J Org Chem. 2009 Sep 18;74(18):6907-14. doi: 10.1021/jo9012223.
Thermodynamic trends in carbon-hydrogen bond activation in nitriles and chloroalkanes at rhodium.
The Journal of organic chemistry
Meagan E Evans, Ting Li, Andrew J Vetter, Ryan D Rieth, William D Jones
Affiliations
Affiliations
- Department of Chemistry, University of Rochester, Rochester, New York 14627, USA.
PMID: 19743881
DOI: 10.1021/jo9012223
Abstract
Several transition-metal systems have been used to establish correlations between metal-carbon and carbon-hydrogen bonds. Here, the [Tp'RhL] fragment, where Tp' = tris(3,5-dimethylpyrazolyl)borate and L = neopentyl isocyanide, is used to investigate C-H bond activation in a series of linear alkylnitriles and chloroalkanes. Using a combination of kinetic techniques, relative free energies can be found for the compounds TpRhL(CH(3))H, Tp'RhL[(CH(2))(n)CN]H (n = 1-5), and Tp'RhL[(CH(2))(m)Cl]H (m = 1, 3, 4, 5). It is found that the CN and Cl substituents dramatically strengthen the M-C bond more than anticipated if in the alpha-position, with the effect on bond strength diminishing substantially as the X group moves further from the metal (i.e, beta, gamma, delta). Examination of M-C vs C-H bond strengths shows that the Tp'RhL(CH(2)X)H compounds (X = phenyl, vinyl, CN, Cl) all show a good correlation, as do the alkyl, aryl, and vinyl derivatives. The compounds in the former group, however, have stronger M-C bonds than expected based on the C-H bond strengths and consequently, their correlation is separate from the other unsubstituted compounds.
Publication Types
