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SPECFIT/32, versions v3.0.26 and v3.0.36; Spectrum Software ssociates: Marlborough, MA, 2000.
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SPECFIT/32, versions v3.0.26 and v3.0.36; Spectrum Software ssociates: Marlborough, MA, 2000.
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87
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55649124141
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to be submitted
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Wu, A.; Datta, A.; Mader, E. A.; Hrovat, D. A.; Borden, W. T.; Mayer, J. M., to be submitted.
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Wu, A.1
Datta, A.2
Mader, E.A.3
Hrovat, D.A.4
Borden, W.T.5
Mayer, J.M.6
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89
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55649108452
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NUTS-NMR Utility Transform Software, Acorn NMR Inc, Livermore, CA
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NUTS-NMR Utility Transform Software, 1D version; Acorn NMR Inc.: Livermore, CA, 2003.
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(2003)
1D version
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90
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55649112312
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2HCN) and were not suitable for line fitting. The two overlapping CH-acac singlets (δ 5.29, 5.32) and other non-singlet aromatic resonances were unable to be line fitted by NUTS, but instead using gNMR software.
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2HCN) and were not suitable for line fitting. The two overlapping CH-acac singlets (δ 5.29, 5.32) and other non-singlet aromatic resonances were unable to be line fitted by NUTS, but instead using gNMR software.
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91
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55649109225
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gNMR software, v4.1.0; Ivory Soft: Rancho Palos Verdes, CA, 1999.
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gNMR software, v4.1.0; Ivory Soft: Rancho Palos Verdes, CA, 1999.
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92
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55649100782
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3.
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3.
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93
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55649110723
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IIimH) = 22.1: ref 27.
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IIimH) = 22.1: ref 27.
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94
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0033748948
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+/0: Mori, Y.; Sakaguchi, Y.; Hayashi, H. J. Phys. Chem. A 2000, 104, 4896.
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+/0: Mori, Y.; Sakaguchi, Y.; Hayashi, H. J. Phys. Chem. A 2000, 104, 4896.
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95
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55649110927
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•) - E(TEMPO-H)]/1.37 ≈-3.
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•) - E(TEMPO-H)]/1.37 ≈-3.
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96
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33845552369
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+/0: Semmelhack, M. F.; Chou, C. S.; Cortes, D. A. J. Am. Chem. Soc. 1983, 105, 4492.
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+/0: Semmelhack, M. F.; Chou, C. S.; Cortes, D. A. J. Am. Chem. Soc. 1983, 105, 4492.
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98
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0000026284
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a conversion from DMSO to MeCN: Chantooni, M. K., Jr.; Kolthoff, I. M. J. Phys. Chem. 1976, 80, 1306.
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a conversion from DMSO to MeCN: Chantooni, M. K., Jr.; Kolthoff, I. M. J. Phys. Chem. 1976, 80, 1306.
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100
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34247221448
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(b) Vuina, D.; Pilepiæ, V.; Ljubas, D.; Sanković, K.; Sajenko, I.; Uršić, S. Tetrahedron Lett. 2007, 48, 3633-3637.
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(2007)
Tetrahedron Lett
, vol.48
, pp. 3633-3637
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Vuina, D.1
Pilepiæ, V.2
Ljubas, D.3
Sanković, K.4
Sajenko, I.5
Uršić, S.6
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102
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55649107092
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BT] = 6.9, where T = 298 K.
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BT] = 6.9, where T = 298 K.
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105
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0029964954
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(c) Jonsson, T.; Glickman, M. H.; Sun, S.; Klinman, J. P. J. Am. Chem. Soc. 1996, 118, 10319.
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(1996)
J. Am. Chem. Soc
, vol.118
, pp. 10319
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Jonsson, T.1
Glickman, M.H.2
Sun, S.3
Klinman, J.P.4
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106
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0013691695
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(a) Gilbert, J. A.; Gersten, S. W.; Meyer, T. J. J. Am. Chem. Soc. 1982, 104, 6872.
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(1982)
J. Am. Chem. Soc
, vol.104
, pp. 6872
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Gilbert, J.A.1
Gersten, S.W.2
Meyer, T.J.3
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107
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0000797811
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(b) Gilbert, J.; Roecker, L.; Meyer, T. J. Inorg. Chem. 1987, 26, 1126.
