Cultural advice

The Australian National University acknowledges, celebrates and pays our respects to the Ngunnawal and Ngambri people of the Canberra region and to all First Nations Australians on whose traditional lands we meet and work, and whose cultures are among the oldest continuing cultures in human history.

Aboriginal and Torres Strait Islander peoples are advised that ANU Library collections may include images, names, voices, and other representations of deceased persons.

Material in the collection may contain terms, language or views that reflect the period in which the item was created and may be considered inappropriate today.

Synthesis and conformational analysis of an a-cyclodextrin [2]-rotaxane

Thumbnail Image

Date

1999

Authors

Easton, Christopher
Lincoln, Stephen F
Meyer, Adam G
Onagi, Hideki

Journal Title

Journal ISSN

Volume Title

Publisher

Royal Society of Chemistry

Abstract

An a-cyclodextrin [2]-rotaxane has been prepared in 10% yield, by threading a-cyclodextrin (a-CD) with (£)-4, 4'diaminostilbene in aqueous solution and capping the included guest through reaction with 2, 4, 6-trinitrobenzene-lsulfonate. ID 'H NMR spectro

Description

Keywords

Citation

URI

http://hdl.handle.net/1885/93776

Collections

ANU Research Publications

Source

Royal Chemical Society Journal Perkin Transactions

Type

Journal article

Book Title

Entity type

Access Statement

License Rights

DOI

Restricted until

DSpace software copyright © 2002-2026 LYRASIS