Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, Moscow 119991, Russia.
Faculty of Technology of Inorganic Substances and High Temperature Materials, Mendeleev University of Chemical Technology of Russia, Moscow 125047, Russia.
Molecules. 2023 Jan 3;28(1):418. doi: 10.3390/molecules28010418.
The chemical immobilization of cobalt(II) ions in a silica aerogel matrix enabled the synthesis of the first representative example of aerogel-based single-ion magnets. For the synthesis of the lyogels, methyl-trimethoxysilane and N-3-(trimethoxysilyl)propyl ethylenediamine were co-hydrolyzed, then the ethylenediamine groups that were immobilized on the silica matrix enabled the subsequent binding of cobalt(II) ions. Lyogels with various amounts of ethylenediamine moieties (0.1-15 mol %) were soaked in isopropanol solutions of cobalt(II) nitrate and further supercritically dried in carbon dioxide to obtain aerogels with a specific surface area of 210-596 m·g, an apparent density of 0.403-0.740 cm·g and a porosity of 60-78%. The actual cobalt content in the aerogels was 0.01-1.50 mmol per 1 g of SiO, which could easily be tuned by the concentration of ethylenediamine moieties in the silica matrix. The introduction of cobalt(II) ions into the ethylenediamine-modified silica aerogel promoted the stability of the diamine moieties at the supercritical drying stage. The molecular prototype of the immobilized cobalt(II) complex, bearing one ethylenediamine ligand [Co(en)(MeCN)(NO)], was synthesized and structurally characterized. Using magnetometry in the DC mode, it was shown that cobalt(II)-modified silica aerogels exhibited slow magnetic relaxation in a nonzero field. A decrease in cobalt(II) concentration in aerogels from 1.5 mmol to 0.14 mmol per 1 g of SiO resulted in a weakening of inter-ion interactions; the magnetization reversal energy barrier likewise increased from 4 to 18 K.
将钴(II)离子化学固定在硅胶气凝胶基质中,使得合成首例基于气凝胶的单离子磁体的代表实例成为可能。为了合成凝胶,首先将甲基三甲氧基硅烷和 N-3-(三甲氧基硅基)丙基乙二胺共同水解,然后固定在硅胶基质上的乙二胺基团可以随后结合钴(II)离子。将具有不同乙二胺部分摩尔数(0.1-15 mol%)的凝胶浸泡在异丙醇溶液中的硝酸钴中,并在二氧化碳中超临界干燥,得到比表面积为 210-596 m·g、表观密度为 0.403-0.740 cm·g 和孔隙率为 60-78%的气凝胶。气凝胶中的实际钴含量为 0.01-1.50 mmol 每 1 g SiO,这可以很容易地通过硅胶基质中的乙二胺部分的浓度来调节。将钴(II)离子引入乙二胺修饰的硅胶气凝胶中,促进了在超临界干燥阶段二胺部分的稳定性。固定化钴(II)配合物的分子原型,带有一个乙二胺配体[Co(en)(MeCN)(NO)],被合成并进行了结构表征。通过直流模式的磁测量表明,钴(II)修饰的硅胶气凝胶在非零磁场中表现出缓慢的磁弛豫。气凝胶中钴(II)浓度从 1.5 mmol 降低到 1 g SiO 中的 0.14 mmol,导致离子间相互作用减弱;磁化反转能量势垒同样从 4 K 增加到 18 K。