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Conformational Flexibility of Hybrid [3]- and [4]-Rotaxanes

[Image: see text] The synthesis, structures, and properties of [4]- and [3]-rotaxane complexes are reported where [2]-rotaxanes, formed from heterometallic {Cr(7)Ni} rings, are bound to a fluoride-centered {CrNi(2)} triangle. The compounds have been characterized by single-crystal X-ray diffraction...

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Autores principales: Lockyer, Selena J., Nawaz, Selina, Brookfield, Adam, Fielding, Alistair J., Vitorica-Yrezabal, Inigo J., Timco, Grigore A., Burton, Neil A., Bowen, Alice M., Winpenny, Richard E. P., McInnes, Eric J. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7605720/
https://www.ncbi.nlm.nih.gov/pubmed/32820906
http://dx.doi.org/10.1021/jacs.0c06547
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author Lockyer, Selena J.
Nawaz, Selina
Brookfield, Adam
Fielding, Alistair J.
Vitorica-Yrezabal, Inigo J.
Timco, Grigore A.
Burton, Neil A.
Bowen, Alice M.
Winpenny, Richard E. P.
McInnes, Eric J. L.
author_facet Lockyer, Selena J.
Nawaz, Selina
Brookfield, Adam
Fielding, Alistair J.
Vitorica-Yrezabal, Inigo J.
Timco, Grigore A.
Burton, Neil A.
Bowen, Alice M.
Winpenny, Richard E. P.
McInnes, Eric J. L.
author_sort Lockyer, Selena J.
collection PubMed
description [Image: see text] The synthesis, structures, and properties of [4]- and [3]-rotaxane complexes are reported where [2]-rotaxanes, formed from heterometallic {Cr(7)Ni} rings, are bound to a fluoride-centered {CrNi(2)} triangle. The compounds have been characterized by single-crystal X-ray diffraction and have the formulas [CrNi(2)(F)(O(2)C(t)Bu)(6)]{(BH)[Cr(7)NiF(8)(O(2)C(t)Bu)(16)]}(3) (3) and [CrNi(2)(F)(O(2)C(t)Bu)(6)(THF)]{(BH)[Cr(7)NiF(8)(O(2)C(t)Bu)(16)]}(2) (4), where B = py-CH(2)CH(2)NHCH(2)C(6)H(4)SCH(3). The [4]-rotaxane 3 is an isosceles triangle of three [2]-rotaxanes bound to the central triangle while the [3]-rotaxane 4 contains only two [2]-rotaxanes bound to the central triangle. Studies of the behavior of 3 and 4 in solution by small-angle X-ray scattering and atomistic molecular dynamic simulations show that the structure of 3 is similar to that found in the crystal but that 4 has a different conformation to the crystal. Continuous wave and pulsed electron paramagnetic resonance spectroscopy was used to study the structures present and demonstrate that in frozen solutions (at 5 K) 4 forms more extended molecules than 3 and with a wider range of conformations.
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spelling pubmed-76057202020-11-03 Conformational Flexibility of Hybrid [3]- and [4]-Rotaxanes Lockyer, Selena J. Nawaz, Selina Brookfield, Adam Fielding, Alistair J. Vitorica-Yrezabal, Inigo J. Timco, Grigore A. Burton, Neil A. Bowen, Alice M. Winpenny, Richard E. P. McInnes, Eric J. L. J Am Chem Soc [Image: see text] The synthesis, structures, and properties of [4]- and [3]-rotaxane complexes are reported where [2]-rotaxanes, formed from heterometallic {Cr(7)Ni} rings, are bound to a fluoride-centered {CrNi(2)} triangle. The compounds have been characterized by single-crystal X-ray diffraction and have the formulas [CrNi(2)(F)(O(2)C(t)Bu)(6)]{(BH)[Cr(7)NiF(8)(O(2)C(t)Bu)(16)]}(3) (3) and [CrNi(2)(F)(O(2)C(t)Bu)(6)(THF)]{(BH)[Cr(7)NiF(8)(O(2)C(t)Bu)(16)]}(2) (4), where B = py-CH(2)CH(2)NHCH(2)C(6)H(4)SCH(3). The [4]-rotaxane 3 is an isosceles triangle of three [2]-rotaxanes bound to the central triangle while the [3]-rotaxane 4 contains only two [2]-rotaxanes bound to the central triangle. Studies of the behavior of 3 and 4 in solution by small-angle X-ray scattering and atomistic molecular dynamic simulations show that the structure of 3 is similar to that found in the crystal but that 4 has a different conformation to the crystal. Continuous wave and pulsed electron paramagnetic resonance spectroscopy was used to study the structures present and demonstrate that in frozen solutions (at 5 K) 4 forms more extended molecules than 3 and with a wider range of conformations. American Chemical Society 2020-08-21 2020-09-16 /pmc/articles/PMC7605720/ /pubmed/32820906 http://dx.doi.org/10.1021/jacs.0c06547 Text en This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Lockyer, Selena J.
Nawaz, Selina
Brookfield, Adam
Fielding, Alistair J.
Vitorica-Yrezabal, Inigo J.
Timco, Grigore A.
Burton, Neil A.
Bowen, Alice M.
Winpenny, Richard E. P.
McInnes, Eric J. L.
Conformational Flexibility of Hybrid [3]- and [4]-Rotaxanes
title Conformational Flexibility of Hybrid [3]- and [4]-Rotaxanes
title_full Conformational Flexibility of Hybrid [3]- and [4]-Rotaxanes
title_fullStr Conformational Flexibility of Hybrid [3]- and [4]-Rotaxanes
title_full_unstemmed Conformational Flexibility of Hybrid [3]- and [4]-Rotaxanes
title_short Conformational Flexibility of Hybrid [3]- and [4]-Rotaxanes
title_sort conformational flexibility of hybrid [3]- and [4]-rotaxanes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7605720/
https://www.ncbi.nlm.nih.gov/pubmed/32820906
http://dx.doi.org/10.1021/jacs.0c06547
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