Synthesis of monoalkoxide monopyrrolyl complexes Mo(NR)(CHR′) (OR″)(pyrrolyl): Enyne metathesis with high oxidation state catalysts

Article abstract of DOI:10.1021/ja075569f

Addition of 1 equiv of ROH to Mo(NAr)(CHCMe₂Ph)(Me₂Pyr)₂ (Ar = 2,6-i-Pr₂C₆H₃, Me₂Pyr = 2,5-dimethylpyrrolyl) in diethyl ether or THF yields Mo(NAr)(CHCMe₂Ph)(OR)(Me

Full text of DOI:10.1021/ja075569f

Published on Web 09/29/2007
Synthesis of Monoalkoxide Monopyrrolyl Complexes Mo(NR)(CHR′)(OR′′)(pyrrolyl):
Enyne Metathesis with High Oxidation State Catalysts
†
,†
†
‡
Rojendra Singh, Richard R. Schrock,* Peter M u¨ ller, and Amir H. Hoveyda
Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, and Department
of Chemistry, Merkert Chemistry Center, Boston College, Chestnut Hill, Massachusetts 02467
Received July 25, 2007; E-mail: rrs@mit.edu
We recently reported the synthesis, characterization, and reac-
tivities of molybdenum bispyrrolyl complexes of the type Mo(NR)-
1
(
2
CHR′)(pyrrolyl)
,5-dimethylpyrrolyl (Me
use of bispyrrolyl species as precursors to bisalkoxide catalysts
of the type Mo(NR)(CHR′)(OR) or Mo(NR)(CHR′)(diolate)
through addition of an alcohol or a diol to Mo(NR)(CHR′)(pyrrolyl)
2
where pyrrolyl is either the parent pyrrolyl or
2
2
Pyr). We are interested primarily in the
3
2
2
complexes. Preliminary experiments suggest that bispyrrolyls are
less reactive toward olefins than bisalkoxide species, but serve as
effective precursors to Mo-based bisalkoxides or diolates.1,2 We
were attracted to the possibility that monoalkoxide monopyrrolyl
species might be intercepted and might prove to be of interest in
their own right. This expectation partly arises from the high
reactivities observed for supported catalysts prepared through
4
Figure 1. POV-ray drawing of 3. Thermal ellipsoids are displayed at 50%
probability level. Hydrogen atoms are omitted. Mo-N(2) ) 1.7364(11) Å,
Mo-C(1) ) 1.8921(13) Å, Mo-O(1) ) 1.9145(10) Å, Mo-N(1) ) 2.0373-
addition of bispyrrolyl species to silica where the predominant
surface species is Mo(NR)(CHR′)(pyrrolyl)(OSisurf). High catalytic
activities have been observed (and also rationalized through
(
11) Å, Mo-N(2)-C(21) ) 172.57(9)°, Mo-O-C(11) ) 143.58(8)°, Mo-
5
theoretical studies ) for these and related pseudotetrahedral metal
C(1)-C(2) ) 139.48(9)°, Mo-N(1)-C(32) ) 135.28(9)°.
complexes that are asymmetric at the metal center. We report here
1
5
complexes that contain smaller alkoxides contain an η - or an η -
the synthesis of species of the type Mo(NR)(CHR′)(OR′′)(pyrrolyl)
1
5
and their use in catalytic enyne metathesis reactions.6
pyrrolyl ligand. It also should be noted that η - and η -pyrrolyl
ligands interconvert readily at room temperature in Mo(NAr)-
Addition of 1 equiv of ROH to Mo(NAr)(CHCMe
Ar ) 2,6-i-Pr ; Me Pyr ) 2,5-Me NC ) in diethyl ether
or THF yields Mo(NAr)(CHCMe Ph)(OR)(Me Pyr) species where
R ) (CH C (1, 22% isolated yield), (CH CH (2, 83%), Ar (3,
1%), (CF CH (4, 45%), or (CF (CH )C (5, 80%) (eq 1). In
2 2 2
Ph)(Me Pyr)
(
(
CHCMe
CHCMe
2
Ph)(Me
2
Pyr)
2
species, and presumably also in Mo(NAr)-
Pyr) species.
(
2
C
6
H
3
2
2
4 2
H
2
Ph)(OR)(Me
2
2
2
Ring-closing of diallyl ether catalyzed by compounds 1-5 (2
mol %) in C was complete within 15-20 min. In a separate
experiment 3 was treated with 10 equiv of diallylether in C at
)
3 3
3 2
)
6 6
D
8
)
3 2
3
)
2
3
6
D
6
room temperature a total of 10 times in sequence. Complete con-
version of the substrate into products was observed in <10 min at
1
each stage according to H NMR spectroscopy. These observations
suggest that monopyrrolyl monoalkoxide catalysts are relatively
stable and long-lived, as observed in the metathesis of propylene
4
by silica-supported catalysts of the same type in a flow reactor.
Mo-based monoalkoxides 1-5 were examined as possible enyne
metathesis catalysts; enynes 6-9 served as substrates in these
studies. Ring-closing enyne metathesis products are proposed to
arise through initial addition of the triple bond to an intermediate
methylene complex to give an R- or a â-substituted metallacy-
clobutene, followed by ring formation and reformation of the
certain cases, Mo(NAr)(CHCMe
from which the Mo(NAr)(CHCMe
be separated by selective crystallization. The syn alkylidene reso-
nances are found in the proton NMR spectrum (C ) at 12.24
1), 12.04 (2), 12.29 (3), 12.34 ppm (4), and 12.45 ppm (5) with
2
Ph)(OR)
2
species are also formed,
2
Ph)(OR)(Me
2
Pyr) species can
6
methylene species in the usual manner. For example, as illustrated
D
6 6
in eq 2, enyne 7 could furnish 7R or 7â as a consequence of initial
R or â addition, respectively. In the case of enyne 9, product 9R
refers to the consequence of addition with the largest substituent
in the R position of the initial metallacyclobutene. The results of
these studies are summarized in Table 1.
Substrate 6 was converted exclusively into 6â, the six-membered
ring analogue of 7â, in good isolated yield within 15 min using 4
(
J
CH ≈ 120 Hz in each case; no alkylidene resonances for anti iso-
mers were observed. Results are likely to vary with the nature of
the imido ligand. Preliminary studies have shown that an adaman-
tylimido analogue of 3 cannot be prepared in a similar manner from
a bispyrrolyl precursor; only the bisphenoxide species is formed.
An X-ray structure of 3 (Figure 1) showed that the alkylidene
5
has the expected syn orientation, but although an η -2,5-dimethyl-
1
pyrrolyl ligand is possible electronically, an η -2,5-dimethylpyrrolyl
is observed, presumably for steric reasons. It is not known whether
†
Massachusetts Institute of Technology.
Merkert Chemistry Center.
‡
12654
9
J. AM. CHEM. SOC. 2007, 129, 12654-12655
10.1021/ja075569f CCC: $37.00 © 2007 American Chemical Society

