Sterically directed functionalization of the redox-active bis(imino)acenaphthene ligand class: An experimental and theoretical investigation

Journal of the American Chemical Society

Volumn 135, Issue 37, 2013, Pages 13939-13946

  Evans, Daniel A ^a   Vargas Baca, Ignacio ^b   Cowley, Alan H ^a  

^a UNIVERSITY OF TEXAS AT AUSTIN   (United States)

^b MCMASTER UNIVERSITY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

DEAROMATIZATION; EPR SPECTROSCOPY; FUNCTIONALIZATIONS; REACTION PATHWAYS; SINGLE CRYSTAL X-RAY DIFFRACTION; STERIC CONGESTION; THEORETICAL INVESTIGATIONS; THEORETICAL STUDY;

LIGANDS; X RAY DIFFRACTION;

CHELATION;

ACENAPHTHENE DERIVATIVE; IMINE;

ALKYLATION; AROMATIZATION; ARTICLE; CHEMICAL STRUCTURE; DENSITY FUNCTIONAL THEORY; ELECTRON SPIN RESONANCE; NUCLEOPHILICITY; OXIDATION REDUCTION REACTION; REACTION ANALYSIS; SINGLE CRYSTAL X RAY DIFFRACTION; SYNTHESIS; THEORETICAL STUDY; X RAY DIFFRACTION;

EID: 84884469940     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja407070y     Document Type: Article

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