The reaction of Fe2(pdt)(CO)6 with two equivalents of Ph2PC6H4NH2 (PNH2) affords the amido hydride HFe2(pdt)(CO)2(PNH2)(PNH) {[H1H]0, pdt2− = CH2(CH2S−)2}. Isolated intermediates in this conversion include Fe2(pdt)(CO)5-(κ1-PNH2) and Fe2(pdt)(CO)4(κ2-PNH2). X-ray crystallographic analysis of [H1H]0 shows that the chelating amino/amido–phosphine ligands occupy trans-dibasal positions. The 31P NMR spectrum indicates that [H1H]0 undergoes rapid proton exchange between the amido and amine centers. No exchange was observed for the hydride. Protonation of [H1H]0 gives [HFe2(pdt)(CO)2(PNH2)2]+ ([H21H]+), which contains two equivalent amino–phosphine ligands. Single-crystal X-ray crystallographic analysis of [H21H]+ also reveals hydrogen bonds between the exo amine protons with a THF molecule and BF4. Deprotonation of [H1H]0 with potassium tert-butoxide gave [HFe2(pdt)(CO)2(PNH)2]− ([1H]−), which was characterized spectroscopically. The complex has time-averaged C2 symmetry with two amido–phosphine ligands. FTIR spectroscopic measurements show that υCO shifts by approximately 20 cm−1 in the series [1H]−, [H1H]0, and [H21H]+. These shifts are comparable to those seen for the S-protonation of the (NC)2(CO)Fe-(μ-Scys)2Ni(Scys)2 site in the [NiFe]-hydrogenases.[1]