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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Rhenium(i) tricarbonyl complex of 5,20-bis(p-tolyl)-10,15-bis(p- methoxyphenyl)-21-selenaporphyrin: First X-ray structural characterization of metal complex of 21-selenaporphyrin
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Rhenium(i) tricarbonyl complex of 5,20-bis(p-tolyl)-10,15-bis(p- methoxyphenyl)-21-selenaporphyrin: First X-ray structural characterization of metal complex of 21-selenaporphyrin

机译:5,20-双(对甲苯基)-10,15-双(对甲氧基苯基)-21-硒卟啉的tri(i)三羰基配合物:21-硒卟啉金属配合物的第一个X射线结构表征

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摘要

Synthesis and first structural characterization of hexa coordinated rhenium(i) tricarbonyl complex of 5,20-bis(p-tolyl)-10,15-bis(p-methoxyphenyl)- 21-selenaporphyrin 3 are described. The Re(i) complex of 21-selenaporphyrin 3 was synthesized by treating free base 21-selenaporphyrin in 1,2-dichlorobenzene with Re(CO)_5Cl at reflux for 7 h and analyzed using mass, NMR, FT-IR, UV-vis and electrochemical techniques. The first structure of metal complex of 21-selenaporphyrin was determined by X-ray single crystal analysis. The crystal structure revealed that the Re(CO)_3 coordinates to two of the three inner nitrogens and one selenium to produce compound 3. The selenophene ring bent towards the Re(i) ion and the selenium is displaced by 0.41 ? from the mean plane of 24-atoms to coordinate with Re(i) ion in η~1- fashion. The 21-selenaporphyrin is distorted in compound 3 compared to free base 21-selenaporphyrin. ~1H and ~(13)C NMR studies indicated that compound 3 exhibits fluxional behaviour in coordination mode of binding in solution. The compound 3 is highly stable and does not undergo decomplexation under acidic conditions. The absorption spectra showed three broad Q-bands and splitted Soret band and electrochemical studies indicated that compound 3 is stable under redox conditions. This journal is
机译:描述了5,20-双(对甲苯基)-10,15-双(对甲氧基苯基)-21-硒卟啉3的六配位rh(i)三羰基配合物的合成和第一结构表征。通过用Re(CO)_5Cl回流处理1,2-二氯苯中的游离碱21-硒卟啉7小时来合成21-硒卟啉3的Re(i)配合物,并使用质量,NMR,FT-IR,UV-可见和电化学技术。通过X射线单晶分析确定21-硒卟啉金属配合物的第一结构。晶体结构表明,Re(CO)_3与三个内部氮原子中的两个和一个硒配位以生成化合物3。硒烯环向Re(i)离子弯曲,硒原子错位了0.41?1。从24个原子的平均平面以η〜1-的方式与Re(i)离子配位。与游离碱21-硒卟啉相比,21-硒卟啉在化合物3中变形。 〜1H和〜(13)C NMR研究表明,化合物3在溶液中的结合配位模式下表现出通量行为。化合物3是高度稳定的,并且在酸性条件下不发生分解。吸收光谱显示三个宽的Q波段和分裂的Soret波段,电化学研究表明化合物3在氧化还原条件下是稳定的。这本日记是

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