4.7 Article

A series of dithiocarbamates for americium, curium, and californium

期刊

DALTON TRANSACTIONS
卷 47, 期 41, 页码 14452-14461

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8dt02658k

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资金

  1. Heavy Element Chemistry Program at LANL by the Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences, U.S. Department of Energy
  2. U.S. Department of Energy
  3. National Nuclear Security Administration of U.S. Department of Energy [DE-AC52-06NA25396]
  4. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Heavy Elements Chemistry Program [DE-FG02-13ER16414]
  5. U.S. Department of Energy (DOE), Office of Science, Basic Energy Sciences (BES) [DE-SC0016568]
  6. Glenn T. Seaborg Institute
  7. LDRD office
  8. U.S. Department of Energy (DOE) [DE-SC0016568] Funding Source: U.S. Department of Energy (DOE)

向作者/读者索取更多资源

Characterizing how actinide properties change across the f-element series is critical for improving predictive capabilities and solving many nuclear problems facing our society. Unfortunately, it is difficult to make direct comparisons across the 5f-element series because so little is known about trans-plutonium elements. Results described herein help to address this issue through isolation of An(S2CNEt2)(3)(N2C12H8) (Am, Cm, and Cf). These findings included the first single crystal X-ray diffraction measurements of Cm-S (mean of 2.86 +/- 0.04 angstrom) and Cf-S (mean of 2.84 +/- 0.04 angstrom) bond distances. Furthermore, they highlight the potential of An(S2CNEt2)(3)(N2C12H8) for providing a test bed for comparative analyses of actinide versus lanthanide bonding interactions.

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