Synthesis and Characterization of <italic style="font-style: italic">S,N</italic>-Heteroacenes by Bischler-Napieralski Reaction

Hong-shuang Guo; Mei-fang Liu; Yi Han; Sheng Han; Yu-lan Chen

doi:10.1007/s10118-016-1846-9

Your Location：

Home >

Browse articles >

Synthesis and Characterization of S,N-Heteroacenes by Bischler-Napieralski Reaction

PAPERS | Updated：2021-05-12

- Synthesis and Characterization of S,N-Heteroacenes by Bischler-Napieralski Reaction
- Synthesis and Characterization of S,N-Heteroacenes by Bischler-Napieralski Reaction
- Chinese Journal of Polymer Science 2016年34卷第11期页码：1319-1329
- Affiliations：
  
  a.School of Chemical and Environmental Engineering, Shanghai Institute of Technology, Shanghai 201418, China
  b.Tianjin Key Laboratory of Molecular Optoelectronic Science, Tianjin University, Tianjin 300072, China
  c.Department of Chemistry, Weifang University, Weifang 261061, China
- Author bio：
  
  Sheng Han(韩生),E-mail:hansheng654321@sina.com
  Yu-lan Chen(陈于蓝),E-mail:chenyl@iccas.ac.cn
- Funds：
  
  the National Natural Science Foundation of China(51503142;21522405;20976105);Shanghai Leading Academic Discipline Project(J51503);Shanghai Municipal Education Commission Boosting Project(15cxy39);the Open Project of the State Key Laboratory of Supramolecular Structure and Materials(SKLSSM201505)
- DOI：10.1007/s10118-016-1846-9
  中图分类号：
- 收稿：2016-05-16，
  
  修回：2016-5-22，
  
  录用：2016-5-25，
  
  纸质出版：2016-11
- Accepted：
Scan QR Code
Hong-shuang Guo, Mei-fang Liu, Yi Han, 等. Synthesis and Characterization of S,N-Heteroacenes by Bischler-Napieralski Reaction[J]. Chinese Journal of Polymer Science, 2016,34(11):1319-1329. DOI: 10.1007/s10118-016-1846-9.

Hong-shuang Guo, Mei-fang Liu, Yi Han, et al. Synthesis and Characterization of S,N-Heteroacenes by Bischler-Napieralski Reaction[J]. Chinese Journal of Polymer Science, 2016, 34(11): 1319-1329. DOI: 10.1007/s10118-016-1846-9.
Hong-shuang Guo, Mei-fang Liu, Yi Han, 等. Synthesis and Characterization of S,N-Heteroacenes by Bischler-Napieralski Reaction[J]. Chinese Journal of Polymer Science, 2016,34(11):1319-1329. DOI: 10.1007/s10118-016-1846-9. DOI：

Hong-shuang Guo, Mei-fang Liu, Yi Han, et al. Synthesis and Characterization of S,N-Heteroacenes by Bischler-Napieralski Reaction[J]. Chinese Journal of Polymer Science, 2016, 34(11): 1319-1329. DOI: 10.1007/s10118-016-1846-9. DOI：

摘要

Abstract

Bischler-Napieralski cyclization has been successfully employed to prepare planar

-heteroacenes (SNHs) with the analogue structures to 1

10-phenanthroline. The opto-/electrical properties and the packing modes of these S

Nheteroacenes were examined

which were dependent on the structure of the fused groups. SNH-based copolymers with high molecular weight and good solubility in common organic solvents or water have been synthesized by Suzuki-Miyaura-Schlüter polycondensation. The photophysical property studies revealed that the copolymers may be a promising chemosensor material.

关键词

Keywords

references

X. Guo, , M. Baumgarten, , K. Müllen, . . Prog. Polym. Sci. , 2013 . 38 1832 DOI: 10.1016/j.progpolymsci.2013.09.005 http://doi.org/10.1016/j.progpolymsci.2013.09.005 .

Y. Zhao, , Y. Guo, , Y. Liu, . . Adv. Mater. , 2013 . 25 5372 DOI: 10.1002/adma.201302315 http://doi.org/10.1002/adma.201302315 .

S. Rochat, , T.M. Swager, . . ACS Appl. Mater. Inter. , 2013 . 5 4488 DOI: 10.1021/am400939w http://doi.org/10.1021/am400939w .

