Issue 17, 2013

Ferrocenyl substituted calixarenes: synthesis, structure and properties

Abstract

A set of ferrocenyl substituted calix[4]arenes were designed and synthesized by the Pd-catalyzed Sonogashira cross coupling reaction. The photophysical and electrochemical data show a substantial electronic interaction between the ferrocene unit and the calixarene core. Calixarenes 5a–5c are non-emissive in nature and the absorption maxima of 5a–5c exhibit a red shifted absorption. The calixarene core exhibits a cone conformation, which was confirmed by 1H NMR and X-ray crystallography. The crystal packing of 5a exhibits a C–H–π bonded 2-D network.

Graphical abstract: Ferrocenyl substituted calixarenes: synthesis, structure and properties

Supplementary files

Article information

Article type
Communication
Submitted
10 Jan 2013
Accepted
19 Feb 2013
First published
20 Feb 2013

RSC Adv., 2013,3, 5785-5788

Ferrocenyl substituted calixarenes: synthesis, structure and properties

R. Sharma, R. Margani, S. M. Mobin and R. Misra, RSC Adv., 2013, 3, 5785 DOI: 10.1039/C3RA00146F

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