Immobilization of Pd nanoparticles with functional ionic liquid grafted onto cross-linked polymer for solvent-free Heck reaction

Article abstract of DOI:10.1039/b913182e

1-Aminoethyl-3-vinylimidazolium bromide ([VAIM]Br) grafted on the cross-linked polymer polydivinylbenzene (PDVB) was synthesized. The copolymers were used as a support to immobilize palladium nanoparticles. The catalyst was characterized by Fourier transform infrared spectroscopy (FT-IR), thermogravimetric (TG) analysis, transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The catalytic performance of the copolymer-supported Pd nanoparticles for the Heck arylation of olefins with different aryl iodides was studied under solvent-free conditions. The results demonstrated that the catalyst was very active and stable under solvent-free conditions, and could be reused after simple separation. The reason for the high activity and stability of the catalyst is discussed.

Full text of DOI:10.1039/b913182e

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PAPER
www.rsc.org/greenchem | Green Chemistry
Immobilization of Pd nanoparticles with functional ionic liquid grafted onto
cross-linked polymer for solvent-free Heck reaction
Gang Liu, Minqiang Hou, Jiyuan Song, Tao Jiang, Honglei Fan, Zhaofu Zhang and Buxing Han*
Received 2nd July 2009, Accepted 15th September 2009
First published as an Advance Article on the web 22nd October 2009
DOI: 10.1039/b913182e
1
-Aminoethyl-3-vinylimidazolium bromide ([VAIM]Br) grafted on the cross-linked polymer
polydivinylbenzene (PDVB) was synthesized. The copolymers were used as a support to
immobilize palladium nanoparticles. The catalyst was characterized by Fourier transform infrared
spectroscopy (FT-IR), thermogravimetric (TG) analysis, transmission electron microscopy (TEM)
and X-ray photoelectron spectroscopy (XPS). The catalytic performance of the
copolymer-supported Pd nanoparticles for the Heck arylation of olefins with different aryl iodides
was studied under solvent-free conditions. The results demonstrated that the catalyst was very
active and stable under solvent-free conditions, and could be reused after simple separation. The
reason for the high activity and stability of the catalyst is discussed.
Introduction
ILs have also been used to stabilize metal nanoparticles.
For example, Safavi and coworkers reported highly efficient
palladium nanocatalysts supported on a phosphorylated IL
Metallic nanoparticles have attracted much attention in the field
of catalysis because they can catalyze many organic reactions
effectively due to the quantum size effect and high ratio of
19
modified xerogel, which could be evenly coated on glass slides.
Dyson and coworkers synthesized a nitrile-functionalized IL,
1–3
surface area to volume. However, the naked nanoparticles
tend to aggregate to form bulk metal because of the impulse
of high surface energy, resulting in a severe decease in catalytic
activity and selectivity. An effective way to solve this problem is
to immobilize the metallic nanoparticles on suitable supports,
[
C
3
CNpy][Tf N], which was an effective immobilization solvent
2
for palladium-catalyzed Suzuki and Stille reactions; TEM anal-
ysis of the nanoparticles extracted from the catalysis solution
showed the stabilizing effect of the IL.
The design and preparation of active and stable catalysts for
Heck reactions under solvent-free conditions is highly desirable,
and consistent with the requirements of green chemistry. It is
20
4–7
and many methods have been developed for this.
The Heck reaction is a very useful route for the formation
8–10
of new C–C bonds in a single operational step.
The wide
21,22
well known that amine groups bind strongly to palladium.
It
functional group tolerance in both reactants allows convenient
application in the total synthesis without protecting groups.
The Heck reaction has mostly been catalyzed by palladium
complexes combined with phosphine ligands in organic sol-
vents under homogeneous conditions. It is known that the
homogeneous systems suffer drawbacks in separation, and
result in environmental problems, especially in the case of
toxic ligands. Therefore, it is desirable to develop cheaper
and environmentally benign heterogeneous catalytic systems.
It is also known that palladium nanoparticles have high
can be expected that the ILs with amine groups on solid supports
should be effective for stabilizing palladium nanoparticles.
Herein we describe the synthesis of a new type of imidazolium
IL with an amine group, and its copolymerization with cross-
linker divinylbenzene. The prepared copolymer was used for the
immobilization of Pd nanoparticles for Heck reaction.
Results and discussion
11,12
Preparation and characterization of the catalyst
catalytic activity for the Heck reaction.
