Carbon monoxide substitutions by trimethyl phosphite in diiron dithiolate complex Fe-Fe bond cleavage, selectivity of the substitutions, crystal structures and electrochemical studies

N.B. Makouf , H.B. Mousser (1) , A. Darchen (2) , A. Mousser

1 UMC - Université frères Mentouri Constantine I
2 ISCR - Institut des Sciences Chimiques de Rennes

The reaction of substitution of carbon monoxide by P(OMe)3 in the complex (μ-η2PhC(S) = C(S)Ph)Fe2(CO)6 1 under thermal activation afforded two colored compounds a binuclear disubstituted complex (μ-PhC(S) = C(S)Ph)Fe2(CO)4 [P(OMe)3]2 2 and a mononuclear iron disubstituted complex (η2PhC(S) = C(S)Ph)Fe(CO)[P(OMe)3]2 3. Mass spectrometry, 1H NMR, IR and electrochemical studies established that two (CO) have been substituted by P(OMe)3 in complexes 2 and 3. The X-ray studies show that the two P(OMe)3 ligands are in apical positions in trans of the iron – iron bound of complex 2 and in equatorial positions in complex 3. However, the substitution reaction of (CO) by P(OMe)3 in complex 1 under electron transfer catalysis (ETC) led to the monosubstituted compound (μ-PhC(S) = C(S)Ph)Fe2(CO)5 [P(OMe)3] 4.

Keywords: Carbon monoxide substitution; Diiron hexacarbonyl complex; Electron transfer catalysis; Single-crystal X-ray study; Thermal activation; [FeFe] hydrogenase

Domains: Chemical Sciences; Chemical Sciences; Organic chemistry

N.B. Makouf, H.B. Mousser, A. Darchen, A. Mousser. Carbon monoxide substitutions by trimethyl phosphite in diiron dithiolate complex Fe-Fe bond cleavage, selectivity of the substitutions, crystal structures and electrochemical studies. Journal of Organometallic Chemistry, 2018, 866, pp.35-42. ⟨10.1016/j.jorganchem.2018.04.005⟩. ⟨hal-01809155⟩