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Tiedemann, B. E. F.; Raymond, K. N. Angew. Chem., Int. Ed. 2007, 46, 4976-4978.
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(2007)
Angew. Chem., Int. Ed
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, pp. 4976-4978
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Tiedemann, B.E.F.1
Raymond, K.N.2
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70
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35048822089
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Pluth, M. D.; Bergman, R. G.; Raymond, K. N. J. Am. Chem. Soc. 2007, 129, 11459-11467.
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(2007)
J. Am. Chem. Soc
, vol.129
, pp. 11459-11467
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Pluth, M.D.1
Bergman, R.G.2
Raymond, K.N.3
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71
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0029815987
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Beissel, T.; Powers, R. E.; Raymond, K. N. Angew. Chem., Int. Ed. 1996, 35, 1084-1086.
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(1996)
Angew. Chem., Int. Ed
, vol.35
, pp. 1084-1086
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Beissel, T.1
Powers, R.E.2
Raymond, K.N.3
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72
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0033526337
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Beissel, T.; Powers, R. E.; Parac, T. N.; Raymond, K. N. J. Am. Chem. Soc. 1999, 121, 4200-4206.
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(1999)
J. Am. Chem. Soc
, vol.121
, pp. 4200-4206
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Beissel, T.1
Powers, R.E.2
Parac, T.N.3
Raymond, K.N.4
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73
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0037124623
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-
In an intermediate example, synchronized racemization of the four homochiral metal centers of an M4L6 diethyl ketipinate-based tetrahedral structure occurs: Saalfrank, R. W, Demleitner, B, Glaser, H, Maid, H, Bathelt, D, Hampel, F, Bauer, W, Teichert, M. Chem, Eur. J. 2002, 8, 2679-2683
-
6 diethyl ketipinate-based tetrahedral structure occurs: Saalfrank, R. W.; Demleitner, B.; Glaser, H.; Maid, H.; Bathelt, D.; Hampel, F.; Bauer, W.; Teichert, M. Chem. - Eur. J. 2002, 8, 2679-2683.
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76
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37049039757
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An alternative model could involve S-nic+ dimers connected by hydrogen bonding this might better explain the observed stoichiometry of the M416 resolution, S-nic+ dimers might intercalate between M416 ligands or might link one tetrahedron to another; as was found in S-nic+-helicate interactions, the 2D NMR study confirms intercalation of the pyridinium ring into the metal catecholate cap of the structures vertices and orientation of the pyrolidine ring toward the naphthalene backbones. However, no more specific information could be deduced. In addition, base must be added to the solution in order to dissolve the precipitated ΔΔΔΔ complex
-
+-helicate interactions, the 2D NMR study confirms intercalation of the pyridinium ring into the metal catecholate cap of the structures vertices and orientation of the pyrolidine ring toward the naphthalene backbones. However, no more specific information could be deduced. In addition, base must be added to the solution in order to dissolve the precipitated ΔΔΔΔ complex.
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77
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4544282884
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5.04; Fujitsu Limited
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CAChe Workstation Pro, 5.04; Fujitsu Limited: 2002.
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(2002)
CAChe Workstation Pro
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-
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79
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37049023949
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6 salt.
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6 salt.
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-
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80
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24444447369
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Tor, Y.; Shanzer, A.; Scherz, A. Inorg. Chem. 1990, 29, 4096-4099.
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(1990)
Inorg. Chem
, vol.29
, pp. 4096-4099
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Tor, Y.1
Shanzer, A.2
Scherz, A.3
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81
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0001035792
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Borgias, B. A.; Barclay, S. J.; Raymond, K. N. J. Coord. Chem. 1986, 15, 109-123.
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(1986)
J. Coord. Chem
, vol.15
, pp. 109-123
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Borgias, B.A.1
Barclay, S.J.2
Raymond, K.N.3
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82
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0001610596
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Karpishin, T. B.; Stack, T. D. P.; Raymond, K. N., J. Am. Chem. Soc. 1993, 115, 182-192.
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(1993)
J. Am. Chem. Soc
, vol.115
, pp. 182-192
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Karpishin, T.B.1
Stack, T.D.P.2
Raymond, K.N.3
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83
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37049014354
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8-, for example, would be expected to demonstrate greater tris-catecholate twist. Twist differences are likely accommodated by distortions in the ligand amide junctions.
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8-, for example, would be expected to demonstrate greater tris-catecholate twist. Twist differences are likely accommodated by distortions in the ligand amide junctions.
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84
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37049033924
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+ salts.
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+ salts.
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86
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0034640627
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Johnson, A. R.; O'Sullivan, B.; Raymond, K. N. Inorg. Chem. 2000, 39, 2652-2660.
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(2000)
Inorg. Chem
, vol.39
, pp. 2652-2660
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Johnson, A.R.1
O'Sullivan, B.2
Raymond, K.N.3
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87
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0012093532
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University of Leeds and University of Florence: Leeds and Florence
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Gans, P.; Sabbatini, A.; Vacca, A. HYPERQUAD2000; University of Leeds and University of Florence: Leeds and Florence, 2000.
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(2000)
HYPERQUAD2000
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Gans, P.1
Sabbatini, A.2
Vacca, A.3
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88
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0030272334
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Gans, P.; Sabbatini, A.; Vacca, A. Talanta 1996, 43, 1739-1753.
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(1996)
Talanta
, vol.43
, pp. 1739-1753
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Gans, P.1
Sabbatini, A.2
Vacca, A.3
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