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Guest recognition enhanced by lateral interactions
A hexacationic triangular covalent organic cage, AzaEx(2)Cage(6+), has been synthesized by means of a tetrabutylammonium iodide-catalyzed S(N)2 reaction. The prismatic cage is composed of two triangular 2,4,6-triphenyl-1,3,5-triazine (TPT) platforms bridged face-to-face by three 4,4′-bipyridinium (B...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531815/ https://www.ncbi.nlm.nih.gov/pubmed/31183063 http://dx.doi.org/10.1039/c9sc00591a |
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author | Jiao, Tianyu Cai, Kang Liu, Zhichang Wu, Guangcheng Shen, Libo Cheng, Chuyang Feng, Yuanning Stern, Charlotte L. Stoddart, J. Fraser Li, Hao |
author_facet | Jiao, Tianyu Cai, Kang Liu, Zhichang Wu, Guangcheng Shen, Libo Cheng, Chuyang Feng, Yuanning Stern, Charlotte L. Stoddart, J. Fraser Li, Hao |
author_sort | Jiao, Tianyu |
collection | PubMed |
description | A hexacationic triangular covalent organic cage, AzaEx(2)Cage(6+), has been synthesized by means of a tetrabutylammonium iodide-catalyzed S(N)2 reaction. The prismatic cage is composed of two triangular 2,4,6-triphenyl-1,3,5-triazine (TPT) platforms bridged face-to-face by three 4,4′-bipyridinium (BIPY(2+)) spacers. The rigidity of these building blocks leads to a shape-persistent cage cavity with an inter-platform distance of approximately 11.0 Å. This distance allows the cage to accommodate two aromatic guests, each of which is able to undergo π–π interactions with one of the two TPT platform simultaneously, in an A–D–D–A manner. In the previously reported prism-shaped cage, the spacers (pillars) are often considered passive or non-interactive. In the current system, the three BIPY(2+) spacers are observed to play an important role in guest recognition. Firstly, the BIPY(2+) spacers are able to interact with the carbonyl group in a pyrene-1-carbaldehyde (PCA) guest, by introducing lateral dipole–cation or dipole–dipole interactions. As a consequence, the binding affinity of the cage towards the PCA guest is significantly larger than that of pyrene as the guest, even although the latter is often considered to be a better π-electron donor. Secondly, in the case of the guest 1,5-bis[2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)ethoxy]naphthalene (BH4EN), the pillars can provide higher binding forces compared to the TPT platform. Hence, peripheral complexation occurs when AzaEx(2)Cage(6+) accommodates BH4EN in MeCN. Thirdly, when both PCA and BH4EN are added into a solution of AzaEx(2)Cage(6+), inclusion and peripheral complexation occur simultaneously to PCA and BH4EN respectively, even though the accommodation of the former guest seems to attenuate the external binding of the latter. This discovery of the importance of lateral interactions highlights the relationship between the electrostatic properties of a highly charged host and its complexation behavior, and as such, provides insight into the design of more complex hosts that bind guests in multiple locations and modes. |
format | Online Article Text |
id | pubmed-6531815 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-65318152019-06-10 Guest recognition enhanced by lateral interactions Jiao, Tianyu Cai, Kang Liu, Zhichang Wu, Guangcheng Shen, Libo Cheng, Chuyang Feng, Yuanning Stern, Charlotte L. Stoddart, J. Fraser Li, Hao Chem Sci Chemistry A hexacationic triangular covalent organic cage, AzaEx(2)Cage(6+), has been synthesized by means of a tetrabutylammonium iodide-catalyzed S(N)2 reaction. The prismatic cage is composed of two triangular 2,4,6-triphenyl-1,3,5-triazine (TPT) platforms bridged face-to-face by three 4,4′-bipyridinium (BIPY(2+)) spacers. The rigidity of these building blocks leads to a shape-persistent cage cavity with an inter-platform distance of approximately 11.0 Å. This distance allows the cage to accommodate two aromatic guests, each of which is able to undergo π–π interactions with one of the two TPT platform simultaneously, in an A–D–D–A manner. In the previously reported prism-shaped cage, the spacers (pillars) are often considered passive or non-interactive. In the current system, the three BIPY(2+) spacers are observed to play an important role in guest recognition. Firstly, the BIPY(2+) spacers are able to interact with the carbonyl group in a pyrene-1-carbaldehyde (PCA) guest, by introducing lateral dipole–cation or dipole–dipole interactions. As a consequence, the binding affinity of the cage towards the PCA guest is significantly larger than that of pyrene as the guest, even although the latter is often considered to be a better π-electron donor. Secondly, in the case of the guest 1,5-bis[2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)ethoxy]naphthalene (BH4EN), the pillars can provide higher binding forces compared to the TPT platform. Hence, peripheral complexation occurs when AzaEx(2)Cage(6+) accommodates BH4EN in MeCN. Thirdly, when both PCA and BH4EN are added into a solution of AzaEx(2)Cage(6+), inclusion and peripheral complexation occur simultaneously to PCA and BH4EN respectively, even though the accommodation of the former guest seems to attenuate the external binding of the latter. This discovery of the importance of lateral interactions highlights the relationship between the electrostatic properties of a highly charged host and its complexation behavior, and as such, provides insight into the design of more complex hosts that bind guests in multiple locations and modes. Royal Society of Chemistry 2019-04-23 /pmc/articles/PMC6531815/ /pubmed/31183063 http://dx.doi.org/10.1039/c9sc00591a Text en This journal is © The Royal Society of Chemistry 2019 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Jiao, Tianyu Cai, Kang Liu, Zhichang Wu, Guangcheng Shen, Libo Cheng, Chuyang Feng, Yuanning Stern, Charlotte L. Stoddart, J. Fraser Li, Hao Guest recognition enhanced by lateral interactions |
title | Guest recognition enhanced by lateral interactions
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title_full | Guest recognition enhanced by lateral interactions
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title_fullStr | Guest recognition enhanced by lateral interactions
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title_full_unstemmed | Guest recognition enhanced by lateral interactions
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title_short | Guest recognition enhanced by lateral interactions
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title_sort | guest recognition enhanced by lateral interactions |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531815/ https://www.ncbi.nlm.nih.gov/pubmed/31183063 http://dx.doi.org/10.1039/c9sc00591a |
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