2021
DOI: 10.1039/d0tb02716b
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A class of water-soluble Fe(iii) coordination complexes as T1-weighted MRI contrast agents

Abstract: Iron-based coordination complexes are showing increasing potentials to be alternatives for T1-weighted magnetic resonance imaging (MRI) and contribute to the safety to the gadolinium-based compounds. In this work, three water-soluble...

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Cited by 13 publications
(14 citation statements)
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“…After fabrication, the 4a -iron complexes were subjected to IR and UV-visible (UV-Vis) spectroscopy. As shown in Figure 3a the formation of iron chelation was verified by a strong stretching vibrational band at about 592 cm −1 ( 7a ) and 591 cm −1 ( 7b ) in the IR spectra, as the hall mark of the Fe-O bond formation [ 31 ]. Moreover, the absorption bands near 486 nm in the UV-Vis absorption spectra of 7a and 7b could be associated with a change in electronic distribution due to d-d transition (Figure S4) [ 31 ].…”
Section: Resultsmentioning
confidence: 99%
“…After fabrication, the 4a -iron complexes were subjected to IR and UV-visible (UV-Vis) spectroscopy. As shown in Figure 3a the formation of iron chelation was verified by a strong stretching vibrational band at about 592 cm −1 ( 7a ) and 591 cm −1 ( 7b ) in the IR spectra, as the hall mark of the Fe-O bond formation [ 31 ]. Moreover, the absorption bands near 486 nm in the UV-Vis absorption spectra of 7a and 7b could be associated with a change in electronic distribution due to d-d transition (Figure S4) [ 31 ].…”
Section: Resultsmentioning
confidence: 99%
“…Changing the coordination groups and/or introducing suitable hydrophilic groups of the previously studied chelators (for example, HBED, EHPG, and TACN) can largely alter the coordination structures of the central iron ions (with or without inner-sphere water ligand), the second coordination sphere environment, as well as the charge of the complexes, which gives rise to the enhance of relaxivities and the improvement of thermodynamic stability. Clinically used iron-sequestering agents with a high biocompatibility and strong binding ability to Fe 3+ could be also a good [68] 1.07 b 1.28 b --MOC-Fe(III) 4 [68] 1.…”
Section: Discussionmentioning
confidence: 99%
“…The recently independent studies from our group [ 68 , 69 ] and the group of Janet R Morrow [ 70 ] demonstrated that water soluble metal–organic cages (MOC) with multiple Fe(III) centers are promising alternatives to prepare multinuclear Fe(III) complexes [ 71 ]. In our study, two water soluble metal-organic cages with two (MOC-Fe(III) 2 ) and four Fe(III) centers (MOC–Fe(III) 4 ) based on the bisbidentate catecholate ligand were prepared ( Figure 11 ) [ 68 ].…”
Section: Multinuclear Fe(iii) Complexesmentioning
confidence: 99%
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