Abstract:
:The purpose of the present study was to evaluate the use of a non-innocent ligand as a surrogate of the anchored [4Fe4S] cubane in a synthetic mimic of the [FeFe] hydrogenase active site. Reaction of 2,3-bis(diphenylphosphino) maleic anhydride (bma) with [Fe(2)(CO)(6)(mu-pdt)] (propanedithiolate, pdt=S(CH(2))(3)S) in the presence of Me(3)NO-2H(2)O afforded the monosubstituted derivative [Fe(2)(CO)(5)(Me(2)NCH(2)PPh(2))(mu-pdt)] (1). This results from the decomposition of the bma ligand and the apparent C-H bond cleavage in the released trimethylamine. Reaction under photolytic conditions afforded [Fe(2)(CO)(4)(bma)(mu-pdt)] (2). Compounds 1 and 2 were characterized by IR, NMR and X-ray diffraction. Voltammetric study indicated that the primary reduction of 2 is centered on the bma ligand.
journal_name
J Inorg Biochemjournal_title
Journal of inorganic biochemistryauthors
Si Y,Charreteur K,Capon JF,Gloaguen F,Pétillon FY,Schollhammer P,Talarmin Jdoi
10.1016/j.jinorgbio.2010.05.011subject
Has Abstractpub_date
2010-10-01 00:00:00pages
1038-42issue
10eissn
0162-0134issn
1873-3344pii
S0162-0134(10)00129-7journal_volume
104pub_type
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