TRANSITION-METAL COMPLEXES WITH SULFUR LIGANDS .102. CHANGES IN CONFIGURATION AND REACTIVITY CAUSED BY ALKYL SUBSTITUENTS-R IN [FE(L)(NRS4)] COMPLEXES (L=CO, NO-)(, NO, PME3, N2H4 R=CH3, CH2CH2CO2CH3, CH2CH2CO2)
D. Sellmann et al., TRANSITION-METAL COMPLEXES WITH SULFUR LIGANDS .102. CHANGES IN CONFIGURATION AND REACTIVITY CAUSED BY ALKYL SUBSTITUENTS-R IN [FE(L)(NRS4)] COMPLEXES (L=CO, NO-)(, NO, PME3, N2H4 R=CH3, CH2CH2CO2CH3, CH2CH2CO2), Inorganica Chimica Acta, 219(1-2), 1994, pp. 75-84
In search for complexes revealing functional and structural characteri
stics of the active sites of nitrogenases the iron(II) complexes [Fe(L
)('NES4')] (E=CH2CH2COOCH3; L=CO (2), PMe3 (11), N2H4 (9)) and [Fe('NE
S4')]x (7), [Fe(L)('NmeS4')] (L=CO (1), PMe3 (10), N2H4 (8), NO (13),
NO' (12)) and [Fe('NMeS4')]x (6), Na[Fe(CO)('NAS4')] (16) (A=CH2CH2COO
-) and {Na[Fe('NAS4')}x (15) as well as the free ligands 'NES4'-H-2-HC
l (5), 'NMeS4'-H-2-HCl (4) and Na3-'NAS4' (14) were synthesized. 1 was
characterized by X-ray structure analysis. It crystallizes in the spa
ce group P2(1)/c with a=753.9(4), b=1283.7(8), c=1931.9(10) pm, beta=9
5.86(4)-degrees, Z=4. Unexpectedly, the [Fe(L)('NRS4')] complexes (R=C
H3, CH2CH2CO2CH3, CH2CH2CO2Na) show different coordination geometries
and considerably higher reactivities in comparison to the correspondin
g [Fe(L)('NHS4')] complexes with the parent ligand 'NHS4'2- (2,2'-bis(
2-mercapto-phenylthio)diethylamine(2-)). These differences can be trac
ed back to the fact that the N atom is a tertiary amine in 'NRS4'2- an
d a secondary amine in the 'NHS4'2- ligand. Repulsive interactions amo
ng the three N substituents in the 'NRS4'2- ligands lead to a weakenin
g of the Fe-N bond, to a meso configuration of the [Fe('NS4')] core an
d ultimately to higher reactivities of the [Fe(L)('NRS4')] complexes i
n comparison to the [Fe(L)('NHS4')] parent compounds. The low-spin com
plexes [Fe(CO)('NMeS4')] (1) and [Fe(CO)('NHS4')] (3) may serve as exa
mples: [Fe(CO)('NHS4')] (3) has C1 symmetry and a short Fe-N distance
(207.2(8) pm), whereas [Fe(CO)(['NMeS4')] (1) reveals C(s) symmetry an
d a long Fe-N bond (218.7(4) pm). Such long Fe-N bonds can only be obs
erved in the parent [Fe(L)('NHS4')] complexes with sigma ligands when
electrons occupy antibonding sigma molecular orbitals.