期刊
INORGANIC CHEMISTRY
卷 56, 期 8, 页码 4555-4567出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.6b03094
关键词
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资金
- COMOCHOL project within the Emergence 2013 program from Projects Initiatives d'excellence Idex UNITI [UT 2014-590]
- CNRS (Chirafun network)
- Ministry of Science and Higher Education in Poland (an Outstanding Young Scientist scholarship)
- National Science Foundation [CHE 1560881, 1265833]
- Center for Computational Research (CCR) at the University at Buffalo for computational resources
- Division Of Chemistry
- Direct For Mathematical & Physical Scien [1265833, 1560881] Funding Source: National Science Foundation
Five tris(beta-diketonato) complexes of ruthenium(III), chromium(III), and cobalt(III) [Ru(Buacac)(3) (1), Ru(Oacac)(3) (2), Cr(Buacac)(3) (3), Cr(Oacac)(3) (4), and Co(Buacac)(3) (5), where Buacac = 3-butylpentane-2,4-dionato and Oacac = 3-octylpentane-2,4-dionato] with a chiral propeller-like structure have been prepared. Ligands and complexes syntheses are presented together with characterization of the compounds by H-1 and C-13 NMR spectroscopy, mass spectrometry, IR, UV-vis, electronic circular dichroism (ECD) spectroscopy, electrochemistry studies, and first-principles calculations. The crystal structures of 1 and 5 have also been obtained and analyzed. A comparison of the H-1 NMR spectra of diamagnetic (ligands and 5) and paramagnetic (1 and 2) species is presented. Optical resolution of the five complexes has been achieved for the first time by supercritical fluid chromatography using a chiral column, giving rise to very high purity grades in all cases. ECD measurements and calculations have led to the assignment of the absolute configuration, Delta or Lambda, of each enantiomer for 1-5. Spectroelectrochemical UV-vis and ECD studies have been performed on ruthenium Lambda-2 and chromium Lambda-4 complexes, revealing their redox-triggered chiroptical switching confirming the noninnocence character of the beta-diketonate ligands.
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