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September 18, 2013Journal of the American Chemical Society65 citations

Aromatizing Olefin Metathesis by Ligand Isolation inside a Metal– Organic Framework

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NVNicolaas A. VermeulenOKOlga KaragiaridiASAmy A. Sarjeant

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Abstract

The aromatizing ring-closing metathesis has been shown to take place inside an extended porous framework. Employing a combination of solvent-assisted linker exchange and postsynthesis modification using olefin metathesis, the noninterpenetrated SALEM-14 was formed and converted catalytically into PAH-MOF-1 with polycyclic aromatic hydrocarbon (PAH) pillars. The metal-organic framework in SALEM-14 prevents "intermolecular" olefin metathesis from occurring between the pillars in the presence of the first generation Hoveyda-Grubbs catalyst, while favoring the production of a PAH, which can be released from the framework under acidic conditions in dimethylsulfoxide.

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Cite This Study

Vermeulen et al. (2013) studied this question.

synapsesocial.com/papers/6a6fc8c33ce530166bc2af92https://doi.org/10.1021/ja407333q
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