Abstract
Pd-NHC-ionic liquid matrix was immobilized into ionic liquid
layers coated on the surface of Fe3 O4 . The
immobilized Pd-NHC was used as a catalyst for Suzuki coupling. The
catalyst exhibited both high catalytic activity and stability for
the coupling between aryl bromide and arylboronic acid in water.
This catalyst was simply recovered by an external permanent magnet
and recycled without a significant loss in the catalytic activity.
Key words
heterogeneous catalysis - Suzuki reaction - palladium - magnetic nanoparticle - ionic liquids
References and Notes
For reviews, see:
1a
Leadbeater NE.
Marco M.
Chem. Rev.
2002,
102:
3217
1b
Yin L.
Liebscher J.
Chem. Rev.
2007,
107:
133
2a
Paul S.
Clark JH.
Green
Chem.
2003,
5:
635
2b
Hardy JJE.
Hubert S.
Macquarrie DJ.
Wilson
AJ.
Green
Chem.
2004,
6:
53
2c
Yang Q.
Ma S.
Li J.
Xiao F.
Xiong H.
Chem. Commun.
2006,
2495
2d
Sayah R.
Glegola K.
Framery E.
Dufaud V.
Adv. Synth. Catal.
2007,
349:
373
2e
Qiu H.
Sarkar SM.
Lee D.-H.
Jin M.-J.
Green Chem.
2008,
10:
37
3a
Wasserscheid P.
Keim W.
Angew.
Chem. Int. Ed.
2000,
39:
3772
3b
Dupont J.
de Souza RF.
Suarez PA.
Z. Chem. Rev.
2002,
102:
3667
3c
Jain N.
Kumar A.
Chauhan S.
Chauhan SMS.
Tetrahedron
2005,
61:
1015
3d
Akiyama T.
Suzuki A.
Fuchibe K.
Synlett
2005,
1024
3e
Ranu BC.
Banerjee S.
Jana R.
Tetrahedron
2007,
63:
776
4
Mehnert CP.
Cook RA.
Dispenziere NC.
Afeworki M.
J. Am.
Chem. Soc.
2002,
124:
12932
5a
Breitenlechner S.
Fleck M.
Müller TE.
Suppan A.
J. Mol. Catal. A
2004,
214:
175
5b
Mehnert CP.
Chem. Eur. J.
2005,
11:
50
5c
Hagiwara H.
Ko KH.
Hoshi T.
Suzuki T.
Chem. Commun.
2007,
2838
6a
Xu C.
Xu K.
Gu H.
Zheng R.
Liu H.
Zhang X.
Guo Z.
Xu B.
J. Am. Chem. Soc.
2004,
126:
9938
6b
Kohler N.
Fryxell GE.
Zhang M.
J.
Am. Chem. Soc.
2004,
126:
7206
6c
Berry CC.
Curtis ASG.
J.
Phys. D: Appl. Phys.
2003,
36:
R198
6d
Park J.
An K.
Hwang Y.
Park J.-G.
Noh H.-J.
Kim J.-Y.
Park J.-H.
Hwang N.-M.
Hyeon T.
Nat. Mater.
2004,
3:
891
7a
Tsang SC.
Caps V.
Paraskevas I.
Chadwick D.
Thompsett D.
Angew. Chem. Int. Ed.
2004,
43:
5645
7b
Yoon T.-J.
Lee W.
Oh Y.-S.
Lee J.-K.
New J. Chem.
2003,
27:
227
7c
Hu A.
Yee TG.
Lin W.
J.
Am. Chem. Soc.
2005,
127:
12486
7d
Dalaigh OC.
Corr AS.
Gun’ko Y.
Connon JS.
Angew.
Chem. Int. Ed.
2007,
46:
4329
For a review, see:
8a
Herrmann WA.
Angew. Chem. Int. Ed.
2002,
41:
1290
8b
Crudden CM.
Allen DP.
Coord. Chem.
Rev.
2004,
248:
2247
9a
Navarro O.
Kelly RA.
Nolan SP.
J.
Am. Chem. Soc.
2003,
125:
16194
9b
Navarro O.
Kaur H.
Mahjoor P.
Nolan SP.
J. Org. Chem.
2003,
69:
3173
9c
Altenhoff G.
Heska R.
Org. Lett.
2004,
6:
3641
9d
Wang AE.
Xie JH.
Wang LX.
Zhou QL.
Tetrahedron
2005,
61:
259
9e
Lee S.-M.
Yoon H.-J.
Kim J.-H.
Chung W.-H.
Lee Y.-S.
Pure
Appl. Chem.
2007,
79:
1553
9f
Qiu H.
Sarkar SM.
Lee D.-H.
Jin M.-J.
Green Chem.
2008,
10:
37
10a
Herrman WA.
Elison M.
Fisher J.
Kocher C.
Artus GRJ.
Angew. Chem.
Int. Ed.
1995,
34:
2371
10b
Deshmukh RR.
Rajagopal R.
Srinivasan KV.
Chem. Commun.
2001,
1544
10c
Kim J.-H.
Kim J.-W.
