TY - JOUR
T1 - Investigations on Organo-Sulfur-Nitrogen Rings and the Thiocyanogen Polymer, (SCN)x
AU - Bowman, W R
AU - Burchell, C J
AU - Kilian, Petr
AU - Slawin, Alexandra Martha Zoya
AU - Wormald, Philip
AU - Woollins, John Derek
PY - 2006/8/16
Y1 - 2006/8/16
N2 - The synthesis and full characterisation of a series of 1,2,4-thiadiazoles is reported. (SCN)(x) has been studied by a variety of techniques and the data compared with 1,2,4-thiadiazole and 1,2,4-dithiazoles. The observed data suggest that the polymer consists of 1,2,4-dithiazole rings linked by nitrogen atoms. For (SCN)(x), the MALDI-TOF mass spectroscopy showed a parent ion at 1149 and a series of peaks with (SCN)(2) repeat units (116 m/z); this result implies that (SCN)(2) may be the monomer unit of the polymer. Its IR spectrum shows a very broad peak with maximum at 1134 cm(-1) consisting of several overlapping peaks in the same region as ring vibrations for 1,2,4-thiadiazole and 1,2,4-dithiazole compounds. Peaks in the Raman spectrum in the range 400480 cm-1 support the presence of disulfide units within the polymer. The solid-state C-13 NMR (99 % C-13-labelled) spectrum is dominated by two singlets of equal intensity at approximately 187 and 184 ppm with low intensity peaks in the range 152-172 ppm, in approximately the same range as both 1,2,4-thiadiazoles and 1,2,4-dithiazoles. The solid-state N-15 NMR (99% N-15 labelled) spectrum displays two major peaks of similar intensity at 236.9 and 197.2 ppm, which are clearly very different environments to those observed in bis(3-bromo-1,2,4-thiadiazol-5-yl) disulfide, but similar to 1,2,4-dithiazoles. The X-ray structures of seven C-S-N systems are reported. Preliminary studies on (SeCN)(x) suggest that literature references to this polymer may be in error with the red solid actually being red selenium.
AB - The synthesis and full characterisation of a series of 1,2,4-thiadiazoles is reported. (SCN)(x) has been studied by a variety of techniques and the data compared with 1,2,4-thiadiazole and 1,2,4-dithiazoles. The observed data suggest that the polymer consists of 1,2,4-dithiazole rings linked by nitrogen atoms. For (SCN)(x), the MALDI-TOF mass spectroscopy showed a parent ion at 1149 and a series of peaks with (SCN)(2) repeat units (116 m/z); this result implies that (SCN)(2) may be the monomer unit of the polymer. Its IR spectrum shows a very broad peak with maximum at 1134 cm(-1) consisting of several overlapping peaks in the same region as ring vibrations for 1,2,4-thiadiazole and 1,2,4-dithiazole compounds. Peaks in the Raman spectrum in the range 400480 cm-1 support the presence of disulfide units within the polymer. The solid-state C-13 NMR (99 % C-13-labelled) spectrum is dominated by two singlets of equal intensity at approximately 187 and 184 ppm with low intensity peaks in the range 152-172 ppm, in approximately the same range as both 1,2,4-thiadiazoles and 1,2,4-dithiazoles. The solid-state N-15 NMR (99% N-15 labelled) spectrum displays two major peaks of similar intensity at 236.9 and 197.2 ppm, which are clearly very different environments to those observed in bis(3-bromo-1,2,4-thiadiazol-5-yl) disulfide, but similar to 1,2,4-dithiazoles. The X-ray structures of seven C-S-N systems are reported. Preliminary studies on (SeCN)(x) suggest that literature references to this polymer may be in error with the red solid actually being red selenium.
KW - nitrogen heterocycles
KW - polymers
KW - structure elucidation
KW - sulfur heterocycles
KW - INORGANIC POLYMERS
KW - PARATHIOCYANOGEN
KW - HETEROCYCLES
KW - OXIDATION
KW - SE
KW - POLYTHIOCYANOGENS
KW - COMPLEXES
KW - CHLORIDES
KW - IODINE
KW - ACID
UR - http://www.scopus.com/inward/record.url?scp=33748302252&partnerID=8YFLogxK
UR - http://www3.interscience.wiley.com/cgi-bin/fulltext/112651137/PDFSTART
U2 - 10.1002/chem.200501528
DO - 10.1002/chem.200501528
M3 - Article
SN - 0947-6539
VL - 12
SP - 6366
EP - 6381
JO - Chemistry - A European Journal
JF - Chemistry - A European Journal
IS - 24
ER -