854927-06-3

Basic information

• Product Name: Cu((C₂H₅)2NC₆H₄NO)3⁽¹⁺⁾*PF₆^(1-)=[Cu((C₂H₅)2NC₆H₄NO)3]PF₆
• Synonyms: Cu((C₂H₅)2NC₆H₄NO)3⁽¹⁺⁾*PF₆^(1-)=[Cu((C₂H₅)2NC₆H₄NO)3]PF₆
• CAS NO: 854927-06-3
• Molecular Weight: 743.212
• Mol File: 854927-06-3.mol

Chemical Properties

• CAS DataBase Reference: Cu((C₂H₅)2NC₆H₄NO)3⁽¹⁺⁾*PF₆^(1-)=[Cu((C₂H₅)2NC₆H₄NO)3]PF₆(CAS DataBase Reference)
• NIST Chemistry Reference: Cu((C₂H₅)2NC₆H₄NO)3⁽¹⁺⁾*PF₆^(1-)=[Cu((C₂H₅)2NC₆H₄NO)3]PF₆(854927-06-3)
• EPA Substance Registry System: Cu((C₂H₅)2NC₆H₄NO)3⁽¹⁺⁾*PF₆^(1-)=[Cu((C₂H₅)2NC₆H₄NO)3]PF₆(854927-06-3)

Safety Data

• Hazardous Substances Data: 854927-06-3(Hazardous Substances Data)

Upstream product

• 64443-05-6 tetrakis(actonitrile)copper(I) hexafluorophosphate 
• 120-22-9 N,N-diethyl-4-nitrosoaniline 

Relevant articles and documents

Nitrosoarene-Cu(I) complexes are intermediates in copper-catalyzed allylic amination

Reactions of nitrosobenzene and N,N′-diethyl-4-nitrosoaniline with [Cu(CH3CN)4]PF6 produce novel homoleptic Cu(I)-nitrosoarene complexes, [Cu(ArNO)3]PF6, 1 (Ar = Ph) and 2 (Ar = 4-Et2NC6H4NO). The X-ray structure of 2 reveals that the copper is coordinated in a severely distorted trigonal planar geometry to the N-atom of the nitrosoarene ligand. Reactions of the PhNO complex 1 with olefins and an olefin/diene mixture provide evidence for its role as an intermediate and possibly the active nitrogen transfer agent in the Cu-catalyzed allylic amination of olefins by aryl hydroxylamines. Copyright

Mechanistic studies of copper(I)-catalyzed allylic amination

The reactions of nitrosobenzene and N,N′-diethyl-4-nitrosoaniline with [Cu(CH3CN)4]PF6 provide novel Cu(I) complexes, [Cu(PhNO)3]PF6 (1) and [Cu(Et 2NPhNO)3]PF6 (2); in 2 the copper atom is N-coordinated to the nitrosoarenes in a distorted trigonal planar geometry. Complex 1 is strongly implicated as a reactive intermediate in the Cu(I)-catalyzed allylic amination of olefins based on (i) its isolation from the catalytic reaction, (ii) its stoichiometric regioselective allylic amination of α-methyl styrene (AMS), (iii) the non-involvement of free PhNO in its amination of AMS, and (iv) its function as a catalyst for the amination of alkenes from phenylhydroxylamine. The reaction between AMS and 1 (80°C, dioxane) is first order in both alkene and 1. Relative rate studies of the reaction of 1 with para substituted AMS derivatives gives a Hammett ρ value of -0.035. Alkene adducts isolated from the reaction of 1 with styrene and α-methylstyrene are formulated as [(PhNO)3Cu(η2- alkene)]PF6 (7,8) on the basis of spectroscopic characterization and thermolysis. PM3 and DFT MO calculations support the role of [(alkene)Cu(RNO)3]+ and (η1- or η3-allyl)Cu(RNO)2(RNHOH)+ complexes as probable catalytic intermediates and address the origin of the distinctive reaction regioselectivity. A mechanistic scheme is proposed which is consistent with the accumulated experimental and computational results.