Reviews

Recent Progress of Naphthalimide-Based Dendrimers

  • LI Long ,
  • MA Cha ,
  • SUN Jin-Sheng ,
  • ZHAO Feng
Expand
  • a Jiangxi Key Laboratory of Organic Chemistry, Jiangxi Science and Technology Normal University, Nanchang 330013;
    b Department of Drilling Fluid, CNPC Drilling Research Institute, Beijing 100083;
    c Research Institute of Petroleum Exploration and Development, Beijing 100083

Received date: 2011-04-22

  Revised date: 2011-08-31

  Online published: 2012-03-09

Supported by

Project supported by the National Natural Science Foundations of China (No. 20903049) and the Natural Science Foundation of Jiangxi Province of China (No. 2009GZH0032).

Abstract

Due to their special luminescent properties and electrical properties, especially their good photoinduced electron transfer properties, naphthalimide-based dendrimers have been attracting considerable attention. Recently, lots of novel naphthalimide- based dendrimers have been synthesized, and they have extensive applications in many fields. In this paper, the recent progress of naphthalimide-based dendrimers is reviewed, and the synthesis and application of some compounds are discussed. These dendrimers have significant values of application in different fields, such as chemsensors, light harvesting antenna materials, organic electroluminescent devices, drug delivery, environmental pollution detection, and so on. Finally, the future development and application of them are also prospected.

Cite this article

LI Long , MA Cha , SUN Jin-Sheng , ZHAO Feng . Recent Progress of Naphthalimide-Based Dendrimers[J]. Chinese Journal of Organic Chemistry, 2012 , 32(02) : 304 -317 . DOI: 10.6023/cjoc115081

References

[1] Bosman, A. W.; Janssen, H. M.; Meijer, E. W. Chem. Rev. 1999, 99, 1665.

[2] Grayson, S. M.; Fréchet, J. M. J. Chem. Rev. 2001, 101, 3819.

[3] Devadoss, C.; Bharathi, P.; Moore, J. S. J. Am. Chem. Soc. 1996, 118, 9635.

[4] Fischer, M.; Vögtle, F. Angew. Chem., Int. Ed. 1999, 38, 884.

[5] Vögtle, F.; Gesterman, S.; Hasse, R.; Schwiert, H.; Windisch, B. Prog. Polym. Sci. 2000, 25, 987.

[6] Jing, X.-B.; Xu, F.; Xu, W.; Yan, C.-G. Chin. J. Org. Chem. 2007, 27, 457 (in Chinese). (景崤壁, 徐峰, 徐伟, 颜朝国, 有机化学, 2007, 27, 457.)

[7] Ma, C.; Li, L.; Sun, J.-S.; Zhao, F.; Li, Y.-L. Chin. J. Org. Chem. 2011, 31, 1977 (in Chinese). (马茶, 李龙, 孙金声, 赵丰, 李易隆, 有机化学, 2011, 31, 1977.)

[8] Jockusch, S.; Ramirez, J.; Sanghvi, K.; Nociti, R.; Turro, N. J.; Tomalia, D. A. Macromolecules 1999, 32, 4419.

[9] Cardona, C. M.; Alvarez, J.; Kaifer, A. E.; McCarley, T. D.; Pandey, S.; Baker, G. A.; Bonzagni, N. J.; Bright, F. V. J. Am. Chem. Soc. 2000, 122, 6139.

[10] Setayesh, S.; Garimsdale, A. C.; Weil, T. J. Am. Chem. Soc. 2001, 123, 946.

[11] Sabine, F.; Timo, K.; Henning, O. Chem. Eur. J. 2004, 10, 1167.

[12] Ma, C.; Li, L.; Cheng, C.-J.; Shen, L. Acta Chim. Sinica 2010, 68, 2135 (in Chinese). (马茶, 李龙, 程传杰, 申亮, 化学学报, 2010, 68, 2135.)

[13] Qian, X.; Zhu, K.; Chen, K. Dyes Pigm. 1989, 11, 13.

[14] Martin, E.; Weigand, R.; Pardo, A. J. Lumin. 1996, 68,157.

[15] Ramachandram, B.; Samanta, A. Chem. Commun. 1997, 1037.

[16] Ma, C.; Li, L.; Cheng, C.-J.; Shen, L. Polym. Mater. Sci. Eng. 2011, 27, 36 (in Chinese). (马茶, 李龙, 程传杰, 申亮, 高分子材料科学与工程, 2011, 27, 36.)

