期刊
FARADAY DISCUSSIONS
卷 220, 期 -, 页码 105-112出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9fd00034h
关键词
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资金
- National Natural Science Foundation of China [21520102003]
- 973 Program [2012CB725302]
- CAS Interdisciplinary Innovation Team
- Hubei Province Natural Science Foundation of China [2017CFA010]
The mechanistic investigation of copper-catalysed transformations has been an important and fundamental task. Herein, we report via XAS and EPR spectroscopy that the sodium bis(trimethylsilyl)amide could reduce Cu(ii) to a Cu(i) species serving as an electron donor. XAS spectroscopy demonstrates that the newly formed Cu(i) species is the Cu[N(TMS)(2)](2)Na ate complex, in which the nitrogen atoms coordinate with copper linearly.
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