pH-Dependent Electrochemically Catalyzed Oxygen Reduction Behaviors of o-Substituted Co(III) Corroles

Wei Tang,^a Yuanyuan Qiu,^b Xiaonan Li,^a@1 Rodah C. Soy,^c John Mack,^c@2 Tebello Nyokong,^c and Xu Liang^b@3

^aDepartment of Children Health Care, Nanjing Children’s Hospital, Nanjing Medical University, 210008 Nanjing, PR China

^bSchool of Chemistry and Chemical Engineering, Jiangsu University, 212013 Zhenjiang, PR China

^cInstitute for Nanotechnology Innovation, Department of Chemistry, Rhodes University, 6140 Makhanda, South Africa

^@1Corresponding author E-mail: xiaonan6189@163.com

^@2Corresponding author E-mail: j.mack@ru.ac.za

^@3Corresponding author E-mail: Liangxu@ujs.edu.cn

DOI: 10.6060/mhc200183l

Macroheterocycles 2020 13(2) 156-162

Herein, a series of three o-substituted Co(III) corroles with electron-donating/withdrawing moieties have been prepared and fully characterized. The different functional substituents at o-position of meso-phenyl rings results in tunable local environment, and unusual pH-dependent electrochemically catalyzed oxygen reduction behaviors were clearly observed.

References:

Click here to expand or collapse this section

1. Ganguly S., Ghosh A. Acc. Chem. Res. 2019, 52, 2003-2014.
https://doi.org/10.1021/acs.accounts.9b00115

2. Lim H., Thomas K.E., Hedman B., Hodgson K.O., Ghosh A., Solomon E.I. Inorg. Chem. 2019, 58, 6722-6730.
https://doi.org/10.1021/acs.inorgchem.9b00128

3. Ghosh A. Chem. Rev. 2017, 117, 3798-3881.
https://doi.org/10.1021/acs.chemrev.6b00590

4. Buckley H.L., Rubin L.K., Chrominski M., McNicholas B.J., Tsen K.H.Y., Gryko D.T., Arnold J. Inorg. Chem. 2014, 53, 7941-7950.
https://doi.org/10.1021/ic500714h

5. Guo Y.X., Gu T.T., Li P.F., Fu B., Sun L., Zhu W.H., Xu H.J., Liang X. Inorg. Chem. Acta 2019, 496, 119067.
https://doi.org/10.1016/j.ica.2019.119067

6. Petrova D.V., Semeikin A.S., Berezina N.M., Berezin M.B., Bazanov M.I. Macroheterocycles 2019, 12, 119-128.
https://doi.org/10.6060/mhc190553s

7. Kosa M., Levy N., Elbaz L., Major D.T. J. Phys. Chem. C 2018, 122, 17686-17694.
https://doi.org/10.1021/acs.jpcc.8b05831

8. Levy N., Mahammed A., Kosa M., Major D.T., Gross Z., Elbaz L. Angew. Chem. Int. Ed. 2015, 54, 14080-14084.
https://doi.org/10.1002/anie.201505236

9. Liang X., Niu Y.J., Zhang Q.C., Mack J., Yi X.Y., Hlatshwayo Z., Nyokong T., Li M.Z., Zhu W.H. Dalton Trans. 2017, 46, 6912-6920.
https://doi.org/10.1039/C7DT00716G

10. Niu Y.J., Li M.Z., Zhang Q.C., Zhu W.H., Mack J., Fomo G., Nyokong T., Liang X. Dyes and Pigments 2017, 142, 416-428.
https://doi.org/10.1016/j.dyepig.2017.02.049

11. Barata J.F.B., Neves M., Faustino M., Tome C., Cavaleiro J. Chem. Rev. 2017, 117, 3192-3253.
https://doi.org/10.1021/acs.chemrev.6b00476

12. Zhang X.F., Wang Y., Zhu W.H., Mack J., Soy R.C., Nyokong T., Liang X. Dyes and Pigments 2020, 175, 108124.
https://doi.org/10.1016/j.dyepig.2019.108124

13. Berezina N.M., Bazanov M.I., Maksimova A.A., Semeikin A.S. Russ. J. Phys. Chem. A 2017, 91(12), 2377-2382.
https://doi.org/10.1134/S0036024417120032

14. Zhu W.H., Huang T.T., Qin M.F., Li M.Z., Mack J., Liang X. J. Electroanal. Chem. 2016, 774, 58-65.
https://doi.org/10.1016/j.jelechem.2016.05.009

15. Berezina N.M., Thao V.T., Berezin D.B., Bazanov M.I. Russ. J. Inorg. Chem. 2017, 62(12), 1617-1621.
https://doi.org/10.1134/S0036023617120051

16. Lei H.T., Li X.L., Meng J., Zheng H.Q., Zhang W., Cao R. ACS Catalysis 2019, 9, 4320-4344.
https://doi.org/10.1021/acscatal.9b00310

17. Li H., Li X.L., Lei H.T., Zhou G.J., Zhang W., Cao R. ChemSusChem 2019, 12, 801-806.
https://doi.org/10.1002/cssc.201802765

18. Stefanelli M., Pomarico G., Tortora L., Nardis S., Fronczek F.R., McCandless G.T., Smith K.M., Manowong M., Fang Y.Y., Chen P., Kadish K.M., Rosa A., Ricciard G., Paolesse R. Inorg. Chem. 2012, 51, 6928-6942.
https://doi.org/10.1021/ic3007926

19. Friedman A., Saltsman I., Gross Z., Elbaz L. Electrochimica Acta 2019, 310, 13-19.
https://doi.org/10.1016/j.electacta.2019.04.096

20. Friedman A., Landau L., Gonen S., Gross Z., Elbaz L. ACS Catalysis 2018, 8, 5024-5031.
https://doi.org/10.1021/acscatal.8b00876

21. Sinha W., Mahammed A., Fridman N., Diskin-Posner Y., Shimon L., Gross Z. Chem. Commun. 2019, 55, 11912-11915.
https://doi.org/10.1039/C9CC06645D

22. Lai W.Z., Cao R., Dong G., Shaik S., Yao J.N., Chen H. J. Phys. Chem. Lett. 2012, 3, 2315-2319.
https://doi.org/10.1021/jz3008535

23. Dogutan D.K., Stoian S.A., McGuire R., Schwalbe M., Teets T., Nocera F.G. J. Am. Chem. Soc. 2011, 133, 131-140.
https://doi.org/10.1021/ja108904s

24. Dogutan D.K., McGuire R.J., Nocera D.G. J. Am. Chem. Soc. 2011, 133, 9178-9180.
https://doi.org/10.1021/ja202138m

25. Li M.Z., Zhu W.H., Mack J., Mkhize S., Nyokong T., Liang X. Chin. J. Struct. Chem. 2017, 36, 367-380.

26. Gouterman M. In: The Porphyrins. Vol. III, Part A (Dolphin D., Ed.) New York: Academic Press, 1978. pp. 1-165.
https://doi.org/10.1016/B978-0-12-220103-5.50008-8

27. Michl J. Tetrahedron 1984, 40, 3845-3934.
https://doi.org/10.1016/S0040-4020(01)99999-5

28. Mack J. Chem. Rev. 2017, 117, 3444-3478.
https://doi.org/10.1021/acs.chemrev.6b00568

Attachment	Size
mhc200183l.pdf	2.65 MB
mhc200183l_supp.pdf	2.02 MB

Журнал "Макрогетероциклы"

Navigation

Languages

News

Search

pH-Dependent Electrochemically Catalyzed Oxygen Reduction Behaviors of o-Substituted Co(III) Corroles

References: