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Journal articles on the topic 'Redox non-innocent ligand'

Author: Grafiati

Published: 4 June 2025

Last updated: 1 August 2025

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1

Braun, Jason D., Paul A. Gray, Baldeep K. Sidhu, Dion B. Nemez, and David E. Herbert. "Zn-Templated synthesis of substituted (2,6-diimine)pyridine proligands and evaluation of their iron complexes as anolytes for flow battery applications." Dalton Transactions 49, no. 45 (2020): 16175–83. http://dx.doi.org/10.1039/d0dt00543f.

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Zn<sup>2+</sup> templating enables synthesis of redox ‘non-innocent’ diimine pyridine ligands with strong electron-withdrawing groups, allowing construction of iron complexes with multiple ligand-based reductions for application in redox flow batteries.

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2

Lehtonen, Ari. "Metal Complexes of Redox Non-Innocent Ligand N,N′-Bis(3,5-di-tertbutyl-2-hydroxy-phenyl)-1,2-phenylenediamine." Molecules 29, no. 5 (2024): 1088. http://dx.doi.org/10.3390/molecules29051088.

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Redox non-innocent ligands react with metal precursors to form complexes where the oxidation states of the ligand and thus the metal atom cannot be easily defined. A well-known example of such ligands is bis(o-aminophenol) N,N′-bis(3,5-di-tertbutyl-2-hydroxy-phenyl)-1,2-phenylenediamine, previously developed by the Wieghardt group, which has a potentially tetradentate coordination mode and four distinct protonation states, whereas its electrochemical behavior allows for five distinct oxidation states. This rich redox chemistry, as well as the ability to coordinate to various transition metals,

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3

Simler, Thomas, Andreas A. Danopoulos, and Pierre Braunstein. "Non-symmetrical, potentially redox non-innocent imino NHC pyridine ‘pincers’ via a zinc ion template-assisted synthesis." Dalton Transactions 46, no. 18 (2017): 5955–64. http://dx.doi.org/10.1039/c7dt01014a.

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A Zn<sup>II</sup>-promoted modular synthesis allows access to new non-symmetrical, redox-active imino NHC pyridine pincer ligands. Radical anionic and dianionic redox states of the ligand are involved in its Fe<sup>II</sup> complexes obtained from FeBr<sub>2</sub>/KC<sub>8</sub>.

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4

Dutta, Debarpan, Suvendu Maity, Suman Kundu, and Prasanta Ghosh. "Mixed-valence di-ruthenium(ii,iii) complexes of redox non-innocent N-aryl-o-phenylenediamine derivatives." Dalton Transactions 50, no. 22 (2021): 7791–803. http://dx.doi.org/10.1039/d1dt00779c.

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5

Hazari, Arijit Singha, Alexa Paretzki, Jan Fiedler, Stanislav Zalis, Wolfgang Kaim та Goutam Kumar Lahiri. "Different manifestations of enhanced π-acceptor ligation at every redox level of [Os(9-OP)L2]n, n = 2+, +, 0, − (9-OP− = 9-oxidophenalenone and L = bpy or pap)". Dalton Transactions 45, № 45 (2016): 18241–51. http://dx.doi.org/10.1039/c6dt03764j.

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6

Wang, Yichen, Jing Li, Li Zhang, et al. "Magnetic on–off switching in redox non-innocent ligand bridged binuclear cobalt complexes." Dalton Transactions 47, no. 48 (2018): 17211–15. http://dx.doi.org/10.1039/c8dt04157a.

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7

Vijaykumar, Gonela, Anand Pariyar, Jasimuddin Ahmed, Bikash Kumar Shaw, Debashis Adhikari, and Swadhin K. Mandal. "Tuning the redox non-innocence of a phenalenyl ligand toward efficient nickel-assisted catalytic hydrosilylation." Chemical Science 9, no. 10 (2018): 2817–25. http://dx.doi.org/10.1039/c7sc04687a.

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8

Chakraborty, Soumi, Arpan Das, Jasimuddin Ahmed, Sayani Barman, and Swadhin K. Mandal. "Designing a Cr-catalyst bearing redox non-innocent phenalenyl-based ligand towards hydrosilylative CO2 functionalization." Chemical Communications 56, no. 89 (2020): 13788–91. http://dx.doi.org/10.1039/d0cc05348a.

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9

Benson, Christopher R., Alice K. Hui, Kumar Parimal, et al. "Multiplying the electron storage capacity of a bis-tetrazine pincer ligand." Dalton Trans. 43, no. 17 (2014): 6513–24. http://dx.doi.org/10.1039/c4dt00341a.