Immobilization of
Pd nanoparticles on solid supports to prepare active and stable
catalytic systems for the Heck reaction is an interesting topic,
and different supports have been used to stabilize the nanoparti-
The route to synthesize the copolymers (PDVB-IL) is presented
in Scheme 1, and the procedures were similar to those for the
copolymerization of 1-vinyl-3-butylimidazolium chloride and
13
14
7,15
cles, such as carbon, hydroxyapatite, molecular sieves, and
23
DVB. In brief, the IL with amine group was first prepared
16,17
polymers.
by the reaction of 1-vinylimidazole and 2-bromoethylamine
hydrobromide to give [VAIM]Br·HBr. This was then copoly-
merized with DVB using azobisisobutyronitrile (AIBN) as the
initiator, and subsequent treatment of the copolymers with
NaOH gave the cross-linked copolymer with IL (PDVB-IL).
To prepare the copolymer-supported Pd nanoparticles (PDVB-
In recent years, ionic liquids (ILs) have been widely studied
owing to their unique properties, such as negligible vapor
18
pressure and high thermal stability. Some functionalized
Beijing National Laboratory for Molecular Sciences, Institute of
Chemistry, Chinese Academy of Sciences, Beijing, 100080, China.
E-mail: hanbx@iccas.ac.cn; Fax: +86-10-62562821;
Tel: +86-10-62562821
IL-Pd), the copolymer was added to aqueous H
with vigorous stirring, giving the catalyst after reduction of the
Pd(II) on the PDVB-IL with NaBH and drying under vacuum.
2
PdCl
4
solution
4
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Scheme 1 Synthesis of the cross-linked polymer-supported ionic liquid.
The prepared copolymers (PDVB-IL) and neat PDVB were
characterized by thermogravimetric analysis. The thermograms
the ILs were copolymerized without hydrobromide, and the
PDVB-IL had a structure shown in Scheme 1.
are shown in Fig. 1. The small weight loss of PDVB-IL before
Fig. 2 shows the FT-IR spectra of the PDVB-IL and PDVB-
IL-Pd. Both spectra showed an asymmetric broad band at
◦
220 C resulted from the loss of the adsorbed water which also
-
1
occurred in the case of neat PDVB. It can be seen from the two
around 3435 cm , which is attributed to the stretching vibration
of the amine groups. It is clear that the band became narrow after
the Pd nanoparticles were supported on the polymers, indicating
the binding of Pd nanoparticles to the polymers through the
◦
thermograms that the weight loss of PDVB-IL between 220 C
◦
and 380 C was due to the elimination of the ILs immobilized
on the polymers, because there was no weight loss for the neat
◦
21
PDVB. Further weight loss at higher temperature (above 380 C)
amine groups. The small change in intensity of the band may
was attributed to the decomposition of PDVB. The amount
of the IL in the PDVB-IL obtained from the thermal analysis
was about 7.0 wt%. The composition of PDVB-IL was also
examined by elemental analysis, and the result indicated that
the content of IL was 7.4 wt%, which was consistent with the
result of thermal analysis. The results of element analysis also
showed that the molar ratio of N/Br was 3, indicating that
result from the change of absorption coefficient of the amino
groups after interaction with Pd particles.
Fig. 2 The FT-IR spectra of PDVB-IL and PDVB-IL-Pd.
Fig. 3 shows the typical SEM and TEM images of the
catalyst (PDVB-IL-Pd). The SEM image (Fig. 3A) shows that
the catalyst was almost amorphous. The dark spots in the TEM
image (Fig. 3B) indicate the presence of palladium nanoparticles
that were bound to the copolymers. The diameter of palladium
Fig. 1 The thermogram of PDVB-IL and pure PDVB.
Fig. 3 SEM (A) and TEM (B) images of the PDVB-IL-Pd; the TEM image (C) of the recovered PDVB-IL-Pd after being reused three times.
6 | Green Chem., 2010, 12, 65–69
6
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nanoparticles was in the range 7–8 nm and the size distribution
was very narrow.
Table 1 Catalytic performance of the catalyst for Heck reaction
a
between iodobenzene and methyl acrylate
The catalyst (PDVB-IL-Pd) was also characterized by XPS
before reaction, and the results are shown in Fig. 4. It can be
seen that the Pd 3d spectrum could be resolved into two spin–
orbit pairs with 3d5/2 binding energies of 335.9 eV and 337.1 eV,
respectively. The peak binding energies of 335.9 eV (Pd 3d5/2) and
◦
Entry
Base
T/ C
Time/h
Yield (%)
3
41.0 eV (Pd 3d3/2) correspond to fully reduced Pd nanoparticles,
1
2
3
4
5
6
7
Et N
NaHCO
120
120
120
120
80
100
140
4
4
4
4
12
12
1
97
3
while the peak at 337.1 eV suggests the presence of the unreduced
Pd ions on the surface of the Pd particles.
from the XPS spectrum that most of Pd was reduced to Pd(0)
because the area of the peak of Pd ion was relatively small.
