Di-metallated platinum carbonyl complexes: platinum-platinum interactions in the solid state
UNSPECIFIED. (2001) Di-metallated platinum carbonyl complexes: platinum-platinum interactions in the solid state. JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS (18). pp. 2678-2682. ISSN 1472-7773Full text not available from this repository.
The reaction of a diphenylpyridine with one equivalent of potassium tetrachloroplatinate in ethanoic acid yields a cyclometallated species which can be induced to undergo a second cyclometallation to give a C<^>N<^>C tridentate species. Carbonyl derivatives of two such compounds have been structurally characterised. The X-ray structure of the complex [2,6-(4'-C6H13OC6H3)(2)C5H3NPt(CO)]. (1), obtained using 2,6-bis(4'-hexyloxyphenyl)pyridine, has no unusual features. In contrast. the structure of the complex [2,6-(C6H4)(2)-4-(4'-C8H17OC6H5)C5H2NPt(CO)], (2), which results when using 4-(4'-octyloxy-phenyl)-2,6-diphenylpyridine, has close intermolecular contacts. with a Pt-Pt "bond" of 3.243(1) Angstrom holding the molecules together as dimers. Compound 2 also exists in another form in the solid state. a form that does not appear to contain Pt-Pt bonds.
|Item Type:||Journal Article|
|Subjects:||Q Science > QD Chemistry|
|Journal or Publication Title:||JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS|
|Publisher:||ROYAL SOC CHEMISTRY|
|Date:||21 September 2001|
|Number of Pages:||5|
|Page Range:||pp. 2678-2682|
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