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10

Kim, Jee Eon, Patrick J. Carroll, and Eric J. Schelter. "Bidentate nitroxide ligands stable toward oxidative redox cycling and their complexes with cerium and lanthanum." Chemical Communications 51, no. 81 (2015): 15047–50. http://dx.doi.org/10.1039/c5cc06052d.

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11

Salojärvi, Esko, Anssi Peuronen, Jani Moilanen, et al. "A diamagnetic iron complex and its twisted sister – structural evidence on partial spin state change in a crystalline iron complex." Dalton Transactions 50, no. 43 (2021): 15831–40. http://dx.doi.org/10.1039/d1dt01607e.

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Diamagnetic Fe complex was made of a redox non-innocent ligand precursor N,N′-bis(3,5-di-tert-butyl-2-hydroxy-phenyl)-1,2-phenylene-diamine and FeCl3. Its phenoxazine derivative was obtained via intra-ligand cyclisation of the parent complex.

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12

Li, Ying-Ying, Xiao-Yan Wang, Hui-Ji Li, et al. "Theoretical study on the mechanism of water oxidation catalyzed by a mononuclear copper complex: important roles of a redox non-innocent ligand and HPO₄²⁻ anion." RSC Advances 13, no. 12 (2023): 8352–59. http://dx.doi.org/10.1039/d3ra00648d.

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13

Ringenberg, Mark R., Swarna Latha Kokatam, Zachariah M. Heiden, and Thomas B. Rauchfuss. "Redox-Switched Oxidation of Dihydrogen Using a Non-Innocent Ligand." Journal of the American Chemical Society 130, no. 3 (2008): 788–89. http://dx.doi.org/10.1021/ja076801k.

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14

Chuang, Yu-Chun, Chou-Fu Sheu, Gene-Hsiang Lee, Yu-Sheng Chen, and Yu Wang. "Charge density studies of 3dmetal (Ni/Cu) complexes with a non-innocent ligand." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 73, no. 4 (2017): 634–42. http://dx.doi.org/10.1107/s2052520617007119.

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High-resolution X-ray diffraction experiments and atom-specific X-ray absorption experiments are applied to investigate a series of square planar complexes with the non-innocent ligand of maleonitriledithiolate (mnt), [S2C2(CN)2]z−, containingM—S bonds. Four complexes of (PyH)z[M(mnt)2]z−, whereM= Ni or Cu,z= 2 or 1 and PyH+= C5NH6+, were studied in order to clarify whether such one-electron oxidation–reduction, [M(mnt)2]2−/[M(mnt)2]1−, is taking place at the metal or the ligand site. Combining the techniques of metalK-,L-edge and SK-edge X-ray absorption spectroscopy with high-resolution X-ra

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15

Duarte, Gabriel M., Jason D. Braun, Patrick K. Giesbrecht, and David E. Herbert. "Redox non-innocent bis(2,6-diimine-pyridine) ligand–iron complexes as anolytes for flow battery applications." Dalton Transactions 46, no. 47 (2017): 16439–45. http://dx.doi.org/10.1039/c7dt03915h.

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16

Lima, Lidiane M. A., Heide Murakami, D. Jackson Gaebler, et al. "Acute Toxicity Evaluation of Non-Innocent Oxidovanadium(V) Schiff Base Complex." Inorganics 9, no. 6 (2021): 42. http://dx.doi.org/10.3390/inorganics9060042.

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The vanadium(V) complexes have been investigated as potential anticancer agents which makes it essential to evaluate their toxicity for safe use in the clinic. The large-scale synthesis and the acute oral toxicity in mice of the oxidovanadium(V) Schiff base catecholate complex, abbreviated as [VO(HSHED)dtb] containing a redox-active ligand with tridentate Schiff base (HSHED = N-(salicylideneaminato)-N’-(2-hydroxyethyl)-1,2-ethylenediamine) and dtb = 3,5-di-(t-butyl)catechol ligands were carried out. The body weight, food consumption, water intake as well biomarkers of liver and kidney toxicity

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17

Khairul, Wan M., Mark A. Fox, Phil A. Schauer, et al. "Ligand redox non-innocent behaviour in ruthenium complexes of ethynyl tolans." Inorganica Chimica Acta 374, no. 1 (2011): 461–71. http://dx.doi.org/10.1016/j.ica.2011.02.043.

