Cyclo[m]pyridine[n]pyrroles: Hybrid Macrocycles That Display Expanded π-Conjugation upon Protonation-Reference-Cited by-同舟云学术

Cyclo[m]pyridine[n]pyrroles: Hybrid Macrocycles That Display Expanded π-Conjugation upon Protonation

Published:2012-02-23 Issue:9 Volume:134 Page:4076-4079
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Zhang Zhan¹,Lim Jong Min²,Ishida Masatoshi²,Roznyatovskiy Vladimir V.¹,Lynch Vincent M.¹,Gong Han-Yuan¹,Yang Xiaoping¹,Kim Dongho²,Sessler Jonathan L.¹²

Affiliation:

1. Department of Chemistry and Biochemistry, 1 University Station-A5300, The University of Texas at Austin, Austin, Texas 78712-0165, United States

2. Department of Chemistry, Yonsei University, Seoul 120-749, Korea

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja211985k

Reference22 articles.

1. Formation and Properties of Cyclo[6]pyrrole and Cyclo[7]pyrrole

2. Nonlinear Optical Properties and Excited-State Dynamics of Highly Symmetric Expanded Porphyrins

3. Redox Behavior of Cyclo[6]pyrrole in the Formation of a Uranyl Complex

4. 18[Hexa(2,6)pyridinocoronand-6]: "Sexipyridine"

5. Cyclosexipyridines

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