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<XML><RECORDS>
<RECORD>
	<REFERENCE_TYPE>0</REFERENCE_TYPE>
	<AUTHORS>
		<AUTHOR>Lahiff, Emer</AUTHOR>
		<AUTHOR>Scarmagnani, Silvia</AUTHOR>
		<AUTHOR>Schazmann, Benjamin</AUTHOR>
		<AUTHOR>Cafolla, Attilio A.</AUTHOR>
		<AUTHOR>Diamond, Dermot</AUTHOR>
	</AUTHORS>
	<YEAR>2010</YEAR>
	<TITLE>Covalent attachment of functional side-groups to polyaniline nanofibres</TITLE>
	<SECONDARY_TITLE>International Journal of Nanomanufacturing</SECONDARY_TITLE>
	<PUBLISHER>Inderscience Publishers</PUBLISHER>
	<VOLUME>5</VOLUME>
	<PAGES>88-99</PAGES>
	<KEYWORDS>
		<KEYWORD>RP1</KEYWORD>
		<KEYWORD>RP2</KEYWORD>
	</KEYWORDS>
	<ABSTRACT>&lt;p&gt;Polyaniline (PAni) is an example of a conducting polymer that can be switched between an insulating and a conductive state. This switching is accompanied by a colour change. Recently, interest has developed in the nanofibre form of PAni as these low dimensional structures have a very high surface area, thus enabling a faster response time. We investigate how the surface chemistry of these nanofibres can be modified by covalently attaching functional side-groups. In particular, we demonstrate the attachment of both amide and carboxylic acid groups. This can be achieved using a simple reflux technique. The modified material retains its nanomorphology and the intrinsic electrochemical, spectroscopic and redox properties of PAni are also preserved. Both acid and amine side-groups are interesting in that they provide a template, which could be further altered to enhance the selectivity of PAni. Acid terminated chains can also be used to introduce self-doping behaviour to PAni.&lt;/p&gt;</ABSTRACT>
	<URL>http://doras.dcu.ie/14979/</URL>
</RECORD>
</RECORDS></XML>