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dc.contributor.editorCanac, Yves
dc.date.accessioned2022-01-11T13:32:30Z
dc.date.available2022-01-11T13:32:30Z
dc.date.issued2021
dc.identifierONIX_20220111_9783036513508_194
dc.identifier.urihttps://directory.doabooks.org/handle/20.500.12854/76458
dc.description.abstractHomogeneous catalysis owes its success, in large part, to the development of a wide range of ligands with well-defined electronic and steric properties, which have thus made it possible to adjust the behavior of many organometallic complexes. However, ligands used in catalysis have long been centered on elements of group 15, and it is only more recently that carbon ligands have proved to be valuable alternatives with the emergence of cyclic diaminocarbenes (NHC).This Special Issue aims to provide a contemporary overview of the advances in carbon ligand chemistry from fundamental aspects to applications.
dc.languageEnglish
dc.subject.classificationbic Book Industry Communication::G Reference, information & interdisciplinary subjects::GP Research & information: general
dc.subject.othercarbenes
dc.subject.otherylides
dc.subject.otherDFT calculations
dc.subject.otherelectronic structure
dc.subject.othercatalysis
dc.subject.otherligands
dc.subject.otherstructure–activity relationship
dc.subject.otherNHC
dc.subject.othernanoparticle
dc.subject.othercalixarene
dc.subject.otherpalladium catalyst
dc.subject.otherSuzuki-Miyaura reaction
dc.subject.otheramino-acids
dc.subject.otherwater
dc.subject.othercarbon ligand
dc.subject.otheramide
dc.subject.othernegative charge
dc.subject.otherphosphonium ylide
dc.subject.otheroxide
dc.subject.otherpincer
dc.subject.othermetathesis
dc.subject.otherruthenium
dc.subject.othernitro catalysts
dc.subject.otherNHC ligands
dc.subject.otherolefins
dc.subject.otherselenonium ylides
dc.subject.otherselenonium salts
dc.subject.otherchirality
dc.subject.otherstereogenic selenium atom
dc.subject.otherasymmetric synthesis
dc.subject.otheroptical resolution
dc.subject.otherreactivity
dc.subject.othermalaria
dc.subject.otherPlasmodium falciparum
dc.subject.othergold
dc.subject.otherNHC-ligands
dc.subject.otherhybrid molecules
dc.subject.otherdrug resistance
dc.subject.otherN-heterocyclic carbene
dc.subject.otherplatinum
dc.subject.othermetal complexes
dc.subject.other195Pt NMR
dc.subject.otherN-heterocyclic carbenes
dc.subject.otherimidazole
dc.subject.otherspectroscopy
dc.subject.otherX-ray
dc.subject.othermercury(II) complex
dc.subject.otherT-shaped
dc.subject.othercarbodiphosphorane
dc.subject.otherphosphorus ylides
dc.subject.otherpincer ligands
dc.subject.othercoordination chemistry
dc.subject.otherCu(I) complex
dc.subject.otherphotoluminescence
dc.subject.othertitanium
dc.subject.otherhafnium
dc.subject.othercopolymerization of epoxide with CO2
dc.subject.otherdensity functional theory
dc.subject.othernatural bond orbitals
dc.subject.otheraromaticity
dc.subject.otherion pairs
dc.subject.otheralkali metals
dc.subject.othertropylidenyl ions
dc.subject.othercyclooctatetraene ions
dc.subject.otherrhodium
dc.subject.otherelectron paramagnetic resonance (EPR) spectroscopy
dc.subject.otherdensity functional theory (DFT)
dc.subject.otherelectrochemistry
dc.subject.othercarbone complexes
dc.subject.othercarbido complexes
dc.subject.othertransition metal complexes
dc.subject.otherchemical bonding
dc.subject.otherpincer ligand
dc.subject.othermacrocycle
dc.subject.otherlithium
dc.subject.otherpotassium
dc.subject.otherintramolecular C-H activation
dc.subject.otherdehydrogenation
dc.subject.othercarbone
dc.subject.otherligand
dc.subject.othergermylene
dc.subject.othercoordination
dc.subject.otherylide
dc.subject.othern/a
dc.titleCarbon Ligands
dc.title.alternativeFrom Fundamental Aspects to Applications
dc.typebook
oapen.identifier.doi10.3390/books978-3-0365-1349-2
oapen.relation.isPublishedBy46cabcaa-dd94-4bfe-87b4-55023c1b36d0
oapen.relation.isbn9783036513508
oapen.relation.isbn9783036513492
oapen.pages311
oapen.place.publicationBasel, Switzerland


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