7267-16-5Relevant articles and documents
Formation of octachloroacenaphthylene in the pyrolysis of decachlorobiphenyl
Bleise,Kleist,Guenther,Schwuger
, p. 655 - 666 (2007/10/03)
The pyrolytic degradation of decachlorobiphenyl (PCB 209) in the temperature range of 700-1000°C and at a pyrolysis time of 10 seconds generated one main chloroaromatic product. This compound has been identified by HPLC-UV, GC-MS, GC-FTIR and 13C-NMR as octachloroacenaphthylene (OCAN). The mechanism of the nearly quantitative formation of octachloroacenaphthylene (OCAN) occurs via a nonachlorobenzobarrylene radical (Z1R) as an intermediate followed by a rearrangement and further dechlorination to form OCAN. Calculations with the program THERM based on the Benson-group-theory indicated that this mechanism is not possible for lower or nonchlorinated biphenyls.
Dicyanpolyine: neue staebchenfoermige Molekuele aus dem Kohlenstoffplasma
Groesser, Thomas,Hirsch, Andreas
, p. 1390 - 1392 (2007/10/02)
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