Reprint
Coordination Chemistry of Silicon
Edited by
March 2019
226 pages
- ISBN978-3-03897-638-7 (Paperback)
- ISBN978-3-03897-639-4 (PDF)
This book is a reprint of the Special Issue Coordination Chemistry of Silicon that was published in
Chemistry & Materials Science
Summary
The chemistry of silicon has always been a field of major concern due to its proximity to carbon on the periodic table. From the molecular chemist’s viewpoint, one of the most interesting differences between carbon and silicon is their divergent coordination behavior. In fact, silicon is prone to form hyper-coordinate organosilicon complexes, and, as conveyed by reports in the literature, highly sophisticated ligand systems are required to furnish low-coordinate organosilicon complexes. Tremendous progress in experimental, as well as computational, techniques has granted synthetic access to a broad range of coordination numbers for silicon, and the scientific endeavor, which was ongoing for decades, was rewarded with landmark discoveries in the field of organosilicon chemistry. Molecular congeners of silicon(0), as well as silicon oxides, were unveiled, and the prominent group 14 metalloid proved its applicability in homogenous catalysis as a supportive ligand or even as a center of catalytic activity. This book focuses on the most recent advances in the coordination chemistry of silicon with transition metals as well as main group elements, including the stabilization of low-valent silicon species through the coordination of electron donor ligands. Therefore, this book is associated with the development of novel synthetic methodologies, structural elucidations, bonding analysis, and also possible applications in catalysis or chemical transformations using related organosilicon compounds.
Format
- Paperback
License
© 2019 by the authors; CC BY-NC-ND license
Keywords
silanetriols; disiloxane tetrols; silsesquioxanes; condensation; molecular cage; platinum; primary silane; hydrido complex; oxidative addition; ligand-exchange reaction; X-ray crystallography; Si–Cl activation; germylene; digermene; digermacyclobutadiene; palladium; cluster; cyclic organopolysilane; template; bridging silylene ligand; isocyanide; hydrogen bonds; silicon; 2-silylpyrrolidines; stereochemistry; X-ray crystallography; Baird’s rule; computational chemistry; excited state aromaticity; Photostability; dye-sensitized solar cell; disilanylene polymer; photoreaction; surface modification; TiO2; silylene; germylene; N-heterocyclic carbene; oxidative addition; siloxanes; host-guest chemistry; supramolecular chemistry; main group coordination chemistry; hydrogen bonding; adsorption; bond activation; bonding analysis; density functional theory; distorted coordination; molecular orbital analysis; silicon surfaces; disilene; functionalization; π-electron systems; silicon; N-heterocyclic carbenes; bromosilylenes; silyliumylidenes; dehydrobromination; silicon cluster; siliconoid; nanoparticle; computation; silicon; N-heterocyclic carbenes; silyliumylidenes; small molecule activation; mechanistic insights; organosilicon; reductant; N-Heterocyclic tetrylene; salt-free; germanium; germanethione; germathioacid chloride; N-heterocyclic carbines; α-chloro-ω-hydrooligosilane; titanium; ruthenium; dehydrogenative alkoxylation; cluster; isomerization; silicon; siliconoid; subvalent compounds; AIM; DFT; intermetallic bond; 29Si NMR spectroscopy; X-ray diffraction; n/a