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18

Orchanian, Nicholas M., Lorena E. Hong, David A. Velazquez, and Smaranda C. Marinescu. "Electrocatalytic syngas generation with a redox non-innocent cobalt 2-phosphinobenzenethiolate complex." Dalton Transactions 50, no. 31 (2021): 10779–88. http://dx.doi.org/10.1039/d0dt03270k.

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19

Chandra, Paul Ganesh. "Catalytic Applications of Transition Metal Complexes Based on o-Aminophenol Ligands." Der Pharma Chemica 14, no. 11 (2022): 11. https://doi.org/10.4172/0975-413X.14.11.14-24.

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Aminophenol based ligands have had a tremendous and continually growing impact on catalysis research. Their utility spans over a number of areas including homogeneous catalysis, small molecule activation, carbon dioxide reduction, and hydrogen evolution processes. For the development of a catalyst metal-ligand covalency is necessary via mutual cooperation and strong electronic coupling between a metal center and coordinating ligands. The role of o-aminophenol based ligands in different metabolic/enzymatic reactions in biological systems is now well documented. Their application is now expandin

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20

Liu, Jiale, Rong-Zhen Liao, Frank W. Heinemann, et al. "Electrocatalytic Hydrogen Evolution by Cobalt Complexes with a Redox Non-Innocent Polypyridine Ligand." Inorganic Chemistry 60, no. 23 (2021): 17976–85. http://dx.doi.org/10.1021/acs.inorgchem.1c02539.

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21

Pakpour, Fatemeh, Elham Safaei, S. Mohammad Azami, Andrzej Wojtczak, and Karolina Kaldunska. "The role of a redox-active non-innocent ligand in additive-free C–C Glaser–Hay and Suzuki coupling reactions by an o-aminophenol palladium(ii) complex." RSC Advances 13, no. 5 (2023): 3278–89. http://dx.doi.org/10.1039/d2ra07252a.

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22

Mele, Andrea, Federica Arrigoni, Luca De Gioia, et al. "Use of the Asymmetrical Chelating N-Donor 2-Imino-Pyridine as a Redox [Fe4S4] Cubane Surrogate at a Di-Iron Site Related to [FeFe]-Hydrogenases." Inorganics 11, no. 12 (2023): 463. http://dx.doi.org/10.3390/inorganics11120463.

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Two complexes, related to the active site of [FeFe]-hydrogenases, [Fe2(CO)4(κ2-pma)(µ-bdt)] (1) and [Fe2(CO)4(κ2-pma)(µ-pdt)] (2) (bdt = benzene-1,2-dithiolate, pdt = propane-1,2-dithiolate) featuring the diaza chelate ligand trans-N-(2-pyridylmethylene)aniline (pma) were prepared, in order to study the influence of such a redox ligand, potentially non-innocent, on their redox behaviours. Both complexes were synthesized by photolysis in moderate yields, and they were characterized by IR, 1H and 13C{1H} NMR spectroscopies, elemental analyses and X-ray diffraction. Their electrochemical study by

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23

Boyle, Jenna, Catherine Breakfield, Leah Buck, Catherine McMahon, and Dominic C. Babbini. "Crystal structure of (1E,1′E)-1,1′-(pyridine-2,6-diyl)bis[N-(2,3,4,5,6-pentafluorophenyl)ethan-1-imine]." Acta Crystallographica Section E Crystallographic Communications 73, no. 7 (2017): 954–56. http://dx.doi.org/10.1107/s2056989017008040.

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The title compound, C21H9F10N3, represents a potential redox non-innocent pyridine diimine ligand system. It consists of a central pyridine ring with two pentafluorophenyl substituted imine groups in positions 2 and 6. The whole molecule is generated by mirror symmetry, the mirror bisecting the N andpara-C atom of the pyridine ring. The perfluorophenyl ring is inclined to the pyridine ring by 73.67 (8)°. In the crystal, molecules stack along theaaxis, but there are no significant intermolecular interactions present.

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24

Khatua, Manas, Bappaditya Goswami, and Subhas Samanta. "Dehydrogenation of amines in aryl-amine functionalized pincer-like nitrogen-donor redox non-innocent ligands via ligand reduction on a Ni(ii) template." Dalton Transactions 49, no. 20 (2020): 6816–31. http://dx.doi.org/10.1039/d0dt00466a.

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25

Colin, Aristide, Yiting Wang, François Lambert, et al. "A Trinuclear Co(II) Complex Based on the Tris-Dioxolene Triphenylene Non-Innocent Bridge: Complementary Redox, Magnetic Behavior and Theoretical Calculations." Magnetochemistry 10, no. 12 (2024): 102. https://doi.org/10.3390/magnetochemistry10120102.