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(1987)
Inorg. Chem
, vol.26
, pp. 1126
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Gilbert, J.1
Roecker, L.2
Meyer, T.J.3
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108
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0000812210
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Binstead, R. A.; McGuire, M. E.; Dovletoglou, A.; Seok, W. K.; Roecker, L. E.; Meyer, T. J. J. Am. Chem. Soc. 1992, 114, 173.
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(1992)
J. Am. Chem. Soc
, vol.114
, pp. 173
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Binstead, R.A.1
McGuire, M.E.2
Dovletoglou, A.3
Seok, W.K.4
Roecker, L.E.5
Meyer, T.J.6
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111
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0029862758
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2 with L = 1,4,7-tribenzyl-7-benzyl-1,4,7- triazacyclononane or 1,4,7-triisopropyl-7-benzyl-1,4,7-triazacyclononane.
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2 with L = 1,4,7-tribenzyl-7-benzyl-1,4,7- triazacyclononane or 1,4,7-triisopropyl-7-benzyl-1,4,7-triazacyclononane.
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112
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0034647213
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Roth, J. P.; Lovell, S.; Mayer, J. M. J. Am. Chem. Soc. 2000, 122, 5486.
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(2000)
J. Am. Chem. Soc
, vol.122
, pp. 5486
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Roth, J.P.1
Lovell, S.2
Mayer, J.M.3
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113
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0141905366
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Yoder, J. C.; Roth, J. P.; Gussenhoven, E. M.; Larsen, A. S.; Mayer, J. M. J. Am. Chem. Soc. 2003, 125, 2629.
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(2003)
J. Am. Chem. Soc
, vol.125
, pp. 2629
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Yoder, J.C.1
Roth, J.P.2
Gussenhoven, E.M.3
Larsen, A.S.4
Mayer, J.M.5
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114
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0000736248
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-1).
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-1).
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116
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0000569158
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Song, J.; Bullock, R. M.; Creutz, C. J. Am. Chem. Soc. 1991, 113, 9862.
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(1991)
J. Am. Chem. Soc
, vol.113
, pp. 9862
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Song, J.1
Bullock, R.M.2
Creutz, C.3
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117
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55649084861
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The self-exchange rate constant for RuIIimH, Ru IIIimH+ is estimated to be between 4 × 10 6 and 1 × 108 M-1 s-1 in MeCN based on the following k(self-exchange) values: (a) 1.4 × 10 8 M-1 s-1 for [Ru(acac)2(4,4′- Me2bpy)]0/, 4.5 × 106 M-1 s-1 for [Ru(hfac)2(4,4′-Me2bpy, 0/, 5.0 × 106 M-1 s-1 for [Ru(hfac)3]-/0, 8.3 × 106 M-1 s-1 for [Ru(bpy)3]2+/3, and 1 × 10 8 M-1 s-1 for [Ru(L)3] 2+/3, L, 3,4,7,8-Me4phen, 3,5,6,8-Me4phen, or 4,7-Me2bpy, hfac, 1,1,1,5,5,5-hexafluoro-2,4-pentanedionato, phen, 1,10-phenanthrolin
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2bpy) [hfac = 1,1,1,5,5,5-hexafluoro-2,4-pentanedionato, phen = 1,10-phenanthroline].
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120
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55649099263
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-1.
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-1.
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123
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0442295106
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For example, see refs 22, 54, and
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For example, see refs 22, 54, and Soper, J. D.; Rhile, I. J.; DiPasquale, A. G.; Mayer, J. M. Polyhedron 2004, 23, 323.
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(2004)
Polyhedron
, vol.23
, pp. 323
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Soper, J.D.1
Rhile, I.J.2
DiPasquale, A.G.3
Mayer, J.M.4
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126
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0034836886
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Iordanova, N.; Decornez, H.; Hammes-Schiffer, S. J. Am. Chem. Soc. 2001, 123, 3723.
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(2001)
J. Am. Chem. Soc
, vol.123
, pp. 3723
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Iordanova, N.1
Decornez, H.2
Hammes-Schiffer, S.3
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127
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55649096478
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3 terms at different temperatures derived from their respective Eyring or van't Hoff equation.
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3 terms at different temperatures derived from their respective Eyring or van't Hoff equation.
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131
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55649091865
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KaleidaGraph, version 3.5; Synergy Software: Reading, PA, 2000
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KaleidaGraph, version 3.5; Synergy Software: Reading, PA, 2000.
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