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Low temperature synthesis study of metal-organic framework CPO-27 : investigating metal, solvent and base effects down to -78 °C

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Morris_2017_DT_CPO_27_AAM.pdf (1.075Mb)
Date
07/07/2017
Author
Vornholt, Simon M.
Henkelis, Susan E.
Morris, Russell E.
Keywords
QD Chemistry
NDAS
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Abstract
CPO-27-M (M = Co, Mg, Ni, Zn) metal-organic frameworks have been successfully synthesized at temperatures down to -78 °C in a range of solvent systems and their crystallinity and morphology analyzed by powder X-ray diffraction and scanning electron microscopy. CPO-27-Mg and -Zn could be synthesized at lower temperatures using MeOH-NaOH as the solvent with CPO-27-Zn showing the most crystalline material at -78 °C. CPO-27-Zn afforded the most crystalline samples of all studies in MeOH-TEA. However, in MeOH a non-porous monomeric [Zn(H2dhtp)(H2O)2] complex was formed when no base was present. In THF with base (NaOH, TEA) the reaction produced crystalline MOFs in a controlled and stable manner at low temperatures, whilst the reagents were insoluble in THF at low temperature when no base was present. SEM was used to analyze the morphologies of the products.
Citation
Vornholt , S M , Henkelis , S E & Morris , R E 2017 , ' Low temperature synthesis study of metal-organic framework CPO-27 : investigating metal, solvent and base effects down to -78 °C ' , Dalton Transactions , vol. 46 , no. 25 , pp. 8298-8303 . https://doi.org/10.1039/C7DT01223C
Publication
Dalton Transactions
Status
Peer reviewed
DOI
https://doi.org/10.1039/C7DT01223C
ISSN
1477-9226
Type
Journal article
Rights
Copyright © 2017, The Royal Society of Chemistry. This work is made available online in accordance with the publisher’s policies. This is the author created, accepted version manuscript following peer review and may differ slightly from the final published version. The final published version of this work is available at https://doi.org/ 10.1039/C7DT01223C
Description
We thank the EPSRC (EP/K005499/1) (EP/K503162/1) for their financial support of this project and the EPSRC Capital for Great Technologies (EP/L017008/1).
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  • University of St Andrews Research
URI
http://hdl.handle.net/10023/13874

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