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Issue 37, 2013
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Complexation behavior of two-coordinated carbon compounds containing fluorenyl ligands

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Abstract

DFT calculations using BP86 in conjunction with the SVP and TZVPP basis sets as well as ab initio calculations at SCS-MP2 have been carried out for six dicoordinated carbon molecules CLL′ where L is a fluorenyl carbene while L′ is a phosphine PH3 (1) or PPh3 (2) or a carbene, i.e. NHCMe (3), benzannulated NHCMe (4), cycloheptatrienylidene (5) and benzannulated cycloheptatrienylidene (6). The complexes of these compounds with one and two AuCl moieties were also calculated. The monoaurated adducts of 1–4 have the AuCl fragment η1 coordinated to the central carbon atom. The complexes 5(AuCl) and 6(AuCl) have AuCl η2 bonded across a C[double bond, length as m-dash]C double bond. Three different bonding modes are found as energy minima for the diaurated species LL′C-(AuCl)2. The AuCl fragments are found to be either both coordinated η1, both coordinated η2 across double bonds, or a combination of the two. According to the electronic structure analysis of the free compounds, 1 and 2 might best be classified as carbenes, 3 and 4 as bent allenes while 5 and 6 are typical allenes. The complexation with AuCl reveals that 1–4 may exhibit chemical behaviour which is typical for carbones and thus, they may be termed “hidden carbones”. The AuCl complexes show that compounds 5 and 6 are classical allenes.

Graphical abstract: Complexation behavior of two-coordinated carbon compounds containing fluorenyl ligands

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Publication details

The article was received on 30 Nov 2012, accepted on 22 May 2013 and first published on 23 May 2013


Article type: Paper
DOI: 10.1039/C3DT32872D
Citation: Dalton Trans., 2013,42, 13349-13356
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    Complexation behavior of two-coordinated carbon compounds containing fluorenyl ligands

    C. Esterhuysen and G. Frenking, Dalton Trans., 2013, 42, 13349
    DOI: 10.1039/C3DT32872D

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