As a result of our ongoing studies on resorcarenes, we obtained three new resorc[5]arene decamethyl ethers containing cyanomethyl side chains together with the three previously described resorc[4]arenes 2a–2c by treatment of 2-(2,4-dimethoxyphenyl)acrylonitrile with BF3·Et2O. From the X-ray crystallographic structure of 3a, molecular mechanics calculations of the three novel stereoisomers in the gas phase, and the NMR spectroscopic data, the three compounds were attributed architectures of partial 1,3-alternate (3a), partial cone (3b) and partial 1,2-alternate (3c). The relative positions of the substituents were determined by DIF NOE experiments.

Cyano-resorc[5]arenes: isolation, conformation and crystal structure

ZAPPIA, GIOVANNI;
2006

Abstract

As a result of our ongoing studies on resorcarenes, we obtained three new resorc[5]arene decamethyl ethers containing cyanomethyl side chains together with the three previously described resorc[4]arenes 2a–2c by treatment of 2-(2,4-dimethoxyphenyl)acrylonitrile with BF3·Et2O. From the X-ray crystallographic structure of 3a, molecular mechanics calculations of the three novel stereoisomers in the gas phase, and the NMR spectroscopic data, the three compounds were attributed architectures of partial 1,3-alternate (3a), partial cone (3b) and partial 1,2-alternate (3c). The relative positions of the substituents were determined by DIF NOE experiments.
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11576/2300875
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