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Suzuki–Miyaura Cross-Coupling Reaction and Potential Applications

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ISBN: 9783038425564 9783038425571 Year: Pages: VIII, 264 Language: English
Publisher: MDPI - Multidisciplinary Digital Publishing Institute
Subject: Chemistry (General)
Added to DOAB on : 2017-12-04 11:24:07
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Suzuki–Miyaura cross-coupling remains a powerful tool in organic synthesis for C–C bond formation and has various industrial applications, for example, the synthesis of pharmaceuticals and materials. Intensive research efforts are being made into finding ways of improving and expanding the scope of this process, and the development of more efficient catalytic systems for this extremely important reaction is still a hot research topic of enormous academic and industrial interest. This Special Issue, consisting of four reviews, two communications and six articles, focuses on recent promising research and novel trends in the broad field of Suzuki–Miyaura cross-coupling employing a range of different palladium catalysts. Homogeneous or heterogeneous catalysis in organic or aqueous medium, using conventional conditions or non-conventional techniques such as microwave and ultrasound irradiation, grinding and photo-activated processes as green chemistry approaches, as well as continuous flow technology are included. The catalysts described herein are unsupported metal complexes, catalysts immobilized on solid supports, ligand-free catalytic systems or metal nanoparticles.

Multi-Walled Carbon Nanotubes

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ISBN: 9783039212293 / 9783039212309 Year: Pages: 184 DOI: 10.3390/books978-3-03921-230-9 Language: eng
Publisher: MDPI - Multidisciplinary Digital Publishing Institute
Subject: Technology (General) --- Chemical Engineering
Added to DOAB on : 2019-08-28 11:21:27
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Since their discovery, multi-walled carbon nanotubes (MWCNTs) have received tremendous attention due to their unique electrical, optical, physical, chemical, and mechanical properties. Remarkable advances have been made in the synthesis, purification, structural characterization, functionalization, and application of MWCNTs. Their particular characteristics make them well suited for a plethora of applications in a number of fields, namely nanoelectronics, nanofluids, energy management, (electro)catalysis, materials science, construction of (bio)sensors based on different detection schemes, multifunctional nanoprobes for biomedical imaging, and sorbents for sample preparation or removal of contaminants from wastewater. They are also useful as anti-bacterial agents, drug delivery nanocarriers, etc. The current relevant application areas are countless. This Special Issue presents original research and review articles that address advances, trends, challenges, and future perspectives regarding synthetic routes, structural features, properties, behaviors, and industrial or scientific applications of MWCNTs in established and emerging areas.

Keywords

water based nanofluid --- carbon-nanotubes --- boundary layer --- heat generation --- thermal radiation --- curved stretching sheet --- numerical solution --- Single-Walled Carbon Nanotube (SWCNT) --- Multi-Walled Carbon Nanotube (MWCNT) --- MHD --- Casson model --- stretching sheet --- non-linear thermal radiation --- HAM --- zeolitic imidazolate framework --- multi-walled carbon nanotubes --- magnetic solid phase extraction --- organochlorine pesticides --- agricultural irrigation water --- Pd-CNT nanohybrids --- functionalized CNTs --- polarity --- semi-homogeneous catalysis --- heck reaction --- nanomaterials --- multi-walled carbon nanotubes --- synthesis methods --- electrochemical properties --- electrochemical sensors --- electroanalysis --- sensing applications --- multiwalled carbon nanotubes --- gold(I) --- gold(III) --- adsorption --- elution --- gold nanoparticles --- adsorption --- multi-walled carbon nanotubes --- nonylphenol --- kinetics --- multi-walled carbon nanotubes --- graphene oxide --- cerium oxide --- lubricating oil additives --- multi-wall carbon nanotube (MWCNT) --- azide-alkyne click chemistry --- RAFT polymerization --- PMMA --- carbon nanotubes --- composites --- radar absorbing materials --- complex permittivity --- chloride diffusion --- cement mortars --- carbon nanotubes --- mechanical properties --- electrical properties --- hydrophobic drugs --- drug delivery --- functionalized carbon nanotubes --- dissolution rate --- nanomedicine --- polymeric composites --- silicone rubber --- Ionic liquid --- carbon materials --- structural --- EMI shielding --- n/a

Catalysts Deactivation, Poisoning and Regeneration

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ISBN: 9783039215461 / 9783039215478 Year: Pages: 254 DOI: 10.3390/books978-3-03921-547-8 Language: eng
Publisher: MDPI - Multidisciplinary Digital Publishing Institute
Subject: Technology (General) --- Chemical Engineering
Added to DOAB on : 2019-12-09 11:49:15
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Catalyst lifetime represents one of the most crucial economic aspects in industrial catalytic processes, due to costly shutdowns, catalyst replacements, and proper disposal of spent materials. Not surprisingly, there is considerable motivation to understand and treat catalyst deactivation, poisoning, and regeneration, which causes this research topic to continue to grow. The complexity of catalyst poisoning obviously increases along with the increasing use of biomass/waste-derived/residual feedstocks and with requirements for cleaner and novel sustainable processes. This book collects 15 research papers providing insights into several scientific and technical aspects of catalyst poisoning and deactivation, proposing more tolerant catalyst formulations, and exploring possible regeneration strategies.

