Didocosyl selenide stabilized recyclable Pd(0) nanoparticles and coordinated palladium(ii) as efficient catalysts for Suzuki-Miyaura coupling

Article abstract of DOI:10.1039/c2dt12256a

First selenium ligand stabilized Pd(0) nanoparticles (～3-5 nm) catalyze Suzuki-Miyaura C-C coupling in short time and are recyclable (up to 94% yield after 5 reuses). The air stable compound [PdCl₂(L1)₂] shows high catalytic efficien

Full text of DOI:10.1039/c2dt12256a

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COMMUNICATION
Didocosyl selenide stabilized recyclable Pd(0) nanoparticles and coordinated
palladium(II) as efficient catalysts for Suzuki–Miyaura coupling†
Gyandshwar Kumar Rao, Arun Kumar, Bharat Kumar and Ajai K. Singh*
Received 25th November 2011, Accepted 2nd February 2012
DOI: 10.1039/c2dt12256a
First selenium ligand stabilized Pd(0) nanoparticles
∼3–5 nm) catalyze Suzuki–Miyaura C–C coupling in short
ligands have been reported in the recent past as important build-
6
a,10
(
ing blocks for catalysts.
The strong electron-donating ability
time and are recyclable (up to 94% yield after 5 reuses). The
air stable compound [PdCl (L1) ] shows high catalytic
of selenium, has made it attractive for designing catalyst frame-
6
a,10
works.
Organic selenides having large alkyl groups may
2
2
−
5
have the combination of electronic and steric properties which
can make them favorable ligands for stabilization of Pd NPs as
well as designing of Pd(II) catalysts. However, they have been so
far unexplored. The large alkyl group as in didocosyl selenide
(L1) is envisaged to minimize the surface deactivation of Pd
NPs by preventing the strong sorption of ligands onto the
surface.
efficiency for this coupling as its 3 × 10 mol% is sufficient
for activated ArBr.
Metal nanoparticles (NPs), more active than their particulate
counterparts due to large surface area, are among the promising
species for efficient catalysis under mild and environmentally
benign conditions. Generally dendrimers, organic/organofluor-
ous ligands, polymers, ionic liquids and surfactants are used to
In this communication we present Suzuki reactions catalyzed
with recyclable Pd(0) NPs, stabilized with (C H ) Se (L1) and
1–4
stabilize such NPs for efficient catalytic organic synthesis. In
the absence of a stabilizing agent they generally tend to aggre-
gate or precipitate losing their catalytic activities. Palladium(0)
NPs stabilized by several agents have been used directly in
22 45 2
highly efficient Pd(II) complex, [PdCl (L1) ].
2
2
The syntheses of L1, its air stable Pd(II)-complex 1 and L1-
stabilized Pd(0) NPs 2–4 have been summarized in Scheme 1.
The centrifugation at 6000 rpm of NPs 2–4 in chloroform does
3
3,4
olefin hydrogenation and various C–C coupling reactions
2
–4
1
13
1
including Suzuki–Miyaura coupling.
This is because palla-
not result in any aggregation (ESI: Fig. S20†). The H, C{ H}
4c,5,6
77
1
dium complexes
of a large number of phosphorus, carbene,
and Se{ H} NMR spectra (ESI: S2, Fig. S7–S12†) of L1 and
diamagnetic complex 1 are consistent with their structures
depicted in Scheme 1. The Pd(0) NPs 2–4 were characterized by
oxime and other ligands are known efficient catalysts for
Suzuki–Miyaura coupling, and in many instances the formation
4
c,6
77
1
of nano-sized species
has been recognized as the pathway.
powder XRD, Se{ H}NMR spectroscopy (Fig. 1), HRTEM
(Fig. 2), TEM-EDX (ESI: Fig. S1–S3†) and SEM (ESI: Fig. S4–
S6†). The size of the NPs is ∼3 nm in the case of 2 whereas
∼5 nm in the case of 3 and 4.
The stabilizing ligands determine the dispersion of the NPs to
a great extent and also affect their catalytic efficiency recyclabil-
ity, composition, solubility and size. They function via ligating
with them. The ligands having strongly coordinating groups
stabilize metal NPs well but may render them catalytically inac-
tive due to strong chemisorptions. For example functional
groups like thiol, amine, carbonyl or hydroxyl, if present in the
The coordination of the ligand L1 via Se with Pd(II) and Pd(0)
77
1
NPs was supported by Se{ H} NMR spectroscopy. The signal
77
in Se NMR spectrum of 1 appears at 257.2 ppm, deshielded by
∼94 ppm with respect to that of free L1 (163.8 ppm). Two
2
a,7
stabilizer, limit the activity
of NPs. The sterically demanding
8
P(n-octyl) also stabilizes NPs of palladium well. Thus to get
3
2
a,c,9
NPs suitable
for multiple reaction cycles, the ligand should
be strong enough to stabilize NPs but should readily allow
access of the reactant to its surface. No ideal stabilizer for Pd
NPs which does not deactivate them at all is known. Therefore,
search of new stabilizers which improve stabilization with
minimal surface deactivation is of current interest. For this
purpose selenium ligands may be good candidates. Such type of
Department of Chemistry, Indian Institute of Technology Delhi, New
Delhi 110016, India. E-mail: aksingh@chemistry.iitd.ac.in, ajai57@
hotmail.com; Fax: +91 11 26581102; Tel: +91 11 26591379
†
Electronic supplementary information (ESI) available: Synthesis and
full characterization of L1 and 1–4; general procedures for the Suzuki
reactions. See DOI: 10.1039/c2dt12256a
Scheme 1 Synthesis of L1, its Pd(II) complex 1 and NPs 2–4.
