Generation and reactivity of sterically hindered iridium carbenes. Competitive α- vs. β-hydrogen elimination in iridium(iii) alkyls
about
β- and α-Hydride abstraction in Gold(I) alkyl complexes.Iridium solutes effect C-H bond activation and C-C bond forming reactions of C6H6-MeOCH2CH2OMe solvent mixtures.Functionalization of 3-Iridacyclopentenes.Iridium(iii) complexes with polypyridine ligands coordinated as N-heterocyclic carbenes. Synthesis, structure and photophysical propertiesReversible Double CH Bond Activation of Linear and Cyclic Ethers To Form Iridium CarbenesTautomerisation of 2-Substituted Pyridines to N-Heterocyclic Carbene Ligands Induced by the 16 e− Unsaturated [TpMe2IrIII(C6H5)2] Moiety
P2860
Generation and reactivity of sterically hindered iridium carbenes. Competitive α- vs. β-hydrogen elimination in iridium(iii) alkyls
description
im Januar 2003 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована у 2003
@uk
name
Generation and reactivity of s ...... ydrogen elimination in iridium
@nl
Generation and reactivity of s ...... ination in iridium(iii) alkyls
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type
label
Generation and reactivity of s ...... ydrogen elimination in iridium
@nl
Generation and reactivity of s ...... ination in iridium(iii) alkyls
@en
prefLabel
Generation and reactivity of s ...... ydrogen elimination in iridium
@nl
Generation and reactivity of s ...... ination in iridium(iii) alkyls
@en
P2860
P50
P356
P1433
P1476
Generation and reactivity of s ...... ination in iridium(iii) alkyls
@en
P2860
P304
P356
10.1039/B303710J
P407
P577
2003-01-01T00:00:00Z