Unidirectional rotary motion in a metal–organic framework
Overcrowded alkene-based light-driven molecular motors are able to perform large-amplitude repetitive unidirectional rotations. Their behaviour is well understood in solution. However, Brownian motion precludes the precise positioning at the nanoscale needed to harness cooperative action. Here, we d...
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| Published in | Nature nanotechnology Vol. 14; no. 5; pp. 488 - 494 |
|---|---|
| Main Authors | , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
London
Nature Publishing Group UK
01.05.2019
Nature Publishing Group |
| Subjects | |
| Online Access | Get full text |
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| Abstract | Overcrowded alkene-based light-driven molecular motors are able to perform large-amplitude repetitive unidirectional rotations. Their behaviour is well understood in solution. However, Brownian motion precludes the precise positioning at the nanoscale needed to harness cooperative action. Here, we demonstrate molecular motors organized in crystalline metal–organic frameworks (MOFs). The motor unit becomes a part of the organic linker (or strut), and its spatial arrangement is elucidated through powder and single-crystal X-ray analyses and polarized optical and Raman microscopies. We confirm that the light-driven unidirectional rotation of the motor units is retained in the MOF framework and that the motors can operate in the solid state with similar rotary speed (rate of thermal helix inversion) to that in solution. These ‘moto-MOFs’ could in the future be used to control dynamic function in crystalline materials.
Overcrowded alkene-based motors are made part of the crystalline structure of a metal–organic framework. It is shown that they retain the same rotatory speed and unidirectionality as in solution. |
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| AbstractList | Overcrowded alkene-based light-driven molecular motors are able to perform large-amplitude repetitive unidirectional rotations. Their behaviour is well understood in solution. However, Brownian motion precludes the precise positioning at the nanoscale needed to harness cooperative action. Here, we demonstrate molecular motors organized in crystalline metal-organic frameworks (MOFs). The motor unit becomes a part of the organic linker (or strut), and its spatial arrangement is elucidated through powder and single-crystal X-ray analyses and polarized optical and Raman microscopies. We confirm that the light-driven unidirectional rotation of the motor units is retained in the MOF framework and that the motors can operate in the solid state with similar rotary speed (rate of thermal helix inversion) to that in solution. These 'moto-MOFs' could in the future be used to control dynamic function in crystalline materials. Overcrowded alkene-based light-driven molecular motors are able to perform large-amplitude repetitive unidirectional rotations. Their behaviour is well understood in solution. However, Brownian motion precludes the precise positioning at the nanoscale needed to harness cooperative action. Here, we demonstrate molecular motors organized in crystalline metal–organic frameworks (MOFs). The motor unit becomes a part of the organic linker (or strut), and its spatial arrangement is elucidated through powder and single-crystal X-ray analyses and polarized optical and Raman microscopies. We confirm that the light-driven unidirectional rotation of the motor units is retained in the MOF framework and that the motors can operate in the solid state with similar rotary speed (rate of thermal helix inversion) to that in solution. These ‘moto-MOFs’ could in the future be used to control dynamic function in crystalline materials. Overcrowded alkene-based motors are made part of the crystalline structure of a metal–organic framework. It is shown that they retain the same rotatory speed and unidirectionality as in solution. Overcrowded alkene-based light-driven molecular motors are able to perform large-amplitude repetitive unidirectional rotations. Their behaviour is well understood in solution. However, Brownian motion precludes the precise positioning at the nanoscale needed to harness cooperative action. Here, we demonstrate molecular motors organized in crystalline metal–organic frameworks (MOFs). The motor unit becomes a part of the organic linker (or strut), and its spatial arrangement is elucidated through powder and single-crystal X-ray analyses and polarized optical and Raman microscopies. We confirm that the light-driven unidirectional rotation of the motor units is retained in the MOF framework and that the motors can operate in the solid state with similar rotary speed (rate of thermal helix inversion) to that in solution. These ‘moto-MOFs’ could in the future be used to control dynamic function in crystalline materials.Overcrowded alkene-based motors are made part of the crystalline structure of a metal–organic framework. It is shown that they retain the same rotatory speed and unidirectionality as in solution. Overcrowded alkene-based light-driven molecular motors are able to perform large-amplitude repetitive unidirectional rotations. Their behaviour is well understood in solution. However, Brownian motion precludes the precise positioning at the nanoscale needed to harness cooperative action. Here, we demonstrate molecular motors organized in crystalline metal-organic frameworks (MOFs). The motor unit becomes a part of the organic linker (or strut), and its spatial arrangement is elucidated through powder and single-crystal X-ray analyses and polarized optical and Raman microscopies. We confirm that the light-driven unidirectional rotation of the motor units is retained in the MOF framework and that the motors can operate in the solid state with similar rotary speed (rate of thermal helix inversion) to that in solution. These 'moto-MOFs' could in the future be used to control dynamic function in crystalline materials.Overcrowded alkene-based light-driven molecular motors are able to perform large-amplitude repetitive unidirectional rotations. Their behaviour is well understood in solution. However, Brownian motion precludes the precise positioning at the nanoscale needed to harness cooperative action. Here, we demonstrate molecular motors organized in crystalline metal-organic frameworks (MOFs). The motor unit becomes a part of the organic linker (or strut), and its spatial arrangement is elucidated through powder and single-crystal X-ray analyses and polarized optical and Raman microscopies. We confirm that the light-driven unidirectional rotation of the motor units is retained in the MOF framework and that the motors can operate in the solid state with similar rotary speed (rate of thermal helix inversion) to that in solution. These 'moto-MOFs' could in the future be used to control dynamic function in crystalline materials. |
| Author | Danowski, Wojciech Roke, Diederik Wezenberg, Sander J. Abdolahzadeh, Shaghayegh Browne, Wesley R. Feringa, Ben L. van Leeuwen, Thomas |
| Author_xml | – sequence: 1 givenname: Wojciech surname: Danowski fullname: Danowski, Wojciech organization: Centre for Systems Chemistry, Stratingh Institute for Chemistry, University of Groningen – sequence: 2 givenname: Thomas surname: van Leeuwen fullname: van Leeuwen, Thomas organization: Centre for Systems Chemistry, Stratingh Institute for Chemistry, University of Groningen – sequence: 3 givenname: Shaghayegh surname: Abdolahzadeh fullname: Abdolahzadeh, Shaghayegh organization: Molecular Inorganic Chemistry Group, Stratingh Institute for Chemistry, University of Groningen – sequence: 4 givenname: Diederik surname: Roke fullname: Roke, Diederik organization: Centre for Systems Chemistry, Stratingh Institute for Chemistry, University of Groningen – sequence: 5 givenname: Wesley R. orcidid: 0000-0001-5063-6961 surname: Browne fullname: Browne, Wesley R. email: w.r.browne@rug.nl organization: Centre for Systems Chemistry, Stratingh Institute for Chemistry, University of Groningen, Molecular Inorganic Chemistry Group, Stratingh Institute for Chemistry, University of Groningen – sequence: 6 givenname: Sander J. orcidid: 0000-0001-9192-3393 surname: Wezenberg fullname: Wezenberg, Sander J. email: s.j.wezenberg@rug.nl organization: Centre for Systems Chemistry, Stratingh Institute for Chemistry, University of Groningen – sequence: 7 givenname: Ben L. orcidid: 0000-0003-0588-8435 surname: Feringa fullname: Feringa, Ben L. email: b.l.feringa@rug.nl organization: Centre for Systems Chemistry, Stratingh Institute for Chemistry, University of Groningen |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30886378$$D View this record in MEDLINE/PubMed |
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| Title | Unidirectional rotary motion in a metal–organic framework |
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