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A trinuclear Co(II)-containing complex was assembled using the non-innocent hexahydroxytriphenylene bridging ligand. Cyclovoltammetry and spectroelectrochemistry studies revealed that the central ligand sustained four reversible redox events, leading to different species with diverse optical behavior. Complementary analysis of the molecular structure confirmed by ab initio theoretical calculations were consistent with the bridge in the tris-semiquinone (sq) state for the trinuclear complex. The exchange coupling among the electrons of the bridge resulted in a spin doublet (s = ½) localized clo

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26

Gandara, Catherine, Christian Philouze, Olivier Jarjayes, and Fabrice Thomas. "Coordination chemistry of a redox non-innocent NHC bis(phenolate) pincer ligand with nickel(II)." Inorganica Chimica Acta 482 (October 2018): 561–66. http://dx.doi.org/10.1016/j.ica.2018.06.046.

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27

Salojärvi, Esko, Anssi Peuronen, Manu Lahtinen, et al. "Series of Near-IR-Absorbing Transition Metal Complexes with Redox Active Ligands." Molecules 25, no. 11 (2020): 2531. http://dx.doi.org/10.3390/molecules25112531.

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New soluble and intensely near-IR-absorbing transition metal (Ti, Zr, V, Ni) complexes were synthesized using a redox non-innocent N,N’-bis(3,5-di-tertbutyl-2-hydroxy-phenyl) -1,2-phenylenediamine (H4L) as a ligand precursor. In all the complexes, ([Ti(Lox)2, [Zr(Lox)2], [V(Lsq1)(HLox)] and [Ni(HLox)2], two organic molecules coordinate to the metal center as tri- or tetradentate ligands. The solid-state structures of the complexes were determined using single crystal XRD, and the compounds were further characterized with Electrospray Ionisation Mass Spectrometry (ESI-MS). Thermoanalytical meas

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28

Queyriaux, N., K. Abel, J. Fize, J. Pécaut, M. Orio, and L. Hammarström. "From non-innocent to guilty: on the role of redox-active ligands in the electro-assisted reduction of CO2 mediated by a cobalt(ii)-polypyridyl complex." Sustainable Energy & Fuels 4, no. 7 (2020): 3668–76. http://dx.doi.org/10.1039/d0se00570c.

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29

Berry, John F., Eckhard Bill, Eberhard Bothe, Thomas Weyhermüller, and Karl Wieghardt. "Octahedral Non-Heme Non-Oxo Fe(IV) Species Stabilized by a Redox-Innocent N-Methylated Cyclam−Acetate Ligand." Journal of the American Chemical Society 127, no. 33 (2005): 11550–51. http://dx.doi.org/10.1021/ja052673t.

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30

Shen, Jingmei, Glenn P. A. Yap, William E. Barker IV, William E. Geiger та Klaus H. Theopold. "An electron transfer series of octahedral chromium complexes containing a redox non-innocent α-diimine ligand". Chem. Commun. 50, № 73 (2014): 10626–29. http://dx.doi.org/10.1039/c4cc03332a.

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31

Jurca, Titel, Wen-Ching Chen, Sheila Michel, Ilia Korobkov, Tiow-Gan Ong, and Darrin S. Richeson. "Solid-State Thermolysis of afac-Rhenium(I) Carbonyl Complex with a Redox Non-Innocent Pincer Ligand." Chemistry - A European Journal 19, no. 13 (2013): 4278–86. http://dx.doi.org/10.1002/chem.201203045.

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32

Ortu, Fabrizio, Hao Zhu, Marie-Emmanuelle Boulon, and David Mills. "Synthesis and Reactivity of a Cerium(III) Scorpionate Complex Containing a Redox Non-Innocent 2,2′-Bipyridine Ligand." Inorganics 3, no. 4 (2015): 534–53. http://dx.doi.org/10.3390/inorganics3040534.

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33

Skara, G., B. Pinter, P. Geerlings, and F. De Proft. "Revealing the thermodynamic driving force for ligand-based reductions in quinoids; conceptual rules for designing redox active and non-innocent ligands." Chemical Science 6, no. 7 (2015): 4109–17. http://dx.doi.org/10.1039/c5sc01140j.

