化学
次黄嘌呤
黄嘌呤
咪唑
原甲酸三乙酯
溴化物
氯化物
药物化学
铁
单体
立体化学
无机化学
有机化学
酶
催化作用
聚合物
作者
Chester M. Mikulski,Monica L. Bayne,Scott Grossman,Michele Gaul,Amy Renn,Donna L. Staley,Nicholas M. Karayannis
标识
DOI:10.1080/00958978909408865
摘要
Abstract Complexes of the type Fe(LH)3LX2 (LH α xanthine or hypoxanthine; X α Cl or Br) were synthesized by refluxing 2:1 molar mixtures of LH and FeX3, in triethyl orthoformate-ethyl acetate for one week. Characterization studies suggest that the new complexes are hexacoordinated and monomeric, involving a cis-FeN4X2 arrangement of the terminal ligands around the Fe3 + ion. The hypoxanthine ligands probably bind via the N7 imidazole nitrogen to Fe(III). In the case of the xanthine complexes, the N7 and N9 imidazole nitrogens are considered as about equally likely to function as the binding site of the terminal neutral and monoanionic xanthine ligands.
科研通智能强力驱动
Strongly Powered by AbleSci AI