-
3
-
-
0000906649
-
-
M. T. Reetz, G. Lohmer, R. Schwickardi, Angew. Chem. 1998, 110, 492-495
-
(1998)
Angew. Chem.
, vol.110
, pp. 492-495
-
-
Reetz, M.T.1
Lohmer, G.2
Schwickardi, R.3
-
5
-
-
0141856236
-
-
A. H. M. de Vries, J. M. C. A. Mulders, J. H. M. Mommers, H. J. W. Hendrickx, J. G. de Vries, Org. Lett. 2003, 5, 3285-3288
-
(2003)
Org. Lett.
, vol.5
, pp. 3285-3288
-
-
De Vries, A.H.M.1
Mulders, J.M.C.A.2
Mommers, J.H.M.3
Hendrickx, H.J.W.4
De Vries, J.G.5
-
6
-
-
34548209359
-
-
M. B. Thathagar, J. E. ten Elshof, G. Rothenberg, Angew. Chem. 2006, 118, 2952-2956
-
(2006)
Angew. Chem.
, vol.118
, pp. 2952-2956
-
-
Thathagar, M.B.1
Ten Elshof, J.E.2
Rothenberg, G.3
-
7
-
-
33746255415
-
-
Angew. Chem. Int. Ed. 2006, 45, 2886-2890.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 2886-2890
-
-
-
8
-
-
33645865241
-
-
For a review see
-
For a review see:, N. T. S. Phan, M. Van Der Sluys, C. W. Jones, Adv. Synth. Catal. 2006, 348, 609-679.
-
(2006)
Adv. Synth. Catal.
, vol.348
, pp. 609-679
-
-
Phan, N.T.S.1
Van Der Sluys, M.2
Jones, C.W.3
-
9
-
-
72149085820
-
-
K. Sawai, R. Tatumi, T. Nakahodo, H. Fujihara, Angew. Chem. 2008, 120, 7023-7025
-
(2008)
Angew. Chem.
, vol.120
, pp. 7023-7025
-
-
Sawai, K.1
Tatumi, R.2
Nakahodo, T.3
Fujihara, H.4
-
10
-
-
53249095970
-
-
Angew. Chem. Int. Ed. 2008, 47, 6917-6919
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 6917-6919
-
-
-
11
-
-
67649616348
-
-
Y.-H. Chen, H.-H. Hung, M. H. Huang, J. Am. Chem. Soc. 2009, 131, 9114-9121.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 9114-9121
-
-
Chen, Y.-H.1
Hung, H.-H.2
Huang, M.H.3
-
12
-
-
77955579407
-
-
P. J. Ellis, I. J. S. Fairlamb, S. F. J. Hackett, K. Wilson, A. F. Lee, Angew. Chem. 2010, 122, 1864-1868
-
(2010)
Angew. Chem.
, vol.122
, pp. 1864-1868
-
-
Ellis, P.J.1
Fairlamb, I.J.S.2
Hackett, S.F.J.3
Wilson, K.4
Lee, A.F.5
-
13
-
-
77749292475
-
-
Angew. Chem. Int. Ed. 2010, 49, 1820-1824
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 1820-1824
-
-
-
14
-
-
78049337805
-
-
A. F. Lee, P. J. Ellis, I. J. S. Fairlamb, K. Wilson, Dalton Trans. 2010, 39, 10473-10482
-
(2010)
Dalton Trans.
, vol.39
, pp. 10473-10482
-
-
Lee, A.F.1
Ellis, P.J.2
Fairlamb, I.J.S.3
Wilson, K.4
-
15
-
-
77952850625
-
-
N. Hoshiya, M. Shimoda, H. Yioshikawa, Y. Yamashita, S. Shuto, M. Arisawa, J. Am. Chem. Soc. 2010, 132, 7270-7772.
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 7270-7772
-
-
Hoshiya, N.1
Shimoda, M.2
Yioshikawa, H.3
Yamashita, Y.4
Shuto, S.5
Arisawa, M.6
-
16
-
-
34548233629
-
-
A. V. Gaikwad, A. Holyuigre, M. B. Thathagar, J. E. ten Elshof, G. Rothenberg, Chem. Eur. J. 2007, 13, 6908-6913
-
(2007)
Chem. Eur. J.
