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  5. Synthesis and photophysical evaluations of fluorescent quaternary bipyridyl-1,8-naphthalimide conjugates as nucleic acid targeting agents
 
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Synthesis and photophysical evaluations of fluorescent quaternary bipyridyl-1,8-naphthalimide conjugates as nucleic acid targeting agents

Author(s)
Ryan, Gary J.  
Elmes, Robert B.P.  
Quinn, Susan J.  
Gunnlaugsson, Thorfinnur  
Uri
http://hdl.handle.net/10197/4324
Date Issued
2012-01-16
Date Available
2013-05-16T10:51:21Z
Abstract
 A family of organic molecules containing the DNA intercalating chromophores, 4-nitro- and 4-amino 1,8-naphthalimide, conjugated to a diquat derivative by an ‘orthogonal’ phenyl spacer have been prepared and characterised. Their binding interactions with double-stranded DNA were studied by a variety of spectroscopic techniques. These charged organic compounds are found to exhibit excellent binding affinities to DNA with binding constants comparable to those exhibited by metal complexes.
Type of Material
Journal Article
Publisher
Taylor & Francis
Journal
Supramolecular Chemistry
Volume
24
Issue
3
Start Page
175
End Page
188
Copyright (Published Version)
2012, Taylor & Francis
Subjects

DNA probes

Naphthalimide

Fluorescence

Sensors

Supramolecular system...

DOI
10.1080/10610278.2011.638381
Language
English
Status of Item
Peer reviewed
This item is made available under a Creative Commons License
https://creativecommons.org/licenses/by-nc-nd/3.0/ie/
File(s)
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Name

2012_Ryan_Supramol.pdf

Size

1.07 MB

Format

Adobe PDF

Checksum (MD5)

7e3cd642b24f156f3b24e47d052e37ec

Owning collection
Chemistry Research Collection

Item descriptive metadata is released under a CC-0 (public domain) license: https://creativecommons.org/public-domain/cc0/.
All other content is subject to copyright.

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