Role of catalytic nitrile decomposition in tricopper complex mediated direct partial oxidation of methane to methanol

被引:5
作者
Moharreri, Ehsan [1 ,2 ]
Jafari, Tahereh [1 ,2 ]
Rathnayake, Dinithi [1 ,2 ]
Khanna, Harshul [1 ,2 ]
Kuo, Chung-Hao [1 ,2 ]
Suib, Steven L. [1 ,2 ]
Nandi, Partha [3 ]
机构
[1] Univ Connecticut, Dept Chem, Storrs, CT 06269 USA
[2] Univ Connecticut, Inst Mat Sci, Storrs, CT 06269 USA
[3] Corp Strategic Res, ExxonMobil Res & Engn, 1545 US 22 East, Annandale, NJ 08801 USA
关键词
HYDROGEN-PEROXIDE; RADZISZEWSKI OXIDATION; OXYGEN; HYDROCARBONS; CONVERSION; ALKANES; ACETONITRILE; SPECTROSCOPY; TEMPERATURE; SELECTIVITY;
D O I
10.1038/s41598-021-98721-2
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Synthetic homogeneous system known to date performing methane to methanol conversion using O-2 as terminal oxidant is unique and based on copper complex with piperazine-based ligand (Cu3L in Fig. 1) in a medium of acetonitrile. Prior work have shown that in order to achieve catalytic turnover, hydrogen peroxide is needed to regenerate the active site. We show in this paper that reaction solvent based on organic nitrile decompose concurrently with methane activation and that in the absence of either acetonitrile, Cu complex or hydrogen peroxide, the catalytic turnover does not happen. We show in this manuscript that the direct methane oxidation to methanol might have been mediated by catalytic Radziszewski oxidation between acetonitrile and H2O2. Additionally we have discovered that in the absence of methane, peroxide mediated acetonitrile decomposition also makes methanol via a background reaction which was hitherto unknown.
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页数:7
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