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1
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For reviews, see: a, Eds: E. W. Abel, F. G. A. Stone, E. Willinson, Pergamon, New York
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For reviews, see: a) E. N. Jacobsen in Comprehensive Organometallic Chemistry II (Eds: E. W. Abel, F. G. A. Stone, E. Willinson), Pergamon, New York, 1995, vol. 12, pp. 1097-1135;
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Katsuki, T.1
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13644249902
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For recent examples, see: a
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For recent examples, see: a) M. S. Taylor, D. N. Zalatan, A. M. Lerchner, E. N. Jacobsen, J. Am. Chem. Soc. 2005, 127, 1313-1317;
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Murahashi, S.-I.1
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c) N. S. Finney, P. J. Pospisil, S. Chang, M. Palucki, R. G. Konsler, K. B. Hansen, E. N. Jacobsen, Angew. Chem. Int. Ed. Engl. 1997, 36, 1720-1723;
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a) T. Niimi, T. Uchida, R. Irie, T. Katsuki, Adv. Synth. Catal. 2001, 343, 79-88;
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See for instance: a) P. G. Cozzi, Chem. Soc. Rev. 2004, 33, 410-421;
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Cozzi, P.G.1
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28044431635
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a) A. W. Kleij, D. M. Tooke, A. L. Spek, J. N. H. Reek, Eur. J. Inorg. Chem. 2005, 4626-4634;
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33645507421
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b) M. Holbach, X. Zheng, C. Burd, C. W. Jones, M. J. Weck, J. Org. Chem. 2006, 71, 2903-2906;
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Holbach, M.1
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27
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34248362335
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c) H. C. Lin, C.-C. Huang, C.-H. Shi, Y.-H. Liao, C.-C. Chen, Y.-C. Lin, Y.-H. Liu, Dalton Trans. 2007, 781-791.
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Lin, H.C.1
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Lin, Y.-C.6
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28
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14844286152
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M. F. Renehan, H.-J. Schanz, E. M. McGarrigle, C. T. Dalton, A. M. Daly, D. G. Dilheany, J. Mol. Catal. A 2005, 231, 205.
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33846540819
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L. Rigamonti, F. Demartin, A. Forni, S. Righetto, A. Pasini, Inorg. Chem. 2006, 45, 10976-10989.
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Rigamonti, L.1
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Pasini, A.5
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32
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85163234074
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A preliminary account of this work was recently published: S. Curreli, E. C. Escudero-Adán, J. Benet-Buchholz, A. W. Kleij, J. Org. Chem. 2007, 72, 7018-7021.
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A preliminary account of this work was recently published: S. Curreli, E. C. Escudero-Adán, J. Benet-Buchholz, A. W. Kleij, J. Org. Chem. 2007, 72, 7018-7021.
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36
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34547697837
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d) A. W. Kleij, M. Kuil, M. Lutz, A. L. Spek, J. N. H. Reek, Inorg. Chem. 2007, 46, 5829-5831.
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Inorg. Chem
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Kleij, A.W.1
Kuil, M.2
Lutz, M.3
Spek, A.L.4
Reek, J.N.H.5
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37
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85163232830
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II salphens in adsorption of alkaloids, see: e E. C. Escudero-Adán, J. Benet-Buchholz, A. W. Kleij, Inorg. Chem. 2008, 47, 4256-4263;
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II salphens in adsorption of alkaloids, see: e) E. C. Escudero-Adán, J. Benet-Buchholz, A. W. Kleij, Inorg. Chem. 2008, 47, 4256-4263;
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38
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43149120222
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f) S. J. Wezenberg, E. C. Escudero-Adán, J. Benet-Buchholz, A. W. Kleij, Inorg. Chem. 2008, 47, 2925-2927.
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Inorg. Chem
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Wezenberg, S.J.1
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Benet-Buchholz, J.3
Kleij, A.W.4
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39
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38949085857
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a) E. C. Escudero-Adán, J. Benet-Buchholz, A. W. Kleij, Inorg. Chem. 2008, 47, 410-412;
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Inorg. Chem
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Escudero-Adán, E.C.1
Benet-Buchholz, J.2
Kleij, A.W.3
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41
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41049086532
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For some recent examples of cooperative bimetallic salen-based catalysis, see: a
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For some recent examples of cooperative bimetallic salen-based catalysis, see: a) C. Mazet, E. N. Jacobsen, Angew. Chem. Int. Ed. 2008, 47, 1762-1765;
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Angew. Chem. Int. Ed
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Mazet, C.1
Jacobsen, E.N.2
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4043107667
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b) G. M. Sammis, H. Danjo, E. N. Jacobsen, J. Am. Chem. Soc. 2004, 126, 9928-9929;
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J. Am. Chem. Soc
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Sammis, G.M.1
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43
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38849126242
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c) X. Zheng, C. W. Jones, M. Weck, Adv. Synth. Catal. 2008, 350, 255-261.