4306 | Dalton Trans., 2012, 41, 4306–4309
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Table 1 Sa uzuki–Miyaura C–C coupling reactions catalyzed by Pd(II)
complex 1
2
Ar–X + PhB(OH) → Ar–Ph (Ar = aryl/heteroaryl; X = Cl/Br)
b
Entry
Aryl/heteroaryl halide
Mol% Pd
t (h)
Yield
c
1
1-Chloro-4-nitrobenzene
1-Chloro-4-nitrobenzene
4-Chlorobenzaldehyde
4-Chloroacetophenone
Chlorobenzene
4-Chlorotoluene
4-Chloroanisole
1-Bromo-4-nitrobenzene
1-Bromo-4-nitrobenzene
4-Bromobenzaldehyde
4-Bromobenzaldehyde
4-Bromobenzaldehyde
4-Bromoacetophenone
Bromobenzene
2
5
5
5
5
5
5
20
17
12
40
24
22
28
20
16
40
36
24
10
15
15
16
16
16
20
15
100
92
95
85
89
89
83
100
94
86
100
92
87
94
84
85
80
91
87
90
2
3
4
5
6
7
8
9
1
1
1
1
1
1
1
1
1
1
2
7
7
1
Fig. 1
Se{ H} NMR spectra of L1 and 1–4.
d,e
−5
3 × 10
10
3 × 10
10
d
−3
d,f
−5
0
1
d,f
−4
−3
2
3
4
5
6
7
8
9
0
10
0.1
0.1
0.1
0.1
1
0.1
0.1
0.1
4-Bromotoluene
4-Bromoanisole
4-Bromoaniline
2-Bromothiophene
2-Bromopyridine
3-Bromoquinoline
a
Reaction conditions: aryl/heteroaryl halide (1.0 mmol), phenylboronic
CO (2.0 equivs.), aq. DMF (3 mL), 100 °C.
Isolated yield after column chromatography. Conversion (57 : 43 ratio
acid (1.3 mmol), K
2
3
b
c
d
2 3
of cross coupled product and N,N-dimethylaminated product). Cs CO
as base. Conversion (50 : 50 ratio of cross coupled product and N,N-
dimethylaminated product). NMR % conversion.
e
f
Table 2 Suzuki–Miyaura C–C coupling reactions catalyzed by Pd(0)
a
NPs
Fig. 2 HRTEM images at 10 nm, 20 nm, 50 nm and 100 nm scale bar.
Ar–X + PhB(OH)
2
→ Ar–Ph (X = Cl or Br)
b
Conversion
7
7
1
signals (Fig. 1) are present in the Se{ H} NMR spectra of 2
and 3 (δ, ppm; 2: 160.2, 257.5 and 3: 160.8, 257.5 ppm). The
deshielded ones around 257 ppm indicate that some ligand mol-
ecules are as strongly coordinated with NPs as with Pd(II) in
complex 1. The signals at ∼160 ppm in the case of 2 and 3 are
due to L1 interacting weakly (or free) with Pd NPs. In the
spectra of 2–4 (Fig. 1) the intensities of the signals reveal that
the ratio of weakly and strongly coordinated L1 is higher for 2
than that of 3. Probably this results in uniformity and dispersion
Entry Aryl halide
t (min) Cycle
2
3
4
1
2
3
4
5
6
7
8
9
1
4-BrC
4-BrC
4-BrC
6
H
6
H
6
H
4
4
4
-OMe
90
90
1
2
3
4
5
1
2
3
4
5
1
2
3
4
5
100
100
100 100
98
85
90
80
100 95
100 97
95
94
89
97
91
89
82
120
120
150
60
120
120
180
180
90 (79)
86 (70)
82 (55)
100
98 (83)
84 (71)
93 (58)
87 (43)
100
100 (96) 98
100 (84) 98
98 (79)
94 (72)
32
c
c
c
-CH
3
82
88
82
7
7
1
of NPs in the case of 2. The Se{ H} NMR spectrum of 4 (Pd:
L1 ratio 4 : 1) suggests that almost all L1 molecules are strongly
coordinated to NPs. The peaks at d ∼2.24 (hkl: 111) and 1.96
0
11
-CHO 20
100 100
1
2
30
45
60
60
100
98
95
88
—
(
(
hkl: 200) observed in their powder XRD (ESI: Fig. S17–S19†
JCPDS ≠ 88–2335)) support the presence of palladium(0) with
13
14
15
16
96
87
17
face-centered cubic structure. The 1 and Pd(0) NPs 2–4 have
been explored as catalysts for Suzuki–Miyaura C–C coupling
reactions of several aryl halides (Tables 1 and 2).
