Hani Amouri, Michel Gruselle
Chirality in Transition Metal Chemistry
Molecules, Supramolecular Assemblies and Materials
Herausgegeben:Woollins, Derek; Atwood, David A.; Crabtree, Robert H.; Mayer, Gerd
Hani Amouri, Michel Gruselle
Chirality in Transition Metal Chemistry
Molecules, Supramolecular Assemblies and Materials
Herausgegeben:Woollins, Derek; Atwood, David A.; Crabtree, Robert H.; Mayer, Gerd
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The first book about chirality as it applies to transition metals, Chirality in Transition Metal Chemistry uses practical applications and real world examples to introduce readers to this new field of inorganic chemistry.
Das neueste Werk in der Serie "Inorganic Chemistry Advanced Textbook" betrachtet die unterschiedlichen Eigenschaften von Enantiomeren von organometallischen und supramolekularen Systemen.
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The first book about chirality as it applies to transition metals, Chirality in Transition Metal Chemistry uses practical applications and real world examples to introduce readers to this new field of inorganic chemistry.
Das neueste Werk in der Serie "Inorganic Chemistry Advanced Textbook" betrachtet die unterschiedlichen Eigenschaften von Enantiomeren von organometallischen und supramolekularen Systemen.
Das neueste Werk in der Serie "Inorganic Chemistry Advanced Textbook" betrachtet die unterschiedlichen Eigenschaften von Enantiomeren von organometallischen und supramolekularen Systemen.
Produktdetails
- Produktdetails
- Inorganic Chemistry: A Textbook Series
- Verlag: Wiley & Sons
- 1. Auflage
- Seitenzahl: 272
- Erscheinungstermin: 1. Dezember 2008
- Englisch
- Abmessung: 241mm x 185mm x 15mm
- Gewicht: 580g
- ISBN-13: 9780470060544
- ISBN-10: 0470060549
- Artikelnr.: 25055448
- Inorganic Chemistry: A Textbook Series
- Verlag: Wiley & Sons
- 1. Auflage
- Seitenzahl: 272
- Erscheinungstermin: 1. Dezember 2008
- Englisch
- Abmessung: 241mm x 185mm x 15mm
- Gewicht: 580g
- ISBN-13: 9780470060544
- ISBN-10: 0470060549
- Artikelnr.: 25055448
Haniel Amouri, was born in Anapolis Goias (Brazil) and obtained his Ph.D. degree (1987) in chemistry from Universite Louis Pasteur Strasbourg (France), with Professor John A. Osborn, on the subject of homogeneous catalysis (hydrogenation). In 1988 he spent one year at Gif-sur-Yvette (France) as a post-doctoral fellow with Dr Hugh Felkin where he studied C-H activation of saturated hydrocarbon with transition metal polyhydrides. In 1992-1993 he spent one year at UC-Berkeley (USA) with Professor K. Peter C. Vollhardt and was working on the synthesis of oligocyclopentadienyl metal complex and their behaviour as electron transfer reagents. He is a Research Director in CNRS and is currently the director of the 'ARC' group (Auto-assemblage, Reconnaissance et Chiralite) of the IPCM at Universite Pierre et Marie Curie Paris-6. His main research interests are chirality, organometallic and coordination chemistry, and he has had over 90 research papers and reviews published in international scientific journals. Michel Gruselle was born in Decazeville (France) and obtained his Ph.D. degree (doctorat d'Etat) in the CNRS laboratory of Thiais, a suburb of Paris, in 1975 with Dr Daniel Lefort where he worked on stereochemical problems in radical chemistry. In 1974 he joined Bianca Tchoubar's group and started working on nitrogen activation by organometallic complexes, and he spent some time collaborating with Prof. A.E. Shilov in Moscow. he is a Research Director in CNRS at Universite Pierre et Marie Curie Paris-6 and was the director of the ARC group (Auto-assemblage, Reconnaissance et Chiralite) at the IPCM from 1996-2000. His main research interests a4re enantioselective synthesis in coordination chemistry and in material science and he has had over 110 research papers and reviews published in international scientific journals.
