发光学报, 2012, 33 (3): 243, 网络出版: 2012-03-17   

主链含萘酰亚胺的聚芳醚型聚合物的合成及其光电性能

Synthesis and Optoelectronic Properties of Aromatic Polyethers with A 1,8-naphthalimide Unit Main Chain
作者单位
1 上海大学材料科学与工程学院 高分子材料系, 上海 200072
2 上海大学材料科学与工程学院 材料研究所, 上海 200072
引用该论文

陈杰, 贺英, 潘照东, 张瑶斐, 朱棣, 顾莹, 王均安. 主链含萘酰亚胺的聚芳醚型聚合物的合成及其光电性能[J]. 发光学报, 2012, 33(3): 243.

CHEN Jie, HE Ying, PAN Zhao-dong, ZHANG Yao-fei, ZHU Di, GU Ying, WANG Jun-an. Synthesis and Optoelectronic Properties of Aromatic Polyethers with A 1,8-naphthalimide Unit Main Chain[J]. Chinese Journal of Luminescence, 2012, 33(3): 243.

参考文献

[1] Hua J L, Qu Y, Jiang Y H, et al. Novel side-chain naphthalimide polyphenylacetylene as a ratiometric fluorescent chemosensor for fluoride ion [J]. J. Polym. Sci. Pol. Chem., 2009, 47(6):1544-1552.

[2] Xu Z, Kim S, Kim H N, et al. A naphthalimide-calixarene as a two-faced and highly selective fluorescent chemosensor for Cu2+or F- [J]. Tetrahedron. Lett., 2007, 48(52):9151-9154.

[3] Rogers J E, Abraham B, Rostkowski A, et al. Mechanisms of photoinitiated cleavage of DNA by 1,8-naphthalimide deri-vatives [J]. Photochem. Photobiol., 2001, 74(4):521-531.

[4] Tao Z F, Qian X H, Wei D Z. 1,8-naphthalimide hydroperoxides as novel intercalating DNA cleavers [J]. Dyes Pigments, 1996, 31(3):245-251.

[5] Yin S G, Liu X Y, Li C X, et al. Electroluminescent properties of naphthalimide derivative thin film devices [J]. Thin Solid Films, 1998, 325(1-2):268-270.

[6] Segura J L, Coya C, Blanco R, et al. Synthesis and tunable emission of novel polyfluorene co-polymers with 1,8-naphthalimide pendant groups and application in a single layer-single component white emitting device [J]. Eur. Polym. J., 2010, 46(8):1778-1789.

[7] Kim H J, Jin J Y, Lee Y S, et al. An efficient luminescence conversion LED for white light emission, fabricated using a commercial InGaN LED and a 1,8-naphthalimide derivative [J]. Chem. Phys. Lett., 2006, 431(4-6):341-345.

[8] Mei C Y, Tu G L, Zhou Q G, et al. Green electroluminescent polyfluorenes containing 1,8-naphthalimide moieties as color tuner [J]. Polymer, 2006, 47(14):4976-4984.

[9] Liu J, Cao J X, Shao S Y, et al. Blue electroluminescent polymers with dopant-host systems and molecular dispersion features:Polyfluorene as the deep blue host and 1,8-naphthalimide derivative units as the light blue dopants [J]. J. Mater. Chem., 2008, 18(14):1659-1666.

[10] Lee J F, Hsu S L C. Green polymer-light-emitting-diodes based on polyfluorenes containing N-aryl-1,8-naphthalimide and 1,8-naphthoilene-arylimidazole derivatives as color tuner [J]. Polymer, 2009, 50(24):5668-5674.

[11] Zhang Yuehua, Zhang Qiping, Shi Wenyan, et al. Synthesis and quantum chemistry study on fluorescence spectra of three 1,8-naphthalimide monomers [J]. Chin. J. Lumin. (发光学报), 2011, 32(5):505-513 (in Chinese).

陈杰, 贺英, 潘照东, 张瑶斐, 朱棣, 顾莹, 王均安. 主链含萘酰亚胺的聚芳醚型聚合物的合成及其光电性能[J]. 发光学报, 2012, 33(3): 243. CHEN Jie, HE Ying, PAN Zhao-dong, ZHANG Yao-fei, ZHU Di, GU Ying, WANG Jun-an. Synthesis and Optoelectronic Properties of Aromatic Polyethers with A 1,8-naphthalimide Unit Main Chain[J]. Chinese Journal of Luminescence, 2012, 33(3): 243.

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