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18
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4544229050
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note
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3 is less reactive by a factor of 5-10.
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19
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15844375540
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G. Roelfes, M. Lubben, K. Chen, R. Y. N. Ho, A. Meetsma, S. Genseberger, R. M. Hermant, R. Hage, S. K. Mandal, V. G. Young, Jr., Y. Zang, H. Kooijman, A. L. Spek, L. Que, Jr., B. L. Feringa, Inorg. Chem. 1999, 38, 1929.
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-
20
-
-
4544388345
-
-
note
-
35% aqueous solution, quantitative analysis by iodometric titration.[20]
-
-
-
-
21
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0000223133
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D. H. R. Barton, V. N. L. Gloahec, H. Patin, F. Launay, New J. Chem. 1998, 22, 559.
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22
-
-
4544258905
-
-
note
-
3CN and fully characterized.
-
-
-
-
23
-
-
4544320669
-
-
note
-
These transitions are attributed to ligand-to-metal charge transfer from the hydroperoxo group.
-
-
-
-
24
-
-
4544365546
-
-
note
-
+, respectively.
-
-
-
-
25
-
-
4544293277
-
-
note
-
4) added to the fully deprotonated form.
-
-
-
-
26
-
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0033926379
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-
27
-
-
4544307943
-
-
note
-
For a related tpen derivative a seven-coordinate peroxo complex was proposed.[27]
-
-
-
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28
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0036007785
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29
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4544265427
-
-
note
-
The comparison of the results of a structure optimization at that level with those of a single-crystal X-ray diffraction study [12] showed that all Fe-N bond lengths are only slightly over-estimated with a mean deviation of 2.5%, while the Fe-Cl bond length is underestimated by 4.6%; that is, the agreement between experiment and theory is acceptable at that level.
-
-
-
-
30
-
-
4544385777
-
-
note
-
All structures were characterized as minima by frequency analysis.
-
-
-
-
31
-
-
4544302151
-
-
note
-
However, the expected structural differences, which correlate well with the different stabilities and reactivities, might have been expected to also lead to significantly different spectroscopic properties. Reasons why this is not so are currently under investigation.
-
-
-
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32
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0032795220
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