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678.84 --- 66.095.26 --- 678-128.2 --- Silicon-containing polymers. Silicones. Organosiloxane polymers. Siloxanes --- Polymerization --- Industries based on macromolecular materials. Rubber industry. Plastics industry--?-128.2 --- 678-128.2 Industries based on macromolecular materials. Rubber industry. Plastics industry--?-128.2 --- 66.095.26 Polymerization --- 678.84 Silicon-containing polymers. Silicones. Organosiloxane polymers. Siloxanes
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Breast implants -- Complications. --- Mammaplasty. --- Silicones -- Toxicology. --- Silicone Gels --- Breast Implants --- Silicones --- Prostheses and Implants --- Siloxanes --- Equipment and Supplies --- Analytical, Diagnostic and Therapeutic Techniques and Equipment --- Organosilicon Compounds --- Polymers --- Biomedical and Dental Materials --- Organic Chemicals --- Macromolecular Substances --- Manufactured Materials --- Chemicals and Drugs --- Technology, Industry, and Agriculture --- Technology, Industry, Agriculture --- Surgery - General and By Type --- Surgery & Anesthesiology --- Health & Biological Sciences --- Breast implants --- Complications. --- Toxicology.
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This reprint reports advances in the topic of Deep Eutectic Solvents regarding their use as green alternatives in different chemical applications. Studies on the extraction/preconcentration processes of pharmacologically relevant molecules, structural spectroscopic studies, and application in gas purification studies are reported. Two relevant reviews are also published in the context of carbon dioxide conversion and their use in the chemistry of transformations. This reprint therefore aims to summarize some of the pertinent issues in DES chemistry through relevant literature references.
absorption --- biogas --- deep eutectic solvents --- siloxanes --- materials --- API formulation --- gas sorbents --- ionothermal synthesis --- organic synthesis --- eutectic mixtures --- hydrogen bond acceptor --- hydrogen bond donor --- design of experiments --- Tauc plot --- band gap energy --- renewable energy --- electrochemical conversion --- carbon dioxide reduction --- functionalized ionic liquids (ILs) --- carbon dioxide transformation --- quercetin --- Deep Eutectic Solvents --- extraction --- preconcentration --- DESs water dilutions --- RP-HPLC-UV --- UHPLC-MS/MS --- recovery
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This reprint reports advances in the topic of Deep Eutectic Solvents regarding their use as green alternatives in different chemical applications. Studies on the extraction/preconcentration processes of pharmacologically relevant molecules, structural spectroscopic studies, and application in gas purification studies are reported. Two relevant reviews are also published in the context of carbon dioxide conversion and their use in the chemistry of transformations. This reprint therefore aims to summarize some of the pertinent issues in DES chemistry through relevant literature references.
Research & information: general --- Chemistry --- absorption --- biogas --- deep eutectic solvents --- siloxanes --- materials --- API formulation --- gas sorbents --- ionothermal synthesis --- organic synthesis --- eutectic mixtures --- hydrogen bond acceptor --- hydrogen bond donor --- design of experiments --- Tauc plot --- band gap energy --- renewable energy --- electrochemical conversion --- carbon dioxide reduction --- functionalized ionic liquids (ILs) --- carbon dioxide transformation --- quercetin --- Deep Eutectic Solvents --- extraction --- preconcentration --- DESs water dilutions --- RP-HPLC-UV --- UHPLC-MS/MS --- recovery --- absorption --- biogas --- deep eutectic solvents --- siloxanes --- materials --- API formulation --- gas sorbents --- ionothermal synthesis --- organic synthesis --- eutectic mixtures --- hydrogen bond acceptor --- hydrogen bond donor --- design of experiments --- Tauc plot --- band gap energy --- renewable energy --- electrochemical conversion --- carbon dioxide reduction --- functionalized ionic liquids (ILs) --- carbon dioxide transformation --- quercetin --- Deep Eutectic Solvents --- extraction --- preconcentration --- DESs water dilutions --- RP-HPLC-UV --- UHPLC-MS/MS --- recovery
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This reprint reports advances in the topic of Deep Eutectic Solvents regarding their use as green alternatives in different chemical applications. Studies on the extraction/preconcentration processes of pharmacologically relevant molecules, structural spectroscopic studies, and application in gas purification studies are reported. Two relevant reviews are also published in the context of carbon dioxide conversion and their use in the chemistry of transformations. This reprint therefore aims to summarize some of the pertinent issues in DES chemistry through relevant literature references.
