Reaction of Fe(CO)(2)(NO)(2) and sparteine/tetramethylethylenediamine (TMEDA) in tetrahydrofuran afforded the electron paramagnetic resonance (EPR)-silent, neutral {Fe(NO)(2)}(10) dinitrosyliron complexes (DNICs) [(sparteine)Fe(NO)(2)] (1) and [(TMEDA) Fe(NO)(2)] (2), respectively. The stable and isolable anionic {Fe(NO)(2)}(9) DNIC [(S(CH2)(3)S)Fe(NO)(2)](-)(4), with a bidentate alkylthiolate coordinated to a {Fe(NO)(2)} motif, was prepared by the reaction of [S(CH2)S-3](2-) and the cationic {Fe(NO)(2)}(9) [(sparteine)Fe(NO)(2)](+) (3) obtained from the reaction of complex 1 and [NO][BF4] in CH3CN. Transformation from the neutral complex 1 to the anionic complex 4 was verified via the cationic complex 3. Here complex 3 acts as an {Fe(NO)(2)}-donor reagent in the presence of thiolates. The EPR spectra of complexes 3 and 4 exhibit an isotropic signal with g = 2.032 and 2.031 at 298 K, respectively, the characteristic g value of {Fe(NO)(2)}(9) DNICs. On the basis of N-O/Fe-N(O) bond lengths of the single-crystal X-ray structures of the {Fe-(NO)(2)}(9)/{Fe(NO)(2)}(10) DNICs, the oxidation level of the {Fe(NO)(2)} core of DNICs can be unambiguously assigned. The mean N-O distances falling in the range of 1.214(6)-1.189(4) angstrom and the Fe-N(O) bond distances in the range of 1.650(7)-1.638(3) angstrom are assigned as the neutral {Fe(NO)(2)}(10) DNICs. In contrast, the mean N-O bond distances ranging from 1.178(3)to1.160(6) angstrom and the mean Fe-N(O) bond distances ranging from 1.695(3) to 1.661(4) angstrom are assigned as the anionic/neutral/cationic {Fe(NO)(2)}(9) DNICs. In addition, an EPR spectrum in combination with the IR v(NO) (the relative position of the v(NO) stretching frequencies and their difference Delta v(NO)) spectrum may serve as an efficient tool for discrimination of the existence of the anionic/cationic/neutral {Fe(NO)(2)}(9) DNICs and the neutral {Fe(NO)(2)}(10) DNICs.