Noncovalent synthesis of melamine-cyanuric/barbituric acid derived nanostructures: Regio- and stereoselection

Citation
P. Timmerman et Lj. Prins, Noncovalent synthesis of melamine-cyanuric/barbituric acid derived nanostructures: Regio- and stereoselection, EUR J ORG C, (17), 2001, pp. 3191-3205
Citations number
44
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
ISSN journal
1434193X → ACNP
Issue
17
Year of publication
2001
Pages
3191 - 3205
Database
ISI
SICI code
1434-193X(200109):17<3191:NSOMAD>2.0.ZU;2-D
Abstract
The hydrogen bond directed self-assembly of calix[4]arene dimelamines and b arbituric or cyanuric acid derivatives gives ready access to organic nanost ructures of nanometer dimensions. The synthesis, characterization, and supr amolecular chirality of these noncovalent assemblies are discussed in detai l, together with means of achieving regio-, diastereo-, and enantioselectio n. Self-organizing behaviour into higher order aggregates on solid surfaces is also described.