Research & information: general --- Chemistry --- absorption --- biogas --- deep eutectic solvents --- siloxanes --- materials --- API formulation --- gas sorbents --- ionothermal synthesis --- organic synthesis --- eutectic mixtures --- hydrogen bond acceptor --- hydrogen bond donor --- design of experiments --- Tauc plot --- band gap energy --- renewable energy --- electrochemical conversion --- carbon dioxide reduction --- functionalized ionic liquids (ILs) --- carbon dioxide transformation --- quercetin --- Deep Eutectic Solvents --- extraction --- preconcentration --- DESs water dilutions --- RP-HPLC-UV --- UHPLC-MS/MS --- recovery
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Breast implants -- Complications. --- Mammaplasty. --- Silicones -- Toxicology. --- Breast implants --- Silicones --- Mammaplasty --- Breast Implants --- Safety --- Prostheses and Implants --- Siloxanes --- Accident Prevention --- Equipment and Supplies --- Organosilicon Compounds --- Polymers --- Accidents --- Organic Chemicals --- Macromolecular Substances --- Biomedical and Dental Materials --- Analytical, Diagnostic and Therapeutic Techniques and Equipment --- Public Health --- Chemicals and Drugs --- Manufactured Materials --- Environment and Public Health --- Health Care --- Technology, Industry, and Agriculture --- Technology, Industry, Agriculture --- Surgery - General and By Type --- Surgery & Anesthesiology --- Health & Biological Sciences --- Complications --- Toxicology --- Complications. --- Toxicology. --- Breast --- Breast reconstruction --- Mammoplasty --- Mastoplasty --- Reconstruction of the breast --- Organosiloxanes --- Siloxane polymers --- Reconstruction --- Surgery, Plastic --- Organosilicon compounds --- Silicon polymers --- Surgery
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Comprising 12 chapters, this book focuses on volatile methylsiloxanes (VMSs), the shorter-chained organosiloxanes, and reviews the main areas and environmental compartments where they have been found and studied. It opens with a detailed description of the structural and functional properties, toxic risks and possible transformations of VMSs in the environment and their main uses in various activities and products, as well as the identification of the main sources of emission. Further chapters examine the analytical strategies and protocols that have been used to address the quantification of VMSs, including the issue of possible cross-contaminations. The book also discusses the presence of VMSs in wastewater treatment plants (WWTPs) and in water bodies, their atmospheric fate and levels in biota, as well as occurrences of VMSs in remote areas of the world. It closes with a comprehensive conclusion and discussion on future directions for upcoming studies. This book is not intended as a finishing line, but rather as an important step towards improving our understanding of VMSs, to fuel new collaborations between research groups and/or with industry and lastly to convince more researchers to explore the mysteries of these ubiquitous, yet understudied, chemicals.
Siloxanes --- Environmental aspects. --- Oxosilanes --- Silicon compounds --- Environmental chemistry. --- Pollution. --- Environment. --- Analytical chemistry. --- Water. --- Environmental Chemistry. --- Pollution, general. --- Environment, general. --- Analytical Chemistry. --- Water, general. --- Hydrology --- Analysis, Chemical --- Analytic chemistry --- Chemical analysis --- Chemistry, Analytic --- Chemistry --- Chemical pollution --- Chemicals --- Contamination of environment --- Environmental pollution --- Pollution --- Contamination (Technology) --- Asbestos abatement --- Bioremediation --- Environmental engineering --- Environmental quality --- Factory and trade waste --- Hazardous waste site remediation --- Hazardous wastes --- In situ remediation --- Lead abatement --- Pollutants --- Refuse and refuse disposal --- Chemistry, Environmental --- Ecology --- Environmental aspects --- Balance of nature --- Biology --- Bionomics --- Ecological processes --- Ecological science --- Ecological sciences --- Environment --- Environmental biology --- Oecology --- Environmental sciences --- Population biology
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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.
