Novel Terpyridine-bridged Parallel Dication Metallo-bisviologens and Their Supramolecular Complexes

Qianqian Liu , Yuan Guo , Tun Wu , Mingzhao Chen , Tingzheng Xie , Pingshan Wang

Chemical Research in Chinese Universities ›› 2019, Vol. 35 ›› Issue (2) : 229 -234.

PDF
Chemical Research in Chinese Universities ›› 2019, Vol. 35 ›› Issue (2) : 229 -234. DOI: 10.1007/s40242-019-8279-2
Article

Novel Terpyridine-bridged Parallel Dication Metallo-bisviologens and Their Supramolecular Complexes

Author information +
History +
PDF

Abstract

By utilizing terpyridine-bridged parallel metallo-complexes as dication metallo-bisviologens, herein we present the synthesis and characterization of two novel supramolecular complexes. 1-Methylpyridin-1-iumterpyridine ligands and their metallo-complexes were first designed and synthesized, and the association of methylpyridiniums with dibenzo-24-crown-8 ether(DB24C8) afforded the desired novel complexes through host-guest interactions. The self-assembly behavior of the supramolecular complexes was comprehensively investigated and could be exploited for further construction of 1D to 3D supramolecular infrastructures.

Keywords

Supramolecular complex / Host-guest interaction / Metallo-viologen / Dibenzo-24-crown-8 ether / Terpyridine

Cite this article

Download citation ▾
Qianqian Liu, Yuan Guo, Tun Wu, Mingzhao Chen, Tingzheng Xie, Pingshan Wang. Novel Terpyridine-bridged Parallel Dication Metallo-bisviologens and Their Supramolecular Complexes. Chemical Research in Chinese Universities, 2019, 35(2): 229-234 DOI:10.1007/s40242-019-8279-2

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Ge Z., Hu J., Huang F., Liu S. Angew. Chem. Int. Ed., 2009, 48: 1798.

[2]

Piepenbrock M. O., Lloyd G. O., Clarke N., Steed J. W. Chem. Rev., 2010, 110: 1960.

[3]

Philp D., Stoddart J. F. Angew. Chem. Int. Ed., 1996, 35: 1154.

[4]

Loeb S. J., Wisner J. A. Angew. Chem. Int. Ed., 1998, 37: 2838.

[5]

Xia B., Zheng B., Han C., Dong S., Zhang M., Hu B., Yu Y., Huang F. Polym. Chem., 2013, 4: 2019.

[6]

Sleiman H., Baxter P. N., Lehn J. M., Airola K., Rissanen K. Inorg. Chem., 1997, 36: 4734.

[7]

Liu Y., Huang Z., Tan X., Wang Z., Zhang X. Chem. Commun., 2013, 49: 5766.

[8]

Tian Y. K., Wang F. Macromol. Rapid Commun., 2014, 35: 337.

[9]

Crowley J. D., Goldup S. M., Lee A. L., Leigh D. A., Mcburney R. T. Chem. Soc. Rev., 2009, 38: 1530.

[10]

Sauvage J. P. Transition Metals in Supramolecular Chemistry, 2007.

[11]

Zhan J., Zhang M., Zhou M., Liu B., Chen D., Liu Y., Chen Q., Qiu H., Yin S. Macromol. Rapid Commun., 2014, 35: 1424.

[12]

Stang P. J., Olenyuk B. Acc. Chem. Res., 1997, 30: 502.

[13]

Olenyuk B., Whiteford J. A., Fechtenkötter A., Stang P. J. Nature, 1999, 398: 796.

[14]

Fyfe M. C. T., Stoddart J. F. Acc. Chem. Res., 1997, 30: 17.

[15]

Newkome G. R., He E. M., Moorefield C. N. Chem. Rev., 1999, 99: 1689.

[16]

Lin C., Xu L., Huang L., Chen J., Liu Y., Ma Y., Ye F., Qiu H., He T., Yin S. Macromol. Rapid Commun., 2016, 37: 1453.

[17]

Zhu Z., Li H., Liu Z., Lei J., Zhang H., Botros Y. Y., Stern C. L., Sarjeant A. A., Stoddart J. F., Colquhoun H. M. Angew. Chem. Int. Ed., 2012, 51: 7231.

[18]

Ashton P. R., Baxter I., Fyfe M. C. T., Raymo F. M., Spencer N., Stoddart J. F., White A. J. P., Williams D. J. J. Am. Chem. Soc., 2016, 120: 2297.

[19]

Pezzato C., Cheng C., Stoddart J. F., Astumian R. D. Chem. Soc. Rev., 2017, 46: 5491.

[20]

Reetz M. T., Niemeyer C. M., Harms K. Angew. Chem., Int. Ed., 1991, 30: 1474.

[21]

Caballero A., Zapata F., White N. G., Costa P. J., Félix V., Beer P. D. Angew. Chem. Int. Ed., 2012, 51: 1876.

[22]

Beer P. D., Gale P. A. Angew. Chem., Int. Ed., 2001, 40: 486.

[23]

Zhu K., Li S., Wang F., Huang F. J. Org. Chem., 2009, 74: 1322.

[24]

Zheng B., Wang F., Dong S., Huang F. Chem. Soc. Rev., 2012, 41: 1621.

[25]

Zhang M., Xu D., Yan X., Chen J., Dong S., Zheng B., Huang F. Angew. Chem., 2012, 124: 7117.

[26]

Dong S., Bo Z., Xu D., Yan X., Zhang M., Huang F. Adv. Mater., 2012, 24: 3191.

[27]

Winter A., Hoeppener S., Newkome G. R., Schubert U. S. Adv. Mater., 2011, 23: 3484.

[28]

Wu T., Guo Y., Yuan J., Jiang Z., Liu D., Wang P. RSC Adv., 2014, 5: 1754.

[29]

Wang Y., Frattarelli D. L., Facchetti A., Cariati E., Tordin E., Ugo R., Zuccaccia C., Macchioni A., Wegener S. L., Stern C. L. J. Phy. Chem. C, 2008, 112: 8005.

[30]

Wang J. L., Li X., Lu X., Hsieh I. F., Cao Y., Moorefield C. N., Wesdemiotis C., Cheng S. Z., Newkome G. R. J. Am. Chem. Soc., 2011, 133: 11450.

[31]

Kubota E., Lee Y. H., Fuyuhiro A., Kawata S., Harrowfield J. M., Yang K., Hayami S. Polyhedron, 2013, 52: 435.

[32]

Gong C., Balanda P. B., Gibson H. W. Macromolecules, 1998, 31: 5278.

[33]

Li J., Ni X., Zhou Z., Leong K. W. J. Am. Chem. Soc., 2003, 125: 1788.

[34]

Tuncel D., Steinke J. H. G. Macromolecules, 2004, 37: 288.

AI Summary AI Mindmap
PDF

125

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/