Cargando…
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...
Autores principales: | , , , , , , , , , |
---|---|
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 |
_version_ | 1783604363326914560 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7605720 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT lockyerselenaj conformationalflexibilityofhybrid3and4rotaxanes AT nawazselina conformationalflexibilityofhybrid3and4rotaxanes AT brookfieldadam conformationalflexibilityofhybrid3and4rotaxanes AT fieldingalistairj conformationalflexibilityofhybrid3and4rotaxanes AT vitoricayrezabalinigoj conformationalflexibilityofhybrid3and4rotaxanes AT timcogrigorea conformationalflexibilityofhybrid3and4rotaxanes AT burtonneila conformationalflexibilityofhybrid3and4rotaxanes AT bowenalicem conformationalflexibilityofhybrid3and4rotaxanes AT winpennyrichardep conformationalflexibilityofhybrid3and4rotaxanes AT mcinnesericjl conformationalflexibilityofhybrid3and4rotaxanes |