c,d
4-ClC
6
H
4
-CHO
24 h
—
a
Reaction conditions: aryl halide (5.0 mmol), phenylboronic acid
CO (8.0 mmol), aq. DMF (12 mL), 100 °C, amount of
(6.0 mmol), K
2
3
The most appropriate base for the functioning of catalyst 1
was found to be K CO /Cs CO (Table 1: entries 8–11). For
2
, 3 or 4 equivalent to 0.5, 1.0 and 1.5 mol% of palladium respectively.
NMR % conversion to coupled product with reference to substrate.
b
2
3
2
3
c
alternatives viz. NEt , NaOAc or Na CO a longer reaction time
Isolated yield after column chromatography (lower to NMR yield by
3
2
3
d
∼
3–5%). Amount of 2, 3 or 4 equivalent to 5.0 mol% of palladium.
was required for reasonable conversions. Further a DMF and
water mixture was found to be the best solvent system for the
reaction. Compound 1 showed catalytic activity for ArCl in the
The NMR yields given in parentheses in the case of 2 correspond to the
time used for first cycle.
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presence of its 2–5 mol%. For aryl bromides 1 showed high cata-
lytic activity as its 3 × 10 to 0.1 mol% was sufficient for good
conversions (Table 1).
In the coupling reaction of 1-chloro-4-nitrobenzene at 2 mol%
loading of catalyst 1, cross coupled product, 4-nitrobiphenyl,
along with N,N-dimethylaminated product (ratio = 57 : 43,
Table 1: entry 1) was obtained. However, at 5 mol% of catalyst
loading, only 4-nitrobiphenyl was obtained in 92% yield
Thus in the case of 1 it is unlikely that catalysis is via Pd nano-
particles as active catalyst. The quenching of the catalytic reac-
−5
tion in the case of
Triphenyphosphine (ESI: S4.3†) also quenched the catalysis
by 3 supporting the results of the Hg test.
3
is as expected for NPs.
11
2
Some Pd(0) NPs stabilized by other ligands are reported to
show somewhat better activity than 2–4 but their preparation
usually includes a series of steps and separations that commonly
result in their low yields. The synthesis of L1 is a simple one
step with good yield, which is a distinct advantage. Various ana-
logues of L1 may be developed, which may constitute a family
of easily accessible ligands suitable for stabilizing various metal
NPs.
(
Table 1: entry 2). The coupling reaction of 1-bromo-4-nitroben-
−5
zene at 3 × 10 mol% loading of 1 and in the presence of
Cs CO3 resulted in the formation of cross-coupled and N,N-
2
dimethylaminated products in equimolar ratio (Table 1: entry 8)
−3
whereas for loading of 10 mol% of catalyst (1) only cross
coupled product 4-nitrobiphenyl in 92% yield (Table 1: entry 9)
was obtained. 4-Bromobenzaldehyde was successfully converted
to biphenyl-4-carboxyaldehyde (yield 86%, Table 1: entry 10) at
In summary newly synthesized [PdCl (n-C H –Se–n-
2
22 45
C H ) ] has been found air stable and highly efficient for
22 45 2
−5
Suzuki coupling as its 3 × 10 mol% is enough for some ArBr.
The catalytic properties for Suzuki coupling of Pd(0) NPs (no
aggregation on centrifugation even at 6000 rpm in chloroform)
stabilized for the first time with a selenium ligand (didocosyl
selenide, L1) vary with Pd : L1 ratio and the NPs are recyclable.
The short reaction time is a distinct feature of 2–4 catalyzed
Suzuki coupling.
−5
3
× 10 mol% loading of catalyst 1 in the presence of Cs CO .
2 3
The results of NPs 2–4 assisted Suzuki coupling (see ESI:
S3.2†) are given in Table 2. The distinct feature of these coup-
ling reactions is the time for maximum conversion which is
found significantly short (20 min to 3 h). The efficiency of 2
was found better than those of 3 and 4 as it was able to catalyze
the reactions to give comparable conversions at lower loading. It
appears that greater shielding of NPs by weakly associated
ligand molecules is favorable for higher catalytic efficiency. The
order of reactivity of NPs towards 4-chlorobenzaldehyde was 2 >
The Council of Scientific and Industrial Research, India sup-
ported the work through the award of SRF/RA and project 01
(2421)10/EMR-II. The authors thank Professor A. K. Ganguli of
IIT Delhi for providing HRTEM as well as powder XRD facility.
