期刊
JOURNAL OF ORGANOMETALLIC CHEMISTRY
卷 693, 期 7, 页码 1177-1185出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jorganchem.2008.01.011
关键词
ferrocenylnaphthalene diimide; double stranded DNA; binding parameter; electrochemical gene detection
Ferrocenylnaphthalene diimide ligands 1-7 were synthesized by joining a piperazino or N-methylamino linker of the naphthalene diimide skeleton with ferrocenecarboxylic, ferroceneacetic, or ferrocenepropionic parts. Their interaction with double stranded DNA (dsDNA) was studied kinetically and electrochemically. Association rate constants of these ligands were found to correlate with their intramolecular stacking ability between the ferrocene and naphthalene diimide planes: ligands which can adopt a stacked conformation in buffer solution were unfavorable in the association with dsDNA, resulting in a smaller association rate constant. Dissociation rate constants of these ligands carrying the bulky piperazino linker were smaller than that of those carrying an N-methylamino one. Binding constants were dictated by the balance of these two factors. These ligands were applied to the electrochemical detection of the amount of dsDNA on the electrode. Ligand 6 having the highest affinity for dsDNA gave rise to the largest current increase upon dsDNA formation in the electrochemical hybridization assay. (C) 2008 Elsevier B.V. All rights reserved.
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