Group 2 Mediated Dehydrocoupling

This book presents an in-depth study into the utility of σ-bond metathesis in Group 2 mediated reactivity. A comprehensive introduction defines the state of the art in both Group 2 mediated catalysis and dehydrocoupling. Structural investigations giving rise to a range of mixed s-block metal hydride...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριος συγγραφέας: Liptrot, David J. (Συγγραφέας)
Συγγραφή απο Οργανισμό/Αρχή: SpringerLink (Online service)
Μορφή: Ηλεκτρονική πηγή Ηλ. βιβλίο
Γλώσσα:English
Έκδοση: Cham : Springer International Publishing : Imprint: Springer, 2016.
Έκδοση:1st ed. 2015.
Σειρά:Springer Theses, Recognizing Outstanding Ph.D. Research,
Θέματα:
Διαθέσιμο Online:Full Text via HEAL-Link
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245 1 0 |a Group 2 Mediated Dehydrocoupling  |h [electronic resource] /  |c by David J. Liptrot. 
250 |a 1st ed. 2015. 
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300 |a XV, 162 p. 169 illus., 3 illus. in color.  |b online resource. 
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490 1 |a Springer Theses, Recognizing Outstanding Ph.D. Research,  |x 2190-5053 
505 0 |a Introduction -- Group 1-Group 2 Bimetallic Alkyls and Hydrides -- Silicon-nitrogen Dehydrocoupling -- Boron-nitrogen Dehydrocoupling -- Single Electron Transfer Steps in Group 2 Catalysis -- Summary -- Future Work. 
520 |a This book presents an in-depth study into the utility of σ-bond metathesis in Group 2 mediated reactivity. A comprehensive introduction defines the state of the art in both Group 2 mediated catalysis and dehydrocoupling. Structural investigations giving rise to a range of mixed s-block metal hydrides including a remarkable dodecabimetallic decahydride are then described. Subsequent extensive mechanistic work focussing on both silicon-nitrogen and boron-nitrogen dehydrocoupling gives insights into both congeneric effects down Group 2 and ligand effects centring upon magnesium. These studies show the striking effects of these factors, as well as the electronic nature of the hydridic coupling partner.  Finally, the unprecedented introduction of single-electron transfer steps into Group 2 catalytic manifolds is described. The use of the stable radical TEMPO to induce single-electron transfer to substituents bound to Group 2 centres coupled with σ-bond metathesis allows a novel hydrogen release from silanes. 
650 0 |a Chemistry. 
650 0 |a Organometallic chemistry. 
650 0 |a Chemistry, Physical and theoretical. 
650 0 |a Catalysis. 
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650 2 4 |a Catalysis. 
650 2 4 |a Organometallic Chemistry. 
650 2 4 |a Theoretical and Computational Chemistry. 
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830 0 |a Springer Theses, Recognizing Outstanding Ph.D. Research,  |x 2190-5053 
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950 |a Chemistry and Materials Science (Springer-11644)