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Russian Chemical Reviews, 2005, Volume 74, Issue 7, Pages 671–683
DOI: https://doi.org/10.1070/RC2005v074n07ABEH000905
(Mi rcr414)
 

This article is cited in 19 scientific papers (total in 19 papers)

Polyquinolines and polyanthrazolines: synthesis and properties

A. L. Rusanova, L. G. Komarovaa, M. P. Prigozhinaa, D. Yu. Likhatchevb

a A. N. Nesmeyanov Institute of Organoelement Compounds of the Russian Academy of Sciences, Moscow
b Materials Research Institute, Autonomous National University of Mexico
Abstract: The advances in the synthesis and studies of the properties of polyquinolines and polyanthrazolines are reviewed. The main attention is given to polymers prepared by the Friedlander reaction from the AB- and AA–BB-type monomers, viz., rigid-rod polyquinolines, polyether quinolines, cardo polyquinolines and polymers containing tetraphenylsilyl and perfluorotetramethylene fragments. The approaches to the design of reactive oligo- and polyquinolines, the terminal groups of which have a curing effect on these systems, are considered. The use of polyquinolines for the preparation of composite and electroluminescent materials is discussed.
Received: 06.02.2004
Bibliographic databases:
Document Type: Article
Language: English
Original paper language: Russian


Citation: A. L. Rusanov, L. G. Komarova, M. P. Prigozhina, D. Yu. Likhatchev, “Polyquinolines and polyanthrazolines: synthesis and properties”, Usp. Khim., 74:7 (2005), 739–752; Russian Chem. Reviews, 74:7 (2005), 671–683
Linking options:
  • https://www.mathnet.ru/eng/rcr414
  • https://doi.org/10.1070/RC2005v074n07ABEH000905
  • https://www.mathnet.ru/eng/rcr/v74/i7/p739
  • This publication is cited in the following 19 articles:
    1. Kim J. Umerani M.J. Kurakake R. Qin H. Ziller J.W. Gorodetsky A.A. Park Y.S., RSC Adv., 11:23 (2021), 13722–13730  crossref  isi
    2. Umerani M.J. Yang H. Pratakshya P. Nowick J.S. Gorodetsky A.A., RSC Adv., 11:23 (2021), 14132–14139  crossref  isi
    3. David J. Dibble, Reina Kurakake, Austin G. Wardrip, Andrew Bartlett, Robert Lopez, Jose Armando Linares, Marcus Firstman, Alexander M. Schmidt, Mehran J. Umerani, Alon A. Gorodetsky, Org. Lett., 20:3 (2018), 502  crossref
    4. Umerani M.J. Dibble D.J. Wardrip A.G. Mazaheripour A. Vargas E. Ziller J.W. Gorodetsky A.A., J. Mater. Chem. C, 4:18 (2016), 4060–4066  crossref  isi  scopus
    5. D.J.. Dibble, M.J.. Umerani, Amir Mazaheripour, Y.S.. Park, J.W.. Ziller, Macromolecules, 2015, 1501161244  crossref  isi  scopus
    6. Avudoddi Venkanna, Kokkirala Swapna, P.V.enkateswar Rao, RSC Adv, 4:29 (2014), 15154  crossref  isi  scopus
    7. P.K.. Bhowmik, A.K.. Nedeltchev, Haesook Han, T.S.oo Jo, J.J.ae Koh, Journal of Photochemistry and Photobiology A: Chemistry, 2014  crossref  isi  scopus
    8. Tanmoy Chanda, Rajiv Kumar Verma, Maya Shankar Singh, Chem. Asian J, 2012, n/a  crossref  isi  scopus
    9. Belen'kii L.I. Gramenitskaya V.N. Evdokimenkova Yu.B., Advances in Heterocyclic Chemistry, Vol 102, Adv. Heterocycl. Chem., 102, ed. Katritzky A., 2011, 1–137  crossref  isi  scopus
    10. Shiri M., Zolfigol M.A., Kruger H.G., Tanbakouchian Z., Advances in Heterocyclic Chemistry, Vol 102, Adv. Heterocycl. Chem., 102, ed. Katritzky A., 2011, 139–227  crossref  isi  elib  scopus
    11. Liu Sh., Wang Q., Jiang P., Liu R., Song G., Zhu H., Yang Sh.-W., Dyes Pigment., 85:1-2 (2010), 51–56  crossref  isi  elib  scopus
    12. Marco-Contelles J., Perez-Mayoral E., Samadi A., Carreiras Maria do Carmo, Soriano E., Chem. Rev., 109:6 (2009), 2652–2671  crossref  isi  elib  scopus
    13. Biao Jiang, Jia-jia Dong, Yun Jin, Xiao-long Du, Min Xu, Eur J Org Chem, 2008:16 (2008), 2693  crossref  isi  scopus
    14. Martinez R., Ramon D.J., Yus M., J. Org. Chem., 73:24 (2008), 9778–9780  crossref  isi  elib  scopus
    15. Waldmann H., Karunakar G.V., Kumar K., Org. Lett., 10:11 (2008), 2159–2162  crossref  isi  elib  scopus
    16. Liang Zhang, Jie Wu, Adv Synth Catal, 349:7 (2007), 1047  crossref  isi  scopus
    17. Ricardo Martínez, Diego J. Ramón, Miguel Yus, Eur J Org Chem, 2007:10 (2007), 1599  crossref  isi  scopus
    18. A. L. Rusanov, L. G. Komarova, M. P. Prigozhina, D. Yu. Likhatchev, ChemInform, 37:6 (2006)  crossref
    19. Rusanov A., Komarova L., Polym. Sci. Ser. B, 47:9-10 (2005), 284–303  isi  elib
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