A novel method for the direct synthesis of crystals of copper phthalocyanine

Dyes and Pigments

Volumn 78, Issue 1, 2008, Pages 84-88

  Xia, Daocheng ^a   Yu, Shukun ^b   Shen, Rensheng ^a   Ma, Chunyu ^a   Cheng, Chuanhui ^a,b   Ji, Dongmei ^b   Fan, Zhaoqi ^a   Wang, Xu ^c   Du, Guotong ^a,b  

^a DALIAN UNIVERSITY OF TECHNOLOGY   (China)

^b JILIN UNIVERSITY   (China)

^c Jilin University   (China)

Author keywords

CuPc; Quinoline; Single crystal; Solvothermal synthesis

Indexed keywords

HYDROCARBONS; SINGLE CRYSTALS; SOLVENTS; SYNTHESIS (CHEMICAL); TEMPERATURE;

COPPER PHTHALOCYANINE; DIIMINOSOINDOLINE; QUINOLINE; SOLVOTHERMAL METHOD;

CRYSTALLINE MATERIALS;

INORGANIC COMPOUND; SOLVENT; TEMPERATURE;

EID: 38349051990     PISSN: 01437208     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dyepig.2007.10.013     Document Type: Article

References (14)

1. Ohmori Y., Tada N., Fujii A., Ueta H., Sawatani T., and Yoshino K. Organic electroluminescent device with R-G-B emission. Thin Solid Films 331 (1998) 89-95
2. Rajagopal A., Hill I., and Kahn A. Electronic properties of metal-organic interfaces with application to electroluminescent devices. Mol Cryst Liq Cryst 322 (1998) 245-252
3. Hung L.S., Lee L.S., Lee C.S., and Lee S.T. Sputter deposition of cathodes in organic light emitting diodes. J Appl Phys 86 (1999) 4607
4. Bao Z., Lovinger A.J., and Dodabalapur A. Organic field-effect transistors with high mobility based on copper phthalocyanine. J Appl Phys Lett 69 (1996) 3066
5. Clarisse C., and Riou M.T. The operation and characteristics of diphthalocyanine field effect transistors. J Appl Phys 69 (1991) 3324
6. Horowitz G. Field-effect transistors based on short organic molecules. J Mater Chem 9 (1999) 2021-2026
7. Laudise R.A., Kloc Ch., Simpkins P.G., and Siegrist T. Physical vapor growth of organic semiconductor. J Cryst Growth 187 (1998) 449-454
8. Wenhai J., Wang X., Yuchun C., Shukun Y., Chunyu M., Kaiqi Y., et al. Single crystal growth of copper phthalocyanine using exaltation-evaporation growth method. J Cryst Growth 15286 (2006) 1-4
9. Brown C.J. Crystal structure of β-copper phthalocyanine. J Chem Soc A (1968) 2488-2493
10. Hoshino A., Takenaka Y., and Miyaji H. Redetermination of the crystal structure of α-copper phthalocyanine grown on KCl. Acta Crystallogr B59 3 (2003) 393-403
11. Erk P., Hengelsberg H., Haddow M.F., and van Gelder R. The innovative momentum of crystal engineering. Cryst Eng Commun 6 78 (2004) 474-483
12. Miyahara T., and Shimizu M. Single crystal growth of organic semiconductors by the repeated solid solvent growth method using melted anthracene as a solvent. J Cryst Growth 229 (2001) 553-557
13. Miyahara T., and Shimizu M. Single crystal growth of organic semiconductors using melted anthracene as a solvent: N,N′-dimethylperylene-3,4:9,10-bis(dicarboximide) and phthalocyanines. J Cryst Growth 226 (2001) 130-137
14. Selvaraj S.L., and Xavier F.P. Growth of phthalocyanine doped anthracene crystal using a three-zone furnace by vacuum sublimation method. J Cryst Growth 225 (2001) 168-172