Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/93265
Title: Characterization of new sulfide ions (C2S3 .+) from ethenedithione by ion-molecule reactions
Authors: Gerbaux, P.
Flammang, R.
Pedersen, C.Th.
Wong, M.W. 
Issue Date: 1999
Citation: Gerbaux, P.,Flammang, R.,Pedersen, C.Th.,Wong, M.W. (1999). Characterization of new sulfide ions (C2S3 .+) from ethenedithione by ion-molecule reactions. Journal of Physical Chemistry A 103 (19) : 3666-3671. ScholarBank@NUS Repository.
Abstract: Collisional activation (high or low translational energy) and neutralization-reionization mass spectrometries appear inefficient for the characterization of the connectivity of isomeric C2S3 .+ ions generated by dissociative ionization of 1,2-dithiolo[4,3-c][1,2]dithiole-3,6-dione (1), 1,2-dithiolo[4,3-c][1,2]dithiole-3-one-6-thione (2), and 1,3,4,6-tetrapentalene-2,5-dione (3). In contrast, ion-molecule reactions (particularly with nitric oxide) readily differentiate the C-sulfide ethenedithione ion, SCCS2 .+ (4), and the S-sulfide ethenedithione ion, SCCSS.+ (5). The collisional activation spectra of these ion-molecule reaction products have been recorded on a new type of hybrid tandem mass spectrometer of sectors-quadrupole-sectors configuration. The characterization of the isomeric C2S3 .+ ions is supported by ab initio calculations at the G2(MP2,SVP) level. The C-sulfide ethenedithione ion is predicted to be more stable than the S-sulfide form by 91 kJ mol-1. The calculated reaction enthalpies for the two isomeric forms C2S3 .+ with nitric oxide support the characterization by ion-molecule reactions.
Source Title: Journal of Physical Chemistry A
URI: http://scholarbank.nus.edu.sg/handle/10635/93265
ISSN: 10895639
Appears in Collections:Staff Publications

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