Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Jiao, Tianyu, Cai, Kang, Liu, Zhichang, Wu, Guangcheng, Shen, Libo, Cheng, Chuyang, Feng, Yuanning, Stern, Charlotte L., Stoddart, J. Fraser, Li, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
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
_version_ 1783420882082856960
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
title_full Guest recognition enhanced by lateral interactions
title_fullStr Guest recognition enhanced by lateral interactions
title_full_unstemmed Guest recognition enhanced by lateral interactions
title_short Guest recognition enhanced by lateral interactions
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
work_keys_str_mv AT jiaotianyu guestrecognitionenhancedbylateralinteractions
AT caikang guestrecognitionenhancedbylateralinteractions
AT liuzhichang guestrecognitionenhancedbylateralinteractions
AT wuguangcheng guestrecognitionenhancedbylateralinteractions
AT shenlibo guestrecognitionenhancedbylateralinteractions
AT chengchuyang guestrecognitionenhancedbylateralinteractions
AT fengyuanning guestrecognitionenhancedbylateralinteractions
AT sterncharlottel guestrecognitionenhancedbylateralinteractions
AT stoddartjfraser guestrecognitionenhancedbylateralinteractions
AT lihao guestrecognitionenhancedbylateralinteractions