Electron transport compound and organic light emitting device comprising the same

Information

  • Patent Application
  • 20070167626
  • Publication Number
    20070167626
  • Date Filed
    January 16, 2007
    17 years ago
  • Date Published
    July 19, 2007
    16 years ago
Abstract
An organic light emitting device having a pyrene based electron transport compound and an electron injecting and transport layer comprising the electron transport compound is provided.
Description
Claims
  • 1. An electron transport compound, having the following chemical formula, wherein A that is substituted or is not substituted is selected from a group consisting of pyridinyl, quinolinyl, isoquinolinyl, quinoxalinyl, bipyridinyl, terpyridinyl, and phenanthrolinyl, andB and C that are substituted or are not substituted are selected from a group consisting of phenyl, biphenyl, naphthyl, fluorenyl, terphenyl, phenanthrolinyl, phenanthryl, and anthryl.
  • 2. The electron transport compound of claim 1, wherein when the A, B, and C are substituted, a substituent of the A, B, and C is selected from a group consisting of aryl, alkyl, aryloxy, alkoxy, allylamino, alkylamino, halogen, and cyano.
  • 3. The electron transport compound of claim 1, wherein when the A, B, and C are substituted, a substituent of the A, B, and C is selected from a group consisting of phenyl, biphenyl, triphenylmethyl, phenylethylidene, diphenylethylidene, phenylmethylidyne, phenoxy, tolyoxy, methyl, ethyl, propyl, i-propyl, t-butyl, cyclohexyl, diphenylamino, morpholine, methoxy, ethoxy, propoxy, butoxy, dimethylamino, diphenylamino, fluorine, and chlorine.
  • 4. An organic light emitting device having an electron injecting and transport layer comprising the electron transport compound of claim 1.
  • 5. The organic light emitting device of claim 4, wherein the electron injecting and transport layer is one or both of an electron injecting layer or an electron transport layer.
  • 6. The organic light emitting device of claim 5, wherein the organic light emitting device comprises an anode, an emitting layer comprising an organic material and a cathode, wherein the electron injecting and transport layer is formed between the emitting layer and a cathode.
  • 7. An electron transport compound, having the following chemical formula, wherein A that is substituted or is not substituted is selected from a group consisting of pyridinyl, quinolinyl, isoquinolinyl, quinoxalinyl, bipyridinyl, terpyridinyl, and phenanthrolinyl, andB and C that are substituted or are not substituted are selected from a group consisting of phenyl, biphenyl, naphthyl, fluorenyl, terphenyl, phenanthrolinyl, phenanthryl, and anthryl.
  • 8. The electron transport compound of claim 7, wherein when the A, B, and C are substituted, a substituent of the A, B, and C is selected from a group consisting of aryl, alkyl, aryloxy, alkoxy, allylamino, alkylamino, halogen, and cyano.
  • 9. The electron transport compound of claim 7, wherein when the A, B, and C are substituted, a substituent of the A, B, and C is selected from a group consisting of phenyl, biphenyl, triphenylmethyl, phenylethylidene, diphenylethylidene, phenylmethylidyne, phenoxy, tolyoxy, methyl, ethyl, propyl, i-propyl, t-butyl, cyclohexyl, diphenylamino, morpholine, methoxy, ethoxy, propoxy, butoxy, dimethylamino, diphenylamino, fluorine, and chlorine.
  • 10. An organic light emitting device having an electron injecting and transport layer comprising the electron transport compound of claim 7.
  • 11. The organic light emitting device of claim 10, wherein the electron injecting and transport layer is one or both of an electron injecting layer or an electron transport layer.
  • 12. The organic light emitting device of claim 11, wherein the organic light emitting device comprises an anode, an emitting layer comprising an organic material and a cathode, wherein the electron injecting and transport layer is formed between the emitting layer and a cathode.
  • 13. An electron transport compound, having the following chemical formula, wherein A that is substituted or is not substituted is selected from a group consisting of pyridinyl, quinolinyl, isoquinolinyl, quinoxalinyl, bipyridinyl, terpyridinyl, and phenanthrolinyl, andB and C that are substituted or are not substituted are selected from a group consisting of phenyl, biphenyl, naphthyl, fluorenyl, terphenyl, methyl, ethyl, propyl, i-propyl, halogen, phenanthrolinyl, phenanthryl, and anthryl.
  • 14. The electron transport compound of claim 13, wherein when the A and B are substituted, a substituent of the A and B is selected from a group consisting of aryl, alkyl, aryloxy, alkoxy, allylamino, alkylamino, halogen, and cyano.
  • 15. The electron transport compound of claim 13, wherein when the A and B are substituted, a substituent of the A and B is selected from a group consisting of phenyl, biphenyl, triphenylmethyl, phenylethylidene, diphenylethylidene, phenylmethylidyne, phenoxy, tolyoxy, methyl, ethyl, propyl, i-propyl, t-butyl, cyclohexyl, diphenylamino, morpholine, methoxy, ethoxy, propoxy, butoxy, dimethylamino, diphenylamino, fluorine, and chlorine.
  • 16. An organic light emitting device having an electron injecting and transport layer comprising the electron transport compound of claim 13.
  • 17. The organic light emitting device of claim 16, wherein the electron injecting and transport layer is one or both of an electron injecting layer or an electron transport layer.
  • 18. The organic light emitting device of claim 17, wherein the organic light emitting device comprises an anode, an emitting layer comprising an organic material and a cathode, wherein the electron injecting and transport layer is formed between the emitting layer and a cathode.
Priority Claims (3)
Number Date Country Kind
10-2006-0004687 Jan 2006 KR national
10-2006-0004688 Jan 2006 KR national
10-2006-0004689 Jan 2006 KR national