C O M M U N I C A T I O N S
Table 1. Enyne Metathesis of Substrates 6, 7, 8, and 9a
conv/products (%b)
entry
cat (time)
subst
R
â
yield (%)
1
2
3
4
5
6
7
8
9
1
1
1
1
1
1
1
1
1 (1.5 h)
2 (1.5 h)
3 (12 h)
4 (15 m)
5 (20 m)
1 (20 m)
2 (20 m)
3 (2 h)
4 (20 m)
5 (20 m)
1 (20 m)
2 (12 h)
3 (12 h)
4 (20 m)
5 (12 h)
2 (1.5 h)
3 (2 h)
6
6
6
6
6
7
7
7
7
7
8
8
8
8
8
9
9
9
9
<5c
<5c
<5c
or 5 (entries 4 and 5). However, 1, 2, or 3 did not afford any ring-
closed product under similar reaction conditions, even though the
initial alkylidenes disappeared immediately. Ru-carbene catalysts
have been reported to afford 6R in this reaction.6
0
100
100
40
20
100
70
68
72
77
79
70
0
60
80
0
30
0
d,e
d,e
,7
d,e
83
70
0
1
2
3
4
5
6
7
100
f
40
50
f
<5c
c
<5
<5c
Treating 7 with 5 mol % of 3 or 5 in benzene-d
6
produced 7â
c
<5
exclusively (entries 8 and 10). In contrast, 7R and 7â were both
<5c
d
observed when 1, 2, or 4 was employed. Ru-carbene complexes
18
19
4 (20 m)
5 (20 m)
40
25
60
75
72
80
d
afford 7R in this reaction.6,7
None of the expected ring-closed enyne metathesis products of
substrate 8 was observed for 1-5 (entries 11-15). Compounds 1
and 2 led to formation of ethylene and what appears to be a dimer
or oligomer mixture, the nature of which has not been elucidated.
In the case of substrate 9, 4 and 5 yield mixtures of the two
possible rings (entries 18 and 19). One might expect this result
since the difference between the two types of initial metallacy-
clobutenes is not as marked compared to yields with substrates that
contain a terminal triple bond. In contrast, 2 and 3 did not lead to
any ring-closed product despite consumption of the initial alkylidene
a
All reactions were performed in C6D6 at 22 °C with 5 mol % catalyst
1
b
loading and followed by H NMR spectroscopy. Based on disappearance
of substrate. c The original alkylidene was consumed. Isolated as a mixture
d
e
of the two products. Some homocoupling of the R product was observed.
The initial alkylidene was consumed and ethylene evolved; the products
could not be identified.
f
oxidation state Mo catalysts. In certain cases, the products that are
observed are different from those obtained through the use of Ru-
based carbenes. It is important to note that all bisalkoxide or diolate
catalysts that we have tried do not lead to controlled enyne
metathesis, but to mixtures of ill-defined, possibly oligomeric,
products. The modular nature of high oxidation state Mo or W
complexes and the sensitivity of M(NR)(CHR′)(X)(Y) complexes
to variations in R, R′, X, and Y continue to open avenues to the
design and development of new catalysts. These investigations are
also in progress and will be the subject of future reports.
9
(entries 16 and 17).
The enyne metathesis results observed here cannot be explained
solely on the basis of the relative sizes of the alkoxide in 1-5, or
upon their electronic properties. It also should be noted that only
