光学学报, 2012, 32 (7): 0731002, 网络出版: 2012-05-18   

两种烷基取代喹吖啶酮衍生物LB膜的荧光特性

Fluorenscence Spectra of Two Kinds of Alkyl Substitution Quinacridone Derivative Langmuir-Blodgett Films
作者单位
1 聊城大学物理科学与信息工程学院, 山东 聊城 252059
2 华东师范大学物理系精密光谱科学与技术国家重点实验室, 上海 200062
摘要
制备了两种烷基取代喹吖啶酮衍生物C6DHQA和C16DMQA的X型Langmuir-Blodgett(LB)膜,采用紫外可见吸收、稳态荧光和时间分辨荧光的方法研究其溶液及LB的光学特性。研究结果表明,C16DMQA比C6DHQA的吸收谱整体红移,说明烷基链加长减小了分子的能级间隔;两者LB膜的吸收谱较溶液整体红移,说明在LB膜中形成了“J-聚集体”。两种材料的溶液及LB膜都有较强的荧光发射,溶液的荧光谱与吸收谱有很好的镜像对称关系,形成LB膜后,镜像对称关系被打破,两者第三个荧光峰相对强度差别很大。C6DHQA溶液中的荧光寿命为21 ns左右,C16DMQA溶液中的荧光寿命为22 ns左右,形成LB膜后,荧光寿命明显较少,两者第三个荧光峰对应的荧光寿命差别较大。其原因应归于C16DMQA分子在基板上的排列更密,分子间的相互作用力强,从而对能级结构的影响更大。
Abstract
Two kinds of alkyl substitution quinacridone derivative C6DHQA and C16DMQA X-type Langmuir-Blodgett (LB) films are prepared. The optical characteristics are studied by UV-visual spectrum, steady state and time resolved fluorescence. The experimental results show that the absorption spectrum of the C16DMQA has a whole red shift compared with C6DHQA′s. It shows that the energy level is lower with the added alkyl chain. The absorption spectrum of their LB films has a whole red shift compared with their solution. It shows that the two kinds molecule formed J-aggregation in LB films. The two kinds of material in chloroform solution and LB films both have strong flourescence emission. The absorption spectrum and the flourescence spetrum of the two kinds of material solution have mirror symmetry. But their LB films′s are asymmetrical. The third peak relative intensity of C6DHQA and C16DMQA LB films has a larger difference. The fluorescence lifetime at three fluorescenct emission peaks of C6DHQA solution is about 21 ns and C16DMQA′s is about 22 ns. It is obviously reduced as in LB films. And it is obviously diffrerent at the third peaks of C6DHQA compared with C16DMQA. All these differences are due to closer-arrangement of C16DMQA molecule on the substrate, the intermolecular interactions stronger and has a bigger influence on its energy level structure than C6DHQA molecule.
参考文献

[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] 时东霞, 季威, 贺肖波 等. 通过不同烷基链取代调控喹吖啶酮分子在Ag(110)表面上的自组装结构[J]. 物理, 2007, 36(1): 11~14

    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] 晋平, 任全胜, 杜俊霞 等. 有丁二酸衍生的有机颜料产品的开发应用及展望[J]. 染料与染色, 2010, 47(5): 1~7

    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] 张慧东, 张萍, 孙迎辉 等. 喹吖啶酮衍生物/介孔分子筛MCM-41组装体的金属离子传感性能研究[J]. 高等学校化学学报, 2006, 27(3): 506~509

    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] 刘云龙, 王文军, 高学喜 等. 稀土夹心双酞菁铥的LB膜及其光谱特性[J]. 光谱学与光谱分析, 2008, 28(2): 422~425

    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

[17] 高学喜, 王文军, 刘云龙 等. 两种偶氮苯化合物LB膜的光谱与非线性光学特性[J]. 中国激光, 2007, 34(9): 1276~1281

    Gao Xuexi, Wang Wenjun, Liu Yunlong et al.. Spectral and nonlinear optical properties of two azobenzene compounds in Langmuir-Blodgett films[J]. Chinese J. Lasers, 2007, 34(9): 1276~1281

[18] 赵剑峰. 氢键功能化有机半导体的合成及其超分子自组装[D].南京:南京邮电大学, 2011. 39~57

    Zhao Jianfeng. Synthesis and Supramolecular Self-Assembly of Hydrogen Bonded Organic Semiconductors[D]. Nanjing: Nanjing University of Posts and Telecommunications, 2011. 39~57

[19] 刘佩华. 可溶性喹吖啶酮类及苝类化合物的合成及其性能研究[D].上海:上海华东理工大学, 2000. 14~23

    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

[20] 刘云龙, 高学喜, 李淑红 等. 一种可溶喹吖啶酮衍生物LB膜的光谱特性[J]. 光散射学报, 2006, 18(2): 168~172

    Liu Yunlong, Gao Xuexi, Li Shuhong et al.. Spectral properties of a novel soluble quinacridone derivative Langmuir-Blodgett films[J]. J. Light Scattering, 2006, 18(2): 168~172

[21] 陆维敏, 陈芳. 谱学基础与结构分析 [M]. 北京:高等教育出版社, 2005. 80

    Lu Weimin, Chen Fang. Fundamental of Spectroscopy and Structure Analysis[M]. Beijing: Higher Education Press, 2005. 80

[22] 黄春辉, 李福友, 黄岩谊. 光电功能超薄膜[M]. 北京:北京大学出版社, 2001. 74~77, 155~162

    Huang Chunhui, Li Fuyou. Huang Yanyi. Ultrathin Films for Optics and Electronics[M].Beijing: Peking University Press, 2001. 74~77, 155~162

高学喜, 王文军, 刘云龙, 徐建华. 两种烷基取代喹吖啶酮衍生物LB膜的荧光特性[J]. 光学学报, 2012, 32(7): 0731002. Gao Xuexi, Wang Wenjun, Liu Yunlong, Xu Jianhua. Fluorenscence Spectra of Two Kinds of Alkyl Substitution Quinacridone Derivative Langmuir-Blodgett Films[J]. Acta Optica Sinica, 2012, 32(7): 0731002.

本文已被 1 篇论文引用
被引统计数据来源于中国光学期刊网
引用该论文: TXT   |   EndNote

相关论文

加载中...

关于本站 Cookie 的使用提示

中国光学期刊网使用基于 cookie 的技术来更好地为您提供各项服务,点击此处了解我们的隐私策略。 如您需继续使用本网站,请您授权我们使用本地 cookie 来保存部分信息。
全站搜索
您最值得信赖的光电行业旗舰网络服务平台!