Lin, C
ORCID: 0000-0001-5609-4358, Darling, GR
ORCID: 0000-0001-9329-9993, Forster, M, McBride, F
ORCID: 0000-0003-2985-3173, Massey, A and Hodgson, A
ORCID: 0000-0001-8677-7467
(2020)
Hydration of a 2D Supramolecular Assembly: Bitartrate on Cu(110)
Journal of the American Chemical Society, 142 (32).
pp. 13814-13822.
ISSN 0002-7863, 1520-5126
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Hydration_TA_230620.pdf - Author Accepted Manuscript Download (9MB) | Preview |
Abstract
Hydration layers play a key role in many technical and biological systems, but our understanding of these structures remains very limited. Here, we investigate the molecular processes driving hydration of a chiral metal-organic surface, bitartrate on Cu(110), which consists of hydrogen-bonded bitartrate rows separated by exposed Cu. Initially water decorates the metal channels, hydrogen bonding to the exposed O ligands that bind bitartrate to Cu, but does not wet the bitartrate rows. At higher temperature, water inserts into the structure, breaks the existing intermolecular hydrogen bonds, and changes the adsorption site and footprint. Calculations show this process is driven by the creation of stable adsorption sites between the carboxylate ligands, to allow hydration of O-Cu ligands within the interior of the structure. This work suggests that hydration of polar metal-adsorbate ligands will be a dominant factor in many systems during surface hydration or self-assembly from solution.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | 3402 Inorganic Chemistry, 3403 Macromolecular and Materials Chemistry, 34 Chemical Sciences |
| Depositing User: | Symplectic Admin |
| Date Deposited: | 22 Jul 2020 08:32 |
| Last Modified: | 01 Mar 2026 03:30 |
| DOI: | 10.1021/jacs.0c04747 |
| Related Websites: | |
| URI: | https://livrepository.liverpool.ac.uk/id/eprint/3094823 |
| Disclaimer: | The University of Liverpool is not responsible for content contained on other websites from links within repository metadata. Please contact us if you notice anything that appears incorrect or inappropriate. |
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