Mixed Metal Acetylides: The PtII Aryl Acetylide '[PtC2H2(CH2NMe2)2-2,6-(C_C)-4]' as a Connective Fragment
Files
Publication date
2000
Authors
Koten, G. van
Back, S.
Gossage, R.A.
Lang, H.
Editors
Advisors
Supervisors
DOI
Document Type
Article
Metadata
Show full item recordCollections
License
Abstract
Using Me3SiCC{Pt}Cl (1; Me3SiCC{Pt} = [Pt(C6H2{CH2NMe2}2-2,6-{CCSiMe3}-4]+) a series of platinum monoacetylides of the type XCC{Pt}CCR [X = SiMe3: 2, R = Ph; 3, R = (5-C5H4)Fe(5-C5H5) (abbreviated as Fc); 4, R = C6H4CN-4; 5, R = C6H4(CCSnMe3)-4; X = H: 7, R = Ph; 8, R = Fc; 9, R = C6H4CN-4] have been prepared. Studies directed towards the coordinative properties of the C2 unit of 1 have been carried out and heterotrimetallic [-(Me3SiCC{Pt}Cl][Co2(CO)6] (10) could be synthesised. The successful attachment of 1 to a Ph3PAu unit leads to linear Ph3PAuCC{Pt}Cl (11). Treatment of 11 with FcCCSnMe3 produces the heterotrimetallic rigid-rod shaped complex Ph3PAuCC{Pt}CCFc (13). Cyclic voltammetric studies carried out on these Ph3PAu-capped molecules show that the attachment of an organometallic entity on either side of the CC{Pt} fragment leads to a facilitation of the PtII/PtIV oxidation.