[1] W. Herbst, K. Hunger. Industrial Organic Pigments (3rd edition)[M]. Weinheim: Wiley-VCH, 2004
[2] Julius Jackson, Westfield. Particle Size Reduction of Quinacridone and Phthalocyanine Pigments[P]. US Patent: 3030370,1962
[3] Herman Gerson, F. John, C. Vincent. Preparation of Quinacridone Pigments[P]. US Patent: 3257405, 1966
[4] S. S. Labana, L. L. Labana. Quinacridones [J]. Chem. Rev., 1967, 67(1): 1~18
[5] Kaiqi Ye, Jia Wang, Hui Sun et al.. Supramolecular structures and assembly and luminescent properties of quinacridone derivatives[J]. J. Phys. Chem. B, 2005, 109(16): 8008~8016
[6] S. E. Shaheen, B. Kippelen, N. Peyghambarian et al.. Energy and charge transfer in organic light-emitting diodes: a soluble quinacridone study[J]. J. Appl. Phys., 1999, 85(11): 80~98
[7] Takeo Wakimoto, Yoshinobu Yonemoto, Jun Funaki et al.. Stability characteristics of quinacridone and coumarin molecules as guest dopants in the organic LEDs[J]. Synthetic Metals, 1997, 91(1-3): 15~19
[8] Shi Dongxia, Ji Wei, He Xiaobo et al.. Modulation of quinacridone derivatives nanostrucures by lateral alkyl chain on Ag(110)[J]. Physics, 2007, 36(1): 11~14
[9] Jin Ping, Ren Quansheng, Du Junxia et al.. Development and prospect of the organic pigments derived from succinic acid [J]. Dyestuffs and Coloration, 2010, 47(5): 1~7
[10] Cristiana Radulescu, I. Ionita, A. M. Hossu. Synthesis of linear bis-thiazolo[2,3-d][8,9-d] trans-quinacridone[J]. Dyes and Pigments, 2005, 65(2): 175~177
[11] Zhang Huidong, Zhang Ping, Sun Yinghui et al.. Metal ion sensing properties of BAEAHQA/MCM-41 assembly[J]. Chemical J. Chinese Universities, 2006, 27(3): 506~509
[12] S. E. Shaheen, G. E. Jabbour, B. Kippelen et al.. Organic light-emitting diode with 20 lm/W efficiency using a triphenyldiamine side-group polymer as the hole transport layer[J]. Appl. Phys. Lett., 2002, 74(21): 3212~3214
[13] J. Li, M. Yahiro, K. Ishida et al.. Influence of doping lacation and width of dimethylquinacridone on the performance of organic light emitting devices[J]. J. Phys. D. Appl. Phys., 2005, 38(3): 392~396
[14] Xunyu Yang, Zhongcheng Mu, Zhiqiang Wang. STM study on quinacridone derivative assemblies: modulation of the two-dimensional structure by coadsorption with dicarboxylic acids[J]. Langmuir, 2005, 21(16): 7225~7229
[15] Zhongcheng Mu, Zhiqiang Wang, Xi Zhang. Two-dimensional suramolecular assemblies of quinacridone derivatives from achiral to chiral racemates and domains[J]. J. Phys. Chem. B, 2004, 108(52): 19955~19959
[16] Liu Yunlong, Wang Wangjun, Gao Xuexi et al.. Spectrum properties of thulium bisphthalocyanine Langmuir-Blodgett films[J]. Spectroscopy and Spectral Analysis, 2008, 28(2): 422~425
[18] Zhao Jianfeng. Synthesis and Supramolecular Self-Assembly of Hydrogen Bonded Organic Semiconductors[D]. Nanjing: Nanjing University of Posts and Telecommunications, 2011. 39~57
[19] Liu Peihua. The Synthesis and the Study of Capability of Soluble Quinacridones and Derivatives[D]. Shanghai: East China University of Science and Technology, 2000. 14~23
[21] Lu Weimin, Chen Fang. Fundamental of Spectroscopy and Structure Analysis[M]. Beijing: Higher Education Press, 2005. 80
[22] Huang Chunhui, Li Fuyou. Huang Yanyi. Ultrathin Films for Optics and Electronics[M].Beijing: Peking University Press, 2001. 74~77, 155~162