کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1322722 1499901 2013 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Ruthenium(III) cyclometallates: Regioselective metallation of 1-pyrenyl in 1-pyrenaldehyde 4-R-benzoylhydrazones
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی معدنی
پیش نمایش صفحه اول مقاله
Ruthenium(III) cyclometallates: Regioselective metallation of 1-pyrenyl in 1-pyrenaldehyde 4-R-benzoylhydrazones
چکیده انگلیسی


• Cycloruthenation of 1-pyrenaldehyde 4-R-benzoylhydrazones (H2pnbhR) was investigated.
• Reactions of [Ru(PPh3)3Cl2], H2pnbhR and NaOAc provided trans-[Ru(pnbhR)(PPh3)2Cl].
• Magnetic, various spectral and redox features of the complexes were determined.
• X-ray structure revealed ortho-metallated 1-pyrenyl moiety of the C,N,O-donor ligand.

Reactions of [Ru(PPh3)3Cl2] with 1-pyrenaldehyde 4-R-benzoylhydrazones (H2pnbhR, where R = H, Me, OMe, Cl and NO2) in presence of NaOAc afford ortho-metallated ruthenium(III) complexes of formula trans-[Ru(pnbhR)(PPh3)2Cl] (1–5). The complexes have been characterized by elemental analysis, magnetic susceptibility, spectroscopic (IR, UV–vis and EPR) and cyclic voltammetric measurements. Molecular structure of 2 (R = Me) determined by single crystal X-ray crystallography shows a distorted octahedral CNOClP2 coordination sphere around the trivalent metal centre assembled by the 1-pyrenyl ortho-C, azomethine-N and amidate-O donor pnbhMe2−, two mutually trans PPh3 and the chloride. Electronic spectra of 1–5 in dichloromethane display several strong bands within 555–276 nm due to ligand to metal charge transfer and ligand centred transitions. The complexes are one-electron paramagnetic (μeff = 1.90–1.99 μB) and display rhombic EPR spectra in frozen (130 K) dichloromethane–toluene (1:1). Cyclic voltammograms of the complexes in dimethylformamide display a ligand substituent sensitive metal centred one electron reduction couple in the E1/2 range −0.24 to −0.31 V (vs. Ag/AgCl).

Cyclometallated ruthenium(III) complexes of formula trans-[Ru(pnbhR)(PPh3)2Cl] (H2pnbhR = 1-pyrenaldehyde 4-R-benzoylhydrazones, where R = H, Me, OMe, Cl and NO2) are reported. The one-electron paramagnetic complexes are EPR and redox active. Crystal structure of the complex with R = Me reveals regioselective ortho-metallation of the 1-pyrenyl fragment of the tridentate pnbhMe2−.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Organometallic Chemistry - Volume 737, 1 August 2013, Pages 7–11
نویسندگان
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