Abstract

Three electronic transitions of the isoelectronic species HC2nH- and HC2n-1N- and one of the neutral polyacetylenes HC2nH (n = 6−12) have been observed by absorption spectroscopy in neon matrixes. Anions produced in an electron impact source were mass-selected and codeposited with excess of neon at 6 K. The HC2nH species were formed from the anions by photodetachment. A well-structured band system at 780 nm for HC12H-, and shifting by regular increments to 1325 nm for HC24H-, is assigned to two overlapping electronic transitions of 2Π ← X2Π symmetry. Another 2Π ← X2Π transition with broader features is observed in the 300−480 nm region. Corresponding transitions are observed for the isoelectronic cyanosubstituted anions HC2n-1N-. The neutral polyacetylenes show a vibrationally well-resolved UV band system attributed to the 1 ← X1 electronic transition. The energy of the electronic transition shows a characteristic inverse dependence on the carbon chain length.

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