2012
DOI: 10.1016/j.ica.2012.01.033
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Insertion of a phospholide unit into a metal–metal bond: Synthesis and X-ray structure of [Ru3(CO)9(μ:η1:η5-PC4H2Me2)(η1-C6H5)]

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Cited by 9 publications
(12 citation statements)
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“…Due to the versatility of phospholes and metal carbonyl complexes, we have been exploring the interaction of both chemical entities. We have found σ-and σ,π-complexes, metal-metal bond cleavage and formation of derivatives where the phosphole ligand have undergone P-P and P-C bonds cleavage, C-H bond activation or partial hydrogenation of phosphorus ring [8,[38][39][40][41][42]. Herein, we have studied the reactivity of 2,5-disubstituted phenylphosphole derivatives with [Re 2 (CO) 8 (CH 3 CN) 2 ] to investigate coordination modes that could afford novel types of rhenium complexes.…”
Section: Introductionmentioning
confidence: 90%
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“…Due to the versatility of phospholes and metal carbonyl complexes, we have been exploring the interaction of both chemical entities. We have found σ-and σ,π-complexes, metal-metal bond cleavage and formation of derivatives where the phosphole ligand have undergone P-P and P-C bonds cleavage, C-H bond activation or partial hydrogenation of phosphorus ring [8,[38][39][40][41][42]. Herein, we have studied the reactivity of 2,5-disubstituted phenylphosphole derivatives with [Re 2 (CO) 8 (CH 3 CN) 2 ] to investigate coordination modes that could afford novel types of rhenium complexes.…”
Section: Introductionmentioning
confidence: 90%
“…The solvents were previously dried and distilled following standard methods [43]. [Re 2 (CO) 8 (CH 3 CN) 2 ], 2,5-bis(2-thienyl)-1phenylphosphole (btpp); 2,5-bis(2-pyridyl)-1-phenylphosphole (bpypp) and 1,2,5triphenylphosphole (tpp) were synthesized according to published procedures [44,45]. NMR spectra were recorded on Bruker Avance AM300 and AM500 spectrometers.…”
Section: General Remarksmentioning
confidence: 99%
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