15-membered rigid macrocyclic ligand for Mn2+ complexation: synthesis and coordination chemical characterization
dc.contributor.advisor | Tircsó, Gyula | |
dc.contributor.author | Baghirova, Aghanana | |
dc.contributor.department | DE--Természettudományi és Technológiai Kar--Kémiai Intézet | |
dc.date.accessioned | 2024-12-20T08:48:24Z | |
dc.date.available | 2024-12-20T08:48:24Z | |
dc.date.created | 2024-11-22 | |
dc.description.abstract | The investigation of Mn²⁺ chelates as alternatives to Gd³⁺-based MRI contrast agents has gained significant attention due to their promising safety and performance profiles. My research focused on the synthesis and coordination chemistry of a novel 15-membered bipyridine-based macrocyclic ligand, 15-BPyN5. The ligand demonstrated excellent thermodynamic stability (log K_MnL = 13.44), high kinetic inertness, and favorable relaxivity properties (r1p/r2p = 3.60/6.60 mM⁻¹s⁻¹). Dissociation studies revealed slow exchange kinetics with Zn²⁺ ions, with half-lives of 79.0 and 28.7 hours at 25°C and 37°C, respectively, attributed to the rigid coordination environment provided by the bipyridine moiety. These properties highlight the potential of [Mn(15-BPyN5)] as a safe and effective MRI contrast agent. This work paves the way for developing non-toxic alternatives to gadolinium-based agents, offering improved safety and imaging performance. | |
dc.description.course | Chemistry | |
dc.description.degree | BSc/BA | |
dc.format.extent | 36 | |
dc.identifier.uri | https://hdl.handle.net/2437/384084 | |
dc.language.iso | en | |
dc.rights.access | Hozzáférhető a 2022 decemberi felsőoktatási törvénymódosítás értelmében. | |
dc.subject | Macrocyclic ligands | |
dc.subject | Mn²⁺ complexation | |
dc.subject | Coordination chemistry | |
dc.subject.dspace | Kémia::Fizikai kémia | |
dc.title | 15-membered rigid macrocyclic ligand for Mn2+ complexation: synthesis and coordination chemical characterization |
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