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Multi-functionalized ferrocenes: –Synthesis and characterization
Ist Teil von
Journal of organometallic chemistry, 2016-02, Vol.804, p.87-94
Ort / Verlag
Elsevier B.V
Erscheinungsjahr
2016
Link zum Volltext
Quelle
Elsevier ScienceDirect Journals Complete
Beschreibungen/Notizen
Ferrocenes with up to four formyl functionalities have been synthesized by selective one- or two-fold ortho-lithiation of 1,1′-di(1,3-dioxan-2-yl)ferrocene followed by the reaction with dimethylformamide. Subsequent deprotection afforded tri- and tetraformyl-ferrocene in good yields. Wittig reactions convert the aldehydes to tri- and tetravinyl-ferrocene. The structures of three formyl-ferrocenes in the solid-state have been determined by single crystal X-ray diffraction. In two of the structures the ferrocene moieties form 1D chains by parallel displaced π-interactions with Cp⋯Cp distances as short as 3.21 Å. Electrochemical measurements (CV) demonstrated an irreversible behavior of the electron-poor multi-formyl ferrocenes. Reducing the measurement temperature down to −40 °C and the usage of [NnBu4][B(C6F5)4] prevents side reactions and hence reversible redox-processes could be obtained. It was found that the number of formyl functionalities correlates with the ferrocenyl's redox potential in a strictly linear fashion.
Ferrocenes with up to four formyl functionalities have been synthesized in good yields. As revealed by X-ray crystallography the C5H3-rings in two examples show strong π interactions with C5H3⋯C5H3 distances as short as 3.21 Å. Electrochemical measurements (CV) demonstrated that the number of formyl functionalities correlates with the ferrocenyl's redox potential in a strictly linear fashion. [Display omitted]
•High yield of multi-functionalized ferrocenes via ortho-lithiation was achieved.•π Interactions leading to a columnar arrangement of the ferrocenes were found.•Reversibility of the redox properties improved using weakly coordinating electrolyes.•A linear correlation between redox potential and number of formyl groups exists.