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A correction was published on 10 March 2014, see Int. J. Mol. Sci. 2014, 15(3), 4255-4256.

Int. J. Mol. Sci. 2013, 14(4), 7468-7479; doi:10.3390/ijms14047468
Article

Synthesis and Characterization of Naphthalenediimide-Functionalized Flavin Derivatives

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1,*  and 2,*
1 Glasgow Centre for Physical Organic Chemistry, WestCHEM, School of Chemistry, University of Glasgow, Glasgow G12 8QQ, UK 2 Department of Chemistry, University of Massachusetts, Amherst, MA 01003, USA
* Authors to whom correspondence should be addressed.
Received: 19 February 2013 / Revised: 22 March 2013 / Accepted: 26 March 2013 / Published: 3 April 2013
(This article belongs to the Special Issue Flavins)
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Abstract

Two acceptor–acceptor dyads have been synthesized featuring a flavin moiety and a naphthalenediimide (NDI) unit. The NDI unit is linked to the flavin through a short spacer group via either the N(3) or N(10) positions of the flavin. We have investigated the UV-Vis and redox properties of these multi-electron accepting systems which indicate that these materials display the collective properties of their component systems. Fluorescence spectroscopy measurements have revealed that their emission properties are dominated by the flavin unit.
Keywords: flavin; naphthalenediimide; redox; optical flavin; naphthalenediimide; redox; optical
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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    Correction (PDF, 150 KB)

    A correction was published on 10 March 2014 http://www.mdpi.com/1422-0067/15/3/4255

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Zainalabdeen, N.; Fitzpatrick, B.; Kareem, M.M.; Nandwana, V.; Cooke, G.; Rotello, V.M. Synthesis and Characterization of Naphthalenediimide-Functionalized Flavin Derivatives. Int. J. Mol. Sci. 2013, 14, 7468-7479.

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