Keywords

hydrogenation --- copper --- catalyst --- water --- deactivation --- octanal --- octanol --- V2O5–WO3/TiO2 catalysts --- poisoning --- sulfur-containing sodium salts --- SO3 --- NO removal --- Cu/SSZ-13 --- NH3-SCR --- sodium ions --- deactivation mechanism --- sulfur poisoning --- coke deposition --- in situ regeneration --- Co-Zn/H-Beta --- NOx reduction by C3H8 --- catalyst deactivation --- diesel --- natural gas --- SEM --- TEM --- poisoning --- oxygen storage capacity --- thermal stability --- cyclic operation --- deactivation --- oxysulfate --- oxysulfide --- Selective Catalytic Reduction (SCR) --- SO2 poisoning --- Low-temperature catalyst --- nitrogen oxides --- nitrous oxide --- dry reforming of methane --- nickel catalysts --- barium carbonate --- deactivation by coking --- catalytic methane combustion --- exhaust gas --- catalyst durability --- Liquefied natural gas --- biogas --- vehicle emission control --- sulfur deactivation --- catalyst deactivation --- aluminum sulfate --- palladium sulfate --- regeneration --- phthalic anhydride --- vanadia-titania catalyst --- unusual deactivation --- physico-chemical characterization --- over-reduction --- vanadia species --- coke deposition --- DeNOx --- MW incinerator --- deactivation --- ammonium sulfates --- regeneration --- washing --- CO2 reforming --- Ni-catalyst --- syngas --- tetragonal zirconia --- phase stabilization --- CPO reactor --- effect of flow rate --- deactivation --- iso-octane --- Rh catalysts --- Rh --- homogeneous catalysis --- catalyst deactivation --- n/a

Amide Bond Activation

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ISBN: 9783039212033 / 9783039212040 Year: Pages: 466 DOI: 10.3390/books978-3-03921-204-0 Language: eng
Publisher: MDPI - Multidisciplinary Digital Publishing Institute
Subject: Science (General) --- Chemistry (General)
Added to DOAB on : 2019-08-28 11:21:27
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The amide bond represents a privileged motif in chemistry. The recent years have witnessed an explosion of interest in the development of new chemical transformations of amides. These developments cover an impressive range of catalytic N–C bond activation in electrophilic, Lewis acid, radical, and nucleophilic reaction pathways, among other transformations. Equally relevant are structural and theoretical studies that provide the basis for chemoselective manipulation of amidic resonance. This monograph on amide bonds offers a broad survey of recent advances in activation of amides and addresses various approaches in the field.

Keywords

fumardiamide --- primaquine --- succindiamide --- Michael acceptor --- biofilm eradication --- antibacterial screening --- antiviral activity --- cytostatic activity --- N,N-dimethylformamide --- DMF --- N,N-dimethylacetamide --- DMAc --- amination --- amidation --- thioamidation --- formylation --- carbonylation --- cyanation --- insertion --- cyclization --- amide --- arynes --- insertion --- activation --- heterocycles --- organic synthesis --- multi-component coupling reaction --- aryl thioamides --- thiourea --- C-H/C-N activation --- C-S formation --- transition-metal-free --- rotational barrier energy --- amide bond --- nuclear magnetic resonance --- kinetic --- density functional theory --- non planar amide --- base-catalyed hydrolysis --- water solvation --- entropy --- transamidation --- amide --- amine --- catalyst --- catalysis --- acylative cross-coupling --- trialkylborane --- amide activation --- palladium --- N-heterocyclic carbene --- ruthenium (Ru) --- N-heterocyclic carbenes (NHCs) --- homogeneous catalysis --- in situ --- amide bonds --- synthesis --- density functional theory --- cis/trans isomerization --- secondary amides --- dipeptides --- steric effects --- tert-butyl --- additivity principle --- amino acid transporters --- amide bond --- gemcitabine prodrug --- metabolic stability --- pancreatic cancer cells --- pharmacokinetics --- peptide bond cleavage --- amide bond resonance --- twisted amides --- enzymes --- metal complexes --- catalysts --- amide C–N bond activation --- nickel catalysis --- amidation --- DFT study --- reaction thermodynamics --- amide resonance --- anomeric effect --- HERON reaction --- pyramidal amides --- physical organic chemistry --- reaction mechanism --- amide --- activation --- amidicity --- carbonylicity --- transamidation --- acyl transfer --- excited state --- Suzuki-Miyaura --- cross-coupling --- aryl esters --- C–O activation --- Pd-catalysis --- amides --- carbanions --- C–H acidity --- nitro-aci tautomerism --- molecular dynamics --- density-functional theory --- alkynes --- C–H bond cleavage --- C–N bond cleavage --- cyclopentadienyl complexes --- N-(1-naphthyl)acetamide --- rhodium --- [2+2+2] annulation --- amide bond --- sulfonamide bond --- alkynes --- addition reaction --- aminoacylation --- aminosulfonylation --- pre-catalysts --- palladium catalysis --- amide bond activation --- ester bond activation --- cross-coupling --- amide bond --- bridged lactams --- twisted amides --- amides --- Winkler-Dunitz parameters --- N–C activation --- hypersensitivity --- nitrogen heterocycles --- distortion --- bridged sultams --- amides --- C-N ? bond cleavage --- sodium --- crown ether --- amide hydrolysis --- model compound --- intramolecular catalysis --- twisted amide --- protease --- intein --- C-H functionalization --- directing groups --- amides --- transition metals --- catalysis

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eng (3)

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2019 (3)

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