Register      Login
Australian Journal of Chemistry Australian Journal of Chemistry Society
An international journal for chemical science
RESEARCH ARTICLE

Copper Complexes of Benzoylacetone Bis-Thiosemicarbazones: Metal and Ligand Based Redox Reactivity*

Jessica K. Bilyj A , Jeffrey R. Harmer B and Paul V. Bernhardt https://orcid.org/0000-0001-6839-1763 A C
+ Author Affiliations
- Author Affiliations

A School of Chemistry and Molecular Biosciences, University of Queensland, Brisbane, Qld 4072, Australia.

B Centre for Advanced Imaging, University of Queensland, Brisbane, Qld 4072, Australia.

C Corresponding author. Email: p.bernhardt@uq.edu.au

Australian Journal of Chemistry 74(1) 34-47 https://doi.org/10.1071/CH20210
Submitted: 30 June 2020  Accepted: 30 July 2020   Published: 9 September 2020

Abstract

Bis-thiosemicarbazones derived from the β-diketone benzoylacetone (H3banR, R = Me, Et, Ph) are potentially tetradentate N2S2 ligands whose coordination chemistry with copper is reported. In the absence of oxygen and in the presence of base they form anionic CuII complexes of the fully deprotonated ligands [CuII(banR)]. Upon exposure to atmospheric oxygen they undergo a complex series of reactions leading to two types of products; one a ligand oxidised ketone complex [CuII(banRO)] and the other an unprecedented dimeric di-CuIII complex [(CuIII(banR))2] depending on the R substituent. Time-resolved UV-vis spectroscopy, cyclic voltammetry, spectroelectrochemistry, and electron paramagnetic resonance (EPR) spectroscopy have been used to identify intermediates on the way to stable products formed under both anaerobic and aerobic conditions. It is found that both ligand-centred and Cu-centred oxidation reactions are occurring in parallel leading to this unusually complicated mixture of products.


References

[1]  B. M. Paterson, J. A. Karas, D. B. Scanlon, J. M. White, P. S. Donnelly, Inorg. Chem. 2010, 49, 1884.
         | Crossref | GoogleScholarGoogle Scholar | 20055473PubMed |

[2]  B. M. Paterson, C. Cullinane, P. J. Crouch, A. R. White, K. J. Barnham, P. D. Roselt, W. Noonan, D. Binns, R. J. Hicks, P. S. Donnelly, Inorg. Chem. 2019, 58, 4540.
         | Crossref | GoogleScholarGoogle Scholar | 30869878PubMed |

[3]  L. E. McInnes, A. Noor, K. Kysenius, C. Cullinane, P. Roselt, C. A. McLean, F. C. K. Chiu, A. K. Powell, P. J. Crouch, J. M. White, P. S. Donnelly, Inorg. Chem. 2019, 58, 3382.
         | Crossref | GoogleScholarGoogle Scholar | 30785268PubMed |

[4]  J. K. Bilyj, J. R. Harmer, P. V. Bernhardt, Eur. J. Inorg. Chem. 2018, 4731.
         | Crossref | GoogleScholarGoogle Scholar |

[5]  P. King, M. Maeder, Reactlab Redox, Ver. 1.1 2014 (J Plus Consulting Pty Ltd: Karawarra, Western Australia).

[6]  P. King, M. Maeder, Reactlab Kinetics, Ver. 1.1 2009 (J Plus Consulting Pty Ltd: Karawarra, Western Australia).

[7]  S. Stoll, A. Schweiger, J. Magn. Reson. 2006, 178, 42.
         | Crossref | GoogleScholarGoogle Scholar | 16188474PubMed |

[8]  G. M. Sheldrick, Acta Crystallogr. Sect. A 2008, 64, 112.
         | Crossref | GoogleScholarGoogle Scholar |

[9]  L. J. Farrugia, J. Appl. Cryst. 1999, 32, 837.
         | Crossref | GoogleScholarGoogle Scholar |

