Issue 6, 1998

3,6-Dihydro[1,2]dithiolo[4,3-c][1,2]dithiole-3,6-dithione and oxo analogues: a comparative study of the thermal (FVP) and electron ionization (EI) induced fragmentations

Abstract

Flash-vacuum pyrolysis (FVP) of the dithiolodithioledithione 2 in the 700–1000 °C temperature range affords carbon subsulfide, carbon disulfide and disulfur with high yields. This has been demonstrated by using a combination of FVP/IR (argon matrix) and FVP/MS(MS) experiments. S[double bond, length half m-dash]C[double bond, length half m-dash]C[double bond, length half m-dash]C[double bond, length half m-dash]C[double bond, length half m-dash]S is generated as ions by dissociative ionization of 2, not as neutrals upon pyrolysis. Similar behaviour is noted for the oxygen analogue 4: pyrolytic formation of carbon subsulfide, carbon oxysulfide and disulfur. It is also demonstrated that, upon dissociative ionization, dithiolodithioledione 3 and thioxodithiolodithiolone 4 constitute an interesting source of new cumulenic ions derived from carbon subsulfide and carbon oxysulfide, tentatively assigned as SCCCS+–S˙ and OCCCS+–S˙ radical cations by collisional activation (high and low energy) experiments and ion–molecule reactions with nitric oxide.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1998, 1403-1406

3,6-Dihydro[1,2]dithiolo[4,3-c][1,2]dithiole-3,6-dithione and oxo analogues: a comparative study of the thermal (FVP) and electron ionization (EI) induced fragmentations

C. Th. Pedersen, R. Flammang, P. Gerbaux and E. Fanghänel, J. Chem. Soc., Perkin Trans. 2, 1998, 1403 DOI: 10.1039/A800654G

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