Shokouhimehr M.
Lee Y.-S.
J. Org. Chem.
2005,
70:
6714
11
Brenna S.
Posset T.
Furrer J.
Blumel J.
Chem. Eur. J.
2006,
12:
2880
12
Surface Modification
of Nano-Fe
3
O
4
To a solution of 1-(3-trimethoxysilylpropyl)-3-methyl-imidazolium
chloride (0.28 g, 1.0 mmol) in toluene was added nano-sized Fe3 O4 (Aldrich,
1.0 g). The mixture was stirred at 100 ˚C for
10 h. After cooling, the nano-Fe3 O4 was magnetically
separated from reaction mixture. Modified Fe3 O4 2 was washed with CH2 Cl2 several
times and dried at 60 ˚C under vacuum. Elemental
analysis and weight gain showed that 0.67 mmol of 1-(3-trimethoxysilylpropyl)-3-methylimidazolium
chloride was anchored on 1.0 g of 2 .
13
Immobilization
of NHC-Pd onto Modified Nano-Fe
3
O
4
2
To a solution of Pd-NHC 1 (195 mg, 0.29 mmol) and 1-butyl-3-methylimidazolium
hexafluorophosphate (165 mg, 0.58 mmol) in CH2 Cl2 (2
mL) modified Fe3 O4 2 (1.0
g) was added. The mixture was sonicated for 15 min at r.t., and then
CH2 Cl2 was slowly removed under reduced pressure. The
resulting powder was washed with Et2 O and dried under vacuum
at 60 ˚C to give Pd-NHC@Fe3 O4 -IL 3 (1.21 g). The Pd content of 0.17 mmol/g
was measured by inductively coupled plasma (ICP) analysis.
For reviews, see:
14a
Miyaura N.
Suzuki A.
Chem. Rev.
1995,
95:
2457
14b
Kotha S.
Lahiri K.
Kashinath D.
Tetrahedron
2002,
58:
9633
14c
Nicolaou KC.
Bulger
PG.
Sarlah D.
Angew. Chem. Int. Ed.
2005,
44:
4442
14d
Phan NTS.
Sluys MVD.
Jones CW.
Adv. Synth. Catal.
2006,
348:
609
15a
Zapf A.
Ehrentraut A.
Beller M.
Angew. Chem. Int. Ed.
2000,
39:
4153
15b
Bedford RB.
Cazin CSJ.
Hazelwood SL.
Angew. Chem. Int.
Ed.
2002,
41:
4120
15c
Liu L.
Zhang Y.
Wang Y.
J.
Org. Chem.
2005,
70:
6122
15d
Churruca F.
SanMartin R.
Inés B.
Tellitu I.
Domínguez E.
Adv.
Synth. Catal.
2006,
348:
1836
15e
Maegawa T.
Kitamira Y.
Udzu T.
Sakurai A.
Tanaka A.
Kobayashi Y.
Endo K.
Bora U.
Kurita T.
Kozaki A.
Monguchi Y.
Sajiki H.
Chem. Eur. J.
2007,
13:
5937
15f
Lee D.-H.
Jung J.-Y.
Lee IM.
Jin M.-J.
Eur. J. Org. Chem.
2008,
356
15g
Billingsley KL.
Buchwald SL.
Angew.
Chem. Int. Ed.
2008,
47:
4695
15h
Phan
NTS.
Styring P.
Green
Chem.
2008,
10:
1055
15i
Suzuki K.
Sawaki T.
Hori Y.
Kobayashi T.
Synlett
2008,
1809
15j
Zotto AD.
Amoroso F.
Baratte W.
Rigo P.
Eur. J. Org.
Chem.
2009,
110
16
General Procedure
for the Suzuki Coupling Reaction
Aryl halide (1.0
mmol), arylboronic acid (1.2 mmol), K3 PO4 (424
mg, 2.0 mmol), TBAB (161 mg, 0.5 mmol), dodecane (40 mg, internal
standard), and catalyst 3 (30 mg, 0.5 mol%) were
mixed in H2 O (2.0 mL). The mixture was stirred at 75 ˚C
in an air atmosphere. The reaction was periodically monitored by
GC. After magnetic separation of the catalyst, the organic material
was twice extracted with Et2 O. The organic phase was
dried over MgSO4 , and the solvent was evaporated under
reduced pressure. The crude was analyzed by GC/GC-MS. The
product was purified by short column chromatography on silica gel.
17
Reuse of Pd-NHC@Fe
3
O
4
-IL
3
In the recycling experiment the reaction was performed
by using a mixture of 4-bromoanisole (187 mg, 1.0 mmol), phenylboronic
acid (134 mg, 1.2 mmol), K3 PO4 (424 mg, 2.0 mmol),
TBAB (161 mg, 0.5 mmol), and catalyst 3 (30
mg, 0.5 mol%) in H2 O (2.0 mL) at 75 ˚C
for 0.7 h. After completion of the reaction, the catalyst was magnetically separated
from the solution. The solution was worked up as described above.
The separated catalyst was successively reused for the next reaction
without any pre-treatment.