Q. Ye, , C. Chi, . . Chem. Mater. , 2014 . 26 4046 DOI: 10.1021/cm501536p http://doi.org/10.1021/cm501536p .

U.H.F. Bunz, , J.U. Engelhart, , B.D. Lindner, , M. Schaffroth, . . Angew. Chem. Int. Ed. , 2013 . 52 3810 DOI: 10.1002/anie.v52.14 http://doi.org/10.1002/anie.v52.14 .

J. Anthony, . . Chem. Rev. , 2006 . 106 5028 DOI: 10.1021/cr050966z http://doi.org/10.1021/cr050966z .

J.E. Anthony, , A. Facchetti, , M. Heeney, , S.R. Marder, , X. Zhan, . . Adv. Mater. , 2010 . 22 3876 DOI: 10.1002/adma.200903628 http://doi.org/10.1002/adma.200903628 .

A. Keerthi, , C. An, , M. Li, , T. Marszalek, , A.G. Ricciardulli, , B. Radha, , F.D. Alsewailem, , K. Müllen, , M. Baumgarten, . . Polym. Chem. , 2016 . 7 1545 DOI: 10.1039/C6PY00023A http://doi.org/10.1039/C6PY00023A .

C. Li, , N.H. Zheng, , H.J. Chen, , J.Y. Huang, , Z.P. Mao, , L.P. Zheng, , C. Weng, , S.T. Tan, , G. Yu, . . Polym. Chem. , 2015 . 6 5393 DOI: 10.1039/C5PY00605H http://doi.org/10.1039/C5PY00605H .

L. Chen, , J. Kim, , T. Ishizuka, , Y. Honsho, , A. Saeki, , S. Seki, , H. Ihee, , D. Jiang, . . J. Am. Chem. Soc. , 2009 . 131 7287 DOI: 10.1021/ja901357h http://doi.org/10.1021/ja901357h .

C. Wetzel, , E. Brier, , A. Vogt, , A. Mishra, , E. Mena-Osteritz, , P. Bäuerle, . . Angew. Chem. Int. Ed. , 2015 . 54 12334 DOI: 10.1002/anie.201502840 http://doi.org/10.1002/anie.201502840 .

S.C. Rasmussen, , S.J. Evenson, . . Prog. Polym. Sci. , 2013 . 38 1773 DOI: 10.1016/j.progpolymsci.2013.04.004 http://doi.org/10.1016/j.progpolymsci.2013.04.004 .

A. Mishra, , D. Popovic, , A. Vogt, , H. Kast, , T. Leitner, , K. Walzer, , M. Pfeiffer, , E. Mena-Osteritz, , P. Bäuerle, . . Adv. Mater. , 2014 . 26 7217 DOI: 10.1002/adma.v26.42 http://doi.org/10.1002/adma.v26.42 .

P. Gao, , X. Feng, , X. Yang, , V. Enkelmann, , M. Baumgarten, , K. Müllen, . . J. Org. Chem. , 2008 . 73 9207 DOI: 10.1021/jo801898g http://doi.org/10.1021/jo801898g .

P. Qin, , H. Kast, , M.K. Nazeeruddin, , S.M. Zakeeruddin, , A. Mishra, , P. Bauerle, , M. Grätzel, . . Energ. Environ. Sci. , 2014 . 7 2981 DOI: 10.1039/C4EE01220H http://doi.org/10.1039/C4EE01220H .

S.I. Kato, , T. Furuya, , A. Kobayashi, , M. Nitani, , Y. Ie, , Y. Aso, , T. Yoshihara, , S. Tobita, , Y. Nakamura, . . J. Org. Chem. , 2012 . 77 7595 DOI: 10.1021/jo301458m http://doi.org/10.1021/jo301458m .

G. Balaji, , S. Valiyaveettil, . . Org. Lett. , 2009 . 11 3358 DOI: 10.1021/ol901133m http://doi.org/10.1021/ol901133m .

C. Wang, , T. Okabe, , G. Long, , D. Kuzuhara, , Y. Zhao, , N. Aratani, , H. Yamada, , Q. Zhang, . . Dyes Pigments. , 2015 . 122 231 DOI: 10.1016/j.dyepig.2015.06.029 http://doi.org/10.1016/j.dyepig.2015.06.029 .

L. Biniek, , B.C. Schroeder, , J.E. Donaghey, , N. Yaacobi-Gross, , R.S. Ashraf, , Y.W. Soon, , C.B. Nielsen, , J.R. Durrant, , T.D. Anthopoulos, , I. McCulloch, . . Macromolecules , 2013 . 46 727 DOI: 10.1021/ma302390z http://doi.org/10.1021/ma302390z .

