Complementary hydrogen bonds and ionic interactions give access to the engineering of organometallic crystals
- 1 January 1999
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in J. Chem. Soc., Dalton Trans.
- No. 1,p. 1-8
- https://doi.org/10.1039/a806069j
Abstract
A crystal synthesis strategy based on a sequence of redox/acid–base/self-assembly/crystallisation processes has been devised and successfully applied to prepare a number of mixed organic/organometallic and organometallic/organometallic crystalline materials. An adequate choice of the building blocks permits design and construction of mono-, two- and three-dimensional superanion framework structures encapsulating organometallic cations. The superanions are generated by partial deprotonation of polyprotic acids from the reaction with the organometallic hydroxides [Cr(η6-C6H6)2][OH] and [Co(η5-C5H5)2][OH], produced in situ by direct oxidation of the neutral complexes [Cr(η6-C6H6)2] and [Co(η5-C5H5)2]. The anionic superstructures are held together by a combination of neutral and interionic O–H · · · O hydrogen bonds, while the interaction with the organometallic cations is based on a profusion of C–H · · · O bonds reinforced via charge assistance.Keywords
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