Targeting synthetic analogues of the metallo-sulfur active sites of nickel enzymes capable of important catalysis
作者:Matt C. Smith、J. Elaine Barclay、Sian C. Davies、David L. Hughes、David J. Evans
DOI:10.1039/b307175h
日期:——
The nickel containing enzymes NiFe-hydrogenase, carbon monoxide dehydrogenase and acetyl-CoA synthase are able to catalyse environmentally, and potentially industrially, important reactions: hydrogen uptake; carbondioxide/carbon monoxide interconversion; and incorporation of carbon monoxide to form acetyl-CoA, respectively. Progress toward the synthesis of nickel–iron complexes with structural features
含镍的酶NiFe氢化酶,一氧化碳脱氢酶和乙酰辅酶A合酶能够催化环境方面以及潜在的工业上重要的反应:氢的吸收;二氧化碳/一氧化碳相互转化;并结合一氧化碳以形成乙酰辅酶A。描述了具有与这些酶的活性位点相关的结构特征的镍铁配合物的合成进展,以及第一个甲基化镍铁双金属配合物[Fe(N S 3)(NO)-S } Ni(CH 3)(dppe)](N S 3 = N(CH 2 CH 2 S)3 3−),与乙酰辅酶A合酶机制中拟议的机制中间体有关。
Smith, Matt C.; Longhurst, Steven; Barclay, J. Elain, Journal of the Chemical Society. Dalton Transactions (2001), 2001, # 9, p. 1387 - 1388
作者:Smith, Matt C.、Longhurst, Steven、Barclay, J. Elain、Cramer, Stephen P.、Davies, Sian C.、Hughes, David L.、Gu, Wei-Wei、Evans, David J.