4.8 Article

Unprecedented Five-Coordinate Iron(IV) Imides Generate Divergent Spin States Based on the Imide R-Groups

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 58, 期 24, 页码 8115-8118

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201903132

关键词

imides; iron; macrocycles; N-heterocyclic carbenes; organometallic chemistry

资金

  1. National Science Foundation [NSF-CAREER/CHE-1254536, CHE-1800237]
  2. National Institute of Health [NIH-R15GM117494-01A]
  3. NSF Predoctoral Fellowship
  4. University of Tennessee

向作者/读者索取更多资源

Three five-coordinate iron(IV) imide complexes have been synthesized and characterized. These novel structures have disparate spin states on the iron as a function of the R-group attached to the imide, with alkyl groups leading to low-spin diamagnetic (S=0) complexes and an aryl group leading to an intermediate-spin (S=1) complex. The different spin states lead to significant differences in the bonding about the iron center as well as the spectroscopic properties of these complexes. Mossbauer spectroscopy confirmed that all three imide complexes are in the iron(IV) oxidation state. The combination of diamagnetism and N-15 labeling allowed for the first N-15 NMR resonance recorded on an iron imide. Multi-reference calculations corroborate the experimental structural findings and suggest how the bonding is distinctly different on the imide ligand between the two spin states.

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