Molecules 2012, 17(10), 12061-12071; doi:10.3390/molecules171012061
Article

Synthesis and Photophysical Study of 2′-Deoxyuridines Labeled with Fluorene Derivatives

1email, 2,* email and 1,* email
Received: 14 September 2012; in revised form: 3 October 2012 / Accepted: 10 October 2012 / Published: 15 October 2012
(This article belongs to the Special Issue Nucleic Acid Analogs)
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.
Abstract: We examined microenvironment-sensitive fluorescent 2′-deoxyuridines labeled with fluorene derivatives that exhibited solvent-dependent photophysical properties. The high sensitivity of the fluorescence shift and the nucleoside intensity dependence on solvent polarity provided information useful for estimating the polarity of the environment surrounding the fluorescent nucleoside.
Keywords: nucleosides; fluorene; fluorescence; dibenzofuran; dibenzothiophene
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MDPI and ACS Style

Cho, H.Y.; Woo, S.K.; Hwang, G.T. Synthesis and Photophysical Study of 2′-Deoxyuridines Labeled with Fluorene Derivatives. Molecules 2012, 17, 12061-12071.

AMA Style

Cho HY, Woo SK, Hwang GT. Synthesis and Photophysical Study of 2′-Deoxyuridines Labeled with Fluorene Derivatives. Molecules. 2012; 17(10):12061-12071.

Chicago/Turabian Style

Cho, Hyun Y.; Woo, Sang K.; Hwang, Gil T. 2012. "Synthesis and Photophysical Study of 2′-Deoxyuridines Labeled with Fluorene Derivatives." Molecules 17, no. 10: 12061-12071.

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