Table 4.
Complex | kex (×106 s−1) | Side chain | Method | Reference |
---|---|---|---|---|
40 | 0.007 | CH2CO2t-Bu | NMR spectroscopyc | [63] |
66 | 0.01 | H | NMR spectroscopyc | [63] |
66 | 0.0083a | H | 1H-NMR spectroscopy | [65] |
67 | 0.005 | CH2Ph | NMR spectroscopyc | [63] |
68 | 0.004 | CH(CH3)Ph | NMR spectroscopyc | [63] |
69 | 0.003 | CH2CO2CH2CH3 | NMR spectroscopyc | [63] |
69 | 0.0013a | CH2CO2CH2CH3 | 1H-NMR spectroscopy | [27] |
70 | 0.002 | CH2CO2nBu | NMR spectroscopyc | [63] |
71 | 0.002 | CH2CO2CH2Ph | NMR spectroscopyc | [63] |
72 | >1 a | 4-heptyl | CEST | [15] |
73 | 0.059 a | 3-pentyl | CEST | [15] |
74 | 0.10 a | t-Bu | CEST | [15] |
75 | 0.027 a | i-Pr | CEST | [15] |
76 | 0.0096 a | C(CH3)2CO2− | CEST | [15] |
77 | 0.0064 a | CH3 | 1H-NMR spectroscopy | [65] |
78 | 0.00077 a | CH2PO(OCH2CH3)2 | 1H-NMR spectroscopy | [66] |
79 | 0.0048 a | C(CH3)2CO2CH2CH3 | CEST | [15] |
80 | 0.015 b | CH2PO32− | 1H-NMR spectroscopy | [27] |
a for the square-antiprism (SAP) isomer in CH3CN, b in water, c the authors did not specify 1H or 17O.