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Although IRCs for the first and second steps should ideally lead to the same intermediate complex, two structures, A-PC1 and A1-PC1, with different water orientations were obtained. Considering the steric hindrance, it is more favorable for the water molecule to attack the C6 atom at the opposition of the C5 methyl group. Since we expect a low barrier for the ring-opening reaction, the energy barriers of steps 1 and 2 were discussed separately
-
Although IRCs for the first and second steps should ideally lead to the same intermediate complex, two structures, A-PC1 and A1-PC1, with different water orientations were obtained. Considering the steric hindrance, it is more favorable for the water molecule to attack the C6 atom at the opposition of the C5 methyl group. Since we expect a low barrier for the ring-opening reaction, the energy barriers of steps 1 and 2 were discussed separately.
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Note that A2-PC1 has one more water molecule than A-PC1, which has no effect on our results because it is the relative energy barriers that are used in our results
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