Abstract
Reported are complexes of the formula Fe(dithiolate)(CO)(2)(diphos) and their use to prepare homo- and heterobimetallic dithiolato derivatives. The starting iron dithiolates were prepared by a one-pot reaction of FeCl(2) and CO with chelating diphosphines and dithiolates, where dithiolate = S(2)(CH(2))(2)(2-) (edt(2-)), S(2)(CH(2))(3)(2-) (pdt(2-)), S(2)(CH(2))(2)(C(CH(3))(2))(2-) (Me(2)pdt(2-)) and diphos = cis-C(2)H(2)(PPh(2))(2) (dppv), C(2)H(4)(PPh(2))(2) (dppe), C(6)H(4)(PPh(2))(2) (dppbz), C(2)H(4)[P(C(6)H(11))(2)](2) (dcpe). The incorporation of (57)Fe into such building block complexes commenced with the conversion of (57)Fe into (57)Fe(2)I(4)( (i) PrOH)(4), which then was treated with K(2)pdt, CO, and dppe to give (57)Fe(pdt)(CO)(2)(dppe). NMR and IR analyses show that these complexes exist as mixtures of all-cis and trans-CO isomers, edt(2-) favoring the former and pdt(2-) the latter. Treatment of Fe(dithiolate)(CO)(2)(diphos) with the Fe(0) reagent (benzylideneacetone)Fe(CO)(3) gave Fe(2)(dithiolate)(CO)(4)(diphos), thereby defining a route from simple ferrous salts to models for hydrogenase active sites. Extending the building block route to heterobimetallic complexes, treatment of Fe(pdt)(CO)(2)(dppe) with [(acenaphthene)Mn(CO)(3)](+) gave [(CO)(3)Mn(pdt)Fe(CO)(2)(dppe)](+) ([3d(CO)](+)). Reduction of [3d(CO)](+) with BH(4)(-) gave the C(s) -symmetric μ-hydride (CO)(3)Mn(pdt)(H)Fe(CO)(dppe) (H3d). Complex H3d is reversibly protonated by strong acids, the proposed site of protonation being sulfur. Treatment of Fe(dithiolate)(CO)(2)(diphos) with CpCoI(2)(CO) followed by reduction by Cp(2)Co affords CpCo(dithiolate)Fe(CO)(diphos) (4), which can also be prepared from Fe(dithiolate)(CO)(2)(diphos) and CpCo(CO)(2). Like the electronically related (CO)(3)Fe(pdt)Fe(CO)(diphos), these complexes undergo protonation to afford the μ-hydrido complexes [CpCo(dithiolate)HFe(CO)(diphos)](+). Low-temperature NMR studies indicate that Co is the kinetic site of protonation.