cluster --- molecular orbital analysis --- bond activation --- X-ray diffraction --- silsesquioxanes --- digermacyclobutadiene --- intermetallic bond --- germanium --- computational chemistry --- ?-electron systems --- isocyanide --- X-ray crystallography --- cyclic organopolysilane --- disilene --- ruthenium --- platinum --- DFT --- Photostability --- silicon surfaces --- stereochemistry --- palladium --- distorted coordination --- 29Si NMR spectroscopy --- organosilicon --- disilanylene polymer --- Si–Cl activation --- adsorption --- AIM --- siliconoid --- nanoparticle --- disiloxane tetrols --- germylene --- hydrogen bonding --- TiO2 --- dehydrogenative alkoxylation --- siloxanes --- 2-silylpyrrolidines --- bonding analysis --- ?-chloro-?-hydrooligosilane --- hydrido complex --- oxidative addition --- photoreaction --- template --- surface modification --- titanium --- bromosilylenes --- host-guest chemistry --- hydrogen bonds --- salt-free --- N-heterocyclic carbines --- silicon cluster --- condensation --- silyliumylidenes --- Baird’s rule --- N-heterocyclic carbenes --- reductant --- main group coordination chemistry --- molecular cage --- subvalent compounds --- isomerization --- silanetriols --- germathioacid chloride --- dehydrobromination --- N-heterocyclic carbene --- mechanistic insights --- ligand-exchange reaction --- bridging silylene ligand --- dye-sensitized solar cell --- silylene --- computation --- functionalization --- silicon --- digermene --- N-Heterocyclic tetrylene --- density functional theory --- primary silane --- small molecule activation --- excited state aromaticity --- germanethione --- supramolecular chemistry
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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.
cluster --- molecular orbital analysis --- bond activation --- X-ray diffraction --- silsesquioxanes --- digermacyclobutadiene --- intermetallic bond --- germanium --- computational chemistry --- ?-electron systems --- isocyanide --- X-ray crystallography --- cyclic organopolysilane --- disilene --- ruthenium --- platinum --- DFT --- Photostability --- silicon surfaces --- stereochemistry --- palladium --- distorted coordination --- 29Si NMR spectroscopy --- organosilicon --- disilanylene polymer --- Si–Cl activation --- adsorption --- AIM --- siliconoid --- nanoparticle --- disiloxane tetrols --- germylene --- hydrogen bonding --- TiO2 --- dehydrogenative alkoxylation --- siloxanes --- 2-silylpyrrolidines --- bonding analysis --- ?-chloro-?-hydrooligosilane --- hydrido complex --- oxidative addition --- photoreaction --- template --- surface modification --- titanium --- bromosilylenes --- host-guest chemistry --- hydrogen bonds --- salt-free --- N-heterocyclic carbines --- silicon cluster --- condensation --- silyliumylidenes --- Baird’s rule --- N-heterocyclic carbenes --- reductant --- main group coordination chemistry --- molecular cage --- subvalent compounds --- isomerization --- silanetriols --- germathioacid chloride --- dehydrobromination --- N-heterocyclic carbene --- mechanistic insights --- ligand-exchange reaction --- bridging silylene ligand --- dye-sensitized solar cell --- silylene --- computation --- functionalization --- silicon --- digermene --- N-Heterocyclic tetrylene --- density functional theory --- primary silane --- small molecule activation --- excited state aromaticity --- germanethione --- supramolecular chemistry
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