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34

Yao, Shenglai, Arseni Kostenko, Yun Xiong, Christian Lorent, Ales Ruzicka, and Matthias Driess. "Changing the Reactivity of Zero‐ and Mono‐Valent Germanium with a Redox Non‐Innocent Bis(silylenyl)carborane Ligand." Angewandte Chemie 133, no. 27 (2021): 14990–94. http://dx.doi.org/10.1002/ange.202103769.

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35

Yao, Shenglai, Arseni Kostenko, Yun Xiong, Christian Lorent, Ales Ruzicka, and Matthias Driess. "Changing the Reactivity of Zero‐ and Mono‐Valent Germanium with a Redox Non‐Innocent Bis(silylenyl)carborane Ligand." Angewandte Chemie International Edition 60, no. 27 (2021): 14864–68. http://dx.doi.org/10.1002/anie.202103769.

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36

Garrido-Barros, Pablo, Ignacio Funes-Ardoiz, Samuel Drouet, Jordi Benet-Buchholz, Feliu Maseras, and Antoni Llobet. "Redox Non-innocent Ligand Controls Water Oxidation Overpotential in a New Family of Mononuclear Cu-Based Efficient Catalysts." Journal of the American Chemical Society 137, no. 21 (2015): 6758–61. http://dx.doi.org/10.1021/jacs.5b03977.

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37

Goudy, Violaine, Arnaud Jaoul, Marie Cordier, Carine Clavaguéra, and Grégory Nocton. "Tuning the Stability of Pd(IV) Intermediates Using a Redox Non-innocent Ligand Combined with an Organolanthanide Fragment." Journal of the American Chemical Society 139, no. 31 (2017): 10633–36. http://dx.doi.org/10.1021/jacs.7b05634.

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38

Jana, Narayan Ch, Sarmistha Adak, Paula Brandão, Tarun Kanti Mandal, and Anangamohan Panja. "Synthesis, structures, electronic properties and DFT calculations of cobalt(II) complexes with a redox non-innocent naphthoquinone ligand." Polyhedron 107 (March 2016): 48–56. http://dx.doi.org/10.1016/j.poly.2015.12.063.

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39

Safaei, Elham, Hadiseh Bahrami, Andrzej Wojtczak, Saman Alavi, and Zvonko Jagličić. "Redox potential tuning by redox-inactive anions in copper(II) complexes of non-innocent o-aminophenol-based ligand containing benzoxazole: Learning from nature." Polyhedron 122 (January 2017): 219–27. http://dx.doi.org/10.1016/j.poly.2016.11.031.

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40

Mikhailov, Ilya K., Zufar N. Gafurov, Alexey A. Kagilev, et al. "Redox Chemistry of Pt(II) Complex with Non-Innocent NHC Bis(Phenolate) Pincer Ligand: Electrochemical, Spectroscopic, and Computational Aspects." Catalysts 13, no. 9 (2023): 1291. http://dx.doi.org/10.3390/catal13091291.

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A Pt(II) complex bearing chelating tridentate bis-aryloxide tetrahydropyrimidinium-based N-heterocyclic carbene (NHC) was synthesized and characterized by using different techniques. Both cyclic voltammetry and differential pulse voltammetry were used to study the electrochemical properties of the complex, revealing two reversible one-electron oxidation processes. The chemical generation and isolation of one-electron-oxidized species were performed oxidizing the initial complex by means of AgBF4. A combination of spectroscopic (UV-Vis/NIR- and EPR-) and theoretical (density functional theory (

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41

Morimoto, Yuma, June Takaichi, Shinichi Hanada та ін. "Redox behavior of novel nickel and palladium complexes supported by trianionic non-innocent ligand containing β-diketiminate and phenol groups". Journal of Porphyrins and Phthalocyanines 19, № 01-03 (2015): 377–87. http://dx.doi.org/10.1142/s1088424615500248.

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A new type of nickel and palladium complexes with non-innocent β-diketiminate ligand having redox active phenol groups, 2,4-di-tert-butyl-6-(((1E,2E)-3-((3,5-di-tert-butyl-2-hydroxyphenyl)amino)-2-nitroallylidene)amino)phenol ( L H 3, fully protonated form) have been developed, and the structure, physical properties, and reactivity of their one-electron and two-electron oxidized complexes, [MII(L•2-)] and [MII(L-)]+ ( M = Ni II or Pd II ) have been examined in detail. The two-electron oxidized forms of both complexes, [MII(L-)]+, exhibited hydrogen atom abstraction ability from 1,4-cyclohexadi

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42

Leconte, Nicolas, Jules Moutet, Khrystyna Herasymchuk, et al. "Mn(iv) and Mn(v)-radical species supported by the redox non-innocent bis(2-amino-3,5-di-tert-butylphenyl)amine pincer ligand." Chemical Communications 53, no. 18 (2017): 2764–67. http://dx.doi.org/10.1039/c7cc00516d.

