Catalytic metathesis of carbon dioxide with heterocumulenes mediated by titanium isopropoxide

Article abstract of DOI:10.1039/b417713d

The insertion of an isopropoxide ligand of titanium isopropoxide into heterocumulenes gives a product that carries out metathesis at elevated temperatures by undergoing insertion of a second heterocumulene in a head to head fashion, followed by an extrusion reaction. The Royal Society of Chemistry 2005.

Full text of DOI:10.1039/b417713d

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COMMUNICATION
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Catalytic metathesis of carbon dioxide with heterocumulenes mediated
by titanium isopropoxide{
Rajshekhar Ghosh and Ashoka G. Samuelson*
Received (in Cambridge, UK) 25th November 2004, Accepted 26th January 2005
First published as an Advance Article on the web 24th February 2005
DOI: 10.1039/b417713d
The insertion of an isopropoxide ligand of titanium isoprop-
oxide into heterocumulenes gives a product that carries out
metathesis at elevated temperatures by undergoing insertion of
a second heterocumulene in a head to head fashion, followed
by an extrusion reaction.
subsequently extrudes a different heterocumulene, other than the
one which was inserted, leading to a metathesis reaction.
Formation of new carbon–carbon double bonds by a metal carbene
catalyzed olefin metathesis has found wide utility in synthetic
1
2
3
chemistry. Stoichiometric or catalytic exchange between multi-
ply bonded substrates has recently been extended to carbon–
heteroatom double bonds. Vanadium oxo and imido complexes
and group 14 complexes have been reported to be catalysts for the
metathesis of phenyl isocyanate to give N,N9-diphenylcarbodi-
Scheme 1 Insertion of two molecules of ArNCO in a head to head
fashion and elimination of carbon dioxide from 1.
The reaction of titanium isopropoxide and phenyl isocyanate led
to the formation of a mixture of complexes (Scheme 2), which was
not possible to separate. The complexes were hydrolyzed and the
TiO2 removed by filtration. The organic products formed by
insertion of the isopropoxide ligand into phenyl isocyanate (3a)
were extracted and characterized. A small amount of (4a), formed
by insertion of carbodiimide into a carbamate, was also isolated
4
imide and carbon dioxide. Carbodiimide metathesis is catalyzed
by a number of complexes leading to the formation of unsym-
5
,6
metrical carbodiimides. Phosphoranes have also been shown to
7
act as catalysts in the metathesis of carbodiimides. Metathesis of
cumulenes with readily available greenhouse gases like carbon
dioxide and carbon monoxide has gained importance as it can
8
generate useful compounds like carbodiimides. Metathesis of
(for crystallographic characterization of 3a and 4a see ESI{){.
carbon dioxide with carbodiimide leading to the formation of
6,9
isocyanates has also been demonstrated. Recently Bergman
et al. have shown the formation of a six membered metallacycle
intermediate by insertion of an isocyanate into the Ir–N bond of
10
an iridium guanidinate in similar reactions.
In this study we report the metathesis reactions of phenyl
isocyanate, carbon dioxide, carbon disulfide and 1,3-diphenyl
carbodiimide using titanium isopropoxide. Isopropoxide insertion
is a key step in these reactions.
The insertion of heterocumulenes into titanium isopropoxides
11,12
had been investigated by several workers in the 1970s.
As part
Scheme 2 Metathesis of two equivalents of aryl isocyanate with titanium
isopropoxide and the products formed on hydrolysis of the reaction
mixture.
of our reinvestigation of the insertion of aryl isocyanates into
titanium isopropoxides, the reaction was carried out at a higher
temperature in refluxing toluene. Along with the inserted
carbamates, we were surprised to find products formed from the
insertion of isopropoxide into carbodiimide. Intermediate forma-
tion of carbodiimide would be possible if the metathesis of two
isocyanate molecules took place. Formation of a six membered
intermediate is likely if a second isocyanate is inserted into the
initial insertion product (Scheme 1). Elimination of carbon
dioxide through the formation of compound 1 would result in
metathesis. This intermediate would be similar to that proposed by
Bergman et al. in their reactions with isocyanates. The intermediate
To find out the effect of carbon dioxide elimination on the
metathesis, the reaction was carried out in a sealed vial in an
atmosphere of carbon dioxide using tetrahydrofuran as the
solvent. As the system was rich in carbon dioxide, it suppresses
the elimination of carbon dioxide and results in reduced metathesis
and insertion products formed from insertion into the metathesis
products. Thus only 27% of the metathesis product was observed
in an atmosphere of carbon dioxide instead of 46% observed in
its absence.
{ Electronic supplementary information (ESI) available: structure of 3a
and 4a, data on metathesis with aryl isocyanates and experimental details.
See http://www.rsc.org/suppdata/cc/b4/b417713d/
*ashoka@ipc.iisc.ernet.in
ð1Þ
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Table 1 Product ratio in metathesis between carbon dioxide with
diphenyl carbodiimide
Table 2 Products obtained in catalytic metathesis and their isolated
yields
a
2
Amount of CO
one equivalent of
for
Ratio of products
Amount and identity