Q.T. Zhang, , J.M. Tour, . . J. Am. Chem. Soc. , 1997 . 119 9624 DOI: 10.1021/ja964223u http://doi.org/10.1021/ja964223u .

Y. Yao, , Q.T. Zhang, , J.M. Tour, . . Macromolecules , 1998 . 31 8600 DOI: 10.1021/ma980761a http://doi.org/10.1021/ma980761a .

Y. Chen, , W. Huang, , C. Li, , Z. Bo, . . Macromolecules , 2010 . 43 10216 DOI: 10.1021/ma1021117 http://doi.org/10.1021/ma1021117 .

Y. Chen, , F. Li, , Z. Bo, . . Macromolecules , 2010 . 43 1349 DOI: 10.1021/ma902375a http://doi.org/10.1021/ma902375a .

C.A. Tolman, , W.C. Seidel, , D.H. Gerlach, . . J. Am. Chem. Soc. , 1972 . 94 2669 DOI: 10.1021/ja00763a019 http://doi.org/10.1021/ja00763a019 .

R.L. Schwiderski. , S.C. Rasmussen, . . J. Org. Chem. , 2013 . 78 .

Q. Li, , J. Li, , R. Yang, , L. Deng, , Z. Gao, , D. Liu, . . Dyes Pigments. , 2011 . 92 .

D.G. Patel, , F. Feng, , Y. Ohnishi, , K.A. Abboud, , S. Hirata, , K.S. Schanze, , J.R. Reynolds, . . J. Am. Chem. Soc. , 2012 . 134 2599 DOI: 10.1021/ja207978v http://doi.org/10.1021/ja207978v .

W.H. Lee, , A.D. Mohanty, , C. Bae, . . ACS Macro Lett. , 2015 . 4 453 DOI: 10.1021/acsmacrolett.5b00145 http://doi.org/10.1021/acsmacrolett.5b00145 .

J. Lee, , B.J. Jung, , S.K. Lee, , J.I. Lee, , H.J. Cho, , H.K., J. Polym. Sci. Shim, . . Part A:Polym. Chem. , 2005 . 43 1845 DOI: 10.1002/(ISSN)1099-0518 http://doi.org/10.1002/(ISSN)1099-0518 .

R.Z. Fu, , X.X. Xu, , Q. Dang, , X. Bai, . . J. Org. Chem. , 2005 . 70 10812 .

T. Yamamoto, , K. Anzai, , T. Iijima, , H. Fukumoto, . . Macromolecules , 2004 . 37 3065 .

W.J. Li, , B. Liu, , Y. Qian, , L.H. Xie, , J. Wang, , S.B. Li, , W. Huang, . . Polym. Chem. , 2013 . 4 1798 .

S. Tokito, , H. Tanaka, , K. Noda, , A. Okada, , Y. Taga, . . Appl. Phys. Lett. , 1997 . 70 1930 .

A. Listorti, , A.D. Esposti, , R.S.K. Kishore, , V. Kalsani, , M. Schmittel, , N. Armaroli, . . J. Phys. Chem. A , 2007 . 111 7710 .

浏览量

Downloads

CSCD

文章被引用时，请邮件提醒。

Submit

工具集

关联资源

Cross-linked Polyamides Prepared through Direct Bulk Michael Addition and Polycondensation from 1,6-Hexanediamine and Methyl Acrylate

Preparation and Characterization of Flexible, Transparent and Thermally Stable Aromatic Co-polyamides

Synthesis of Poly(butylene terephthalate)-Poly(tetramethylene glycol) Copolymers Using Terephthalic Acid as Starting Material: A Comparation between Two Synthetic Strategies

Thermally Stable and Organo-soluble Polyamides Containing Triazine Rings and Ether Linkages in the Main Chain: Synthesis and Characterization

Organosoluble Aliphatic-Aromatic Poly(ether-amide)s Based on Pyridine Moiety in the Main Chain: Synthesis, Characterization and Thermal Studies

Synthesis and Characterization of S,N-Heteroacenes by Bischler-Napieralski Reaction

Synthesis and Characterization of S,N-Heteroacenes by Bischler-Napieralski Reaction

DOI：10.1007/s10118-016-1846-9

摘要

Abstract

关键词

Keywords

references