Elrod Lee Taylor, Kim Eunsuk
Department of Chemistry , Brown University , Providence , Rhode Island 02912 , United States.
Inorg Chem. 2018 Mar 5;57(5):2594-2602. doi: 10.1021/acs.inorgchem.7b02956. Epub 2018 Feb 14.
The reduction of nitrate (NO) to nitrite (NO) is of significant biological and environmental importance. While Mo(O) and Mo(O) complexes that mimic the active site structure of nitrate reducing enzymes are prevalent, few of these model complexes can reduce nitrate to nitrite through oxygen atom transfer (OAT) chemistry. We present a novel strategy to induce nitrate reduction chemistry of a previously known catalyst Mo(O)(SN) (2), where SN = bis(4- tert-butylphenyl)-2-pyridylmethanethiolate, that is otherwise incapable of achieving OAT with nitrate. Addition of nitrate with the Lewis acid Sc(OTf) (OTf = trifluoromethanesulfonate) to 2 results in an immediate and clean conversion of 2 to Mo(O)(SN) (1). The Lewis acid additive further reacts with the OAT product, nitrite, to form NO and O. This work highlights the ability of Sc additives to expand the reactivity scope of an existing Mo(O) complex together with which Sc can convert nitrate to stable gaseous molecules.
将硝酸盐(NO)还原为亚硝酸盐(NO)具有重要的生物学和环境意义。虽然模拟硝酸盐还原酶活性位点结构的Mo(O)和Mo(O)配合物很常见,但这些模型配合物中很少有能通过氧原子转移(OAT)化学将硝酸盐还原为亚硝酸盐的。我们提出了一种新策略,以诱导先前已知的催化剂Mo(O)(SN)(2)(其中SN = 双(4-叔丁基苯基)-2-吡啶基甲硫醇盐)发生硝酸盐还原化学,否则该催化剂无法与硝酸盐实现氧原子转移。向2中加入硝酸盐和路易斯酸Sc(OTf)(OTf = 三氟甲磺酸盐)会导致2立即且完全转化为Mo(O)(SN)(1)。路易斯酸添加剂进一步与氧原子转移产物亚硝酸盐反应,形成NO和O。这项工作突出了Sc添加剂扩展现有Mo(O)配合物反应活性范围的能力,Sc可与该配合物一起将硝酸盐转化为稳定的气态分子。