Non-covalent synthesis of organic nanostructures

Share/Save/Bookmark

Prins, Leonard J. and Timmerman, Peter and Reinhoudt, David N. (1998) Non-covalent synthesis of organic nanostructures. Pure and Applied Chemistry, 70 (8). pp. 1459-1468. ISSN 0033-4545

open access
[img]
Preview
PDF
759kB
Abstract:This review describes the synthesis, characterization and functionalization of hydrogen bonded, box-like assemblies. These assemblies are formed upon mixing bismelamine calix[4]arenes with a complementary barbiturate in apolar solvents. Various techniques for the characterization have been used, like 'H NMR spectroscopy, X-ray crystallography and a novel MALDI-TOF MS technique. The use of cyanurates instead of barbiturates results in the formation of three conformational isomers. The ratio in which these assemblies are formed depends on the N-substituent of the cyanurate. Substituting the bismelamine calix[4]arenes with a variety of functional groups enables the formation of assemblies in which functionalities are gathered around a box-like cavity. Mixing these homomeric assemblies creates a dynamic combinatorial library of heteromeric assemblies.
Item Type:Article
Additional information:Plenary lecture presented at the 12th International Conference on Organic Synthesis (ICOS-12), Venice, Italy, 28 June–2 July 1998
Copyright:© 1998 IUPAC
Research Group:
Link to this item:http://purl.utwente.nl/publications/11050
Official URL:http://www.iupac.org/publications/pac/70/8/1459/
Export this item as:BibTeX
EndNote
HTML Citation
Reference Manager

 

Repository Staff Only: item control page

Metis ID: 105969