Abstract
The sterically encumbered NacNac ligand, [HC(MeCNAr)2]− (Ar = 2,6-i-Pr2C6H3), was investigated as a platform for supporting Lu-halide complexes, sought for their potential capability of being further converted into hydrocarbyl derivatives via metathetical chemistries with alkali metal alkyls. These substituted analogs were targeted as potentially viable candidates for alkane elimination chemistries, with an eye towards the formation of an isolable Lu-alkylidene fragment.
Original language | English |
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Pages (from-to) | 187-190 |
Number of pages | 4 |
Journal | Journal of Organometallic Chemistry |
Volume | 857 |
DOIs | |
State | Published - Feb 15 2018 |
Externally published | Yes |
Funding
ADS acknowledges the G.T. Seaborg Institute at Los Alamos National Laboratory for funding a Postdoctoral Fellowship. Los Alamos National Laboratory is operated by Los Alamos National Security, LLC, for the National Nuclear Security Administration of the U.S. Department of Energy under contract DE-AC5206NA25396.
Funders | Funder number |
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G.T. Seaborg Institute | |
U.S. Department of Energy | DE-AC5206NA25396 |
National Nuclear Security Administration | |
Los Alamos National Laboratory |
Keywords
- Alkyl
- Alkylidene
- Chloride/Halide
- Lutetium
- NacNac