File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Nanoscale borromeates

TitleNanoscale borromeates
Authors
Issue Date2005
Citation
Journal of Organic Chemistry, 2005, v. 70, n. 20, p. 7956-7962 How to Cite?
AbstractIn addition to a parent zinc(II) Borromean ring (BR) complex, the preparation and characterization of two hexasubstituted BR complexes with either 4-acetoxymethylphenyl or 4-methylthiophenyl substituents associated in turn with all six pyridyl rings has been achieved convergently in good yields by appealing to the dynamic features of the reactions between primary amino groups in a preformed acyclic ligand and 2,6-diformylpyridine. Two molecules of the acyclic ligands react with two molecules of 2,6-diformylpyridine to form a cyclic [2 + 2] tetraimine in the presence of Zn(II) ions as templates in 2-propanol at 70 °C. The successful preparation of the two derivatives by convergent template-directed syntheses opens up opportunities to self-assemble, under equilibrium control, numerous nanoscale metallo-organic particles with potentially useful properties. © 2005 American Chemical Society.
Persistent Identifierhttp://hdl.handle.net/10722/332626
ISSN
2021 Impact Factor: 4.198
2020 SCImago Journal Rankings: 1.200
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChichak, Kelly S.-
dc.contributor.authorPeters, Andrea J.-
dc.contributor.authorCantrill, Stuart J.-
dc.contributor.authorStoddart, J. Fraser-
dc.date.accessioned2023-10-06T05:13:00Z-
dc.date.available2023-10-06T05:13:00Z-
dc.date.issued2005-
dc.identifier.citationJournal of Organic Chemistry, 2005, v. 70, n. 20, p. 7956-7962-
dc.identifier.issn0022-3263-
dc.identifier.urihttp://hdl.handle.net/10722/332626-
dc.description.abstractIn addition to a parent zinc(II) Borromean ring (BR) complex, the preparation and characterization of two hexasubstituted BR complexes with either 4-acetoxymethylphenyl or 4-methylthiophenyl substituents associated in turn with all six pyridyl rings has been achieved convergently in good yields by appealing to the dynamic features of the reactions between primary amino groups in a preformed acyclic ligand and 2,6-diformylpyridine. Two molecules of the acyclic ligands react with two molecules of 2,6-diformylpyridine to form a cyclic [2 + 2] tetraimine in the presence of Zn(II) ions as templates in 2-propanol at 70 °C. The successful preparation of the two derivatives by convergent template-directed syntheses opens up opportunities to self-assemble, under equilibrium control, numerous nanoscale metallo-organic particles with potentially useful properties. © 2005 American Chemical Society.-
dc.languageeng-
dc.relation.ispartofJournal of Organic Chemistry-
dc.titleNanoscale borromeates-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/jo050969b-
dc.identifier.scopuseid_2-s2.0-25444487281-
dc.identifier.volume70-
dc.identifier.issue20-
dc.identifier.spage7956-
dc.identifier.epage7962-
dc.identifier.isiWOS:000232166800017-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats