| /paper/doi/10.1016/j.saa.2009.04.017 | 0.000000 | 0.000000 |
| INIT | 0.002310 | 0.002310 |
| _initView | 0.008241 | 0.010551 |
| _initViewBasic | 0.001021 | 0.011572 |
| _initSiteModules | 0.001510 | 0.013082 |
| _initRouters | 0.001650 | 0.014732 |
| pre dispatch _ | 0.027290 | 0.042022 |
| LC::doiAction START | 0.000186 | 0.042208 |
| LC::doiAction END to showListing | 0.185994 | 0.228202 |
| LC::showListing START | 0.000005 | 0.228207 |
| LC::showListing get reviews START | 0.005302 | 0.233509 |
| ES Review Search START | 0.014677 | 0.248186 |
| ES Review Search END | 0.007179 | 0.255365 |
| LC::showListing get reviews END | 0.002008 | 0.257373 |
| Done | 0.111026 | 0.368399 |
Kinetic study works well. Ligand synthesis can be improved.
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...