An overly anionic metal coordination environment eliminates the T-weighted response of quinol-containing MRI contrast agent sensors to H2O2
An overly anionic metal coordination environment eliminates the T-weighted response of quinol-containing MRI contrast agent sensors to H2O2
复制标题
过度阴离子金属配位环境消除了含对苯二酚的 MRI 造影剂传感器对 H2O2 的 T 加权响应
DOI:
10.1016/j.ica.2019.119045
复制
发表时间:
2019
影响因子:
2.8
通讯作者:
Goldsmith, Christian R.
中科院分区:
文献类型:
--
作者:
Hutchinson, Tessa E.;Bashir, Adam;Yu, Meng;Beyers, Ronald J.;Goldsmith, Christian R.
A previously reported quinol- and Mn(II)-containing MRI contrast agent sensor for H2O2has the drawback of releasing the metal ion upon oxidation of the organic ligand. The release of potentially neurotoxic Mn(II) limits the sensor’sin vivoapplicability. We preparedN,N′-bis(2,5-dihydroxybenzyl)ethanediamine-N,N′-diacetic acid (H6qc1) as a substitute ligand that could potentially remain bound to the metal ion after oxidation of the quinol portions to more weakly metal-bindingpara-quinones. The carboxylic acid groups deprotonate at ambient pH, providing a more anionic coordination environment that stabilizes its Mn(II) complex in water. Although the more anionic coordination sphere doesn’t introduce air sensitivity, it does render the metal center more susceptible to oxidation by hydrogen peroxide, as evidenced by electron paramagnetic resonance. The oxidation of the metal to less paramagnetic Mn(III) is proposed to lower ther1enough to completely counter any increase inT1-weighted relaxivity that would result from improved aquation.
登录
查看更多内容
DOI:
--
发表时间:
1996
期刊:
影响因子:
--
作者:
Antonio Cusanelli;U. Frey;D. Richens;A. Merbach
通讯作者:
A. Merbach
影响因子:
15
作者:
Loving GS;Mukherjee S;Caravan P
通讯作者:
Caravan P
影响因子:
2.9
作者:
Eskici, Goezde;Axelsen, Paul H.
通讯作者:
Axelsen, Paul H.
影响因子:
15
作者:
Goldsmith, CR;Cole, AP;Stack, TDP
通讯作者:
Stack, TDP
影响因子:
4.6
作者:
Meng Yu;Meghan Ward;Alicja Franke;Stephen L Ambrose;Z. Whaley;Thomas Miller Bradford;J. Gorden;R. Beyers;R. Cattley;I. Ivanović‐Burmazović;D. Schwartz;Christian R. Goldsmith
通讯作者:
Christian R. Goldsmith