Synthesis of CH<sub>3</sub>K in the Gas Phase:  Structural and Mechanistic Trends for Monomeric, Unsolvated CH<sub>3</sub>M and HCCM (M = Li, Na, K)

Douglas B. Grotjahn, T. C. Pesch, M. A. Brewster, L. M. Ziurys

Journal of the American Chemical Society · 2000 · 33 citations · 29 references

Concepts

Abstract

Monomeric, solvent-free CH 3 K has been made in the gas phase and its precise structure determined by millimeter/submillimeter spectroscopy, from which the following parameters were deduced: C−K and C−H bond lengths are 2.633 and 1.135 Å, respectively, and the H−C−H angle is 107.0°. The structure completes a series with those reported for CH 3 Na and CH 3 Li, showing the expected decrease in metal−carbon bond length (2.633 to 2.299 to 1.961 Å) ascending the periodic table, but little change in the H−C−H bond angles, which are all near 107°. The latter observation on these simple monomeric species clearly differs from the range of 104.8−108.2° reported for oligomeric CH 3 M samples in the solid phase, which feature several metal−carbon contacts, showing the importance of measurements on monomeric species. Synthetic details for the methyl compounds and HCCM (M = Li, Na, K) are also discussed. Preparation of HCCLi from HCCBr and Li vapor produced LiBr but possible intermediate radical HCC • was not detected, suggesting synchronous reduction of the C−Br bond. The linear structure of HCCM is contrasted with nonlinear structures of LiCCLi (predicted theoretically), NaCN, and KCN, using Coulombic arguments to explain the different molecular geometries.

References

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