
Journal of Organometallic Chemistry p. 27 - 40 (1997)
Update date:2022-08-05
Topics:
Butler
Hobson
Coles
Hursthouse
Malik, K. M. Abdul
The synthesis of a series of ferrocenylanthracene derivatives is described, utilising the palladium catalysed coupling reaction of 1,1′-bis(chlorozincio)ferrocene with halo-anthracenes. Bis-1,1′-(9-anthracenyl)ferrocene (1) was characterised by single crystal X-ray diffraction and shows an eclipsed ferrocenyl geometry. X-ray crystallographic studies indicate that there are no clear stacking interactions of either an intra-or intermolecular nature between the anthracenyl rings in the structure. A series of 9-and 10-disubstituted ferrocenylanthracene derivatives has also been prepared. In each case the palladium catalyst (Pd(dppf)Cl2) is recovered in a modified form, e.g. as the [(dppf)PdBr(9-anthracenyl)] complex in the synthesis of bis-1,1′-(9-anthracenyl)ferrocene. The single crystal X-ray structure of one such palladium complex [(dppf)PdBr-{9-(10-chloroanthracenyl)}] (15a) has been determined in a case where chloride/bromide exchange had occurred in the palladium complex intermediate. The potential application of compound 1 as synthon for the construction of a molecular sensing device is discussed. Cyclic voltammetry and fluorescence studies have been carried out for selected derivatives.
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Doi:10.1016/S0960-894X(98)00746-X
(1999)Doi:10.1016/j.jorganchem.2008.04.033
(2008)Doi:10.1055/s-1997-3250
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(2015)Doi:10.1021/ic970225j
(1997)Doi:10.1246/cl.1997.801
(1997)