Syntheses of a series of electron donor and electron acceptor derivatives

Article abstract of DOI:10.1080/00397919308011221

New electron donor and electron acceptor compounds have been prepared suitable for direct covalent attachment to a photosensitizer or other synthetic subunit. In each case, a saturated three-carbon chain separates a reactive functional group (an alkyl bromide, an amine, or an alcohol) from the electron donor (a phenylenediamine) or electron acceptor (a viologen).

Full text of DOI:10.1080/00397919308011221

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Syntheses of a Series of
Electron Donor and Electron
Acceptor Derivatives
Christoph Hoefler a , Nadeem A. Kizilbash a & Carl C.
Wamser a
a Department of Chemistry , Portland State
University , Portland, Oregon, 97207-0751, U.S.A.
Published online: 24 Sep 2006.
To cite this article: Christoph Hoefler , Nadeem A. Kizilbash & Carl C. Wamser (1993)
Syntheses of a Series of Electron Donor and Electron Acceptor Derivatives, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 23:9, 1339-1349, DOI: 10.1080/00397919308011221
To link to this article: http://dx.doi.org/10.1080/00397919308011221
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