کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1321657 | 1499900 | 2013 | 4 صفحه PDF | دانلود رایگان |
• A stable dinuclear Pd (II) complex bearing a bridging diarylene ligand was synthesized by double oxidative addition reaction.
• The complex can be used as an initiator to prepare the well-defined polymer.
• The functional group could be incorporated into in the middle of polymer main chain.
Dinuclear Pd(II) complex DiPd–DPE with a bridging ligand C6H4OC6H4-4,4′ was successfully synthesized by double oxidative addition reaction of Pd(PCy3)4 with 4,4′-dibromodiphenyl ether in good yield. X-ray crystal structure analysis reveals that the Pd atoms have the nearly square-planar coordination geometry with the similar bond lengths of two Pd–Br as well as four Pd–P, implying that two Pd(II) centers have similar reactivity. Using the dinuclear Pd(II) complex DiPd–DPE as an initiator, novel polyfluorene (PF) with a defined group (C6H4OC6H4-4,4′) in the middle of polymer main chain was prepared, demonstrated by MALDI-TOF analysis.
A stable dinuclear Pd (II) complex with a bridging diarylene ligand was successfully synthesized by double oxidative addition reaction. Especially, the complex can be used as an initiator to prepare a new-type conjugated polymer bearing the functional group in the center of polymeric main chain via the chain-growth polycondensation.Figure optionsDownload as PowerPoint slide
Journal: Journal of Organometallic Chemistry - Volume 738, 15 August 2013, Pages 55–58