4.8 Article

ATerminal Iron Nitrilimine Complex: Accessing the Terminal Nitride through Diazo N-N Bond Cleavage

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 58, 期 51, 页码 18547-18551

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201910428

关键词

diazo compounds; iron; N-heterocyclic carbenes; N-N activation; terminal nitrides

资金

  1. Swiss National Science Foundation
  2. Fonds der Chemischen Industrie
  3. German-American Fulbright Commission
  4. Friedrich-Alexander-University ErlangenNgrnberg (FAU)

向作者/读者索取更多资源

A novel method for the N-N bond cleavage of trimethylsilyl diazomethane is reported for the synthesis of terminal nitride complexes. The lithium salt of trimethylsilyl diazomethane was used to generate a rare terminal nitrilimine transition metal complex with partially occupied d-orbitals. This iron complex 2 was characterized by CHN combustion analysis, H-1 and C-13 NMR spectroscopic analysis, single-crystal X-ray crystallography, SQUID magnetometry, Fe-57 Mossbauer spectroscopy, and computational analysis. The combined results suggest a high-spin d(6) (S=2) electronic configuration and an allenic structure of the nitrilimine ligand. Reduction of 2 results in release of the nitrilimine ligand and formation of the iron(I) complex 3, which was characterized by CHN combustion analysis, H-1 NMR spectroscopic analysis, and single-crystal X-ray crystallography. Treatment of 2 with fluoride salts quantitatively yields the diamagnetic Fe-IV nitride complex 4, with concomitant formation of cyanide and trimethylsilyl fluoride through N-N bond cleavage.

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