Syntheses, Structures,
and Luminescent Properties
of Dipyridylamine-Functionalized Anthracene and Its Complexes
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Abstract
A novel multidentate ligand with 2,2′-dipyridylamine
functionalities,
1,8-bis[4-(2,2′-dipyridylamino)phenylacetylenyl]anthracene
(<b>1</b>), has been synthesized through a double Sonogashira
coupling reaction and characterized by NMR spectroscopic, elemental,
and X-ray diffraction analyses. Compound <b>1</b> can bind to
either one metal center as a tetradentate ligand or two metal centers
as a double-bidentate ligand. In the double-bidentate mode, the distance
between the two metal centers may vary significantly. Compound <b>1</b> displays bright blue luminescence in the solid state and
in solution with a quantum efficiency of 64% relative to 9,10-diphenylanthracene.
While the dirhodium complex of <b>1</b> shows no luminescence,
the two zinc complexes of <b>1</b> display blue luminescence
with quantum efficiencies slightly lower than that of <b>1</b>. Organic light-emitting devices (OLEDs) using <b>1</b> as
the emitter show a maximum current efficiency of 7 cd/A