期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 135, 期 13, 页码 4938-4941出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja400836u
关键词
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资金
- NIH [GM070757]
- Beckman Institute
- Gordon and Betty Moore Foundation
- Sanofi-Aventis BRP at Caltech
- Office of Biological and Environmental Research
- NIH NIGMS [P41GM103393]
- NCRR [P41RR001209]
The synthesis and characterization of Fe-diphosphineborane complexes are described in the context of N-2 functionalization chemistry. Iron aminoimides can be generated at room temperature under 1 atm N-2 and are shown to react with E-H bonds from PhSiH3 and H-2. The resulting products derive from delivery of the E fragment to N alpha and the H atom to B. The flexibility and lability of the Fe-BPh interactions in these complexes engender this reactivity.
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