Browse > Article
http://dx.doi.org/10.12925/jkocs.2002.19.2.5

Synthesis and Characteristics of Diphosphine-digold complexes as Light-Emitting Materials  

Kim, Jun-Ho (Dept. of Electrical Information & Control Engineering, Hongik University)
Sohn, Byung-Chung (Dept. of Chemical Engineering, Hongik University)
Ha, Yun-Kyoung (Dept. of Science, College of Engineering, Hongik University)
Publication Information
Journal of the Korean Applied Science and Technology / v.19, no.2, 2002 , pp. 103-107 More about this Journal
Abstract
Diphosphine dinuclear gold(I) complexes were synthesized from the reaction of bridged diphosphines and gold ions. As a bridged diphosphine, 1,2-bis(diphenylphosphino)metbane (dppm) or 1,1'-Bis(diphenylphosphino) ferrocene (dppf) was introduced. As anionic ligands, CI was first coordinated to Au, resulting in (diphosphine)$(AuCl)_{2}$. Then, the ligand, SPh, was substituted for Cl in the chloride complex to give (diphosphine)$(AuSPh)_{2}$. As a result, three digold complexes, (dppm)$(AuCl)_{2}$. (I), (dppf)$(AuCl)_{2}$. (II), and (dppf)$(AuSPh_{2}$. (III) were prepared in this study. The thermal properties were investigated at first hand to confirm that the gold complexes were in fact formed. The digold complexes were decomposed above $200^{\circ}C$ while the ligand, dppm or dppf, melts under $180^{\circ}C$ The photoluminescence (PL) spectra of the spin-coated thin films showed the maximum peak at 590, 595, and 540nm for the complex, I, II, and III, respectively. These complexes were found to give the orange color phosphorescence. Therefore, these digold complexes can be candidates for orange-red phosphorescent materials in organic electroluminescent devices (OELD). Further studies on application of the complexes as a dopant in an emitting layer are in progress in our laboratory.
Keywords
diphosphine digold complex; phosphorescence; efficiency; OLED;
Citations & Related Records
연도 인용수 순위
  • Reference
1 Y. Hamada, H. Kanno, T. Sano, M. Fujita, Fujii, Y. Nishnio, H. Takahashi, T. Usuki, and K. Shibata, Appl. Phys. Lett., 72, 1939 (1998)   DOI   ScienceOn
2 C. M. Che, W. T. Wong, T. F. Lai, and H. L. Kwong, J. Chem Soc. Chem. Commun, 243 (1989)
3 Z. Assefa, B. G. McBumett, R. J. Staples, and J. P. Fackler, Jr., Inorg. Chem., 34, 4965 (1995)   DOI   ScienceOn
4 A. Houlton, R. M. G. Roberts, J. Silver, and R. V. Parish, J. Organomet. Chem, 418, 269 (1991)   DOI   ScienceOn
5 C. W. Tang, Information Display, 10, 16 (1996)
6 C. W. Tang and S. A. Van Slyke, Appl. Phys. Lett., 51, 913 (1987)   DOI
7 Y. Ma, X. Zhou, J. Shen, H. Y. Chao, and C. M. Che, Appl. Phys. Lett., 74, 1361 (1999)   DOI   ScienceOn
8 Y. Hamada, IEEE Transactions on Electron Devices, 44 (1997)
9 J. M. Forward, D. Bohmann, J. P. Fackler, Jr., and R. J. Staples, Inorg. Chem. 34, 6330 (1995)   DOI
10 Z. Assefa, B. G. McBumett, R. J. Staples, J. P. Fackler, Jr., B. Assmann, K. Angennaier, and H. Schmidbaur, Inorg. Chem, 34, 75 (1995)   DOI   ScienceOn
11 C. H. Chen and J. Shi, Coord. Chem. Rev., 171, 161 (1998)   DOI