Aromatic isoprenoids from the 25–65 Ma saline lacustrine formations in the western Qaidam Basin, NW China
详细信息    查看全文
文摘
Abundant aryl isoprenoids have been detected in source rock extracts from the 25–65 Ma saline lacustrine formations in the western Qaidam Basin, NW China. Identification was based mainly on comparison of mass spectra and gas chromatographic behaviour with literature data. Two pseudohomologous series in the range C13–C40 were assigned as 2,3,6- and 2,3,4-trimethyl monoaryl isoprenoids. The C40 2,3,4-trimethylaryl isoprenoid, okenane, was the most abundant component of the series, while its C40 2,3,6-trimethylaryl isomer, chlorobactane, was present in low abundance. Two C40 monoaromatic isoprenoids with a cyclohexyl ring were tentatively assigned as β-isorenieratane and β-renierapurpurane. One C40 diaryl isoprenoid was identified as isorenieratane. Identification of okenane, chlorobactane and isorenieratane was confirmed by co-elution experiments using synthetic standards. In addition, two novel series of aryl isoprenoids in the C12–C39 range were tentatively assigned as 2,6- and 2,3-dimethylaryl isoprenoids. The C39 2,3-dimethylaryl isoprenoid homologue was the most abundant component of the series, while the C39 2,6-dimethylaryl isomer was only present in low abundance. Two C39 monoaromatic bicyclic compounds were tentatively assigned as 2,6- and 2,3-dimethylaryl isoprenoids with a terminal cyclohexyl ring. Furthermore, a minor C38 component was tentatively assigned as a diaryl isoprenoid with a 2,3-/2,3-dimethyl substitution pattern. These dimethylaryl isoprenoids seem to be formed by demethylation of their parent trimethylaryl isoprenoid counterparts, the location of the demethylated position being exclusively at C-3, C-4 or C-6 of the aromatic ring. This specificity points to a biologically-mediated process (as opposed to an abiotic, maturity-related transformation) that needs to be further investigated.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700