Titlebook: Catalysis by Unique Metal Ion Structures in Solid Matrices; From Science to Appl Gabriele Centi,Blanka Wichterlová,Alexis T. Bell Book 2001

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Asymmetric Oxidation of Sulphide on Metal Ion Planted in Mesoporous MCM-41,the proton exchanges with metal cation. Ti-MCM- 41 was the most active among the metal ion-planted MCM-41 for catalytic asymmetric oxidation of sulphide with hydrogen peroxide in the presence of optically active tartaric acid in dichloromethane.

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Book 2001udingthe distribution of framework Al atoms in Si-rich zeolites,distribution and siting of charge-exchanged metal cations, electronic,adsorptive and catalytic properties of metal cations, and correlationof metal cation structure and siting with catalytic activity.

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1568-2609 ects, includingthe distribution of framework Al atoms in Si-rich zeolites,distribution and siting of charge-exchanged metal cations, electronic,adsorptive and catalytic properties of metal cations, and correlationof metal cation structure and siting with catalytic activity.978-0-7923-6875-5978-94-010-0782-5Series ISSN 1568-2609

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José Baptista,Filipe Lima,Adelaide Cerveirasignificant role in the photocatalytic decomposition of NO, i.e., an electron transfer from the s orbital of the excited state of Cu. or Ag. ions into the π. antibonding orbital of NO initiates the decomposition reaction of NO.

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Photocatalysis of Cations Incorporated within Zeolites,significant role in the photocatalytic decomposition of NO, i.e., an electron transfer from the s orbital of the excited state of Cu. or Ag. ions into the π. antibonding orbital of NO initiates the decomposition reaction of NO.

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Book 2001from the same cationic species containedin a bulk oxide or supported on amorphous carriers. This subject istreated to an extensive review, showing how an understanding of it isessential to the development of a new generation of solid catalysts.There are also exciting opportunities to shape the catal

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Electronic Structure of Transition-Metal Ion Containing Zeolites,dvanced to a level, still rapidly developing, where relatively large systems, including periodic systems, can be handled by all-electron calculations from the first principles. It is now possible to optimize geometries of zeolites with different cations and framework substituents and to predict their structural and electronic properties.

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