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• W3024915440 startingPage "1700" @default.
• W3024915440 abstract "A detailed DFT study involving 50 intermediates, 26 transition states, a range of spin multiplicities and 3 MECPs explains the products (and their distribution) of the reaction of cyclohexyl isocyanide with the Cr–Cr quintuple-bonded complex [LCr]2 (L = N,N′-bis(2,6-diisopropylphenyl-1,4-diazadiene). Using methyl isocyanide as the prototypical isocyanide and [LCr]2 (L = N,N′-bis(2,6-dimethyl-1,4-diazadiene) as the quintuple-bonded system, mechanistic pathways for the formation of diamagnetic [LCr(MeNC)4] (2b) and paramagnetic [L2Cr2[C4(NMe)4](MeNC)2] (3b) and [L2Cr2[C6(NMe)6]] (4b) with an excess of isocyanide and of a paramagnetic product of C–H activation (5b) with 4 equiv of isocyanide are obtained. The ground-state electronic configurations of different products are discussed using an electron-counting scheme. Barriers for minimum energy crossing points (MECPs) and for different transition states control the experimental product distributions." @default.
• W3024915440 created "2020-05-21" @default.
• W3024915440 creator A5030851922 @default.
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• W3024915440 date "2020-05-11" @default.
• W3024915440 modified "2023-10-16" @default.
• W3024915440 title "DFT Study of C–C and C–N Coupling on a Quintuple-Bonded Cr₂ Template: MECP (Minimum Energy Crossing Point) Barriers Control Product Distribution" @default.
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• W3024915440 doi "https://doi.org/10.1021/acs.organomet.9b00841" @default.
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