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  2. File:Au Carbene.pdf - Wikipedia

    en.wikipedia.org/wiki/File:Au_Carbene.pdf

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  3. Carbene - Wikipedia

    en.wikipedia.org/wiki/Carbene

    Carbene radicals, in which the carbene is bonded to an open-shell metal with the carbene carbon possessing a radical character. Carbene radicals have features of both Fischer and Schrock carbenes, but are typically long-lived reaction intermediates. The "second generation" of the Grubbs catalysts for alkene metathesis features an NHC ligand.

  4. Category:Carbenes - Wikipedia

    en.wikipedia.org/wiki/Category:Carbenes

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  5. Fischer carbene - Wikipedia

    en.wikipedia.org/wiki/Fischer_carbene

    A Fischer carbene is a type of transition metal carbene complex, which is an organometallic compound containing a divalent organic ligand. In a Fischer carbene, the carbene ligand is a σ-donor π-acceptor ligand. Because π-backdonation from the metal centre is generally weak, the carbene carbon is electrophilic.

  6. Carbyne - Wikipedia

    en.wikipedia.org/wiki/Carbyne

    Carbyne molecules are generally found to be in electronic doublet states: the non-bonding electrons on carbon are arranged as one radical (unpaired electron) and one electron pair, leaving a vacant atomic orbital, rather than being a triradical (the quartet state).

  7. Transition metal carbene complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_carbene...

    Examples include (CO) 5 W=COMePh and (OC) 5 Cr=C(NR 2)Ph. Orbital interaction in a Fisher carbene. The carbene electrons are donated to a sigma bond, and weak pi-backbonding occurs. Fisher carbene complexes are related to the singlet form of carbenes, where both electrons occupy the same sp 2 orbital at the carbon. This lone pair donates to a ...

  8. Methylene (compound) - Wikipedia

    en.wikipedia.org/wiki/Methylene_(compound)

    Methylene (IUPAC name: Methylidene, also called carbene or methene) is an organic compound with the chemical formula CH 2 (also written [CH 2] and not to be confused with compressed hydrogen, which is also denoted CH 2). It is a colourless gas that fluoresces in the mid-infrared range, and only persists in dilution, or as an adduct.

  9. Transition metal carbyne complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_carbyne...

    The net reaction gives a transition metal carbene complex: L n M≡CR + HX → L n (X)M=CHR. These complexes can also undergo photochemical reactions. In some carbyne complexes, coupling of the carbyne ligand to a carbonyl is observed. Protonation of the carbyne carbon and conversion of the carbyne ligand into a π-allyl. [13]