The content of Pd in the catalyst was 2.3 wt%, as determined by
the ICP-AES method.
3
<2
<2
<2
<2
73
2
+
21,24
CH
3
COONa
It can be seen
NaOH
2
+
Et
3
Et
3
Et
3
N
N
N
2
+
98
a
The molar ratio of iodobenzene/methyl acrylate/base/Pd is
: 1.5 : 1.5 : 0.0002.
1
Table 2 Heck reaction of haloarenes with olefins in the presence of
a,b
PDVB-IL-Pd
1
2
Entry
R
R
Time/h
Yield (%)
1
2
3
4
5
6
7
8
H
H
H
4-F
4-Cl
4-OH
4-OMe
4-Me
H
Me
Et
Bu
4
5
6
3
2
1
3
6
4
4
4
97
94
95
93
94
98
96
93
95
95
94
Me
Me
Me
Me
Me
Me
Me
Me
c
9
1
1
c
0
1
H
H
Fig. 4 XPS spectrum of the Pd 3d edge of the PDVB-IL-Pd sample.
c
a
b
The molar ratio of haloarene/olefin/Et
The reaction was performed without solvent at 120 C. Entries 9, 10
3
N/Pd is 1 : 1.5 : 1.5 : 0.0002.
c
◦
Catalytic Heck reactions
and 11 are the results of reusing the catalyst for the second, third and
fourth times under the reaction conditions of entry 1.
The catalytic activity of the PDVB-IL-Pd for Heck reactions
was investigated under solvent-free conditions. It is known that
a base is required for Heck reactions. The effect of Et
3
N and
high conversion increased from 4 h to 6 h (entries 1–3, Table 2).
This may be due to the steric hindrance effect that reduced the
reaction rate.
some inorganic bases on the reaction of iodobenzene and methyl
◦
acrylate was studied at 120 C. The results showed that the
catalyst was very active and selective for the reaction in the
In order to investigate the effect of substituted groups
of iodobenzene on the Heck reaction, various substituted
iodobenzenes were studied. The coupling reaction of both
electron-deficient and electron-rich iodobenzenes with olefins
can proceed with high yields using the catalyst. Iodobenzenes
with electron-donating groups, such as methyl, gave reduced
reaction rates, and longer reaction times were required for a
high yield. Groups with a lone electron pair (e.g. -OH, -OMe,
-F, -Cl) in the iodobenzenes affect the electron cloud density of
benzene ring and the coordination of Pd with the benzene ring,
ultimately accelerating the reaction rate, as can be seen from
entries 1 and 4–8 of Table 2.
presence of Et N (entry 1, Table 1), while the reaction rate was
3
very slow when inorganic bases were used (entries 2–4, Table 1).
The main reason for this is that the solubility of the inorganic
bases in the reaction system was very poor, while Et N is miscible
3
with the substrates. This indicates that the solubility of the bases
in the reaction mixture is crucial for the Heck reaction. Using
Et N as the base, the effect of temperature on the reaction was
3
studied. The results demonstrated that the activity of the catalyst
increased with temperature as the temperature increased from
◦
8
0 to 140 C (entries 1 and 5–7 of Table 1), with the activity
◦
◦
being very high at 120 C and 140 C.
The catalytic activity of the catalyst for the arylation of
different olefins with iodobenzene was tested under solvent-free
conditions; the results are given in Table 2. The iodobenzene was
very active with electron-poor olefins such as methyl, ethyl and
butyl acrylate. As the size of the substituted group of acrylate
ester increased from methyl to butyl, the reaction time needed for
The reusability of the catalyst was tested using iodobenzene
and methyl acrylate as the substrates. After each run, the catalyst
was recovered by filtration, followed by washing with ethanol
(10 mL ¥ 3). After drying, the catalyst was reused directly
for the next run. The results for the three repeated runs are
also presented in Table 2. The activity of the catalyst remained
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unchanged after it was reused three times, indicating that the
catalyst was not only very active, but also very stable. There are
several reasons for the excellent stability of the catalyst. First,
the PDVB-IL was not soluble in the reactants and the product
because it was a cross-linked polymer; second, it was thermally
was recrystallized three times before use. Other chemicals were
used as received. All the chemicals were A.R. grade.
