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Carbene mesoionic

For imidazolium salts 1, an alternative pathway with deprotonation and carbene generation at the C4/C5-position was observed previously the carbenes thus generated are called abnormal carbenes [79-81]. Likewise, suitably substituted imidazo[l,5-a]pyridinium salts can be deprotonated to mesoionic carbenes 10b and the corresponding silver, iridium and rhodium complexes were formed. [Pg.13]

Fig. 9 Pd l,2,3-triazol-5-ylidene mesoionic carbene PEPPSI complexes. Fig. 9 Pd l,2,3-triazol-5-ylidene mesoionic carbene PEPPSI complexes.
To conclude this section just a quick word about triazolium cation derivatives of 1,2,3-triazoles [87]. They have also been investigated and show application for functional ionic liquids and precursors of mesoionic carbenes for catalytic purposes, or as units of supramolecular assemblies and molecular machines. [Pg.469]

The Cu(l) complex formed by a mesoionic carbene and a phenanthroline has been generated in situ to perform copper-catalysed azide-alkyne cycloaddition in alcoholic solvent and without the need for a reducing reagent. ... [Pg.185]

Poly-NHC Ligands Containing Abnormal, Remote, or Mesoionic Carbenes 216... [Pg.203]

The statements abnormal and mesoionic carbenes (aNHCs and MICs) are synonyms and are referred to free carbenes for which it is not possible to draw a structure resonance formula without formal charges (Fig. 6). Differ-endy, remote carbenes (rNHCs) are carbenes without any heteroatom in the a and positions of the carbene center. These three types of ligands are characterized by a different structure with respect to the one usuaUy owned by NHCs. In the case of normal carbenes (nNHCs), the carbene donor is stabilized by the presence in the a and a positions of two heteroatoms. To emphasize this difference, aNHCs, MICs, and rNHCs are also caUed... [Pg.216]

Guisado-Barrios G, Bouf rdJ, Donnadieu B, Bertrand G. Bis(l, 2,3-triazol-5-ylidenes) (i-bitz) as stable 1,4-bidentate ligands based on mesoionic carbenes (MICs). Organometallics. 2011 30 6017-6021. [Pg.274]

Maity R, Hohloch S, Su C-Y, Van der Meer M, Sarkar B. Cyclometalated mono- and dinuclear Ir complexes with cHck -derived triazoles and mesoionic carbenes. Chem Eur J. 2014 20 9952-9961. [Pg.277]

Maity R, Van der Meet M, Sarkar B. Redox-active mrJtinuclear Pd(II) complexes with bis- and tris-mesoionic carbenes. Dalton Trans. 2015 44 46-49. [Pg.278]

Lee W-T, Dickie DA, Metta-Magan AJ, Smith JM. A tripodal bgand constructed from mesoionic carbene donors. Inorg Chem. 2013 52 12842-12846. [Pg.278]

Zamora MT, Ferguson MJ, Cowie M. Di-mesoionic carbene-bridged complexes of Rh2, It2 and Rhir a stepwise metalation strategy for the synthesis of di-MIC-bridges mixed-metal systems. Organometallics. 2012 31 5384-8395. [Pg.281]

Figure 1.10 Chiral triazolium salts 113-114, mesoionic carbenes 115-116 and dicationic triazolium salt 117. Figure 1.10 Chiral triazolium salts 113-114, mesoionic carbenes 115-116 and dicationic triazolium salt 117.

See other pages where Carbene mesoionic is mentioned: [Pg.155]    [Pg.299]    [Pg.60]    [Pg.505]    [Pg.297]    [Pg.322]    [Pg.505]    [Pg.308]    [Pg.204]    [Pg.205]    [Pg.210]    [Pg.231]    [Pg.15]    [Pg.50]    [Pg.126]    [Pg.211]   
See also in sourсe #XX -- [ Pg.155 ]




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