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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Electron deficient nonplanar beta-octachlorovanadyl-porphyrin as a highly efficient and selective epoxidation catalyst for olefins
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Electron deficient nonplanar beta-octachlorovanadyl-porphyrin as a highly efficient and selective epoxidation catalyst for olefins

机译:电子不足的非平面β-八氯钒氧-卟啉作为烯烃的高效选择性环氧化催化剂

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摘要

We have synthesized 2,3,7,8,12,13,17,18-octachloro-meso-tetraphenylporphyrinatooxidovanadium(IV) (VOTPPCl8) and characterized by various spectroscopic (UV-Vis, IR and EPR) techniques, MALDI-TOF mass spectrometry and elemental analysis. The DFT optimized structure of VOTPPCl8 in CH3CN exhibited a highly nonplanar saddle shape conformation of the porphyrin macrocycle. The cyclic voltammogram of VOTPPCl8 showed a 500 mV anodic shift in the first ring reduction potential and 220 mV in the first ring oxidation potential compared to VOTPP indicating the electron deficient nature of the porphyrin p-system and further proving the existence of a nonplanar conformation of the macrocycle in solution. Further, VOTPPCl8 exhibited very high thermal stability till 390 degrees C as indicated in its thermogram. The oxidation state of the metal ion (V-IV) was confirmed by EPR spectroscopy and VOTPPCl8 exhibited an axial spectrum which corresponds to the axially compressed d(xy)(1) configuration. VOTPPCl8 was utilised for the selective epoxidation of various olefins in good yields with very high TOF numbers (6566-9650 h(-1)) in the presence of H2O2 as an oxidant and NaHCO3 as a promoter in a CH3CN/H2O mixture. The oxidoper-oxidovanadium(V) species is expected to be the intermediate during the catalytic reaction which is probed by V-51 NMR spectroscopy and MALDI-TOF mass analysis. Notably, VOTPPCl8 is stable after the catalytic reaction and doesn't form a mu-oxo dimer due to the highly electron deficient nonplanar porphyrin core and can be reused for several cycles.
机译:我们已经合成了2,3,7,8,12,13,17,18-八氯-间位-四苯基卟啉对氧化钒(IV)(VOTPPCl8),并通过各种分光镜(UV-Vis,IR和EPR)技术进行了表征,MALDI-TOF质量光谱分析和元素分析。 CH3CN中VOTPPCl8的DFT优化结构显示了卟啉大环的高度非平面鞍形构象。与VOTPP相比,VOTPPCl8的循环伏安图显示,第一环还原电势的阳极位移为500 mV,第一环氧化电势的阳极位移为220 mV,这表明卟啉p系统具有电子缺陷性质,并进一步证明存在非平面构象。解决方案中的宏周期。此外,如其热分析图中所示,VOTPPCl8表现出很高的热稳定性,直到390摄氏度为止。通过EPR光谱法确认了金属离子(V-IV)的氧化态,并且VOTPPCl8表现出对应于轴向压缩的d(xy)(1)构型的轴向光谱。在H3O2作为氧化剂和NaHCO3作为促进剂的情况下,在CH3CN / H2O混合物中,使用VOTPPCl8以很高的TOF值(6566-9650 h(-1))以高收率选择性地进行各种烯烃的选择性环氧化。预计oxyoper-oxidovanadium(V)物种是催化反应过程中的中间产物,可通过V-51 NMR光谱和MALDI-TOF质量分析进行探测。值得注意的是,由于高度缺乏电子的非平面卟啉核,VOTPPCl8在催化反应后稳定并且不会形成mu-oxo二聚体,并且可以重复使用多个周期。

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