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  Managing Hydrogen Bonding in Clathrate Hydrates by Crystal Engineering

Shin, K., Moudrakovski, I. L., Ratcliffe, C. I., & Ripmeester, J. A. (2017). Managing Hydrogen Bonding in Clathrate Hydrates by Crystal Engineering. Angewandte Chemie International Edition, 56(22), 6171-6175.

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 Creators:
Shin, K., Author
Moudrakovski, I. L.1, Author           
Ratcliffe, C. I., Author
Ripmeester, J. A., Author
Affiliations:
1Max Planck Institute for Solid State Research, Heisenbergstraße 1, Stuttgart, Germany, ou_persistent13              

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Free keywords: crystal engineering; hydrates; methanol; powder X-ray diffraction; water chemistry
 Abstract: Methanol is one of the most common inhibitors for clathrate hydrate formation. Crystalline clathrate hydrates containing methanol were synthesized and analyzed by powder X-ray diffraction and C-13 NMR spectroscopy. The data obtained demonstrate that methanol can be a helper guest for forming structure I, structure II, and structure H clathrate hydrates, as long as the lattice framework contains NH4F. The latter acts as a lattice stabilizer by providing sites for strong hydrogen bonding of the normally disruptive methanol hydroxy group. NH4F and methanol can be considered key materials for crystal engineering of clathrate hydrates, as the modified lattices allow preparation of hydrates of non-traditional water-soluble guests such as alcohols and diols. Methanol takes on the role of an unconventional helper guest. This extends clathrate chemistry to a realm where neither hydrophobic guests nor high pressures are required. This also suggests that more stable lattices can be engineered for applications such as gas storage.

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Language(s): eng - English
 Dates: 2017
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 734945
ISI: 000401326300028
 Degree: -

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Title: Angewandte Chemie International Edition
Source Genre: Journal
 Creator(s):
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Publ. Info: WEINHEIM : WILEY-V C H VERLAG GMBH
Pages: - Volume / Issue: 56 (22) Sequence Number: - Start / End Page: 6171 - 6175 Identifier: ISSN: 1433-7851