LEADER 01072nam0 22002771i 450 001 UON00463642 005 20231205105134.931 100 $a20160122d1955 |0itac50 ba 101 $afre 102 $aFR 105 $a|||| ||||| 200 1 $aˆLe ‰cardinal$fHenry Morton Robinson$gtraduction de Geneviève Hurel 210 $aParis$cDel Duca$d1955 215 $a701 p.$d17 cm. 316 $aValore stimato$5IT-UONSI Francese1 L.P.ROBI 410 1$1001UON00459635$12001 $aˆLe ‰livre de poche$1210 $aParis$cDel Duca$v1687-1689 620 $aFR$dParis$3UONL002984 700 1$aROBINSON$bHenry Morton$3UONV191792$0286141 702 1$aHUREL$bGeneviève$3UONV229902 712 $aDel Duca$3UONV266185$4650 801 $aIT$bSOL$c20240220$gRICA 899 $aSIBA - SISTEMA BIBLIOTECARIO DI ATENEO$2UONSI 912 $aUON00463642 950 $aSIBA - SISTEMA BIBLIOTECARIO DI ATENEO$dSI Francese 1 L.P. ROBI $eSI SFR2964 7 Valore stimato 996 $aCardinal$91398137 997 $aUNIOR LEADER 04306nam 2201357z- 450 001 9910557372703321 005 20220111 035 $a(CKB)5400000000042164 035 $a(oapen)https://directory.doabooks.org/handle/20.500.12854/76458 035 $a(oapen)doab76458 035 $a(EXLCZ)995400000000042164 100 $a20202201d2021 |y 0 101 0 $aeng 135 $aurmn|---annan 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 00$aCarbon Ligands$eFrom Fundamental Aspects to Applications 210 $aBasel, Switzerland$cMDPI - Multidisciplinary Digital Publishing Institute$d2021 215 $a1 online resource (311 p.) 311 08$a3-0365-1350-7 311 08$a3-0365-1349-3 330 $aHomogeneous 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. 517 $aCarbon Ligands 606 $aResearch and information: general$2bicssc 610 $a195Pt NMR 610 $aalkali metals 610 $aamide 610 $aamino-acids 610 $aaromaticity 610 $aasymmetric synthesis 610 $acalixarene 610 $acarbenes 610 $acarbido complexes 610 $acarbodiphosphorane 610 $acarbon ligand 610 $acarbone 610 $acarbone complexes 610 $acatalysis 610 $achemical bonding 610 $achirality 610 $acoordination 610 $acoordination chemistry 610 $acopolymerization of epoxide with CO2 610 $aCu(I) complex 610 $acyclooctatetraene ions 610 $adehydrogenation 610 $adensity functional theory 610 $adensity functional theory (DFT) 610 $aDFT calculations 610 $adrug resistance 610 $aelectrochemistry 610 $aelectron paramagnetic resonance (EPR) spectroscopy 610 $aelectronic structure 610 $agermylene 610 $agold 610 $ahafnium 610 $ahybrid molecules 610 $aimidazole 610 $aintramolecular C-H activation 610 $aion pairs 610 $aligand 610 $aligands 610 $alithium 610 $amacrocycle 610 $amalaria 610 $amercury(II) complex 610 $ametal complexes 610 $ametathesis 610 $aN-heterocyclic carbene 610 $aN-heterocyclic carbenes 610 $an/a 610 $ananoparticle 610 $anatural bond orbitals 610 $anegative charge 610 $aNHC 610 $aNHC ligands 610 $aNHC-ligands 610 $anitro catalysts 610 $aolefins 610 $aoptical resolution 610 $aoxide 610 $apalladium catalyst 610 $aphosphonium ylide 610 $aphosphorus ylides 610 $aphotoluminescence 610 $apincer 610 $apincer ligand 610 $apincer ligands 610 $aPlasmodium falciparum 610 $aplatinum 610 $apotassium 610 $areactivity 610 $arhodium 610 $aruthenium 610 $aselenonium salts 610 $aselenonium ylides 610 $aspectroscopy 610 $astereogenic selenium atom 610 $astructure-activity relationship 610 $aSuzuki-Miyaura reaction 610 $aT-shaped 610 $atitanium 610 $atransition metal complexes 610 $atropylidenyl ions 610 $awater 610 $aX-ray 610 $aylide 610 $aylides 615 7$aResearch and information: general 700 $aCanac$b Yves$4edt$01318571 702 $aCanac$b Yves$4oth 906 $aBOOK 912 $a9910557372703321 996 $aCarbon Ligands$93033415 997 $aUNINA