Journal article
Entrapment of ferrocenes within supramolecular, deep-cavity resorcin[4]arenes
Chemical communications (Cambridge, England), Vol.2000(6), pp.517-518
2000
DOI: 10.1039/a909745g
Abstract
Using a template-based method to molecular self-assembly, the ability of ferrocene (FcH) and two of its acetylated derivatives [FcAc, 1,1′-Fc(Ac)2] to induce formation of a supramolecular deep cavity based upon C-methylcalix[4]resorcinarene 1 and 4,4′-bipyridine 2, 1·2(2), 3, is revealed; equatorial inclusion of 1,1′-Fc(Ac)2 within 3 promotes a change in conformation of the guest.
Details
- Title: Subtitle
- Entrapment of ferrocenes within supramolecular, deep-cavity resorcin[4]arenes
- Creators
- Leonard R MacGillivrayHeather A SpinneyJennifer L ReidJohn A Ripmeester
- Resource Type
- Journal article
- Publication Details
- Chemical communications (Cambridge, England), Vol.2000(6), pp.517-518
- DOI
- 10.1039/a909745g
- NLM abbreviation
- Chem Commun (Camb)
- ISSN
- 1359-7345
- eISSN
- 1364-548X
- Publisher
- Royal Society of Chemistry
- Language
- English
- Date published
- 2000
- Academic Unit
- Pharmaceutical Sciences and Experimental Therapeutics; Chemistry
- Record Identifier
- 9984216722102771
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