CaltechAUTHORS
  A Caltech Library Service

Redox Control of the Binding Modes of an Organic Receptor

Frasconi, Marco and Fernando, Isurika R. and Wu, Yilei and Liu, Zhichang and Liu, Wei-Guang and Dyar, Scott M. and Barin, Gokhan and Wasielewski, Michael R. and Goddard, William A., III and Stoddart, J. Fraser (2015) Redox Control of the Binding Modes of an Organic Receptor. Journal of the American Chemical Society, 137 (34). pp. 11057-11068. ISSN 0002-7863. https://resolver.caltech.edu/CaltechAUTHORS:20150909-100621676

[img] PDF - Supplemental Material
See Usage Policy.

3421Kb
[img] Crystallographic Info File (CIF) - Supplemental Material
See Usage Policy.

1207Kb
[img] Crystallographic Info File (CIF) - Supplemental Material
See Usage Policy.

85Kb
[img] Crystallographic Info File (CIF) - Supplemental Material
See Usage Policy.

244Kb
[img] Crystallographic Info File (CIF) - Supplemental Material
See Usage Policy.

501Kb

Use this Persistent URL to link to this item: https://resolver.caltech.edu/CaltechAUTHORS:20150909-100621676

Abstract

The modulation of noncovalent bonding interactions by redox processes is a central theme in the fundamental understanding of biological systems as well as being ripe for exploitation in supramolecular science. In the context of host–guest systems, we demonstrate in this article how the formation of inclusion complexes can be controlled by manipulating the redox potential of a cyclophane. The four-electron reduction of cyclobis(paraquat-p-phenylene) to its neutral form results in altering its binding properties while heralding a significant change in its stereoelectronic behavior. Quantum mechanics calculations provide the energetics for the formation of the inclusion complexes between the cyclophane in its various redox states with a variety of guest molecules, ranging from electron-poor to electron-rich. The electron-donating properties displayed by the cyclophane were investigated by probing the interaction of this host with electron-poor guests, and the formation of inclusion complexes was confirmed by single-crystal X-ray diffraction analysis. The dramatic change in the binding mode depending on the redox state of the cyclophane leads to (i) aromatic donor–acceptor interactions in its fully oxidized form and (ii) van der Waals interactions when the cyclophane is fully reduced. These findings lay the foundation for the potential use of this class of cyclophane in various arenas, all the way from molecular electronics to catalysis, by virtue of its electronic properties. The extension of the concept presented herein into the realm of mechanically interlocked molecules will lead to the investigation of novel structures with redox control being expressed over the relative geometries of their components.


Item Type:Article
Related URLs:
URLURL TypeDescription
http://dx.doi.org/10.1021/jacs.5b05618DOIArticle
http://pubs.acs.org/doi/10.1021/jacs.5b05618PublisherArticle
http://pubs.acs.org/doi/suppl/10.1021/jacs.5b05618PublisherSupporting Information
ORCID:
AuthorORCID
Frasconi, Marco0000-0003-2010-175X
Fernando, Isurika R.0000-0002-8135-3072
Wu, Yilei0000-0001-6756-1855
Liu, Zhichang0000-0003-3412-512X
Liu, Wei-Guang0000-0002-6633-7795
Goddard, William A., III0000-0003-0097-5716
Stoddart, J. Fraser0000-0003-3161-3697
Additional Information:© 2015 American Chemical Society. Received: May 31, 2015; Published: August 3, 2015. We thank Dr. Amy Sarjeant and Charlotte C. Stern for solving the single-crystal X-ray structures. This research is part (Project 32-949) of the Joint Center of Excellence in Integrated Nano-Systems (JCIN) at King Abdulaziz City for Science and Technology (KACST) and Northwestern University (NU). The authors thank both KACST and NU for their continued support of this research. M.R.W. and S.M.D. acknowledge support from the National Science Foundation (NSF) under Grant No. CHE-1266201. W.G.L. and W.A.G. were supported by NSF-EFRI-ODISSEI 1332411. Y.W. thanks the Fulbright Scholar Program for a Research Fellowship and also acknowledges additional support from a Ryan Fellowship awarded under the auspices of the NU International Institute of Nanotechnology (IIN). The authors declare no competing financial interest.
Funders:
Funding AgencyGrant Number
King Abdulaziz City for Science and Technology (KACST)UNSPECIFIED
Northwestern UniversityUNSPECIFIED
NSFCHE-1266201
NSF1332411
Fulbright Scholar ProgramUNSPECIFIED
Ryan FellowshipUNSPECIFIED
Issue or Number:34
Record Number:CaltechAUTHORS:20150909-100621676
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20150909-100621676
Official Citation:Redox Control of the Binding Modes of an Organic Receptor Marco Frasconi, Isurika R. Fernando, Yilei Wu, Zhichang Liu, Wei-Guang Liu, Scott M. Dyar, Gokhan Barin, Michael R. Wasielewski, William A. Goddard, III, and J. Fraser Stoddart Journal of the American Chemical Society 2015 137 (34), 11057-11068 DOI: 10.1021/jacs.5b05618
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:60118
Collection:CaltechAUTHORS
Deposited By: Tony Diaz
Deposited On:09 Sep 2015 21:07
Last Modified:03 Oct 2019 08:53

Repository Staff Only: item control page