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	<dc:title xml:lang="en-US">Synthesis of an E-BODIPY based fluorescent Co-polymer containing organoboron quinolate units</dc:title>
	<dc:creator>Hewavitharanage, Priya</dc:creator>
	<dc:creator>Nzeata, Prince</dc:creator>
	<dc:creator>Wiggins, Jeffrey</dc:creator>
	<dc:subject xml:lang="en-US">BODIPY</dc:subject>
	<dc:subject xml:lang="en-US">Stokes shift</dc:subject>
	<dc:subject xml:lang="en-US">Fluorescence</dc:subject>
	<dc:subject xml:lang="en-US">Donor-acceptor</dc:subject>
	<dc:subject xml:lang="en-US">Energy transfer</dc:subject>
	<dc:subject xml:lang="en-US">Organoboron quinolate</dc:subject>
	<dc:description xml:lang="en-US">A novel fluorescent co-polymer with an organoboron quinolate and an E-BODIPY (BODIPY: 4,4-difluoro-4-bora-3a-4a-diaza-s-indacene) moiety was synthesized with the aim of producing a donor-acceptor polymeric system where the organoboron quinolate acts as the donor and the E-BODIPY moiety is the acceptor. The polymer has three prominent absorption bands: 264 nm (corresponding to the organoboron quinolate), 397 nm (corresponding to the organoboron quinolate and BODIPY) and 516 nm (corresponding to the E-BODIPY moiety). Excitation of the organoboron quinolate at 264 nm resulted in emission at 525 nm, giving a 261 nm Stokes shift. Energy transfer from the donor (organoboron quinolate) unit to the acceptor (BODIPY) explains the origin of this large Stokes shift.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2012-03-31</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
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	<dc:identifier>10.5155/eurjchem.3.1.13-16.543</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 3 No. 1 (2012): March 2012; 13-16</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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