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Adv. Synth. Catal
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Zheng, X.1
Jones, C.W.2
Weck, M.3
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44
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85163224703
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We use the term nonsymmetrical here to designate the symmetry within each salen unit
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We use the term "nonsymmetrical" here to designate the symmetry within each salen unit.
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45
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85163234425
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Here, the isomer with the highest symmetry is isolated, which relates to the exo-exo compound.
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Here, the isomer with the highest symmetry is isolated, which relates to the exo-exo compound.
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46
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85163224757
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Crystal data for compound 26: Formula 2(C52H 50N8O14S2Zn2) ·7(C2H6OS, M, 2958.81, monoclinic, C2/c (No. 15, a, 36.4392(10) Å, b, 9.5882(3) Å, c, 38.4521(11) Å, β, 99.921(1)°, V, 13233.7(7) Å3, Z, 4, ρcalcd, 1.485 g/cm3, F(000, 6152, crystal size 0.15 x 0.20 x 0.30 mm, T, 100 K, θmin-max, 2.7-35.8°, total/unique data, 34311/18891, Rint, 0.046, observed data [I > 2.0σI, 12770, Nref/Npar, 18891/894, R/wR/S, 0.0588/0.1607/1.03, max. and av. shift/error, 0.00, 0.00, min. and max. resd. dens, 0.74, 1.88 e/Å3
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3.
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47
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85163225653
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Crystal data for compound 30: Formula (C60H 66N8O14S2Zn2) ·12(C2H6OS)·(C2H 6OS)·2(H2O, M, 3688.09, triclinic, P1 (No. 2, a, 14.7497(9) Å, b, 16.5770(9) Å, c, 19.9117(12) Å, α, 79.456(3)°, β, 74.018(3)o, γ, 73.347(3)°, V, 4455.3(5) Å3, Z, 1, ρcalcd, 1.375 g/cm3, F(000, 1938, crystal size 0.10 x 0.20 x 0.30 mm, T, 100 K, θmin-max, 2.6-31.3°, total/unique data, 65510/26748, Rint, 0.052, observed data [I > 2.0σI, 17287, N ref/Npar, 26748/1069, R/wR/S, 0.0855/0.2670/1.03, max. and av. shift/error, 0.00, 0.00, min. and max. resd. dens, 3.31, 2.50 e/Å3
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3.
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48
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85163230883
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Crystal data for compound 31·bipy: Formula (C 33H31Cl2N3O2Zn) ·5(C4H8O, M, 998.42, triclinic, P1 (No. 2, a, 9.6480(6) Å, b, 16.1632(9) Å, c, 17.5764(9) Å, α, 87.570(3)°, β, 74.285(3)°, γ, 74.177(3)°, V, 2537.0(3) Å3, Z, 2, ρcalcd, 1.307 g/cm3, F(000, 1060, crystal size 0.05 x 0.05 x 0.40 mm, T, 100 K, θmin-max, 2.8-30.9°, total/unique data, 23805/13472, Rint= 0.048, observed data [I > 2.0σI, 9787, N ref/Npar, 13472/696, R/wR/S, 0.0696/0.2116/1.04, max. and av. shift/error, 0.00, 0.00, min. and max. resd. dens, 1.21, 2.00 e/Å3
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3.
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49
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23744473315
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a) A. W. Kleij, M. Kuil, D. M. Tooke, M. Lutz, J. N. H. Reek, Chem. Eur. J. 2005, 11, 4743-4750;
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Kleij, A.W.1
Kuil, M.2
Tooke, D.M.3
Lutz, M.4
Reek, J.N.H.5
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51
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0035907450
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c) G. A. Morris, H. Zhou, C. L. Stern, S. T. Nguyen, Inorg. Chem. 2001, 40, 3222-3227.
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Morris, G.A.1
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Stern, C.L.3
Nguyen, S.T.4
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53
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32244439080
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K. H. Chang, C.-C. Huang, Y.-H. Liu, Y.-H. Hu, P.-T. Chou, Y.-C. Lin, Dalton Trans. 2004, 1731-1738.
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Chang, K.H.1
Huang, C.-C.2
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Hu, Y.-H.4
Chou, P.-T.5
Lin, Y.-C.6
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54
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4944260323
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C. Baleizao, B. Gigante, H. Garcia, A. Corma, Tetrahedron 2004, 60, 10461-10468.
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Baleizao, C.1
Gigante, B.2
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Corma, A.4
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