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Homogeneous catalysis.

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"Catalysis Communications aims to provide rapid publication of significant, novel, and timely research results [on] homogeneous, heterogeneous, and enzymatic catalysis."--Publisher

Enzymology --- biotechnologie --- bioengineering --- Biotechnology --- Catalysis --- Catalyse --- Periodicals. --- Périodiques --- Chemistry --- Engineering --- Chemical Engineering --- General and Others --- Kinetics --- Physical Chemistry --- Catalysis. --- biochemie --- katalysatoren --- enzymen --- homogeneous catalysis --- heterogeneous catalysis --- enzymatic catalysis --- Physical & Theoretical Chemistry --- Activation (Chemistry) --- Chemistry, Physical and theoretical --- Surface chemistry

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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.

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

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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.

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