• DOI:10.1021/JA0713633
• Corpus ID: 41409460

Selective activation and functionalization of linear alkanes initiated under ambient conditions by a tungsten allyl nitrosyl complex.

@article{Tsang2007SelectiveAA,
  title={Selective activation and functionalization of linear alkanes initiated under ambient conditions by a tungsten allyl nitrosyl complex.},
  author={Jenkins Y. K. Tsang and Miriam S. A. Buschhaus and Peter Legzdins},
  journal={Journal of the American Chemical Society},
  year={2007},
  volume={129 17},
  pages={
          5372-3
        }
}

• Jenkins Y. K. Tsang, M. Buschhaus, P. Legzdins
• Published 7 April 2007
• Chemistry
• Journal of the American Chemical Society

The new tungsten allyl nitrosyl complex, Cp*W(NO)(η3-CH2CHCHMe)(CH2CMe3) (1) (Cp* = η5-C5Me5; Me = CH3), selectively activates the terminal C−H bonds of n-pentane at room temperature and forms the thermally stable compound, Cp*W(NO)(η3-CH2CHCHMe)(CH2CH2CH2CH2Me) (2), from which the n-pentyl ligand may be selectively released as 1-iodopentane by treatment with I2. Current experimental evidence suggests that the C−H activation chemistry derived from 1 proceeds via two distinct steps:  (1) formation of the intermediate η2-diene complex, Cp*W(NO)(η2-CH2CHCHCH2) (A) via intramolecular β-H elimination of neopentane from 1, and (2) incorporation of n-pentane into A via intermolecular β-H addition to produce 2. Intermediate A can be trapped by PMe3 as the Cp*W(NO)(η2-CH2CHCHCH2)(PMe3) adduct (3), and the solid-state molecular structures of 1, 2, and 3 have been established by single-crystal X-ray crystallographic analyses.