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Charge-Density Induced Discrimination of Halides with a Rigid Dinuclear Copper(II) Complex

preprint
submitted on 03.05.2020, 06:47 and posted on 06.05.2020, 05:28 by Md Mhahabubur Rhaman, Mohammad Hasan, Zulfikhar A. Ali, Douglas Powell, Ritesh Tandon, Bryan Wong, Alamgir Hossain

A rigid dinuclear copper(II) complex L based on furan spacers has been synthesized and studied for its binding interactions with halides by colorimetric studies, UV-Vis titrations, and density functional theory (DFT) calculations. Our results from the titration studies demonstrate that L binds each of the halides in the order of fluoride > chloride > bromide > iodide, correlating directly with the charge density of the respective halide. Fully unconstrained DFT geometry optimizations have been carried out on both the isolated L as well as the anion-bound motifs. Binding energies (DE) were calculated for each of the optimized geometries, yielding an attractive DE of -92.39, -27.14, -23.16, and -13.37 kcal/mol for fluoride, chloride, bromide, and iodide, respectively, which is in accord with our experimental results. The compound has been further investigated for its biocompatibility on HeLa cells, demonstrating an excellent cell viability up to 500 µM concentration.

Funding

US Department of Defense (Grant Number W911NF-19-1-0006)

Office of Naval Research (Grant N00014-18-1-2740)

American Heart Association (Award No. 14SDG20390009)

History

Email Address of Submitting Author

usagi@alum.mit.edu

Institution

University of California-Riverside

Country

United States

ORCID For Submitting Author

0000-0002-3477-8043

Declaration of Conflict of Interest

no conflict of interest

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