摘要
合成了咪唑基尾式卟啉──5-邻[4-(1-咪唑基)丁氧基]苯基-10,15,20-三苯基卟啉(o-ImBPTPP)及其铁(Ⅲ)配合物[Fe(Ⅲ)(o-ImBPTPP)Cl],以元素分析、质谱、1HNMR、IR和紫外可见吸收光谱等进行了表征。初步研究了在氯仿和苯中某些含氮配体与铁(Ⅲ)配合物的轴向配位性质。结果表明,Fe(Ⅲ)(o-ImBPTPP)Cl通常与含氮配体生成低自旋的六配位加合物,但在苯溶液中与咪唑作用时,一定条件下还能生成稳定的高自旋五配位加合物。
A imidazolyl tailed porphyrin,5-[o-(1-imidazolyl) butoxy]phenyl-10,15,20-triphenyl porphyrin(o-ImBPTPP),and its iron(Ⅲ) coordination compound(Fe(Ⅲ)(o-ImBPTPP)Cl) were synthesized and identified by elementary analysis and mass spectrometry.The structures were confirmed by IR、1H NMR and UV-vis spectrometries.The coordinations of Fe(Ⅲ)(o-ImBPTPP) Cl with some nitrogeous ligands were studied.Usually Fe(Ⅲ)(o-ImBPTPP)Cl formed low-spin six-coordinate adducts with nitrogeous,but it could form a stable high-spin five-coordinate adduct with imidazole in benzene when the concentration of imidazole was lower.
出处
《高等学校化学学报》
CSCD
北大核心
1995年第2期163-167,共5页
Chemical Journal of Chinese Universities
基金
国家自然科学基金
广东省自然科学基金
南京大学配位化学国家重点实验室资助
兰州大学应用有机化学国家重点实验室资助
关键词
尾式卟啉
合成
性质
铁配合物
Tailed porphyrin
Tailed iron(Ⅲ) porphyrin
Synthesis
Properties