, vol.13
, pp. 6908-6913
-
-
Gaikwad, A.V.1
Holyuigre, A.2
Thathagar, M.B.3
Ten Elshof, J.E.4
Rothenberg, G.5
-
17
-
-
62549109731
-
-
S. MacQuarrie, J. H. Horton, J. Barnes, K. McEleney, H.-P. Loock, C. M. Crudden, Angew. Chem. 2008, 120, 3324-3328
-
(2008)
Angew. Chem.
, vol.120
, pp. 3324-3328
-
-
MacQuarrie, S.1
Horton, J.H.2
Barnes, J.3
McEleney, K.4
Loock, H.-P.5
Crudden, C.M.6
-
18
-
-
53549131956
-
-
Angew. Chem. Int. Ed. 2008, 47, 3279-3282.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 3279-3282
-
-
-
20
-
-
0000840737
-
-
C. Amatore, A. Jutand, F. Khalil, M. A. M'Barki, L. Mottier, Organometallics 1993, 12, 3168-3178.
-
(1993)
Organometallics
, vol.12
, pp. 3168-3178
-
-
Amatore, C.1
Jutand, A.2
Khalil, F.3
M'Barki, M.A.4
Mottier, L.5
-
21
-
-
0000975959
-
-
Synthesis of biaryls via the cross-coupling reaction of arylboronic acids":, JAI, New York
-
"Synthesis of biaryls via the cross-coupling reaction of arylboronic acids":, N. Miyaura, Advances in Metal-Organic Synthesis, Vol. 6, JAI, New York, 1998, pp. 187-243
-
(1998)
Advances in Metal-Organic Synthesis
, vol.6
, pp. 187-243
-
-
Miyaura, N.1
-
23
-
-
39749179066
-
-
F. Alonso, I. P. Beletskaya, M. Yus, Tetrahedron 2008, 64, 3047-3101
-
(2008)
Tetrahedron
, vol.64
, pp. 3047-3101
-
-
Alonso, F.1
Beletskaya, I.P.2
Yus, M.3
-
25
-
-
72949108920
-
-
Angew. Chem. Int. Ed. 2009, 48, 9240-9261
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 9240-9261
-
-
-
27
-
-
79951662418
-
-
C. Amatore, A. Jutand, G. Le Duc, Chem. Eur. J. 2011, 17, 2492-2503.
-
(2011)
Chem. Eur. J.
, vol.17
, pp. 2492-2503
-
-
Amatore, C.1
Jutand, A.2
Le Duc, G.3
-
28
-
-
83755192970
-
-
note
-
The observed kinetic laws (Figure 1 and Figure S1 in the Supporting Information) establish that the reaction proceeds without significant induction period as if the concentration of catalytic species were rapidly maintained at a constant value during the reaction course; this constant value depends on the number of monolayers. According to one possible mechanism each type of NP acts as a reservoir in fast equilibrium with the soluble palladium species ("fast" with respect with the overall kinetics). Such behavior would maintain a time-constant ML-dependent catalyst(s) concentration in the solution and compensate automatically for their expected low life-time in the absence of suitable ligands.
-
-
-
-
32
-
-
34748833496
-
-
Z. Q. Tian, B. Ren, J. F. Li, Z. L. Yang, Chem. Commun. 2007, 3514-3534
-
(2007)
Chem. Commun.
, pp. 3514-3534
-
-
Tian, Z.Q.1
Ren, B.2
Li, J.F.3
Yang, Z.L.4
-
33
-
-
78449272460
-
-
H. Kim, K. M. Kosuda, R. P. Van Duyne, P. C. Stair, Chem. Soc. Rev. 2010, 39, 4820.
-
(2010)
Chem. Soc. Rev.
, vol.39
, pp. 4820
-
-
Kim, H.1
Kosuda, K.M.2
Van Duyne, R.P.3
Stair, P.C.4
-
34
-
-
78449272460
-
-
Note that the slanted background of the SERS spectrum recorded after catalytic runs (Figure 2-b, blue) is characteristic of the fluorescent background due to adsorbed aromatic moieties
-
Note that the slanted background of the SERS spectrum recorded after catalytic runs (Figure 2-b, blue) is characteristic of the fluorescent background due to adsorbed aromatic moieties:, H. Kim, K. M. Kosuda, R. P. Van Duyne, P. C. Stair, Chem. Soc. Rev. 2010, 39, 4820.
