An Unusual Conversion of Paramagnetic [3-Cl-3,3,8-{Ph2P(CH2)nPPh-µ-(C6H4-ortho)}-1,2-(CH3)2-closo-3,1,2-RuIIIC2B9H8] (n = 3 and 4) to Form the First 18-Electron P-Phenylene ortho-Cycloboronated closo-Ruthenacarboranes with a Dioxygen Ligand
Autor: | Igor T. Chizhevsky, Dmitrii I. D’yachihin, Alexander Y. Kostukovich, Ivan A. Godovikov, Fedor M. Dolgushin, Alexander F. Smol'yakov |
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Jazyk: | angličtina |
Rok vydání: | 2014 |
Předmět: |
NMR-spectra
oxygen-type ligands Chemistry Transition metal dioxygen complex Ligand Organic Chemistry Pharmaceutical Science ruthenacarboranes Analytical Chemistry X-ray diffraction NMR spectra database lcsh:QD241-441 Paramagnetism Crystallography chemistry.chemical_compound lcsh:Organic chemistry Chemistry (miscellaneous) Phenylene Yield (chemistry) Drug Discovery X-ray crystallography Molecular Medicine Physical and Theoretical Chemistry Benzene |
Zdroj: | Molecules, Vol 19, Iss 6, Pp 7094-7103 (2014) Molecules; Volume 19; Issue 6; Pages: 7094-7103 |
ISSN: | 1420-3049 |
Popis: | Treatment of [3-Cl-3,3,8-[Ph2P(CH2)nPPh-µ-(C6H4-ortho)]-1,2-Me2-closo-3,1,2-RuIIIC2B9H8] (1, n = 3; 2, n = 4) with an excess of KOH in a 1:1 benzene/methanol mixture at room temperature in air affords new dioxygen closo-ruthenacarborane complexes [3-(η2-O2)-3,3,8-[Ph2P(CH2)nPPh-µ-(C6H4-ortho)]-1,2-Me2-closo-3,1,2-RuIIIC2B9H8] (3, n = 3) and (4, n = 4) in 42.5% and 45.8% yield respectively. The structures of dioxygen complexes 3 and 4 were established by single-crystal X-ray diffraction. The IR and multinuclear NMR data [1H, 13C{1H}, 31P{1H} and 11B{1H}] along with 2D HSQC correlation spectra for the new dioxygen closo-ruthenacarboranes are discussed. |
Databáze: | OpenAIRE |
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