Timeline for How to compare the bond lengths of an peroxide complex before and after oxidation?
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| Sep 14, 2017 at 11:53 | history | edited | andselisk♦ |
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| Sep 14, 2017 at 11:13 | answer | added | andselisk♦ | timeline score: 4 | |
| Sep 14, 2017 at 10:09 | comment | added | Jan | @IvanNeretin I wouldn’t exactly call cobalt(III) ‘unusually high’ … | |
| Sep 14, 2017 at 10:08 | history | edited | Jan | CC BY-SA 3.0 |
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| Sep 14, 2017 at 10:08 | answer | added | Jan | timeline score: 4 | |
| Apr 27, 2017 at 5:03 | history | edited | Martin - マーチン♦ | CC BY-SA 3.0 |
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| Apr 26, 2017 at 18:54 | history | bumped | CommunityBot | This question has answers that may be good or bad; the system has marked it active so that they can be reviewed. | |
| Mar 27, 2017 at 18:28 | history | tweeted | twitter.com/StackChemistry/status/846428848627560448 | ||
| Mar 27, 2017 at 17:04 | comment | added | Ivan Neretin | Exactly. So in fact, the reasoning goes the other way around: first we find the distances, then we use those to deduce the oxidation states. | |
| Mar 27, 2017 at 16:19 | comment | added | orthocresol | this is a case of the so-called "non-innocent" ligand: there is no way of knowing how $\ce{O2}$ as a ligand behaves without actually doing experiments on it (spectroscopy, diffraction, etc). | |
| Mar 27, 2017 at 16:11 | history | edited | TrY iS CheM | CC BY-SA 3.0 |
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| Mar 27, 2017 at 12:55 | comment | added | Ivan Neretin | We can't. It is a borderline case. With transition metals in unusually high oxidation states, you can never tell for sure by looking at the formula alone. | |
| Mar 27, 2017 at 12:12 | history | asked | TrY iS CheM | CC BY-SA 3.0 |