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Title: A spectroscopic study of the reaction of Cu atoms with CO in a rotating cryostat: Evidence for the formation of CuCO, Cu(CO) sub 3 , and Cu sub 2 (CO) sub 6

Journal Article · · Journal of Physical Chemistry; (USA)
DOI:https://doi.org/10.1021/j100338a026· OSTI ID:5296687
; ; ;  [1]
  1. National Research Council, Ottawa, Ontario (Canada)

Reaction of {sup 63}Cu atoms with CO has been studied in inert hydrocarbon matrices in a rotating cryostat at 77 K at EPR, FTIR, and UV/visible spectroscopy. CuCO and Cu(CO){sub 3} have been identified by EPR spectroscopy. CuCO has the magnetic parameters a{sub 63} = 3961 MHz, a{sub 13} = 191 MHz, and g = 1.9966 and is a linear molecule with most of the unpaired spin located in an sp-hybridized orbital on Cu. It is unstable and disappears rapidly above 77 K. Cu(CO){sub 3} is a planar trigonal {pi} radical with a {sup 2}A{sub 2}{prime}{prime} electronic ground state and a{sub 17} = 11.2 MHz which indicates significant unpaired spin population on the ligands. It has three infrared bands at 1998, 1988, and 1978 cm{sup {minus}1} which are assigned to the CO stretching mode of a D{sub 3h} molecule in three different trapping sites and is significantly more stable than CuCO. There are no bands in the FTIR spectra from Cu(CO){sub 2}. Cu{sub 2}(CO){sub 6} is formed in significant yields in adamantane and cyclohexane at 77 K and has a major CO stretching mode at 2035 cm{sup {minus}1}. Optical spectra of Cu(CO){sub 3} and Cu{sub 2}(CO){sub 6} in adamantane have {sup 2}A{sub 1}{prime} {l arrow} {sup 2}A{sub 2}{prime}{prime} and {sigma}* {l arrow} {sigma} electronic transitions at 565 and 405 nm, respectively.

OSTI ID:
5296687
Journal Information:
Journal of Physical Chemistry; (USA), Vol. 93:1; ISSN 0022-3654
Country of Publication:
United States
Language:
English