| 1H
NMR |
13C
NMR |
|
| CH3COCH3 | 2.09 (s) | 206.6 (s), 30.8 (s) |
| CHCl3 | 7.32 (s) | 77.9 (s) |
| C6H5Cl | 7.26-7.37 (m) | 134.5 (s), 130.2 (s), |
| C6H5CH3 | 7.12-7.26 (m), 2.34 (s) | 128.9
(s), 126.9 (s) \138.4 (s), 129.4 (s), 128.6 (s), 125.6 (s), 21.6 (s) |
| C6H6 | 7.36 (s) | 128.6 (s) |
| n-Hexane | 1.26-1.32 (m), 0.89 (t, 3J = 7.0) | 32.1 (s), 23.1 (s), 14.3 (s) |
| n-Pentane | 1.24-1.33 (m), 0.89 (t, 3J = 7.0) | 34.5 (s), 22.7 (s), 14.2 (s) |
| CH3OH | 3.37 (s) | 50.2 (s) |
| Et2O | 3.44 (q, 3J = 7.0), 1.15 (t, 3J = 7.0) | 66.0 (s), 15.5 (s) |
| THF | 3.68 (m), 1.82 (m) | 68.1 (s), 25.9 (s) |
| H2O | 1.53 (s) | |
| Silicone | 0.08 (s) | |
| Apiezon M | 1.26 (s, br), 0.86 (m, br) | |
| Apiezon N | 2.12 (s), 1.26 (m, br), 0.88 (m, br) | |
| MeCN | 1.949
(s) |
117.0 (s) |
| PMe3 | 0.98 (d) | |
| C6H5Br | 7.50 (d), 7.30 (t), 7.26 (t) | |
| C6Me6 | 2.20 (s) |
1H and 13C
NMR spectra were recorded at ambient temperature. Chemical shifts are
reported relative to SiMe4 and were determined by reference
to the residual solvent resonances, 5.32 (t) for 1H and
53.8 (quint) for 13C, respectively. All coupling constants
are given in Hertz.