期刊
ORGANOMETALLICS
卷 30, 期 14, 页码 3704-3707出版社
AMER CHEMICAL SOC
DOI: 10.1021/om200508k
关键词
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资金
- NSF Center for Enabling New Technologies through Catalysis (CENTC)
Tuning the aryl substituents of N,N'-diaryl-2,3-dimethyl-1,4-diaza-1,3-butadiene (DAB) ligands promotes the challenging C-C bond-forming reductive elimination from Pt-IV diimine complexes [(DAB)Pt(CH3)(3)(solvent)](+) (2) under mild conditions. Experimental results and density functional calculations indicate that 2,6-aryl substitution promotes reductive elimination by facilitating dissociation of the coordinating solvent by close to 10 kcal mol(-1), but too much steric bulk inhibits the formation of 2 in the one-electron outersphere oxidation of (DAB)Pt(CH3)(2) (1).
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