Preparation of [VAIM]Br·HBr
◦
To prepare the basic IL [VAIM]Br·HBr, 1-vinylimidazole(9.42 g,
stable up to about 220 C (Fig. 1), which was much higher
0
.10 mol) and acetonitrile (50 mL) were added to a two-necked
than the reaction temperature; third, the amine groups in the
PDVB-IL interacted strongly with Pd particles by coordination,
which anchored the Pd nanoparticles stably on the support. The
TEM image of the catalyst after being used four times is shown in
Fig. 3C. The aggregation of the Pd particles in the used catalyst
was not obvious, supporting the argument above.
flask equipped with a magnetic stirrer. The mixture was refluxed
◦
at 78 C under a nitrogen atmosphere. 2-Bromoethylamine
hydrobromide (20.50 g, 0.10 mol) was added into the flask
stepwise over 24 h. Then, the reaction mixture was cooled
down, the liquid was poured out and the solid was washed
with anhydrous ethanol three times to remove the unreacted
starting materials. After drying under vacuum, 1-aminoethyl-3-
The mechanism of the Heck reaction employing supported Pd
25
nanoparticles as catalysts has been discussed in the literature.
vinylimidazolium bromide hydrobromide ([VAIM]Br·HBr) was
Many authors have reported the leaching of Pd during the
reaction. In order to investigate the mechanism in our catalytic
system, we conducted a filtration test for the Heck reaction
between iodobenzene and methyl acrylate using PDVB-IL-Pd
as catalyst. After 2 h (the reaction was completed in 4 h), the
reaction was stopped and the reaction mixture was centrifuged
at 16000 rpm for 20 min. Then the mixture without the solid
catalyst was allowed to continue under the same conditions for
another 2 h, and the conversation found to increase from 60%
to 73%. This suggests that the leaching of active Pd species from
the solid supports occurred to some extent, but the dissolved
Pd redeposited back onto the polymers after the iodobenzene
was completely consumed. This argument was confirmed by
our ICP-AES analysis, which showed that the content of Pd
in the catalyst before and after reaction was 2.30% and 2.23%,
respectively.
1
obtained. H NMR (400 MHz, D
2
O) d: 3.52 (m, 2H), 4.65 (m,
2
7
H), 5.47 (dd, 1H), 5.84 (dd, 1H), 7.17 (dd, 1H), 7.71 (s, 1H),
.87 (s, 1H), 9.23 (s, 1H). Positive ion ESI-MS: m/z 138.1. Anal.
Br : N, 14.0; C, 28.1; H, 4.3; Br, 53.5. Found:
Calcd for C
7
H
13
N
3
2
C, 25.9; H, 4.4; N, 13.2; Br, 54.9.
Our experiment showed that the isolated [VAIM]Br could
be obtained by neutralization of [VAIM]Br·HBr by NaOH. In
the experiment, [VAIM]Br·HBr (10 mmol) was dissolved in the
water (10 mL) and then equimolar NaOH (10 mmol) was added.
The solution was stirred for 6 h at r.t. followed by vaporization of
the water under vacuum. Then the obtained viscous liquid was
dissolved in MeOH (20 mL) with stirring for 1 h. The solution
was filtered, and ionic liquid [VAIM]Br was obtained after the
MeOH in the filtrate was evaporated. The identity of [VAIM]Br
1
was confirmed by NMR. H NMR (300 MHz, DMSO) d: 2.78
(
m, 2H), 4.12 (m, 2H), 5.27 (dd, 1H), 5.88 (dd, 1H), 7.20 (dd,
1
H), 7.79 (s, 1H), 8.11 (s, 1H), 9.47 (s, 1H).
Conclusion
Preparation of PDVB-IL
We synthesized DVB cross-linked copolymer with chemically
supported IL [VAIM]Br. The copolymer was proved to be an
effective supporter for palladium nanoparticles. The nanocat-
alysts immobilized on the copolymers showed high catalytic
activity in the Heck reaction for various substrates. The catalyst
was very stable and could be easily separated from the products
and reused because of the insoluble nature of the cross-linked
copolymer and the coordination force between the amine group
and the palladium nanoparticles. We believe that this route can
be used to support some other metallic nanocatalysts on a highly
cross-linked polymer matrix to prepare active, stable catalysts for
different reactions.
