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Please use this identifier to cite or link to this item: http://hdl.handle.net/10805/2319

Title: The Olefin Metathesis Reaction in the Synthesis of Resorc[4]arenes with Intriguing Architectures
Authors: Ghirga, Francesca
Tutor: Botta, Bruno
Keywords: Supramolecular chemistry
Metathesis reaction
Fullerenes
Resorcarenes
Issue Date: 28-Jan-2014
Abstract: Tetramerization of (E)-2,4-dimethoxycinnamic acid ω-undecenyl ester with ethereal BF3 gave three stereoisomers which were assigned as the chair, cone, and 1,2-alternate conformations. When the three resorc[4]arenes were submitted to olefin metathesis using the second generation Grubbs catalyst, different intra- and inter-molecular products were isolated, depending on conformation and reaction conditions. Molecular modeling studies showed that a basket-like resorc[4]arene, obtained by olefin metathesis of the cone resorc[4]arene ω-undecenyl ester, provide efficient shape complementarity to fullerenes C60 and C70 . Both self-assembly and encapsulation phenomena were demonstrated by UV spectroscopy.
URI: http://hdl.handle.net/10805/2319
Appears in PhD:SCIENZE FARMACEUTICHE

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