3
(yields of biphenyl-4-carboxaldehyde: 32 and 17% respect-
ively) at 5 mol% loading of catalyst. The conversion of the sub-
strate was almost negligible when 4 was used as a catalyst at
similar loading. The higher ligand to Pd ratio in 2 makes better
dispersion of NPs which probably results in its higher activity.
The recyclability (ESI: S3.2†) of Pd(0) NPs (2–4) was studied
for coupling of 4-bromoanisole, 4-bromotoluene and 4-bromo-
benzaldehyde. The conversions were lowered when reaction time
was kept same for each higher cycle but with prolonged reaction
time these remained reasonably intact even for fifth cycle
Notes and references
1 For reviews, see: (a) J. Dupont and J. D. Scholten, Chem. Soc. Rev.,
2010, 39, 1780; (b) Y. Gu and G. Li, Adv. Synth. Catal., 2009, 351, 817;
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1
2
814; (d) D. Astruc, M.-C. Daniel and J. Ruiz, Chem. Commun., 2004,
637.
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Synth. Catal., 2008, 350, 846; (c) R. Tatumi, T. Akita and H. Fujihara,
Chem. Commun., 2006, 3349; (d) L. Wu, B. L. Li, Y. Y. Huang, H.
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C. Khemtong and J. Hu, Chem. Commun., 2004, 398; (f) K. R. Gopidas,
J. K. Whitesell and M. A. Fox, Nano Lett., 2003, 3, 1757;
(Table 2). The NPs of palladium stabilized with L1 are needed
in more amounts than that of 1 for getting comparable conver-
sion in Suzuki coupling.
(
2
g) M. Moreno-Manas, R. Pleixats and S. Villarroya, Organometallics,
001, 20, 4524; (h) Y. Li, X. M. Hong, D. M. Collard and M. A. El-
Generally molecular complexes have been found to be more
efficient in comparison to NPs (except in situ generated ones)
but recyclability of NPs is a distinct advantage as observed pre-
sently. The TEM image of nano-particles obtained after using 2
for five times is shown in Fig. 2. Their size (∼5 nm) and dis-
persion both suggest that aggregation of nano-particles is not
extensive which probably results in their recyclability.
Sayed, Org. Lett., 2000, 2, 2385.
3
4
For reviews, see: (a) D. Astruc, F. Lu and J. R. Aranzaes, Angew. Chem.,
Int. Ed., 2005, 44, 7852; (b) A. Roucoux, J. Schulz and H. Patin, Chem.
Rev., 2002, 102, 3757.
For reviews, see: (a) A. Fihri, M. Bouhrara, B. Nekoueishahraki, J.-
M. Basset and V. Polshettiwar, Chem. Soc. Rev., 2011, 40, 5181;
(b) D. Astruc, Inorg. Chem., 2007, 46, 1884; (c) N. T. S. Phan, M. Van
Der Sluys and C. W. Jones, Adv. Synth. Catal., 2006, 348, 609.
To understand further the catalysis by Pd(0) NPs hot filtration
5
6
For reviews, see: (a) A. John and P. Ghosh, Dalton Trans., 2010, 39,
7183; (b) E. Alacid, D. A. Alonso, L. Botella, C. Nájera and M.
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11
experiments were carried out with 3 (1 mol%). When the reac-
tion mixture was filtered hot, after 60% conversion (occurred in
1
0 min), the reaction continued in filtrate at a lower rate (ESI:
S4.1†) indicating that some palladium was leached from the NPs
during catalysis. The amount of leached palladium estimated by
flame AAS was found to be 0.5% of the initial catalyst loading.
11
A mercury poisoning test was performed (ESI: S4.2†) on a
representative coupling reaction of 4-bromoanisol with phenyl-
boronic acid using 1 (0.1 mol%) and 3 (1 mol%) as catalyst
under optimal conditions. The biaryl product was obtained in
7
8
V. Mazumder and S. Sun, J. Am. Chem.Soc., 2009, 131, 4588.
S. U. Son, Y. Jang, K. Y. Yoon, E. Kang and T. Hyeon, Nano Lett., 2004,
1
00% yield when 1 was used as catalyst even in the presence of
4, 1147.
an excess of Hg and with 3 only traces of product were obtained.
9 F. Lu, J. Ruiz and D. Astruc, Tetrahedron Lett., 2004, 45, 9443.
4308 | Dalton Trans., 2012, 41, 4306–4309
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This journal is © The Royal Society of Chemistry 2012
Dalton Trans., 2012, 41, 4306–4309 | 4309