ABSTRACT: Described are the syntheses of several Ni(?-SR)2Fe complexes, including hydride derivatives, in a search for improved models for the active site of [NiFe]-hydrogenases. The nickel(II) precursors include (i) nickel with tripodal ligands: Ni(PS3)- and Ni(NS3)- (PS33- = tris(phenyl-2-thiolato)phosphine, NS33- = tris(benzyl-2-thiolato)amine), (ii) traditional diphosphine-dithiolates, including chiral diphosphine R,R-DIPAMP, (iii) cationic Ni(phosphine-imine/amine) complexes, and (iv) organonickel precursors Ni( o-tolyl)Cl(tmeda) and Ni(C6F5)2. The following new nickel precursor complexes were characterized: PPh4[Ni(NS3)] and the dimeric imino/amino-phosphine complexes [NiCl2(PCH?NAn)]2 and [NiCl2(PCH2NHAn)]2 (P = Ph2PC6H4-2-). The iron(II) reagents include [CpFe(CO)2(thf)]BF4, [Cp*Fe(CO)(MeCN)2]BF4, FeI2(CO)4, FeCl2(diphos)(CO)2, and Fe(pdt)(CO)2(diphos) (diphos = chelating diphosphines). Reactions of the nickel and iron complexes gave the following new Ni-Fe compounds: Cp*Fe(CO)Ni(NS3), [Cp(CO)Fe(?-pdt)Ni(dppbz)]BF4, [( R,R-DIPAMP)Ni(?-pdt)(H)Fe(CO)3]BArF4, [(PCH?NAn)Ni(?-pdt)(Cl)Fe(dppbz)(CO)]BF4, [(PCH2NHAn)Ni(?-pdt)(Cl)Fe(dppbz)(CO)]BF4, [(PCH?NAn)Ni(?-pdt)(H)Fe(dppbz)(CO)]BF4, [(dppv)(CO)Fe(?-pdt)]2Ni, {H[(dppv)(CO)Fe(?-pdt)]2Ni]}BF4, and (C6F5)2Ni(?-pdt)Fe(CO)2(dppv) (DIPAMP = (CH2P(C6H4-2-OMe)2)2; BArF4- = [B(C6H3-3,5-(CF3)2]4-)) Within the context of Ni-(SR)2-Fe complexes, these new complexes feature new microenvironments for the nickel center: tetrahedral Ni, chirality, imine, and amine coligands, and Ni-C bonds. In the case of {H[(dppv)(CO)Fe(?-pdt)]2Ni}+, four low-energy isomers are separated by ?3 kcal/mol, one of which features a biomimetic HNi(SR)4 site, as supported by density functional theory calculations.
