Since the classic work Metal-Catalyzed Oxidations of Organic Compounds (edited by R A Sheldon and J K Kochi, 1991), no book has been devoted to advances in the field of biomimetic oxidations, which was created nearly 18 years ago. This expanding research field is covered in this volume. All the different aspects of the modeling of oxidations catalyzed by metalloenzymes are dealt with.This invaluable book will be useful to postgraduates as well as researchers in academia and industry, and will also benefit second year university students.
This new edition describes the state of the art regarding metal complexes of N4-ligands, such as porphyrins and phthalocyanines. Volume 2 focuses on the electro assisted use of N4 complexes as biomimetic models for studying several biological redox processes. It focuses on molecular oxygen transport and catalytic activation to mimic monooxygenase enzymes of the cytochrome P450 in particular. It also examines N4 complexes’ use as catalysts for the oxidative degradation of various types of pollutants (organo-halides, for example) and residual wastes. The remarkable activity of these complexes towards a large number of significantly relevant biological compounds makes them excellent candidates as electrode modifiers for electrochemical sensing. This volume also discusses applications of N4 Macrocyclic Metal Complexes to photoelectrochemistry and photocatalysis, and concludes with an exciting section on Electrosynthesis of N4.
How I Feel books help children ages 2-6 recognize and identify their emotions and give them a vocabulary to describe what they are feeling. If children can name an emotion, they are on their way to understanding it. And when children can talk about what they are feeling, their parents will be better able to help them.Features: -- 8 x 8 24-page hardcover or -- softcover full-color picture book -- Each book includes an activity card and reusable stickers -- Question-answer format stimulates conversation between parent and child
This volume provides an in-depth overview of the chemistry of metalloporphyrins as oxidation catalysts in chemical and biological systems. It discusses practical techniques for the synthesis of metalloporphyrins and introduces useful methods of immobilization to improve their synthetic utility. Detailed discussions of underlying mechanistic features are provided.
Reviews the physiochemical properties of natural and synthetic porphyrins, phthalocyanine and its polymers, and their numerous complexes. Analyzes specific features of the processes of their formation and dissociation, the mechanisms of these processes, and conditions for further coordination on metalloporphyrins. Treats their ionization and dissociation, structural aspects, electronic effects of coordination and their manifestation in the optical, coordination, acid-base and oxidation-reduction properties.
Oxidative catalysis by metalloporphyrin systems occupies a prominent role in the current research in the fields of chemical and biological catalysis. Our particular interest and approach has been to collect in the same volume papers dealing with both the chemical and biological aspects of the reactivity of heme systems because of the realization that a better understanding of the complementary discipline can be extremely useful for the researchers from either field. The current progress of the research on synthetic metalloporphyrin catalysts has led to the development of several systems that are able to reproduce the heme-enzyme mediated oxygenation and oxidation reactions, at least in terms of reaction types, mechanisms and often rates. These achievements have stimulated the of creating metalloporphyrin catalysts which are both ambitious project efficient and stable enough to become competitive for large-scale industrial processes. Although this project is still far from being realized, the efforts in this direction parallel those aimed at the application of heme enzymes to chemical technologies, e. g. for the mild, selective oxidation of organics or the detoxification of pollutants. Both the two approaches will be advantageous because while the enzyme systems can achieve selectivities which are probably unattainable by synthetic catalysts, the latter can be active under experimental conditions that would readily inactivate the enzymes.
