Transition metal complex compound and organic electroluminescence device using the compound

Abstract
Provided are an organic electroluminescence device having high luminous efficiency and a long emission lifetime, and a transition metal complex compound realizing the organic electroluminescence device. In the transition metal complex compound, three ligands are crosslinked with a crosslinking group having a saturated cyclic structure or a saturated polycyclic structure in a tripod manner. The organic electroluminescence device includes an organic thin film layer composed of one or multiple layers including at least a light emitting layer, the organic thin film layer being interposed between a pair of electrodes. In the organic electroluminescence device, at least one layer of the organic thin film layer contains the transition metal complex compound.
Description

BRIEF DESCRIPTION OF THE DRAWINGS

[FIG. 1] A view showing 1H-NMR spectrum data on Metal Complex Compound 8 obtained in Example 1.


[FIG. 2] A view showing 13C-NMR spectrum data on Metal Complex Compound 8 obtained in Example 1.


[FIG. 3] A view showing the emission spectrum of Metal Complex Compound 8.


[FIG. 4] A view showing the X-ray crystallography of Metal Complex Compound 8.


[FIG. 5] A view showing 1H-NMR spectrum data on Metal Complex Compound 15 obtained in Example 2.


[FIG. 6] A view showing 13C-NMR spectrum data on Metal Complex Compound 15 obtained in Example 2.


[FIG. 7] A view showing the emission spectrum of Metal Complex Compound 15.


Claims
  • 1. A transition metal complex compound represented by the following general formula (1):
  • 2. A transition metal complex compound according to claim 1, wherein the crosslinking group X comprises a cycloalkane residue.
  • 3. A transition metal complex compound according to claim 2, wherein the crosslinking group X comprises a cyclohexane residue.
  • 4. A transition metal complex compound according to claim 3, wherein the crosslinking group X (in a broken line) comprises the following structure (2):
  • 5. A transition metal complex compound according to claim 4, wherein all of Ra to Ri each represent a hydrogen atom.
  • 6. A transition metal complex compound according to claim 1, wherein at least one of L2, L4, and L6 represents a group having carbene carbon.
  • 7. A transition metal complex compound according to claim 1, wherein L2, L4, and L6 represent a group having carbene carbon.
  • 8. An organic electroluminescence device, comprising an organic thin film layer composed of one or multiple layers including at least a light emitting layer, the organic thin film layer being interposed between an anode and a cathode, wherein at least one layer of the organic thin film layer contains the transition metal complex compound according to claim 1.
  • 9. An organic electroluminescence device according to claim 8, wherein the light emitting layer contains the transition metal complex compound as a light emitting material.
  • 10. An organic electroluminescence device according to claim 8, wherein the light emitting layer contains the transition metal complex compound as a dopant.
  • 11. An organic electroluminescence device according to claim 8, wherein: at least one of an electron injecting layer and an electron transporting layer is placed between the light emitting layer and the cathode; andat least one of the electron injecting layer and the electron transporting layer contains a n-electron-deficient, nitrogen-containing heterocyclic derivative as a main component.
  • 12. An organic electroluminescence device according to claim 8, wherein a reducing dopant is added to an interfacial region between the cathode and the organic thin film layer.
Priority Claims (2)
Number Date Country Kind
019794/2006 Jan 2006 JP national
175427/2006 Jun 2006 JP national