| /paper/doi/10.1016/j.saa.2009.04.017 | 0.000000 | 0.000000 |
| INIT | 0.000222 | 0.000222 |
| _initView | 0.000902 | 0.001124 |
| _initViewBasic | 0.000164 | 0.001288 |
| _initSiteModules | 0.000151 | 0.001439 |
| _initRouters | 0.000152 | 0.001591 |
| Sess + | 0.001472 | 0.003063 |
| Sess _ | 0.000096 | 0.003159 |
| pre dispatch _ | 0.000142 | 0.003301 |
| LC::doiAction START | 0.000254 | 0.003555 |
| LC::doiAction END to showListing | 0.194252 | 0.197807 |
| LC::showListing START | 0.000003 | 0.197810 |
| LC::showListing get reviews START | 0.000018 | 0.197828 |
| ES Review Search START | 0.000710 | 0.198538 |
| ES Review Search END | 0.009287 | 0.207825 |
| LC::showListing get reviews END | 0.001198 | 0.209023 |
| Done | 0.049794 | 0.258817 |
Kinetic study works well. Ligand synthesis can be improved.
Summary:
This paper reports an interesting property of the O, N and S donor ligand 2-(2’-Hydroxy-3’-methoxyphenyl)benzothiazole which makes it switch chelating donor sites from O, S (at pH < 5.0) to O, N (above pH 5.0) while reacting with Cu(II) acetate in a 3:1...