2026-07-09T01:32:41Zhttps://riubu.ubu.es/oai/request

oai:riubu.ubu.es:10259/78132023-09-19T00:05:35Zcom_10259_6168com_10259_5086com_10259_2604com_10259_3593com_10259_5822col_10259_6169col_10259_3594col_10259_5823

Parra de la Parra, Sandra de la Tamayo Ramos, Juan Antonio Rubio Presa, Rubén Perez Antolin, Daniel Ruiz Fernández, Virginia Sanz Díez, Roberto Rumbo Lorenzo, Carlos Ventosa Arbaizar, Edgar 2023-09-18T10:08:42Z 2023-09-18T10:08:42Z 2023-09 1864-5631 http://hdl.handle.net/10259/7813 10.1002/cssc.202300626 1864-564X Viologen-derivatives are the most widely used redox organic molecules for neutral pH negative electrolyte of redox flow batteries. However, the long-established toxicity of the herbicide methyl-viologen raises concern for deployment of viologen-derivatives at large scale in flow batteries. Herein, we demonstrate the radically different cytotoxicity and toxicology of a series of viologen-derivatives in in vitro assays using model organisms representative of human and environmental exposure, namely human lung carcinoma epithelial cell line (A549) and the yeast Saccharomyces cerevisiae. The results show that safe viologen derivatives can be molecularly engineered, representing a promising family of negolyte materials for neutral redox flow batteries. eng http://creativecommons.org/licenses/by-nc-nd/4.0/ info:eu-repo/semantics/openAccess Attribution-NonCommercial-NoDerivatives 4.0 Internacional Cytotoxicity Toxicology Viologen derivatives Anolyte Redox flow battery On the Tunability of Toxicity for Viologen‐Derivatives as Anolyte for Neutral Aqueous Organic Redox Flow Batteries info:eu-repo/semantics/article