Harnessing the active site triad: merging hemilability, proton responsivity, and ligand-based redox-activity

被引:12
作者
Baumgardner, Douglas F. [1 ]
Parks, Wyatt E. [1 ]
Gilbertson, John D. [1 ]
机构
[1] Western Washington Univ, Dept Chem, Bellingham, WA 98225 USA
关键词
BOND ACTIVATION; WATER OXIDATION; IRON CATALYST; NITRIC-OXIDE; COMPLEX; ELECTRON; REDUCTION; NITRATE; O-2; HYDROSILYLATION;
D O I
10.1039/c9dt04470a
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Metalloenzymes catalyze many important reactions by managing the proton and electron flux at the enzyme active site. The motifs utilized to facilitate these transformations include hemilabile, redox-active, and so called proton responsive sites. Given the importance of incorporating and understanding these motifs in the area of coordination chemistry and catalysis, we highlight recent milestones in the field. Work incorporating the triad of hemilability, redox-activity, and proton responsivity into single ligand scaffolds will be described.
引用
收藏
页码:960 / 965
页数:6
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