Abstract
Abstract A series of bisethynyl compounds, IX and XII, were prepared by a modified ethynylation using N-methyl-2-pyrrolidone in good yields. Intramolecular oxidative coupling of the bisethynyl compounds has been achieved with high-dilution technique to give relatively good yields of highly strained or strainless [m.n]paracyclophadiynes I and cyclic diacetylenes XIII. From the comparison of the electronic spectra of these diacetylenic compounds, it is concluded that abnormal spectra of Ic and Id are attributed to the transannular π-electronic interaction between benzene nucleus and diacetylenic unit rather than the ring strain in the molecules. In addition, a marked down-field shift of aromatic protons in Ic compared with the other paracyclophadiynes is explained in terms of the transannular shielding effect of diacetylenic linkage.
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