Abstract
Condensation of Fe(2)(SH)(2)(CO)(6), acetaldehyde, and (NH(4))(2)CO(3) affords the methyl-substituted azadithiolate Fe(2)[(SCHMe)(2)NH](CO)(6) (1). The complex exists mainly (~95%) as the meso diastereomer, but the d,l diastereoisomers could be detected. DFT calculations predict that the meso isomer would be 2.5 kcal/mol more stable than the d,l isomer due to conventional nonbonding interactions between the methyl groups and the ring hydrogen atoms. Crystallographic analysis of meso-1 confirms that the two methyl groups are equatorial, constraining the diferraazadithiolate bicycle to a conformation that desymmetrizes the diiron center. The lowered symmetry is confirmed by the observation of two (13)C NMR signals in the FeCO region under conditions of fast turnstile rotation at the Fe(CO)(3) groups. The pK(a) value of the amine in 1 is 7.89 (all pK(a)'s determined in MeCN solution), which is similar to a redetermined value for Fe(2)[(SCH(2))(2)NH](CO)(6) (2, pK(a) = 7.98) and only slightly less basic than the tertiary amine Fe(2)[(SCH(2))(2)NMe](CO)(6) (pK(a) = 8.14). Substitution of 1 with PMe(3) proceeded via the intermediacy of two isomers of Fe(2)[(SCHMe)(2)NH](CO)(5)(PMe(3)), affording Fe(2)[(SCHMe)(2)NH](CO)(4)(PMe(3))(2) (3). (31)P NMR spectra confirm that the two PMe(3) ligands in 3 are nonequivalent, consistent with the desymmetrizing effect of the dithiolate. The pK(a) value of the amine in 3 was found to be 11.3. Using triphenylphosphine, we prepared Fe(2)[(SCHMe)(2)NH](CO)(5)(PPh(3)) as a single regioisomer.