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. Author manuscript; available in PMC: 2021 Nov 14.
Published in final edited form as: Inorg Chem. 2021 Sep 7;60(18):13759–13783. doi: 10.1021/acs.inorgchem.1c01754

Table 1.

Reactivity of synthetic and enzymatic FeIV–oxido complexes with C-H substrates.

Spin state Complex Substrate Reactivitya References
1 [FeIV(O)TMC(MeCN)]2+ DHA (0.016)
CHD (0.018)
88,114
[FeIV(O)TPA*(MeCN)]2+b DHA (0.042) 117
[FeIV(O)N4Py]2+ DHA (2)
CHD (1.3)
88
2 [FeIV(O)TMG3tren]2+ DHA (0.090)
CHD (1.2)
88
[FeIVH3buea(O)] No reactivity 115
[FeIV(O)tpaPh] CHD (1.4) 90
[FeIV(O)(TQA)(MeCN)]2+ Cyclohexane (0.37, −40 °C)
DHA (200, −80 °C)
102
TauD-J Taurine (kobs = 13 s−1, 5 °C, aqueous) 37
a

Unless specified, rate constants (k2, M−1 s−1) were measured in MeCN at −30 °C.

b

TPA* = tris(4-methoxy-3,5-dimethylpyridyl-2-methyl)amine.