Literature DB >> 15161291

Dynamic devices. Shape switching and substrate binding in ion-controlled nanomechanical molecular tweezers.

Anne Petitjean1, Richard G Khoury, Nathalie Kyritsakas, Jean-Marie Lehn.   

Abstract

As examples of supramolecular devices performing chemical (ionic, molecular) control of binding events and models of related natural systems, two molecular conformational switches are described, which display cation-controlled nanomechanical motion coupled to substrate binding and release. The substrate binding relies on donor/acceptor interactions, provided by intercalation between planar sites located at the extremities of the switching units, whereas cation complexation is responsible for conformational regulation. The terpyridine py-py-py-based receptor is activated toward substrate binding upon complexation of a zinc(II) cation and operates in a two-state process. The replacement of the central pyridine by a 4,6-disubstituted pyridimine as in py-pym-py induces a state reversal and yields a new receptor which binds a substrate in the absence of cation, and releases it when copper(I) is introduced, following a three-step process. These systems represent effector-triggered supramolecular switching devices leading toward multistate nanomechanical chemical systems. These two systems illustrate the use of simple conformational switches in the binding site and allosteric regulation of substrate affinity.

Entities:  

Year:  2004        PMID: 15161291     DOI: 10.1021/ja031915r

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


  18 in total

Review 1.  Artificial Molecular Machines.

Authors:  Sundus Erbas-Cakmak; David A Leigh; Charlie T McTernan; Alina L Nussbaumer
Journal:  Chem Rev       Date:  2015-09-08       Impact factor: 60.622

2.  Conformational changes and chiroptical switching of enantiopure bis-helicenic terpyridine upon Zn(2+) binding.

Authors:  Helena Isla; Monika Srebro-Hooper; Marion Jean; Nicolas Vanthuyne; Thierry Roisnel; Jamie L Lunkley; Gilles Muller; J A Gareth Williams; Jochen Autschbach; Jeanne Crassous
Journal:  Chem Commun (Camb)       Date:  2016-04-07       Impact factor: 6.222

3.  Control of Nanospaces with Molecular Devices.

Authors:  Fabien Durola; Henry Dube; Dariush Ajami; Julius Rebek
Journal:  Supramol Chem       Date:  2011-01       Impact factor: 1.688

4.  Glycoluril-Derived Molecular Clips are Potent and Selective Receptors for Cationic Dyes in Water.

Authors:  Nengfang She; Damien Moncelet; Laura Gilberg; Xiaoyong Lu; Vladimir Sindelar; Volker Briken; Lyle Isaacs
Journal:  Chemistry       Date:  2016-08-05       Impact factor: 5.236

5.  Theoretical study on noncovalent interaction of molecular tweezers by Zn(II) salphen-azo-crown ether triads receptor.

Authors:  Hui Li; Xin Zheng; Zishang Jia; Xueye Wang
Journal:  J Mol Model       Date:  2020-02-01       Impact factor: 1.810

6.  The ouroborand: a cavitand with a coordination-driven switching device.

Authors:  Fabien Durola; Julius Rebek
Journal:  Angew Chem Int Ed Engl       Date:  2010-04-19       Impact factor: 15.336

Review 7.  Nucleoside, nucleotide and oligonucleotide based amphiphiles: a successful marriage of nucleic acids with lipids.

Authors:  Arnaud Gissot; Michel Camplo; Mark W Grinstaff; Philippe Barthélémy
Journal:  Org Biomol Chem       Date:  2008-03-05       Impact factor: 3.876

8.  Anthracene functionalized terpyridines - synthesis and properties.

Authors:  Falk Wehmeier; Jochen Mattay
Journal:  Beilstein J Org Chem       Date:  2010-05-27       Impact factor: 2.883

9.  High-Yielding Flow Synthesis of a Macrocyclic Molecular Hinge.

Authors:  Christopher D Jones; Laurence J Kershaw Cook; David Marquez-Gamez; Konstantin V Luzyanin; Jonathan W Steed; Anna G Slater
Journal:  J Am Chem Soc       Date:  2021-05-07       Impact factor: 15.419

10.  The multiple roles of histidine in protein interactions.

Authors:  Si-Ming Liao; Qi-Shi Du; Jian-Zong Meng; Zong-Wen Pang; Ri-Bo Huang
Journal:  Chem Cent J       Date:  2013-03-01       Impact factor: 4.215

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