Please use this identifier to cite or link to this item:
|Title:||Synthesis, characterization, and application of cationic water-soluble oligofluorenes in DNA-hybridization detection|
|Authors:||Liu, B. |
Fluorescence resonance energy transfer (FRET)
|Citation:||Liu, B., Dishari, S.K. (2008-08-18). Synthesis, characterization, and application of cationic water-soluble oligofluorenes in DNA-hybridization detection. Chemistry - A European Journal 14 (24) : 7366-7375. ScholarBank@NUS Repository. https://doi.org/10.1002/chem.200701906|
|Abstract:||A simple and efficient approach was developed for the synthesis of a series of cationic water-soluble oligofluorenes up to a chain length of a heptamer. Bromoalkyl-substituted fluorenyl boronic esters as the key intermediates were synthesized by using a modified Miyaura reaction. With an increasing number of repeat units (trimer to hexamer), the size-specific oligomers have shown redshifts in both the absorption and emission maxima. The emission maximum reaches the limit for the hexamer in both water and buffer solution. The quantum yields of the oligomers decreased with increased oligomer size in water. Both fluorescence quenching of the oligomers by 9,10-anthraquinone-2,6-disulfonate and the fluorescence resonance energy transfer experiments with the oligomers as the donor and fluorescein (Fl)-labeled double-stranded DNA (dsDNA-Fl) as the acceptor revealed the chain-length-dependent behavior. The Stern-Volmer quenching constant increased with the molecular size, whereas the highest donor-sensitized Fl emission was observed for the hexamer. These size-specific oligomers also served as a model to study the structure-property relationships for cationic polyfluorenes. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA,.|
|Source Title:||Chemistry - A European Journal|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Jul 16, 2018
WEB OF SCIENCETM
checked on Jun 20, 2018
checked on Jun 29, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.