To prepare the DVB-cross-linked polymers with the supported
IL (PDVB-IL), DVB (1.95 g, 15 mmol), AIBN (0.05 g)
and [VAIM]Br·HBr (0.45 g, 1.5 mmol) were dissolved in
ethanol/water (100 ml, 3 : 1 v/v) under nitrogen. The mixture
◦
was refluxed at 100 C with stirring. After 24 h, a white solid
formed was filtrated and was washed with THF, acetone, and
methanol. The final product was treated with equimolar NaOH
◦
and washed with water before being dried in vacuum at 60 C for
12 h. Element analysis: C, 84.4; H, 7.8; N, 1.5; Br, 2.7. The PDVB
without the ionic liquid was synthesized by direct polymerization
of DVB under the same conditions.
Preparation of PDVB-IL-Pd
Experimental
PdCl
00 mL) with stirring for 24 h. PDVB-IL (1.00 g) was added to
the aqueous solution of H PdCl (0.02 M, 50 mL) in a 100 mL
2
(2 mmol) was dissolved in the solution of HCl (0.04 M,
1
Materials
2
4
Azobis(isobutyronitrile) (AIBN), methanol, acetone, acetoni-
flask with vigorous stirring. The mixture was stirred for 12 h and
then filtered. The solid catalysts were then dispersed in water
(20 mL) and reduced by a fresh aqueous solution (10 mL) of
trile, ethanol, PdCl , tetrahydrofuran (THF), methyl acrylate,
2
ethyl acrylate, n-butyl acrylate, sodium hydroxide, sodium
bicarbonate, sodium acetate, triethylamine, iodobenzene,
NaBH (0.185 g, 5 mmol) at room temperature. The resulting
4
4
-fluoroiodobenzene, 4-chloro-1-iodobenzene, 4-iodophenyl
grey catalysts were washed with water (10 mL ¥ 3) and ethanol
(10 mL ¥ 3) respectively, then dried under vacuum at 60 C for
24 h. The content of Pd in the catalyst was 2.30 wt%, which was
determined using ICP-AES.
◦
methyl ether and 4-iodophenol were provided by Beijing Chem-
ical Company. Divinylbenzene (DVB) was purchased from
Fluka, and 1-vinylimidazole was provided by Aldrich. AIBN
6
8 | Green Chem., 2010, 12, 65–69
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Catalytic reaction
Chinese Academy of Sciences (KJCX2.YW.H16) for financial
support.
The Heck reaction was carried out in a 6 mL stainless steel
reactor with a magnetic stirrer. In the experiment, aryl halide
References
(
1 mmol), vinylic substrate (1.5 mmol), triethylamine (1.5 mmol)
and Pd catalyst (1.0 mg) were added into the reactor. Then
the reactor was heated to the desired temperature in an air
bath under stirring. After reaction, the reactor was cooled by
a ice bath. The products were collected using DMF as solvent
after centrifuging the catalysts from the suspension. The liquid
phase was analyzed by GC (Agilent 4890 D) equipped with a
flame-ionized detector, and biphenyl was used as the internal
standard. The formation of product was confirmed by GC-MS
1 M. Turner, V. B. Golovko, O. P. H. Vaughan, P. Abdulkin, A.
Berenguer-Murcia, M. S. Tikhov, B. F. G. Johnson and R. M.
Lambert, Nature, 2008, 454, 981–983.
2
A. A. Herzing, C. J. Kiely, A. F. Carley, P. Landon and G. J.
Hutchings, Science, 2008, 321, 1331–1335.
3 V. Cimpeanu, M. Kocevar, V. I. Parvulescu and W. Leitner, Angew.
Chem., Int. Ed., 2009, 48, 1085–1088.
4
D. Astruc, F. Lu and J. R. Aranzaes, Angew. Chem., Int. Ed., 2005,
4, 7852–7872.
4
5 R. W. J. Scott, O. M. Wilson and Richard M. Crooks, J. Phys. Chem.
B, 2005, 109, 692–704.
(
QP2010). All the reactions were conducted three times and the
6
Handbook of heterogeneous catalysis, 2nd edn, ed. G. Ertl,
H. Kn o¨ zinger and J. Weitkamp, Wiley-VCH, 2008.
experimental errors were less than ±2%. In the catalyst recycling
experiments, the catalyst was reused after washing with ethanol
7
V. L. Budarin, J. H. Clark, R. Luque, D. J. Macquarrie and R. J.
White, Green Chem., 2008, 10, 382–387.
◦
(
10 mL ¥ 3) and drying at 60 C for 6 h.
