Literature DB >> 23865381

Ex(2)Box: interdependent modes of binding in a two-nanometer-long synthetic receptor.

Michal Juríček1, Jonathan C Barnes, Edward J Dale, Wei-Guang Liu, Nathan L Strutt, Carson J Bruns, Nicolaas A Vermeulen, Kala C Ghooray, Amy A Sarjeant, Charlotte L Stern, Youssry Y Botros, William A Goddard, J Fraser Stoddart.   

Abstract

Incorporation of two biphenylene-bridged 4,4'-bipyridinium extended viologen units into a para-phenylene-based cyclophane results in a synthetic receptor that is ~2 nm long and adopts a box-like geometry. This cyclophane, Ex(2)Box(4+), possesses the ability to form binary and ternary complexes with a myriad of guest molecules ranging from long π-electron-rich polycyclic aromatic hydrocarbons, such as tetracene, tetraphene, and chrysene, to π-electron-poor 2,6-dinitrotoluene, 1,2,4-trichlorobenzene, and both the 9,10- and 1,4-anthraquinone molecules. Moreover, Ex(2)Box(4+) is capable of forming one-to-one complexes with polyether macrocycles that consist of two π-electron-rich dioxynaphthalene units, namely, 1,5-dinaphtho[38]crown-10. This type of broad molecular recognition is possible because the electronic constitution of Ex(2)Box(4+) is such that the pyridinium rings located at the "ends" of the cyclophane are electron-poor and prefer to enter into donor-acceptor interactions with π-electron-rich guests, while the "middle" of the cyclophane, consisting of the biphenylene spacer, is more electron-rich and can interact with π-electron-poor guests. In some cases, these different modes of binding can act in concert to generate one-to-one complexes which possess high stability constants in organic media. The binding affinity of Ex(2)Box(4+) was investigated in the solid state by way of single-crystal X-ray diffraction and in solution by using UV-vis and NMR spectroscopy for 12 inclusion complexes consisting of the tetracationic cyclophane and the corresponding guests of different sizes, shapes, and electronic compositions. Additionally, density functional theory was carried out to elucidate the relative energetic differences between the different modes of binding of Ex(2)Box(4+) with anthracene, 9,10-anthraquinone, and 1,4-anthraquinone in order to understand the degree with which each mode of binding contributes to the overall encapsulation of each guest.

Entities:  

Year:  2013        PMID: 23865381     DOI: 10.1021/ja4052763

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  6 in total

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2.  Biphen[n]arenes.

Authors:  Huanqing Chen; Jiazeng Fan; Xiaoshi Hu; Junwei Ma; Shilu Wang; Jian Li; Yihua Yu; Xueshun Jia; Chunju Li
Journal:  Chem Sci       Date:  2014-09-17       Impact factor: 9.825

3.  Assembly and Adsorption Properties of Seven Supramolecular Compounds with Heteromacrocycle Imidazolium.

Authors:  Yuan-Yuan Li; Fu-Rong Wang; Zi-Yan Li; Zhen-Ning Yan; Yun-Yin Niu
Journal:  ACS Omega       Date:  2019-05-22

4.  A facile and efficient route to one-pot synthesis of new cyclophanes using vinamidinium salts.

Authors:  Nooshin Golzar; Abdolmohammad Mehranpour; Najmeh Nowrouzi
Journal:  RSC Adv       Date:  2021-04-13       Impact factor: 3.361

5.  Oxatub[4]arene: a smart macrocyclic receptor with multiple interconvertible cavities.

Authors:  Fei Jia; Zhenfeng He; Liu-Pan Yang; Zhi-Sheng Pan; Min Yi; Ren-Wang Jiang; Wei Jiang
Journal:  Chem Sci       Date:  2015-09-14       Impact factor: 9.825

6.  Feeding a Molecular Squid: A Pliable Nanocarbon Receptor for Electron-Poor Aromatics.

Authors:  Rafał Frydrych; Tadeusz Lis; Wojciech Bury; Joanna Cybińska; Marcin Stępień
Journal:  J Am Chem Soc       Date:  2020-08-28       Impact factor: 15.419

  6 in total

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