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Updated: May 18, 2026
![Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-(phosphinetriyl)tripiperidine]}palladium Under Mild Reaction Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F51444.jpg&w=3840&q=50)
Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-(phosphinetriyl)tripiperidine]}palladium Under Mild Reaction Conditions
Published on: March 20, 2014
Co(III) imidos exhibiting spin crossover and C-H bond activation
Evan R King1, Graham T Sazama, Theodore A Betley
1Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138, USA.
Abstract:
The reaction of ((Ar)L)Co(py) with (t)BuN(3) afforded the isolable three-coordinate Co-imido complex ((Ar)L)Co(N(t)Bu), which is paramagnetic at room temperature. Variable-temperature (VT) (1)H NMR spectroscopy, VT crystallography, and magnetic susceptibility measurements revealed that ((Ar)L)Co(N(t)Bu) undergoes a thermally induced spin crossover from an S = 0 ground state to a quintet (S = 2) state. The reaction of ((Ar)L)Co(py) with mesityl azide yielded an isolable S = 1 terminal imido complex that was converted into the metallacycloindoline ((Ar)L)Co(κ(2)-NHC(6)H(2)-2,4-Me(2)-6-CH(2)) via benzylic C-H activation.
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