Sample Originator: J. H. R. Tucker, Mark E. Light, Michael B. Hursthouse, S. J. Green, G. Gasser, S. R. Collinson, Simon J. Coles and J. Westwood.


Identification Number:10.5258/ecrystals/83
Date Created:26 October 2000
Deposited On:21 Jan 2008 15:28
Deposited By:A.N. Admin

Depositor Comments

A series of ferrocene-containing amidopyridyl receptors, in two regioisomeric forms (1,1' and 1,3), have been shown to bind cyclic organic molecules in chloroform through complementary hydrogen-bonding interactions. Complexation was monitored by NMR spectroscopy and by cyclic voltammetry. The magnitude of the host-guest binding strength and the redox response to complexation depend on both the type and the relative position of the amidopyridyl groups on the cyclopentadienyl rings of the ferrocene.

Data collection parameters

Chemical formula
Crystal morphology
Crystal system
Space group symbol
Cell length a
Cell length b
Cell length c
Cell angle alpha
Cell angle beta
Cell angle gamma
Data collection temperature

Refinement results

Solution figure of merit
R Factor (Obs)
R Factor (All)
Weighted R Factor (Obs)
Weighted R Factor (All)

Citation: Tucker, J. H. R. and Light, Mark E. and Hursthouse, Michael B. and Green, S. J. and Gasser, G. and Collinson, S. R. and Coles, Simon J. and Westwood, J. (2000) University of Southampton, Crystal Structure Report Archive. (doi:10.5258/ecrystals/83)
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