Issue 11, 2025

Spectroscopic evidence of the interaction of titanium(iv) coordination complexes with a phosphate head group in phospholipids

Abstract

Biological membranes are potentially involved in the transport of metal ions, such as Ti(IV), and, sometimes, their associated ligands. Understanding the interactions of Ti(IV) ions and complexes with biological membranes provides a basis for elucidating the action mechanism of titanium anticancer drugs. Herein, we investigated the interactions of two neutral titanium(IV) complexes, viz. [H2Ti(Cat)3] (1) and [H2Ti(Napht)3] (2), incorporated into DOPC multi-bilayers using ATR-FTIR spectroscopy. Infrared results showed that complexes 1 and 2, when interacting with DOPC multi-bilayers, highly affected the hydration of the lipid phosphate group and its mobility, revealing that the phosphate group is the main group involved in the interactions of complexes 1 and 2 with DOPC phospholipids. NMR studies involving complex 1 and DOPC dissolved in deuterated DMSO solution were performed, and interactions between the Ti complex and DOPC phosphate group could be evidenced. DFT calculations of model complexes were in good agreement with experimental data, and the stability of three model complexes was estimated. On the basis of the obtained data, it can be suggested that the oxygen atom(s) of the phosphato group of the DOPC ligand acted as donor atoms for Ti.

Graphical abstract: Spectroscopic evidence of the interaction of titanium(iv) coordination complexes with a phosphate head group in phospholipids

Supplementary files

Article information

Article type
Paper
Submitted
23 Oct 2024
Accepted
24 Dec 2024
First published
30 Dec 2024
This article is Open Access
Creative Commons BY license

Dalton Trans., 2025,54, 4556-4565

Spectroscopic evidence of the interaction of titanium(IV) coordination complexes with a phosphate head group in phospholipids

M. Scarpi-Luttenauer, Z. Boubegtiten-Fezoua, P. Hellwig, A. Chaumont, B. Vincent, L. Barloy and P. Mobian, Dalton Trans., 2025, 54, 4556 DOI: 10.1039/D4DT02966F

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