The effect of fluorination on the luminescent behaviour of 8-hydroxyquinoline boron compounds.
File(s)Britovsek, G - The effect of flourination (ESI).pdf (104.26 KB) Britovsek, G - The effect of flourination.pdf (968.74 KB)
Supporting information
Accepted version
Author(s)
Hellstrom, SL
Ugolotti, J
Britovsek, GJP
Jones, TS
White, AJP
Type
Journal Article
Abstract
B quinolinate compds. with different degrees of fluorination {Ph2BQ 1, (4-F-C6H4)2BQ 2 and (C6F5)2BQ 3 (Q is 8-quinolinate)} were prepd. and their electronic and luminescent behavior was studied in a variety of org. light emitting device structures. Cyclic voltammetry studies showed a decrease in ionization potential with the degree of fluorination. Electroluminescence (EL) measurements showed increasingly red shifted exciplex emission, originating from the different B compds. interacting with the hole transporting layer. In layered devices, the B compds. 1-3 are inferior in their EL performance compared to Al tris(8-quinolinoate) (AlQ3). However, when the B compds. 1, 2 or 3 are doped into a 4,4'-bis(carbazol-9-yl)diphenyl (CBP) host, emission solely attributable to 1-3 is obsd. In such devices, the B compds. 1 and 2 outperform AlQ3 as an emitter at low to moderate current densities. [on SciFinder(R)]
Date Issued
2008
Citation
New J. Chem., 2008, 32 (8), pp.1379-1387
ISSN
1144-0546
Publisher
Royal Society of Chemistry
Start Page
1379
End Page
1387
Journal / Book Title
New J. Chem.
Volume
32
Issue
8
Copyright Statement
© The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2008
Description
13.09.12 KB. Accepted version, to be add to spiral, embargo period as elapsed.
Identifier
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000259038200014&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
Subjects
fluorination luminescence behavior hydroxyquinoline boron compd