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Effects of molecular confinement on structure and catalytic behaviour of metal phthalocyanine complexes encapsulated in zeolite-Y

机译:分子限制对Y型沸石中金属酞菁配合物结构和催化性能的影响

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Metal phthalocyanine complexes (MPc; M = V, Co and Cu) encapsulated in zeolite-Y have beenprepared by “in situ ligand synthesis” method and characterized by chemical and thermal analysesand FT-IR, diffuse reflectance UV-vis and EPR spectroscopic techniques. The studies haveprovided evidence for the encapsulation of MPc inside the supercages of zeolite-Y. The Pc moietyundergoes distortion from square planarity on encapsulation. Spectroscopic studies havedifferentiated the encapsulated and surface adsorbed MPc molecules. The encapsulated complexesexhibited enhanced styrene epoxidation activity with tert-butylhydroperoxide (TBHP) than the“neat” complexes in homogeneous medium. A comparative study has revealed that the activity andproduct selectivity of the encapsulated complexes vary with the central metal atom.
机译:通过“原位配体合成”方法制备了包裹在Y型沸石中的金属酞菁配合物(MPc; M = V,Co和Cu),并通过化学和热分析以及FT-IR,漫反射紫外可见和EPR光谱技术对其进行了表征。研究为MPc在Y型沸石超笼中的包埋提供了证据。在封装过程中,Pc部分经历了正方形平面的扭曲。光谱研究已区分了封装和表面吸附的MPc分子。与均相介质中的“纯”配合物相比,被包裹的配合物在叔丁基过氧化氢(TBHP)的作用下具有更高的苯乙烯环氧化活性。一项比较研究表明,包封的配合物的活性和产物选择性随中心金属原子而变化。

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