Entry of aryl isocyanate
Isolated
yield (%)
a
Time/h
2
5
3
6
Entry
diphenyl carbodiimide
Time/h
2a
3a
5
1
2
3
4
a
20 eq. PhNCO
20 eq. 4-TolNCO
40 eq. PhNCO
100 eq. PhNCO
24
24
48
96
29 57
16 74
18 70
4
0
0
0
10 84
11 73
12 76
1
2
3
4
a
1.2 eq.
24
24
12
48
36
45
72
75
52
50
23
22
5
5
5
5
1.4 eq. CO
2.4 eq. CO
2.4 eq. CO
2
2
2
8
89
3
72
Reactions have been carried out under toluene reflux with 1eq.
Reactions have been carried out in a sealed vial in tetrahydrofuran
at 110 uC.
i
Ti(O Pr) .
i
as the solvent with 1 eq. of Ti(O Pr)
4
4
Since metathesis of phenyl isocyanate was suppressed in the
presence of carbon dioxide, we decided to study the metathesis of
carbon dioxide with other heterocumulenes such as diphenyl
carbodiimide (eqn. (1)). These reactions were carried out in sealed
vials in tetrahydrofuran as the solvent, at 110 uC. In the reaction of
the carbodiimide and carbon dioxide, the metathesis product was
phenyl isocyanate which was isolated as the inserted product
quantities of titanium isopropoxide (Scheme 3). In the catalytic
reactions, the isolated yield was moderate (Table 2). The unreacted
isocyanate was generally isolated as the urea on workup. The yield
was found to decrease when the reaction was carried out with
higher amounts of isocyanates. Surprisingly, the isolated yield was
lower for the 4-methylphenyl isocyanate in comparison with the
phenyl isocyanate under similar conditions. These reactions show
that titanium isopropoxide can be utilized to catalytically convert
isocyanates to the carbodiimides.
(Table 1).
The product ratio was only dependent on the amount of carbon
dioxide used in the reaction. Thus, doubling the amount of carbon
dioxide resulted in twice the amount of 2a while the amount of 3a
was reduced and the side product formed was not affected. The
reaction had reached equilibrium in 24 h and continuing the
reaction for a longer time (48 h) did not change the ratio of 2a
and 3a (entries 3 and 4). The product ratios are thus equilibrium
ratios and are not kinetically controlled.
In summary, we have encountered a metathesis reaction that
could be of considerable value in utilizing carbon dioxide.
Metathesis and insertion products can be isolated when stoichio-
metric amounts of aryl isocyanates and titanium isopropoxides
react with each other in refluxing toluene. Elimination of carbon
dioxide is a key step. Since the reaction is completely reversible, the
metathesis of carbodiimides with carbon dioxide can be conducted
leading to the formation of isocyanates. The metathesis reaction is
faster for heterocumulenes which insert readily. It also occurs
between two heterocumulenes when one of them inserts, whereas
the other only reacts with the first insertion product and not with
the isopropoxide. We have demonstrated that this reaction can be
carried out in a catalytic fashion.
In an attempt to probe the importance of insertion prior to
metathesis, a metathesis reaction with carbon disulfide was
attempted with carbodiimide. We have shown that carbon
13
disulfide does not undergo insertion into titanium isopropoxide.
Surprisingly small amounts of the metathesis product, phenyl
isothiocyanate (4%) and isopropyl phenyl thiocarbamate (4%),
were obtained upon insertion of isopropoxide into phenyl
isothiocyanate, along with 87% of compound 3a.
We acknowledge the Department of Science and Technology,
India (DST) for financial support and FIST program of the DST
for the 400 MHz NMR facility.
We have recently observed that the insertion product from
carbon dioxide and titanium isopropoxide can be isolated only in
14
the presence of trace quantities of water. In the absence of water,
under the metathesis reaction conditions reported here with carbon
dioxide and diphenyl carbodiimide, only insertion of diphenyl
carbodiimide was possible. Metathesis between diphenyl carbodi-
imide and carbon disulfide or carbon dioxide probably occurs
through the intermediate formed by insertion of diphenyl
Rajshekhar Ghosh and Ashoka G. Samuelson*
Department of Inorganic and Physical Chemistry, Indian Institute of
Science, Bangalore 560 012, India. E-mail: ashoka@ipc.iisc.ernet.in;
Fax: 91-80-23601552; Tel: 91-80-22932663
Notes and references
12
carbodiimide followed by reaction with weakly coordinated
carbon disulfide or carbon dioxide.
˚
O, M 5 254.3, triclinic, a 5 8.9335(18) A,
{
Compound 3a: C16
˚
H
18
N
2
˚
b 5 9.5181(19) A, c 5 9.5609(19) A, a 5 110.127(3)u, b 5 99.664(3)u,
3
˚
¯
c 5 101.080(3)u, V 5 724.5(3) A , 293(2) K, space group P1, Z 5 2,
To find out if these metathesis reactions can be carried out in a
catalytic fashion, the reactions were carried out with small
-1
m 5 0.074 mm , 7559 reflections measured, 2835 independent reflections
int 5 0.0594) which were used for all calculations, R1 5 0.0496,
wR2 5 0.1292 (observed data). Compound 4a: C23 , M 5 373.44,
(R
23 3 2
H N O
˚
˚
˚
triclinic, a 5 9.505(5) A, b 5 10.689(6) A, c 5 10.748(6) A, a 5 81.385(9)u,
3
˚
b 5 71.862(9)u, c 5 88.352(9)u, V 5 1025.9(10) A , 293(2) K, space group
-1
¯
P1, Z 5 2, m 5 0.078 mm , 10794 reflections measured, 4038 independent
reflections (Rint 5 0.0563) which were used for all calculations, R1 5 0.0398,
wR2 5 0.0982 (observed data). CCDC 252216 and 252217. See http://
www.rsc.org/suppdata/cc/b4/b417713d/ for crystallographic data in .cif or
other electronic format.
1
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