کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1324334 1499889 2014 12 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Planar-chiral phosphino alkenylferrocenes – Synthesis, solid-state structure and electrochemistry
ترجمه فارسی عنوان
فسفینوکلنیلفروکوسن فلاواریا چیرال ؟؟ سنتز، ساختار حالت جامد و الکتروشیمی
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی معدنی
چکیده انگلیسی


• Synthesis of various phosphino alkenylferrocenes.
• X-ray crystallography.
• Linear correlation of E°′ and σpara.
• Diferrocenyl ethylene characterized as weakly coupled class II system.

The synthesis and characterization of phosphino alkenylferrocenes of type [Fe(η5-C5H3–2-PR′2–(E)-CH = CHR)(η5-C5H5)] (R = C6H5, 4-Cl–C6H4, 4-OMe–C6H4, 4-Me–C6H4, 4-CN–C6H4, 4-Ac–C6H4, Fc; R′ = Ph, MeFur, Cy, o-Tol, 3-Cl–C6H4; Fc = Fe(η5-C5H5)(η5-C5H4), MeFur = 5-methylfuran-2-yl, o-Tol = 2-tolyl) and the molecular structure of representative examples in the solid state are discussed. The alkenyl unit has been built up either by Heck–Mizoroki C,C cross coupling or Horner–Wadsworth–Emmons olefination. The electrochemical characterization of the sulphur-protected phosphino (phenylvinyl)-ferrocenes revealed a linear correlation between the redox potentials of the metallocenyl units (E°′) and the σpara Hammett parameters of the phenylene-bonded substituents. In contrast, the σ-donor properties of the phosphine moieties are not affected as could be demonstrated by analysis of the 1J(31P,77Se) coupling constants of the respective selenophosphines. In diferrocenyl ethylene [Fe(η5-C5H3–2-P(S)Ph2–(E)-CHCHFc)(η5-C5H5)] both ferrocenyl units are oxidized separately. In situ spectroelectrochemical measurements revealed that inter-valence charge transfer interactions contribute to the observed redox splitting of 495 mV and that the formed mono-cation can be classified as weakly coupled class II system according to Robin and Day.

The synthesis, properties and solid-state structure of [Fe(η5-C5H3–2-PR′2–(E)-CHCHR)(η5-C5H5)] is discussed. Electrochemical characterization of the sulphur-protected phosphino (phenylvinyl)ferrocenes revealed a linear correlation between E°′ and the σpara parameters of the phenylene-bonded substituents. In-situ spectroelectrochemical studies showed that mono-cationic diferrocenyl ethylene (R = Fc) is a weakly coupled class II system.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Organometallic Chemistry - Volume 751, 1 February 2014, Pages 742–753
نویسندگان
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