syn alkylidene isomers have been observed so far; nothing is known
2 2
about anti isomers of Mo(NAr)(CHCMe Ph)(OR)(Me Pyr) and
related species, the relative reactivity of syn and anti isomers, and
the rate of interconversion of syn and anti isomers, all important
issues for imido alkylidene catalysts of Mo and W that are generally
difficult to address experimentally.3d Finally, the role of the hapticity
of the pyrrolyl in enyne metathesis is not known.
A potentially important property of the monoalkoxide compounds
reported here is chirality at the metal center.8 Therefore, an
enantiomerically pure alcohol should generate a mixture of dia-
stereomers that may or may not interconvert rapidly. Upon addition
Acknowledgment. This research was funded by the National
Science Foundation (CHE-0138495 and CHE-0554734 to R.R.S.)
and the NIH (GM-59426 to R.R.S. and A.H.H.). R.S. thanks Dr.
Zachary J. Tonzetich for helpful discussions and Dr. Tatiana
Pilyugina (Ph.D. Thesis, MIT, 2007) for a sample of 10.
Supporting Information Available: Experimental details for the
synthesis of all compounds and X-ray studies in CIF format. This
material is available free of charge via the Internet at http://pubs.acs.org.
2 2 2 2
of 10 to Mo(NAr)(CHCMe Ph)(Me Pyr) , Mo(NAr)(CHCMe Ph)-
References
(
(
(
1) Hock, A.; Schrock, R. R.; Hoveyda, A. H. J. Am. Chem. Soc. 2006, 128,
6373.
2) Singh, R.; Czekelius, C.; Schrock, R. R.; M u¨ ller, P. Organometallics 2007,
6, 2528.
3) (a) Schrock, R. R.; Czekelius, C. C. AdV. Synth. Catal. 2007, 349, 55. (b)
Schrock, R. R. Angew. Chem., Int. Ed. 2006, 45, 3748. (c) Schrock, R.
R.; Hoveyda, A. H. Angew. Chem., Int. Ed. 2003, 42, 4592. (d) Schrock,
R. R. Chem. ReV. 2002, 102, 145.
1
2
(
2
OR*)(Me Pyr) (11) is isolated in 43% yield (where OR* is the
(
4) Blanc, R.; Berthoud, R.; Salameh, A.; Basset, J.-M.; Cop e´ ret, C.; Singh,
alkoxide derived from 10) as a mixture of two diastereomers with
R.; Schrock, R. R. J. Am. Chem. Soc. 2007, 129, 8434.
alkylidene proton resonances at 10.67 ppm (75%) and 11.79 ppm
(5) Poater, A.; Solans-Monfort, X.; Cop e´ ret, C.; Eisenstein, O. J. Am. Chem.
Soc. 2007, 129, 8207.
(25%). Recrystallization leads to a different ratio of diastereomers,
(
(
(
6) Diver, S. T.; Giessert, A. J. Chem. ReV. 2004, 104, 1317.
7) Mori, M.; Sakakibara, N.; Kinoshita, A. J. Org. Chem. 1998, 63, 6082.
thus confirming that diastereomers of 11 do not interconvert readily.
The consequences for asymmetric metathesis reactions remain to
be established and are the subject of ongoing investigations in these
laboratories.
To the best of our knowledge, the reactions reported here are
the first enyne metathesis reactions to be promoted by high
8) See also: Van Veldhuizen, J. J.; Garber, S. B.; Kingsbury, J. S.; Hoveyda,
A. H. J. Am. Chem. Soc. 2002, 124, 4954.
(9) See also: Cortez, G. A.; Baxter, C. A.; Schrock, R. R.; Hoveyda, A. H.
Org. Lett. 2007, 9, 2871.
JA075569F
J. AM. CHEM. SOC.
9
VOL. 129, NO. 42, 2007 12655