-
(2010)
Chem. Soc. Rev.
, vol.39
, pp. 4820
-
-
Kim, H.1
Kosuda, K.M.2
Van Duyne, R.P.3
Stair, P.C.4
-
35
-
-
79851502079
-
-
F. Wang, C. Li, L.-D. Sun, H. Wu, T. Ming, J. Wang, J. C. Yu, C.-H. Yan, J. Am. Chem. Soc. 2011, 133, 1106-1111
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 1106-1111
-
-
Wang, F.1
Li, C.2
Sun, L.-D.3
Wu, H.4
Ming, T.5
Wang, J.6
Yu, J.C.7
Yan, C.-H.8
-
36
-
-
83755192971
-
-
note
-
We did not use a strong surfactant as in Ref. [13a] so that the Pd excess residual was smaller (11-%) than that reported by Wang et al.
-
-
-
-
37
-
-
2342651240
-
-
J. Wang, H. F. M. Boelens, M. B. Thathagar, G. Rothenberg, ChemPhysChem 2004, 5, 93-98.
-
(2004)
ChemPhysChem
, vol.5
, pp. 93-98
-
-
Wang, J.1
Boelens, H.F.M.2
Thathagar, M.B.3
Rothenberg, G.4
-
38
-
-
83755192969
-
-
For a comparably remarkable situation, see: Ref. [1c] and
-
For a comparably remarkable situation, see: Ref. [1c] and
-
-
-
-
39
-
-
78649918300
-
-
P. F. Larsson, C. Bolm, P. O. Norrby, Chem. Eur. J. 2010, 16, 13613-13616
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 13613-13616
-
-
Larsson, P.F.1
Bolm, C.2
Norrby, P.O.3
-
41
-
-
77956240378
-
-
Y. Ding, F. R. Fan, Z. Q. Tian, Z. L. Wang, J. Am. Chem. Soc. 2010, 132, 12480-12486.
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 12480-12486
-
-
Ding, Y.1
Fan, F.R.2
Tian, Z.Q.3
Wang, Z.L.4
-
42
-
-
72849122229
-
-
For a similar conclusion about the innocuousness of the aryl halide in Heck reactions catalyzed by Pd NPs, see e.g
-
For a similar conclusion about the innocuousness of the aryl halide in Heck reactions catalyzed by Pd NPs, see e.g.:, A. Karam, J. C. Alonso, T. I. Gerganova, P. Ferreira, N. Bion, J. Barrault, F. Jerome, Chem. Commun. 2009, 7000-7002.
-
(2009)
Chem. Commun.
, pp. 7000-7002
-
-
Karam, A.1
Alonso, J.C.2
Gerganova, T.I.3
Ferreira, P.4
Bion, N.5
Barrault, J.6
Jerome, F.7
-
43
-
-
33645456834
-
-
L. Durán Pachõn, M. B. Thathagar, F. Hartl, G. Rothenberg, Phys. Chem. Chem. Phys. 2006, 8, 151
-
(2006)
Phys. Chem. Chem. Phys.
, vol.8
, pp. 151
-
-
Durán Pachõn, L.1
Thathagar, M.B.2
Hartl, F.3
Rothenberg, G.4
-
44
-
-
79952659758
-
-
P. P. Fang, S. Duan, X.-D. Lin, J. R. Anema, J.-F. Li, O. Buriez, Y. Ding, F.-R. Fan, D.-Y. Wu, B. Ren, Z. L. Wang, C. Amatore, Z.-Q. Tian, Chem. Sci. 2011, 2, 531.
-
(2011)
Chem. Sci.
, vol.2
, pp. 531
-
-
Fang, P.P.1
Duan, S.2
Lin, X.-D.3
Anema, J.R.4
Li, J.-F.5
Buriez, O.6
Ding, Y.7
Fan, F.-R.8
Wu, D.-Y.9
Ren, B.10
Wang, Z.L.11
Amatore, C.12
Tian, Z.-Q.13
|