Synthesis of di-, tri- and tetranuclear platinum(II) and copper(I) acetylide complexes
| Autor: | Petra Zoufalá, Amaya del Villar, Heinrich Lang, Gerd Rheinwald, Sami Klaib |
|---|---|
| Rok vydání: | 2007 |
| Předmět: |
chemistry.chemical_classification
Stereochemistry Organic Chemistry Center (category theory) Alkyne chemistry.chemical_element Triple bond Biochemistry Copper Inorganic Chemistry Crystallography chemistry.chemical_compound chemistry Copper(I) acetylide Materials Chemistry Moiety Molecule Physical and Theoretical Chemistry Platinum |
| Zdroj: | Journal of Organometallic Chemistry. 692:4168-4176 |
| ISSN: | 0022-328X |
| DOI: | 10.1016/j.jorganchem.2007.06.034 |
| Popis: | Heterobimetallic {cis-[Pt](μ-σ,π-C CPh)2}[Cu(N CMe)]BF4 (3a: [Pt] = (bipy)Pt, bipy = 2,2′-bipyridine; 3b: [Pt] = (bipy′)Pt, bipy′ = 4,4′-dimethyl-2,2′-bipyridine) is accessible by the reaction of cis-[Pt](C CPh)2 (1a: [Pt] = (bipy)Pt, 1b: [Pt] = (bipy′)Pt]) with [Cu(N CMe)4]BF4 (2). Substitution of N CMe by PPh3 (4) can be realized by the reaction of 3a with 4, whereby [{cis-[Pt](μ-σ,π-C CPh)2}Cu(PPh3)]BF4 (5) is formed. On prolonged stirring of 3 and 5, respectively, N CMe and PPh3 are eliminated and tetrametallic {[{cis-[Pt](η2-C CPh)2}Cu]2}(BF4)2 (6) is produced. Addition of an excess of N CMe to 6 gives heterobimetallic 3a. When instead of N CMe or PPh3 chelating molecules such as bipy (7) are reacted with 3a then the heterobimetallic π-tweezer molecule [{cis-[Pt](μ-σ,π-C CPh)2}Cu(bipy)]BF4 (8) is formed. Treatment of 8 with another equivalent of 7 produced [Cu(bipy2)]BF4 (9) along with [Pt](C CPh)2. However, when 3b is reacted with 1b in a 1:1 molar ratio then 10 and 11 of general composition [{[Pt](C CPh)2}2Cu]BF4 are formed. These species are isomers and only differ in the binding of the PhC C units to copper(I). A possible mechanism for the formation of 10 and 11 is presented. The solid state structures of 6, 10 and 11 are reported. In 11 the [{cis-[Pt](μ-σ,π-C CPh)2}2Cu]+ building block is set-up by two nearly orthogonal positioned bis(alkynyl) platinum units which are connected by a Cu(I) ion, whereby the four carbon–carbon triple bonds are unsymmetrical coordinated to Cu(I). In trimetallic 10 two cis-[Pt](C CPh)2 units are bridged by a copper(I) center, however, only one of the two PhC C ligands of individual cis-[Pt](C CPh)2 fragments is η2-coordinated to Cu(I) giving rise to the formation of a [(η2-C CPh)2Cu]+ moiety with a linear alkyne–copper–alkyne arrangement (alkyne = midpoint of the C C triple bond). In 6 two almost parallel oriented [Pt](C CPh)2 planes are linked by two copper(I) ions, whereby two individual PhC C units, one associated with each Pt building block, are symmetrically π-coordinated to Cu. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|
Full Text from ScienceDirect