract

The viability of self-assembly as a new concept for the synthesis of novel materials is being vindicated by the creation of increasingly complicated molecular and supramolecular architectures. The extrapolation from alternating donor/acceptor stacks of aromatic rings in the solid state to polycatenanes, polyrotaxanes and double helices in the solution state requires the precise control of molecular recognition processes. This precision is demonstrated by the template-directed synthesis of a wide range of catenanes and rotaxanes. It emerges that, provided the building blocks contain enough molecular information to induce formation of continuously ordered stacks in the crystalline state, then it is possible to exploit this “intelligence” in the self-assembly of exotic macromolecules and polymeric supermolecules in solution.

Original languageEnglish (US)
Pages (from-to)2351-2359
Number of pages9
JournalPure and Applied Chemistry
Volume65
Issue number11
DOIs
StatePublished - Jan 1 1993

ASJC Scopus subject areas

  • Chemistry(all)
  • Chemical Engineering(all)

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