化学
旋转交叉
堆积
氧化铟锡
氢键
电极
脱质子化
氧化还原
结晶学
质子化
分子间力
苯甲酸
羧酸
氧化物
无机化学
分子
高分子化学
物理化学
有机化学
离子
作者
Takuya Shiga,Yamato Sato,Minami Tachibana,Hiroki Sato,Takuto Matsumoto,Hajime Sagayama,Reiji Kumai,Youichi Murakami,Graham N. Newton,Hiroki Oshio
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2018-10-31
卷期号:57 (22): 14013-14017
被引量:19
标识
DOI:10.1021/acs.inorgchem.8b01856
摘要
Two carboxyl-substituted iron(II) grids, one protonated, [Fe 4 (HL) 4 ](BF 4 ) 4 ·4MeCN·AcOEt ( 1 ), and the other deprotonated, [Fe 4 (L) 4 ]·DMSO·EtOH ( 2 ), where H 2 L = 4-{4,5-bis[6-(3,5-dimethylpyrazol-1-yl)pyrid-2-yl]-1 H -imidazol-2-yl}benzoic acid, were synthesized. Single-crystal X-ray structure analyses reveal that both complexes have a tetranuclear [2 × 2] grid structure. 1 formed one-dimensional chains through intermolecular hydrogen bonds between the carboxylic acid units of neighboring grids, while 2 formed two-dimensional layers stabilized by π–π-stacking interactions. 1 showed spin transition between the 3HS-1LS and 1.5HS-2.5LS states around 200 K, while 2 showed spin-crossover between the 4LS and 2LS-2HS states above 300 K. A modified indium–tin oxide (ITO) electrode was fabricated by soaking the ITO in a solution of 1 . The resultant electrode showed reversible redox waves attributed to the original redox processes of iron(II)/iron(III).
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