Research Article
Synthesis, Characterization, Semiempirical and Biological Activities of Organotin(IV) Carboxylates with 4-Piperidinecarboxylic Acid
Table 5
13C NMR dataa of organotin complexes 1–5.
| | Carbon number | Chemical shift (ppm) | HL | 1 | 2 | 3 | 4 | 5 |
| | 1 | 178.2 | 179.5 | 179.1 | 179.6 | 179.8 | 179.7 | 2 | 42.6 | 42.1 | 42.8 | 42.4 | 42.6 | 42.8 | 3, | 24.2 | 27.3 | 27.7 | 27.2 | 27.9 | 27.2 | 4, | 51.1 | 51.3 | 51.6 | 51.5 | 51.8 | 51.2 |
| Sn–R | | — | 24.6 593.1, 567.3 | 25.7 541.1, 516.3 | 135.2 56.4 | −2.0 395.6 | 138.06 583.1, 557.3 | | — | — | 27.7 39.0 | 141.2 | | 128.99 61.4, 59.0 | | — | — | 26.2 117.3, 112.6 | 129.1 88.2 | | 136.57 44.3 | | — | — | 14.2 | 130.2 56.6 | | 129.94 12.5 |
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Chemical shifts () in ppm. 119/117Sn, 13C in Hz is listed in square brackets. See Scheme 1.
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