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The electron-rich pincer ligand 1 has been synthesized and chelated to manganese, affording 2 in high yield. Complex 2 comprises two iminosemiquinone radicals coordinated to a Mn(iv) ion. Its two electron oxidation produces 22+, which is a stable Mn(v)-iminosemiquinone radical complex.

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43

Musella, Elisa, Angelo Mullaliu, Thomas Ruf, et al. "Detailing the Self-Discharge of a Cathode Based on a Prussian Blue Analogue." Energies 13, no. 15 (2020): 4027. http://dx.doi.org/10.3390/en13154027.

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Prussian Blue analogues (PBAs) are a promising class of electrode active materials for batteries. Among them, copper nitroprusside, Cu[Fe(CN)5NO], has recently been investigated for its peculiar redox system, which also involves the nitrosyl ligand as a non-innocent ligand, in addition to the electroactivity of the metal sites, Cu and Fe. This paper studies the dynamics of the electrode, employing surface sensitive X-ray Photoelectron spectroscopy (XPS) and bulk sensitive X-ray absorption spectroscopy (XAS) techniques. XPS provided chemical information on the layers formed on electrode surface

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44

Oberoi, Deepa, Parveen Dagar, Uday Shankar, et al. "Design, synthesis, and characterization of an Fe(ii)-polymer of a redox non-innocent, heteroatomic, polydentate Schiff's base ligand: negative differential resistance and memory behaviour." New Journal of Chemistry 42, no. 23 (2018): 19090–100. http://dx.doi.org/10.1039/c8nj04106g.

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45

Wang, Denan, Danushka M. Ekanayake, Sergey V. Lindeman, Cláudio N. Verani, and Adam T. Fiedler. "Multielectron Redox Chemistry of Transition Metal Complexes Supported by a Non-Innocent N3 P2 Ligand: Synthesis, Characterization, and Catalytic Properties." European Journal of Inorganic Chemistry 2018, no. 37 (2018): 4133–41. http://dx.doi.org/10.1002/ejic.201800843.

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46

Vaddypally, Shivaiah, Ian G. McKendry, Warren Tomlinson, Joseph P. Hooper, and Michael J. Zdilla. "Electronic Structure of Manganese Complexes of the Redox-Non-innocent Tetrazene Ligand and Evidence for the Metal-Azide/Imido Cycloaddition Intermediate." Chemistry - A European Journal 22, no. 30 (2016): 10548–57. http://dx.doi.org/10.1002/chem.201600531.

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47

Kundu, Animesh, Suman Kr Dey, Subhasis Dey, Anakuthil Anoop, and Sukanta Mandal. "Mononuclear Ruthenium-Based Water Oxidation Catalyst Supported by Anionic, Redox-Non-Innocent Ligand: Heterometallic O–O Bond Formation via Radical Coupling Pathway." Inorganic Chemistry 59, no. 2 (2019): 1461–70. http://dx.doi.org/10.1021/acs.inorgchem.9b03258.

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48

Dede, Yavuz, Xinhao Zhang, Maria Schlangen, Helmut Schwarz, and Mu-Hyun Baik. "A Redox Non-Innocent Ligand Controls the Life Time of a Reactive Quartet Excited State - An MCSCF Study of [Ni(H)(OH)]+." Journal of the American Chemical Society 131, no. 35 (2009): 12634–42. http://dx.doi.org/10.1021/ja902093f.

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Corcos, Amanda R., Omar Villanueva, Richard C. Walroth, et al. "Oxygen Activation by Co(II) and a Redox Non-Innocent Ligand: Spectroscopic Characterization of a Radical–Co(II)–Superoxide Complex with Divergent Catalytic Reactivity." Journal of the American Chemical Society 138, no. 6 (2016): 1796–99. http://dx.doi.org/10.1021/jacs.5b12643.

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Roy, Puspendu, Apurba Sau Mondal, Ajoy Kumar Pramanik, and Tapan Kumar Mondal. "Ruthenium carbonyl complex of a redox non-innocent ONS donor azophenol ligand: Electrochemistry, photophysical property, electronic structure and catalytic activity towards oxidation of alcohols." Journal of Organometallic Chemistry 828 (January 2017): 1–9. http://dx.doi.org/10.1016/j.jorganchem.2016.11.012.

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