REAL

Exploring a Rigid Macrocyclic Ligand Bearing Malonate Pendants for Gd(III) Complexation: the Coordination Chemistry of [Gd(OPDMA)]−

Debretsion, Abraham Estifanos and Bunda, Szilvia and Lihi, Norbert and Papp, Gábor Csaba and Pallier, Agnés and Jakabné Tóth, Éva and Kálmán, Ferenc Krisztián (2025) Exploring a Rigid Macrocyclic Ligand Bearing Malonate Pendants for Gd(III) Complexation: the Coordination Chemistry of [Gd(OPDMA)]−. INORGANIC CHEMISTRY, 64 (21). pp. 10594-10602. ISSN 0020-1669

[img] Text
IC_2025_64_10594_10602.pdf - Published Version
Restricted to Repository staff only

Download (3MB) | Request a copy

Abstract

The emergence of nephrogenic systemic fibrosis, clearly linked to the in vivo dissociation of Gd(III)-based MRI contrast agents (CA), has promoted intensive research to identify safe CA candidates. Towards this goal, we have designed the novel ligand H4OPDMA, which combines a rigidified macrocycle, low total ligand basicity, and malonate pendant arms to increase the number of donor atoms. Thanks to these design elements, H4OPDMA is capable of forming a Gd(III) chelate with high thermodynamic stability and kinetic inertness. Indeed, the conditional stability of [Gd(OPDMA)]- (pGd = 14.8; pH 7.4, cGdL = 10-5 M) calculated for physiological conditions is comparable to that of [Gd(DTPA)]2- (pGd = 15.6), and its dissociation half-life is estimated to be 3.2 years at 37 °C and pH 7.4, making it an exceptionally inert chelate. Moreover, the water proton relaxation enhancement efficacy of [Gd(OPDMA)]- (r1 = 4.5 mM-1 s-1, 25°C, 20 MHz) is similar to that of clinical MRI contrast agents. Luminescence lifetime measurements and 17O NMR data confirmed the presence of one water molecule in the inner sphere of the metal ion (q = 1), which undergoes relatively fast exchange (kex298 = (73 ± 12) × 106 s-1). The fast water exchange can likely be related to an associatively activated mechanism, as suggested by the negative activation entropy, ΔS⧧ = -(7 ± 1) J mol-1 K-1. In accordance with this, DFT calculations indicate an eight-coordinated structure for the Gd(III) ion, involving one water molecule and seven donor atoms of the OPDMA4-, while one carboxylate group remains uncoordinated.

Item Type: Article
Additional Information: Department of Physical Chemistry, University of Debrecen, Egyetem tér 1., Debrecen, H-4032, Hungary Doctoral School of Chemistry, Stipendium Hungaricum Program, University of Debrecen, Egyetem tér 1., Debrecen, H-4010, Hungary HUN-REN−UD Mechanisms of Complex Homogeneous and Heterogeneous Chemical Reactions Research Group, Department of Inorganic and Analytical Chemistry, University of Debrecen, Egyetem tér 1, Debrecen, H-4032, Hungary Centre de Biophysique Moléculaire, CNRS, Université d’Orléans, rue Charles Sadron, Orléans, 45071 Cedex 2, France Export Date: 27 May 2025; Cited By: 0; Correspondence Address: S. Bunda; Department of Physical Chemistry, University of Debrecen, Debrecen, Egyetem tér 1., H-4032, Hungary; email: bunda.szilvia@science.unideb.hu; N. Lihi; HUN-REN−UD Mechanisms of Complex Homogeneous and Heterogeneous Chemical Reactions Research Group, Department of Inorganic and Analytical Chemistry, University of Debrecen, Debrecen, Egyetem tér 1, H-4032, Hungary; email: lihi.norbert@science.unideb.hu; F.K. Kálmán; Department of Physical Chemistry, University of Debrecen, Debrecen, Egyetem tér 1., H-4032, Hungary; email: kalman.ferenc@science.unideb.hu; CODEN: INOCA
Uncontrolled Keywords: IN-VIVO; LIGANDS; DISSOCIATION; MRI CONTRAST AGENTS; CONTRAST AGENT; NEPHROGENIC SYSTEMIC FIBROSIS; chelation; Water molecule; Carboxylation; Malonates; Macro-cyclic ligands; Intensive research; Co-ordination chemistries; Donor atoms;
Subjects: Q Science / természettudomány > QD Chemistry / kémia
SWORD Depositor: MTMT SWORD
Depositing User: MTMT SWORD
Date Deposited: 22 Sep 2025 11:31
Last Modified: 22 Sep 2025 11:31
URI: https://real.mtak.hu/id/eprint/224796

Actions (login required)

Edit Item Edit Item