Multiplicity control in the polygeminal diazeniumdiolation of active hydrogen bearing carbons: Chemistry of a new type of trianionic molecular propeller
N. Arulsamy et Ds. Bohle, Multiplicity control in the polygeminal diazeniumdiolation of active hydrogen bearing carbons: Chemistry of a new type of trianionic molecular propeller, J AM CHEM S, 123(44), 2001, pp. 10860-10869
Over a century ago, Traube reported the reaction of four nitric oxides with
acetone and sodium ethoxide to yield sodium methanebis(diazene-N-oxide-N'-
hydroxylate) and sodium acetate. However, when this reaction is carried out
in the presence of nitric oxide at slightly elevated pressures (35-40 psi)
, a product corresponding to the addition of six nitric oxides, sodium meth
anetris(diazene-N-oxide-N'-hydroxylate), forms as the main product in addit
ion to a trace of the previously observed sodium methanebis(diazene-N-oxide
-N'-hydroxylate) and sodium acetate. The corresponding potassium salts form
when potassium hydroxide is employed as the base, while lithium hydroxide
results in the formation of lithium methanebis(ldiazene-Noxide-Al'-hydroxyl
ate) exclusively. Nitric oxide reacts with 3,3-dimethylbutan-2-one in the p
resence of sodium and potassium hydroxide in methanol to yield sodium and p
otassium 3,3-dimethylbutan-2-one-1,1,1-tris(diazene-N-oxide-N'-hydroxylate)
, respectively. In contrast, the reaction in the presence of lithium hydrox
ide forms lithium methanebis(diazene-N-oxide-N'-hydroxylate) and lithium pi
valate. The differential reactivity of nitric. oxide with acetone and 3,3-d
imethylbutan-2-one in the presence of the three bases is attributed to comp
eting hydrolytic reactions of the acetyl and trimethylacetyl group-containi
ng intermediates. A mechanism is proposed for the nitric oxide addition to
active methyl groups in these reactions, where the product distribution bet
ween the di- and trisubstituted methanes is under kinetic control of the co
mpeting reactions. The products are characterized by NMR and IR spectroscop
y, differential scanning calorimetry, and elemental analysis. Two different
ially hydrated forms of potassium methanetris(diazene-N-oxide-N'-hydroxylat
e) are characterized by single-crystal X-ray diffraction. From the metathes
is reaction of the silver salt of methanetris(diazene-N-oxide-N'-hydroxylat
e) with ammonium iodide, the corresponding ammonium salt is isolated in 59%
yield, but only trace amounts of methylated products form in the reaction
of the silver salt with methyl iodide. Density functional calculations (B3L
YP/6-311++G**) are used to evaluate the bonding, ground-state structures, a
nd energy landscape for the different conformers of methanetris(diazene-N-o
xide-N'-hydroxylate)(3-) trianion, a new type of a molecular propeller, and
its corresponding triprotonated acid.