| 11259012 |
Sinnecker S, Brauer M, Koch W, Anders E: Cs (2) fixation by carbonic anhydrase model systems-a new substrate in the catalytic cycle. Inorg Chem. 2001 Feb 26;40(5):1006-13.
The conversion of CS (2) with common carbonic anhydrase model systems has been studied using Hartree-Fock and density-functional theory methods employing the 6-311+G basis set. The calculated geometries and energetical parameters for [L (3) ZnOH](+)/CS (2) model systems (L = NH (3), imidazole) are compared with those obtained previously for the CO (2) hydration. While the same reaction mechanism applies for both heterocumulenes, the hypothetical conversion of CS (2) to give [L (3) ZnSC (O) SH](+) is characterized by a higher barrier and is much more exothermic than the corresponding CO (2) reaction cascade. Due to the increased number of heteroatoms, additional intermediates and product structures (compared with those involved in the CO (2) conversion) must be taken into account and have been analyzed in detail. The smaller electrophilicity of CS (2) is the reason for the higher activation energies, while the significantly increased exothermicity is due to the strong zinc (II)/sulfur interaction. The reversibility and therefore the existence of a catalytic cycle which could allow comparable CS (2) transformations must be questioned. Nevertheless, an interesting field of stoichiometric zinc-mediated CS (2) transformations is conceivable. |
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