期刊
CHEMICAL COMMUNICATIONS
卷 54, 期 73, 页码 10276-10279出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8cc04409k
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资金
- U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences Separations and Analysis program [DE-SC0017259]
- University of Pennsylvania
- National Science Foundation Graduate Research Fellowship Program
- Center for Undergraduate Research & Fellowships at the University of Pennsylvania
- Camille and Henry Dreyfus Postdoctoral Program in Environmental Chemistry
A methoxy-substituted tripodal hydroxylamine ligand, H(3)TriNOx(OMe), was synthesized and coordinated to rare earth cations for separation purposes. Metrics of the resulting complexes were investigated and compared with their parent TriNOx(3-) counterparts for determination of the molecular basis for the described rare earth separation system. Addition of an electron donating group to the aryl backbone resulted in a more electron rich ligand that increased the equilbrium constant for complex dimerization five-fold. The new separation system yielded efficient Nd/Dy separations in toluene rather than benzene.
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