The reactions of indoline (I) and tetrahydroquinoline (THQ) with Os-3(
CO)(10)(CH3CN)(2) (1) have been studied. Reaction of 1 with I at ambie
nt temperatures gives Os-3(CO)(10)(mu-H)(mu-eta(2)-C3H7NH) (2), which
decarbonylates thermally to give a mixture of the tautomeric complexes
Os-3(CO)(9)(mu-H)(2)(mu(3)-eta(3)-C8H7N) (3 and 4) whose structures d
iffer by having a mu-alkylidene-imino bonding mode (3) vs a mu-amido-a
ryl bonding mode (4). The conversion of 2 to 3 and 4 follows strictly
first-order kinetics and equilibrium constant K(4/3)=6. Further thermo
lysis of 3 or 4 yields the dehydrogenated cluster Os-3(CO)(9)(mu-H)(2)
(mu(3)-eta(2)-C8H4-NH) (5). In the case of THQ reacting with 1, no dir
ect analog of 2 is observed but a directly analogous pair of tautomers
Os-3(CO)(9)(mu-H)(mu(3)-eta(2)-C9H9N) (6 and 7) are obtained. In addi
tion, the product Os-3(CO)(10)(mu-H)(mu-eta(1)-C9H10N(CH3)CN) (8) is o
btained, which is the result of an apparent nucleophilic attack of THQ
on the coordinated acetonitrile of 1. Thermolysis of 7 yields the deh
ydrogenation product Os-3(CO)(10)(mu-H)(mu-eta(2)-C9H8N) (10), which m
aintains the eta(2)-C(8)-N bonding to the metal core, in sharp contras
t to 5. Thermolysis of 8 yields Os-3(CO)(8)(mu-H)(2)(mu(3)-eta(2)-C9H9
N(CH3)CN) (11) in which the acetonitrile nitrogen caps the trimetallic
core and the C-H bond at C(8) has been activated. Reaction of 3 and 6
with CF3SO3H or CF3CO2H reveals reversible protonation at the nitroge
n of the coordinated I or THQ. Protonation of 7 on the other hand take
s place at the metal core but 7H(+) gradually rearranges to 6H(+) whic
h yields 6 on deprotonation. The solid-state structures of 4, 6, and 1
0 are reported. In sharp contrast to the above results, isotetrahydroq
uinoline (ITHQ) reacts with 1 to give the mu-imidoyl cluster Os-3(CO)(
10)(mu-H)(mu-eta(2)-C9H8N)(13), which decarbonylates to give the mu(3)
-imidoyl cluster Os-3(CO)(9)(mu-H)(mu(3)-eta(2)-C9H8N)(14). The therma
l behavior and dynamics of these complexes are discussed in the contex
t of current models for hydrodenitrification.