8
9
M. T. Reetz and J. G. de Vries, Chem. Commun., 2004, 1559.
C. Amatore and A. Jutand, Acc. Chem. Res., 2000, 33, 314–
Characterization
3
21.
0 M. Lombardo, M. Chiarucci and C. Trombini, Green Chem., 2009,
1, 574–579.
1
1
1
1
The FT-IR spectra were collected on a Bruker Tensor 27
spectrometer in KBr pellet form. SEM examination was carried
out on a scanning electron microscope (JEOL, JSM-4300)
operated in a high-vacuum mode at 15 kV, which provided
general textural information of the samples. The SEM sample
was sputter-coated with gold before observation. TEM obser-
vation was performed on a transmission electron microscope
1
1 Y. Wan, H. Y. Wang, Q. f. Zhao, M. Klingstedt, O. Terasaki and D. Y.
Zhao, J. Am. Chem. Soc., 2009, 131, 4541–4550.
2 R. T. Tao, S. D. Miao, Z. M. Liu, Y. Xie, B. X. Han, G. M. An and
K. L. Ding, Green Chem., 2009, 11, 96–101.
3 T. Maegawa, Y. Kitamura, S. Sako, T. Udzu, A. Sakurai, A. Tanaka,
Y. Kobayashi, K. Endo, U. Bora, T. Kurita, A. Kozaki, Y. Monguchi
and Hironao Sajiki, Chem. Eur. J., 2007, 13, 5937–5943.
4 K. Mori, T. Hara, T. Mizugaki, K. Ebitani and K. Kaneda, J. Am.
Chem. Soc., 2004, 126, 10657–10666.
5 L. Djakovitch and K. Koehler, J. Am. Chem. Soc., 2001, 123, 5990–
5999.
6 S. Ko and J. Jang, Angew. Chem., Int. Ed., 2006, 45, 7564–7567.
7 B. Karimi, S. Abedi, J. H. Clark and V. Budarin, Angew. Chem., Int.
Ed., 2006, 45, 4776–4779.
8 T. Welton, Coord. Chem. Rev., 2004, 248, 2459–2477.
19 A. Safavi, N. Maleki, N. Iranpoor, H. Firouzabadi, A. R. Banazadeh,
R. Azadi and F. Sedaghati, Chem. Commun., 2008, 6155–6157.
0 D. B. Zhao, Z. F. Fei, T. J. Geldbach, R. Scopelliti and P. J. Dyson,
J. Am. Chem. Soc., 2004, 126, 15876–15882.
21 S. Mandal, D. Roy, R. V. Chaudhari and M. Sastry, Chem. Mater.,
2004, 16, 3714–3724.
2 R. M. Crooks, M. Zhao, L. Sun, V. Chechnik and L. K. Yeung, Acc.
Chem. Res., 2001, 34, 181.
3 Y. Xie, Z. F. Zhang, T. Jiang, J. L. He, B. X. Han, T. B. Wu and K. L.
Ding, Angew. Chem., Int. Ed., 2007, 46, 7255–7258.
1
1
(
JEOL, JEM 1011) at an operating voltage of 100 kV, and
the images were electronically captured using a CCD camera.
X-ray photoelectron spectroscopy data of the as-prepared
samples were obtained with an ESCALab220i-XL electron
spectrometer from VG Scientific using 300 W MgKa radiation.
1
1
-
9
The base pressure was about 3 ¥ 10 mbar. The binding
energies were referenced to the C 1s line at 284.8 eV from
adventitious carbon. TG measurements were performed on a
thermal analyzer (NETZSCH STA 409 PC/PG) with a heating
1
2
◦
-1
rate of 3 C min . The loading content of Pd in the catalysts
was determined by ICP-AES (VISTAMPX); the samples were
dissolved in aqua regia beforehand. The elemental composition
of the polymer was determined using a Flash EA1112 analyzer.
2
2
2
4 K. R. Priolkar, P. Bera, P. R. Sarode, M. S. Hegde, S. Emura,
R. Kumashiro and N. P. Lalla, Chem. Mater., 2002, 14, 2120–
Acknowledgements
2
128.
The authors are grateful to the National Natural Science
Foundation of China (20533010, 20773144) and the
2
5 X. M. Ma, Y. X. Zhou, J. C. Zhang, A. L. Zhu, T. Jiang and B. X.
Han, Green Chem., 2008, 10, 59–66.
This journal is © The Royal Society of Chemistry 2010
Green Chem., 2010, 12, 65–69 | 69