Cargando…

Synthesis and Dynamics of Nanosized Phenylene–Ethynylene–Butadiynylene Rotaxanes and the Role of Shape Persistence

Phenylacetylene‐based [2]rotaxanes were synthesized by a covalent‐template approach by aminolysis of the corresponding prerotaxanes. The wheel and the bulky stoppers are made of phenylene–ethynylene–butadiynylene macrocycles of the same size. The stoppers are large enough to enable the synthesis and...

Descripción completa

Detalles Bibliográficos
Autores principales: Schweez, Christopher, Shushkov, Philip, Grimme, Stefan, Höger, Sigurd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4797704/
https://www.ncbi.nlm.nih.gov/pubmed/26836984
http://dx.doi.org/10.1002/anie.201509702
_version_ 1782422007135076352
author Schweez, Christopher
Shushkov, Philip
Grimme, Stefan
Höger, Sigurd
author_facet Schweez, Christopher
Shushkov, Philip
Grimme, Stefan
Höger, Sigurd
author_sort Schweez, Christopher
collection PubMed
description Phenylacetylene‐based [2]rotaxanes were synthesized by a covalent‐template approach by aminolysis of the corresponding prerotaxanes. The wheel and the bulky stoppers are made of phenylene–ethynylene–butadiynylene macrocycles of the same size. The stoppers are large enough to enable the synthesis and purification of the rotaxane. However, the wheel unthreads from the axle at elevated temperatures. The deslipping kinetics and the activation parameters were determined. We described theoretically the unthreading by state‐of‐the‐art DFT‐based molecular‐mechanics models and a string method for the simulation of rare events. This approach enabled us to characterize in detail the unthreading mechanism, which involves the folding of the stopper during its passage through the wheel opening, a process that defies intuitive geometrical considerations. The conformational and energetic features of the transition allowed us to infer the molecular residues controlling the disassembly timescale.
format Online
Article
Text
id pubmed-4797704
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-47977042016-03-21 Synthesis and Dynamics of Nanosized Phenylene–Ethynylene–Butadiynylene Rotaxanes and the Role of Shape Persistence Schweez, Christopher Shushkov, Philip Grimme, Stefan Höger, Sigurd Angew Chem Int Ed Engl Communications Phenylacetylene‐based [2]rotaxanes were synthesized by a covalent‐template approach by aminolysis of the corresponding prerotaxanes. The wheel and the bulky stoppers are made of phenylene–ethynylene–butadiynylene macrocycles of the same size. The stoppers are large enough to enable the synthesis and purification of the rotaxane. However, the wheel unthreads from the axle at elevated temperatures. The deslipping kinetics and the activation parameters were determined. We described theoretically the unthreading by state‐of‐the‐art DFT‐based molecular‐mechanics models and a string method for the simulation of rare events. This approach enabled us to characterize in detail the unthreading mechanism, which involves the folding of the stopper during its passage through the wheel opening, a process that defies intuitive geometrical considerations. The conformational and energetic features of the transition allowed us to infer the molecular residues controlling the disassembly timescale. John Wiley and Sons Inc. 2016-02-02 2016-03-01 /pmc/articles/PMC4797704/ /pubmed/26836984 http://dx.doi.org/10.1002/anie.201509702 Text en © 2016 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Communications
Schweez, Christopher
Shushkov, Philip
Grimme, Stefan
Höger, Sigurd
Synthesis and Dynamics of Nanosized Phenylene–Ethynylene–Butadiynylene Rotaxanes and the Role of Shape Persistence
title Synthesis and Dynamics of Nanosized Phenylene–Ethynylene–Butadiynylene Rotaxanes and the Role of Shape Persistence
title_full Synthesis and Dynamics of Nanosized Phenylene–Ethynylene–Butadiynylene Rotaxanes and the Role of Shape Persistence
title_fullStr Synthesis and Dynamics of Nanosized Phenylene–Ethynylene–Butadiynylene Rotaxanes and the Role of Shape Persistence
title_full_unstemmed Synthesis and Dynamics of Nanosized Phenylene–Ethynylene–Butadiynylene Rotaxanes and the Role of Shape Persistence
title_short Synthesis and Dynamics of Nanosized Phenylene–Ethynylene–Butadiynylene Rotaxanes and the Role of Shape Persistence
title_sort synthesis and dynamics of nanosized phenylene–ethynylene–butadiynylene rotaxanes and the role of shape persistence
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4797704/
https://www.ncbi.nlm.nih.gov/pubmed/26836984
http://dx.doi.org/10.1002/anie.201509702
work_keys_str_mv AT schweezchristopher synthesisanddynamicsofnanosizedphenyleneethynylenebutadiynylenerotaxanesandtheroleofshapepersistence
AT shushkovphilip synthesisanddynamicsofnanosizedphenyleneethynylenebutadiynylenerotaxanesandtheroleofshapepersistence
AT grimmestefan synthesisanddynamicsofnanosizedphenyleneethynylenebutadiynylenerotaxanesandtheroleofshapepersistence
AT hogersigurd synthesisanddynamicsofnanosizedphenyleneethynylenebutadiynylenerotaxanesandtheroleofshapepersistence