[10]  C. F. Macrae, I. J. Bruno, J. A. Chisholm, P. R. Edgington, P. McCabe, E. Pidcock, L. Rodriguez-Monge, R. Taylor, J. van de Streek, P. A. Wood, J. Appl. Cryst. 2008, 41, 466.
         | Crossref | GoogleScholarGoogle Scholar |

[11]  M. Akbar Ali, P. V. Bernhardt, M. A. H. Brax, J. England, A. J. Farlow, G. R. Hanson, L. L. Yeng, A. H. Mirza, K. Wieghardt, Inorg. Chem. 2013, 52, 1650.
         | Crossref | GoogleScholarGoogle Scholar | 23324063PubMed |

[12]  A. R. Cowley, J. R. Dilworth, P. S. Donnelly, A. D. Gee, J. M. Heslop, Dalton Trans. 2004, 2404.
         | Crossref | GoogleScholarGoogle Scholar | 15303151PubMed |

[13]  M. Salehi, R. Kia, A. Khaleghian, J. Coord. Chem. 2012, 65, 3007.
         | Crossref | GoogleScholarGoogle Scholar |

[14]  R. K. Sherwood, C. L. Kent, B. O. Patrick, W. S. McNeil, Chem. Commun. 2010, 46, 2456.
         | Crossref | GoogleScholarGoogle Scholar |

[15]  M. Amirnasr, R. Vafazadeh, A. H. Mahmoudkhani, Can. J. Chem. 2002, 80, 1196.
         | Crossref | GoogleScholarGoogle Scholar |

[16]  S.-X. Liu, Y.-L. Feng, Polyhedron 1996, 15, 4195.
         | Crossref | GoogleScholarGoogle Scholar |

[17]  X. Pang, H. Du, X. Chen, X. Wang, X. Jing, Chem. – Eur. J. 2008, 14, 3126.
         | Crossref | GoogleScholarGoogle Scholar | 18232044PubMed |

[18]  D. Xu, B. Chen, K. Chen, C. Chen, K. Miki, N. Kasai, Bull. Chem. Soc. Jpn. 1989, 62, 2384.
         | Crossref | GoogleScholarGoogle Scholar |

[19]  M. Salehi, F. Rahimifar, M. Kubicki, A. Asadi, Inorg. Chim. Acta 2016, 443, 28.
         | Crossref | GoogleScholarGoogle Scholar |

[20]  T. I. A. Gerber, E. Hosten, O. Knoesen, P. Mayer, J. Coord. Chem. 2007, 60, 2369.
         | Crossref | GoogleScholarGoogle Scholar |

[21]  J. K. Bilyj, N. V. Silajew, G. R. Hanson, J. R. Harmer, P. V. Bernhardt, Dalton Trans. 2019, 48, 15501.
         | Crossref | GoogleScholarGoogle Scholar | 31304485PubMed |

[22]  F. H. Allen, Acta Crystallogr. Sect. B 2002, 58, 380.
         | Crossref | GoogleScholarGoogle Scholar |

[23]  L. Yang, D. R. Powell, R. P. Houser, Dalton Trans. 2007, 955.
         | Crossref | GoogleScholarGoogle Scholar | 17308676PubMed |

[24]  B. J. Hathaway, D. E. Billing, Coord. Chem. Rev. 1970, 5, 143.
         | Crossref | GoogleScholarGoogle Scholar |

[25]  J. Peisach, W. E. Blumberg, Arch. Biochem. Biophys. 1974, 165, 691.
         | Crossref | GoogleScholarGoogle Scholar | 4374138PubMed |

[26]  V. B. Arion, N. V. Gerbeleu, V. G. Levitsky, Y. A. Simonov, A. A. Dvorkin, P. N. Bourosh, J. Chem. Soc., Dalton Trans. 1994, 1913.
         | Crossref | GoogleScholarGoogle Scholar |

[27]  D. Laziz, C. Beghidja, N. Baali, B. Zouchoune, A. Beghidja, Inorg. Chim. Acta 2019, 497, 119085.
         | Crossref | GoogleScholarGoogle Scholar |

[28]  A. Mukhopadhyay, S. Pal, Eur. J. Inorg. Chem. 2009, 4141.
         | Crossref | GoogleScholarGoogle Scholar |