Publication Type : Journal Article
Publisher : Journal of Organometallic Chemistry
Source : Journal of Organometallic Chemistry, Volume 689, Number 25, p.4791 - 4802 (2004)
Url : http://www.sciencedirect.com/science/article/pii/S0022328X04007454
Keywords : Bioorganometallic chemistry
Campus : Coimbatore
School : School of Engineering
Department : Chemistry, Sciences
Year : 2004
Abstract : pA new chiral ferrocene-labelled tyrosine PNA monomernbsp;1nbsp;has been synthesised in good yield in both racemic and enantiomerically pure forms. It is suitable for insertion in various positions of PNA oligomers, a possibility that has been preliminarily demonstrated by synthesising the dimernbsp;16.nbsp;Moreover, in view of possible applications to nucleic acid detection, a preliminary voltammetric investigation on the electrochemical activity of monomernbsp;1nbsp;and its synthetic precursors has been carried out in DMF. It appears that, despite the bulkiness of the PNA monomer backbone, its insertion on the ferrocene group only moderately lowers the latter’s diffusion coefficients and peak currents, thus affording voltammetric detection limits in the order of 10−6–10−7 M./p
Cite this Research Publication : C. Baldoli, Falciola, L., Licandro, E., Maiorana, S., Mussini, P., Dr. Prasanna Ramani, Rigamonti, C., and Zinzalla, G., “A new ferrocene conjugate of a tyrosine PNA monomer: synthesis and electrochemical properties”, Journal of Organometallic Chemistry, vol. 689, pp. 4791 - 4802, 2004.