Foreword by Alex von Zelewsky 1.Introduction 2 Chirality and enantiomers
2.1 Chirality 2.2 Enantiomers and racemic compounds 2.3 Absolute
configurations and system descriptors 2.4 Physical properties of
enantiomers and racemics 2.5 Principles of resolution and preparation of
enantiomers 2.6 Summary 3 Some examples of chiral organometallic complexes
and asymmetric catalysis 3.1 Chirality at metal half-sandwich compounds 3.2
Chiral-at-metal complexes in organic synthesis 3.3 Asymmetric catalysis by
chiral complexes 4 Chiral recognition in organometallic and coordination
compounds 4.2 Chiral recognition using the chiral anion strategy: 4.3 Brief
introduction to DNA discrimination by octahedral polypyridyl metal
complexes: 5 Chirality in supramolecular coordination compounds 5.1
Self-assembly of chiral polynuclear complexes from achiral building units.
5.2 Chirality transfer in polynuclear complexes: Enantioselective Synthesis
6 Chiral enantiopure molecular materials 6.1 General considerations 6.2
Conductors 6.3 Metallomesogens 6.4 Porous metal-organic coordination
networks (MOCN) 6.5 Molecular magnets 6.6 Chiral surfaces 6.7 Summary
2.1 Chirality 2.2 Enantiomers and racemic compounds 2.3 Absolute
configurations and system descriptors 2.4 Physical properties of
enantiomers and racemics 2.5 Principles of resolution and preparation of
enantiomers 2.6 Summary 3 Some examples of chiral organometallic complexes
and asymmetric catalysis 3.1 Chirality at metal half-sandwich compounds 3.2
Chiral-at-metal complexes in organic synthesis 3.3 Asymmetric catalysis by
chiral complexes 4 Chiral recognition in organometallic and coordination
compounds 4.2 Chiral recognition using the chiral anion strategy: 4.3 Brief
introduction to DNA discrimination by octahedral polypyridyl metal
complexes: 5 Chirality in supramolecular coordination compounds 5.1
Self-assembly of chiral polynuclear complexes from achiral building units.
5.2 Chirality transfer in polynuclear complexes: Enantioselective Synthesis
6 Chiral enantiopure molecular materials 6.1 General considerations 6.2
Conductors 6.3 Metallomesogens 6.4 Porous metal-organic coordination
networks (MOCN) 6.5 Molecular magnets 6.6 Chiral surfaces 6.7 Summary
Foreword by Alex von Zelewsky 1.Introduction 2 Chirality and enantiomers
2.1 Chirality 2.2 Enantiomers and racemic compounds 2.3 Absolute
configurations and system descriptors 2.4 Physical properties of
enantiomers and racemics 2.5 Principles of resolution and preparation of
enantiomers 2.6 Summary 3 Some examples of chiral organometallic complexes
and asymmetric catalysis 3.1 Chirality at metal half-sandwich compounds 3.2
Chiral-at-metal complexes in organic synthesis 3.3 Asymmetric catalysis by
chiral complexes 4 Chiral recognition in organometallic and coordination
compounds 4.2 Chiral recognition using the chiral anion strategy: 4.3 Brief
introduction to DNA discrimination by octahedral polypyridyl metal
complexes: 5 Chirality in supramolecular coordination compounds 5.1
Self-assembly of chiral polynuclear complexes from achiral building units.
5.2 Chirality transfer in polynuclear complexes: Enantioselective Synthesis
6 Chiral enantiopure molecular materials 6.1 General considerations 6.2
Conductors 6.3 Metallomesogens 6.4 Porous metal-organic coordination
networks (MOCN) 6.5 Molecular magnets 6.6 Chiral surfaces 6.7 Summary
2.1 Chirality 2.2 Enantiomers and racemic compounds 2.3 Absolute
configurations and system descriptors 2.4 Physical properties of
enantiomers and racemics 2.5 Principles of resolution and preparation of
enantiomers 2.6 Summary 3 Some examples of chiral organometallic complexes
and asymmetric catalysis 3.1 Chirality at metal half-sandwich compounds 3.2
Chiral-at-metal complexes in organic synthesis 3.3 Asymmetric catalysis by
chiral complexes 4 Chiral recognition in organometallic and coordination
compounds 4.2 Chiral recognition using the chiral anion strategy: 4.3 Brief
introduction to DNA discrimination by octahedral polypyridyl metal
complexes: 5 Chirality in supramolecular coordination compounds 5.1
Self-assembly of chiral polynuclear complexes from achiral building units.
5.2 Chirality transfer in polynuclear complexes: Enantioselective Synthesis
6 Chiral enantiopure molecular materials 6.1 General considerations 6.2
Conductors 6.3 Metallomesogens 6.4 Porous metal-organic coordination
networks (MOCN) 6.5 Molecular magnets 6.6 Chiral surfaces 6.7 Summary