ic300673k_si_002.cif (47.33 kB)
Cationic Iridium Complexes with Intramolecular π–π Interaction and Enhanced Steric Hindrance for Solid-State Light-Emitting Electrochemical Cells
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posted on 2012-11-19, 00:00 authored by Hsiao-Fan Chen, Wen-Yi Hung, Shou-Wei Chen, Ting-Chih Wang, Shih-Wei Lin, Shu-Hua Chou, Chih-Teng Liao, Hai-Ching Su, Hsiao-An Pan, Pi-Tai Chou, Yi-Hung Liu, Ken-Tsung WongCationic iridium complexes incorporated 4,5-diaza-9,9′-spirobifluorene
as N∧N ancillary ligands, in which one (2) or two (3) phenyl groups were introduced onto 4,5-diazafluorene
to afford intraligand π–π interactions. The X-ray
crystal structures of complexes 2 and 3 show
that the pendant phenyl ring forms strong intramolecular face-to-face
π-stacking with the difluorophenyl ring of the cyclometalated
ligand with distances of 3.38 Å for complex 2 and
3.40 and 3.46 Å for complex 3. This π–π
stacking interaction minimizes the expansion of the metal–ligand
bonds in the excited state, resulting in a longer device lifetime
in the light-emitting electrochemical cell (LEC) devices.
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intraliganddevice lifetimecyclometalated ligandelectrochemicalintramolecularEnhanced Steric Hindrance3.40difluorophenyl ringLECCellsCationicIntramolecularcomplexes 23.46 ÅInteraction3 showinteractiondiazafluoreneCationic Iridium Complexespendant phenyl ring formscrystaliridiumElectrochemicaldiaza3.38 Åbond
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