下面是文献里的一段话，能不能帮我翻一下，自己翻译的老是感觉有些意思不是特别明白. 先谢谢了
Depending on the position of the substituent in the arene ring, the benzoic acid can undergo either ortho-hydroxylation (forming salicylates) or oxidative decarboxylation followed by hydroxylation at the ipso-carbon (making phenols). The salicylates obtained from ortho-hydroxylation are excellent bidentate ligands and form stable iron(III) complexes that exclude the possibility of catalytic turnover. However, as reported in this paper, the phenolates obtained from ipso-hydroxylation are more susceptible to displacement by substrate, and multiple turnovers of phenol formation are observed for benzoic acids with electron withdrawing substituents. 返回小木虫查看更多