Investigations of Bis(alkylthiocarbamato)copper Linkage Isomers

• Published in: Inorganic chemistry Vol. 61; no. 20; pp. 7715 - 7719
• Main Authors: Bajaj, Kritika, Andres, Sarah A., Hofsommer, Dillon T., Galib, Mirza, Mashuta, Mark S., Bennett, Brian, Narayanan, Badri, Buchanan, Robert M., Bates, Paula J., Grapperhaus, Craig A.
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 23.05.2022; American Chemical Society (ACS)
• Subjects: Chemistry
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/acs.inorgchem.2c00371

Linkage isomers are coordination compounds with the same composition but different donor atoms, resulting in distinct physical and electronic structures. A pair of linkage isomers, CuL 555 and CuL 465 , derived from phenylglyoxal bis­(ethylthiocarbamate) were synthesized, isolated, and characterized by structural, electrochemical, and spectroscopic methods. The isomers are stable in solution under ambient conditions, but CuL 465 converts to CuL 555 in acid, consistent with quantum-chemical calculations. The complexes were screened against a lung adenocarcinoma cell line (A549) and a nonmalignant lung fibroblast cell line (IMR-90) to evaluate the antiproliferation activity. CuL 555 and CuL 465 possessed EC50 values of 0.113 ± 0.030 and 0.115 ± 0.038 μM for A549 and 1.87 ± 0.29 and 0.77 ± 0.22 μM for IMR-90, respectively.