[17] Miller, L. L.; Zinger, B.; Schlechte, J. S. Chem. Mater. 1999, 11, 2313.

[18] Du, P.; Zhu, W. H.; Xie, Y. Q.; Zhao, F.; Ku, C. F.; Cao, Y.; Chang, C. P.; Tian, H. Macromolecules 2004, 37, 4387.

[19] Sun, J.-Y.; Wang, X.-X. Chem. J. Chin. Univ. 2008, 29, 519 (in Chinese). (孙金余, 王溪溪, 高等学校化学学报, 2008, 29, 519.)

[20] Bojinov, V. B.; Georgiev, N. I.; Nikolov, P. S. J. Photochem. Photobiol., A 2008, 193, 129.

[21] Miller, L. L.; Hashimoto, T.; Tabakovic, I.; Swanson, D. R.; Tomalia, D. A. Chem. Mater. 1995, 7, 9.

[22] Duan, R. G.; Miller, L. L.; Tomalia, D. A. J. Am. Chem. Soc. 1995, 117, 10783.

[23] Grabchev, I.; Qian, X. H.; Bojinov, V.; Xiao, Y.; Zhang, W. Polymer 2002, 43, 5731.

[24] Serin, J. M.; Brousmiche, D. W.; Fréchet, J. M. J. Chem. Commun. 2002, 2605.

[25] Grabchev, I.; Bojinov, V.; Chovelon, J. M. Polymer 2003, 44, 4421.

[26] Grabchev, I.; Chovelon, J. M.; Bojinov, V.; Ivanova, G. Tetrahedron 2003, 59, 9591.

[27] Grabchev, I.; Betcheva, R.; Bojinov, V.; Staneva, D. Eur. Polym. J. 2004, 40, 1249.

[28] Grabchev, I.; Staneva, D.; Betcheva, R. Polym. Degrad. Stab. 2006, 91, 2257.

[29] Cross, J. P.; Lauz, M.; Badger, P. D.; Petoud, S. J. Am. Chem. Soc. 2004, 126, 16278.

[30] Chen, Q. Q.; Lin, L.; Chen, H. M.; Yang, S. P.; Yang, L. Z.; Yu, X. B. J. Photochem. Photobiol., A 2006, 180, 69.

[31] Yang, S. P.; Lin, L.; Yang, L. Z.; Chen, J. M.; Chen, Q. Q.; Di, C.; Yu, X. B. J. Lumin. 2007, 126, 515.

[32] Sali, S.; Grabchev, I.; Chovelon, J. M.; Ivanova, G. Spectrochim. Acta, Part A 2006, 65, 591.

[33] Grabchev, I.; Sali, S.; Chovelon, J. M. Chem. Phys. Lett. 2006, 422, 547.

[34] Grabchev, I.; Dumas, S.; Chovelon, J. M.; Nedelcheva, A. Tetrahedron 2008, 64, 2113.

[35] Grabchev, I.; Bosch, P.; McKenna, M.; Staneva, D. J. Photochem. Photobiol., A 2009, 201, 75.

[36] Grabchev, I.; Dumas, S.; Chovelon, J. M. Dyes Pigm. 2009, 82, 336.

[37] Tang, J. G.; Yang, H.; Liu, J. X.; Wang, Y.; Yin, X. J.; Wang, R.; Huang, L. J.; Huang, Z. Opt. Mater. 2010, 32, 1417.

[38] Scutaru, A. M.; Krüger, M.; Wenzel, M.; Richter, J.; Gust, R. Bioconjugate Chem. 2010, 21, 2222.

[39] Bojinov, V. B.; Georgiev, N. I.; Nikolov, P. S. J. Photochem. Photobiol., A 2008, 197, 281.

[40] Georgiev, N. I.; Bojinov, V. B.; Nikolov, P. S. Dyes Pigm. 2009, 81, 18.

[41] McKenna, M. D.; Grabchev, I.; Bosch, P. Dyes Pigm. 2009, 81, 180.

[42] Georgiev, N. I.; Bojinov, V. B.; Marinova, N. Sens. Actuators, B 2010, 150, 655.

[43] Georgiev, N. I.; Bojinov, V. B. Dyes Pigm. 2010, 84, 249.
Outlines

/