Angewandte Chemie International Edition
10.1002/anie.201904672
COMMUNICATION
[
[
[
25]
26]
27]
D. S. Bohle, Curr. Opin. Chem. Biol. 1998, 2, 194–200.
S. Goldstein, G. Merényi, in Methods Enzymol., 2008, pp. 49–61.
C. Molina, R. Kissner, W. H. Koppenol, Dalton Trans. 2013, 42,
Hovhannisyan, Inorg. Chem. 2013, 52, 12046–56.
R. Cao, L. T. Elrod, R. L. Lehane, E. Kim, K. D. Karlin, J. Am.
Chem. Soc. 2016, 138, 16148–16158.
D. Maiti, D.-H. Lee, A. A. Narducci Sarjeant, M. Y. M. Pau, E. I.
Solomon, K. Gaoutchenova, J. Sundermeyer, K. D. Karlin, J. Am.
Chem. Soc. 2008, 130, 6700–6701.
D. S. Bohle, P. A. Glassbrenner, B. Hansert, in Methods Enzymol.,
1996, pp. 302–311.
W. Lo, Y. Lee, J. M. Tsai, S. Beckman, Chem. Phys. Lett. 1995,
242, 147–152.
J. S. Woertink, L. Tian, D. Maiti, H. R. Lucas, R. a Himes, K. D.
Karlin, F. Neese, C. Würtele, M. C. Holthausen, E. Bill, et al., Inorg.
Chem. 2010, 49, 9450–9.
J. M. Tsai, J. J. G. Harrison, J. C. Martin, T. P. Hamilton, M. Van
Der Woerd, M. J. Jablonsky, J. S. Beckman, J. Am. Chem. Soc.
1994, 116, 4115–4116.
H. Tsai, T. P. Hamilton, J. M. Tsai, M. Van Der Woerd, J. G.
Harrison, M. J. Jablonsky, J. S. Beckman, W. H. Koppenol, J. Phys.
Chem. 1996, 100, 15087–15095.
[48]
[49]
9898–9905.
[
[
[
[
28]
29]
30]
31]
S. Serrano-Luginbuehl, R. Kissner, W. H. Koppenol, Chem. Res.
Toxicol. 2018, 31, 721–730.
Y. Sheng, I. A. Abreu, D. E. Cabelli, M. J. Maroney, A. F. Miller, M.
Teixeira, J. S. Valentine, Chem. Rev. 2014, 114, 3854–3918.
S. Herold, W. H. Koppenol, Coord. Chem. Rev. 2005, 249, 499–
[50]
[51]
[52]
5
06.
M. P. Schopfer, J. Wang, K. D. Karlin, Inorg. Chem. 2010, 49,
267–6282.
6
[
[
32]
33]
J. Su, J. T. Groves, Inorg. Chem. 2010, 49, 6317–6329.
K. J. Koebke, D. J. Pauly, L. Lerner, X. Liu, A. A. Pacheco, Inorg.
Chem. 2013, 52, 7623–7632.
K. Gogoi, S. Saha, B. Mondal, H. Deka, S. Ghosh, B. Mondal, Inorg.
Chem. 2017, 56, 14438–14445.
[53]
[54]
[55]
[
[
[
34]
35]
36]
A. Yokoyama, K.-B. Cho, K. D. Karlin, W. Nam, J. Am. Chem. Soc.
2013, 135, 14900–14903.
P. Kumar, Y. Lee, L. Hu, J. J. Chen, Y. Jun, J. Yao, H. Chen, K. D.
Karlin, W. Nam, Y. J. Park, et al., J. Am. Chem. Soc. 2016, 138,
Calculating the anharmonicity constant based on these two observed
Raman frequencies leads to a frequency corrected for anharmonicity
of 692 cm–1 well matched by the DFT frequency calculations for the
cis-PN1 optimized geometry.
A. Kalita, P. Kumar, B. Mondal, Chem. Commun. 2012, 48, 4636–
4638.
7753–7762.
[
37]
S. Hong, P. Kumar, K. Bin Cho, Y. M. Lee, K. D. Karlin, W. Nam,
Angew. Chemie - Int. Ed. 2016, 55, 12403–12407.
T. S. Kurtikyan, P. C. Ford, Chem. Commun. 2010, 46, 8570–8572.
M. P. Schopfer, B. Mondal, D. Lee, A. A. N. Sarjeant, K. D. Karlin, J.
Am. Chem. Soc. 2009, 131, 11304–11305.
[56]
[57]
[
[
38]
39]
Unlike a previous report using the same system where a putative
cupryl (generated via O
donor) performs intramolecular hydroxylation,
2
and H-atom donor or directly via an O-atom
[62]
[40]
[41]
[42]
[43]
A. Kalita, P. Kumar, B. Mondal, Chem. Commun. 2012, 48, 4636–
no such reaction
4
638.
A. Kalita, R. C. Deka, B. Mondal, Inorg. Chem. 2013, 52, 10897–
03.
takes place in the present study as evidenced by ESI-MS.
W. K. Wilmarth, D. M. Stanbury, J. E. Byrd, H. N. Po, C. Chua,
Coord. Chem. Rev. 1983, 51, 155–179.
W. H. Koppenol, J. J. Moreno, W. A. Pryor, H. Ischiropoulos, J. S.
Beckman, Chem. Res. Toxicol. 1992, 5, 834–842.
A. Kunishita, H. Ishimaru, S. Nakashima, T. Ogura, S. Itoh, J. Am.
Chem. Soc. 2008, 130, 4244–4245.
T. A. Betley, D. A. Iovan, A. T. Wrobel, A. A. McClelland, A. B.
Scharf, G. A. Edouard, T. A. Betley, Chem. Commun. 2017, 53, 1–
44.
D. Maiti, D.-H. Lee, K. Gaoutchenova, C. Würtele, M. C. Holthausen,
A. A. Narducci Sarjeant, J. Sundermeyer, S. Schindler, K. D. Karlin,
Angew. Chemie Int. Ed. 2008, 47, 82–85.
[58]
[59]
[60]
[61]
9
B. Mondal, S. Saha, D. Borah, R. Mazumdar, B. Mondal, Inorg.
Chem. 2019, 58, 1234–1240.
G. Y. Park, S. Deepalatha, S. C. Puiu, D.-H. Lee, B. Mondal, A. A.
Narducci Sarjeant, D. del Rio, M. Y. M. Pau, E. I. Solomon, K. D.
Karlin, J. Biol. Inorg. Chem. 2009, 14, 1301–11.
S. K. Sharma, A. W. Schaefer, H. Lim, H. Matsumura, P. Moënne-
Loccoz, B. Hedman, K. O. Hodgson, E. I. Solomon, K. D. Karlin, J.
Am. Chem. Soc. 2017, 139, 17421–17430.
[
44]
[62]
[
[
45]
46]
P. K. Wick, R. Kissner, W. H. Koppenol, Helv. Chim. Acta 2000, 83,
748–754.
T. S. Kurtikyan, S. R. Eksuzyan, V. A. Hayrapetyan, G. G.
Martirosyan, G. S. Hovhannisyan, J. A. Goodwin, J. Am. Chem.
Soc. 2012, 134, 13861–70.
[
47]
T. S. Kurtikyan, S. R. Eksuzyan, J. A. Goodwin, G. S.
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