Abstract

Methyltriacetylene - the largest methylated polyacetylene detected in deep space - has been synthesized in the gas phase via the bimolecular reaction of the 1-propynyl radical with diacetylene under single-collision conditions. The barrier-less route to methyltriacetylene represents a prototype of a polyyne chain extension through a radical substitution mechanism and provides a novel low temperature route, in which the propynyl radical piggybacks a methyl group to be incorporated into methylated polyynes. This mechanism overcomes a key obstacle in previously postulated reactions of methyl radicals with unsaturated hydrocarbon, which fail the inclusion of methyl groups into hydrocarbons due to insurmountable entrance barriers thus providing a fundamental understanding on the electronic structure, chemical bonding, and formation of methyl-capped polyacetylenes. These species are key reactive intermediates leading to carbonaceous nanostructures in molecular clouds like TMC-1.

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