No abstract

A new class of cyclic hydrocoppers(I) with the general formula CunHn (n = 3-6), resembling the cyclic hydrocarbon analogues, were predicted by means of DFT calculations to be stable molecules adopting a perfect planar configuration of high-symmetry characteristic of the aromatic systems.

The two-electron oxidation reactions of the [NBu 4 ] 2 [(C 6 F 5 ) 2 M(µ-PPh 2 ) 2 M′(C 6 F 5 ) 2 ] (M ) M′ ) Pt, 1a; M ) M′ ) Pd, 1b; M ) Pt, M′ ) Pd, 1c) complexes using I 2 as oxidant have been investigated by experimental and electronic structure calculation methods. The geometric and energetic reaction profiles in a vacuum have been investigated at the B3LYP/LANL2DZ level. The first step of the oxidation processes involves the oxidative addition of I 2 to one of the four-coordinate M(II) metal centers yielding a five-coordinate intermediate with square pyramidal stereochemistry. The oxidized [(I)L 2 M(µ-PH 2 ) 2 M′L 2 ] -(L ) CN) complex converts to a more stable intermediate involving a planar dimetallacycle five-membered ring, which through a reactant-like transition state surmounting a relatively low barrier of 18.5, 8.7, and 8.9 kcal/mol for Pt 2 , PtPd, and Pd 2 compounds, respectively, yields the final product. At this stage an unusual intramolecular reductive coupling of one of the ancillary ligands with a bridging phosphido ligand takes place, affording the "M(II)(µ-PH 2 )(µ-I)M′(II)" framework. This process is exoergic by 11.4, 18.2, and 18.8 kcal/mol for Pt 2 , PtPd, and Pd 2 compounds, respectively. For the Pt 2 and PtPd complexes removal of the iodide ligand from the oxidized iodo complexes yields the very unusual [L 2 M III (µ-PH 2 ) 2 M′ III L 2 ] (L ) CN or C 6 F 5 ) complexes. In contrast, [L 2 Pd III (µ-PH 2 ) 2 Pd III L 2 ] does not exist as local minima in the PES, but the [L 2 -Pd II (µ-PH 2 )Pd II (PH 2 L)L] species was identified, resulting from the intramolecular reductive coupling promoted by the iodide ligand abstraction. This species could be considered as an intermediate for the reverse intramolecular oxidative addition of the PH 2 L ligand promoted by iodide abstraction with Ag + ions. Finally, the molecular structure of the [(C 6 F 5 ) 2 Pt(µ-PPh 2 )(µ-I)Pd(C 6 F 5 ){PPh 2 (C 6 F 5 )}] complex has been established by X-ray crystallography.