Carbon Ligands : From Fundamental Aspects to Applications
Homogeneous 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 centere...
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Basel, Switzerland
MDPI - Multidisciplinary Digital Publishing Institute
2021
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|---|---|---|---|
| 001 | doab_20_500_12854_76458 | ||
| 005 | 20220111 | ||
| 020 | |a books978-3-0365-1349-2 | ||
| 020 | |a 9783036513508 | ||
| 020 | |a 9783036513492 | ||
| 024 | 7 | |a 10.3390/books978-3-0365-1349-2 |c doi | |
| 041 | 0 | |a English | |
| 042 | |a dc | ||
| 072 | 7 | |a GP |2 bicssc | |
| 100 | 1 | |a Canac, Yves |4 edt | |
| 700 | 1 | |a Canac, Yves |4 oth | |
| 245 | 1 | 0 | |a Carbon Ligands : From Fundamental Aspects to Applications |
| 260 | |a Basel, Switzerland |b MDPI - Multidisciplinary Digital Publishing Institute |c 2021 | ||
| 300 | |a 1 electronic resource (311 p.) | ||
| 506 | 0 | |a Open Access |2 star |f Unrestricted online access | |
| 520 | |a Homogeneous 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. | ||
| 540 | |a Creative Commons |f https://creativecommons.org/licenses/by/4.0/ |2 cc |4 https://creativecommons.org/licenses/by/4.0/ | ||
| 546 | |a English | ||
| 650 | 7 | |a Research & information: general |2 bicssc | |
| 653 | |a carbenes | ||
| 653 | |a ylides | ||
| 653 | |a DFT calculations | ||
| 653 | |a electronic structure | ||
| 653 | |a catalysis | ||
| 653 | |a ligands | ||
| 653 | |a structure-activity relationship | ||
| 653 | |a NHC | ||
| 653 | |a nanoparticle | ||
| 653 | |a calixarene | ||
| 653 | |a palladium catalyst | ||
| 653 | |a Suzuki-Miyaura reaction | ||
| 653 | |a amino-acids | ||
| 653 | |a water | ||
| 653 | |a carbon ligand | ||
| 653 | |a amide | ||
| 653 | |a negative charge | ||
| 653 | |a phosphonium ylide | ||
| 653 | |a oxide | ||
| 653 | |a pincer | ||
| 653 | |a metathesis | ||
| 653 | |a ruthenium | ||
| 653 | |a nitro catalysts | ||
| 653 | |a NHC ligands | ||
| 653 | |a olefins | ||
| 653 | |a selenonium ylides | ||
| 653 | |a selenonium salts | ||
| 653 | |a chirality | ||
| 653 | |a stereogenic selenium atom | ||
| 653 | |a asymmetric synthesis | ||
| 653 | |a optical resolution | ||
| 653 | |a reactivity | ||
| 653 | |a malaria | ||
| 653 | |a Plasmodium falciparum | ||
| 653 | |a gold | ||
| 653 | |a NHC-ligands | ||
| 653 | |a hybrid molecules | ||
| 653 | |a drug resistance | ||
| 653 | |a N-heterocyclic carbene | ||
| 653 | |a platinum | ||
| 653 | |a metal complexes | ||
| 653 | |a 195Pt NMR | ||
| 653 | |a N-heterocyclic carbenes | ||
| 653 | |a imidazole | ||
| 653 | |a spectroscopy | ||
| 653 | |a X-ray | ||
| 653 | |a mercury(II) complex | ||
| 653 | |a T-shaped | ||
| 653 | |a carbodiphosphorane | ||
| 653 | |a phosphorus ylides | ||
| 653 | |a pincer ligands | ||
| 653 | |a coordination chemistry | ||
| 653 | |a Cu(I) complex | ||
| 653 | |a photoluminescence | ||
| 653 | |a titanium | ||
| 653 | |a hafnium | ||
| 653 | |a copolymerization of epoxide with CO2 | ||
| 653 | |a density functional theory | ||
| 653 | |a natural bond orbitals | ||
| 653 | |a aromaticity | ||
| 653 | |a ion pairs | ||
| 653 | |a alkali metals | ||
| 653 | |a tropylidenyl ions | ||
| 653 | |a cyclooctatetraene ions | ||
| 653 | |a rhodium | ||
| 653 | |a electron paramagnetic resonance (EPR) spectroscopy | ||
| 653 | |a density functional theory (DFT) | ||
| 653 | |a electrochemistry | ||
| 653 | |a carbone complexes | ||
| 653 | |a carbido complexes | ||
| 653 | |a transition metal complexes | ||
| 653 | |a chemical bonding | ||
| 653 | |a pincer ligand | ||
| 653 | |a macrocycle | ||
| 653 | |a lithium | ||
| 653 | |a potassium | ||
| 653 | |a intramolecular C-H activation | ||
| 653 | |a dehydrogenation | ||
| 653 | |a carbone | ||
| 653 | |a ligand | ||
| 653 | |a germylene | ||
| 653 | |a coordination | ||
| 653 | |a ylide | ||
| 653 | |a n/a | ||
| 856 | 4 | 0 | |a www.oapen.org |u https://mdpi.com/books/pdfview/book/3894 |7 0 |z Get Fullteks |
| 856 | 4 | 0 | |a www.oapen.org |u https://directory.doabooks.org/handle/20.500.12854/76458 |7 0 |z DOAB: description of the publication |