期刊
CHEMICAL SCIENCE
卷 8, 期 11, 页码 7545-7551出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7sc02780j
关键词
-
资金
- SERB, New Delhi [EMR/2014/00016]
- IISER-Kolkata (Start-up Grant)
- UGC-New Delhi
The iron complex [(bTAML)Fe-III-OH2](-) (1) selectively catalyses the photocatalytic hydroxylation and epoxidation reactions of alkanes and alkenes, respectively, using water as the oxygen-atom source. Upon the oxidation of unactivated alkanes, which included several substrates including natural products, hydroxylation was observed mostly at the 3 degrees C-H bonds with 3 degrees : 2 degrees selectivity up to similar to 100 : 1. When alkenes were used as the substrates, epoxides were predominantly formed with high yields. In the presence of H-2 O-18, more than 90% of the O-18-labelled oxygen atoms were incorporated into the hydroxylated and epoxide product indicating that water was the primary oxygen source. Mechanistic studies indicate the formation of an active [{(bTAML)Fe-IV}(2)-mu-oxo](2-) (2) dimer from the starting complex 1 via PCET. The subsequent disproportionation of 2 upon addition of substrate, leading to the formation of Fe-V(O), renders the high selectivity observed in these reactions.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据