2004
DOI: 10.1002/ejic.200300137
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Synthesis, Structure, and Redox Properties of a New Aqua Ruthenium Complex Containing the Tridentate [9]aneS3 and the Didentate 1,10‐Phenanthroline Ligands

Abstract: The synthesis of a new Ru−H 2 O complex [Ru(phen)-(H 2 O)([9]aneS 3 )](ClO 4 ) 2 , 2, (phen = 1,10-phenanthroline, [9]aneS 3 = 1,4,7-trithiacyclononane) is described. The complex is characterized by UV/Vis and 1-D and 2-D NMR spectroscopy in solution. The complex has been further characterized in the solid-state by X-ray diffraction analysis which displays a distorted octahedral coordination geometry around the Ru metal center. The cyclic voltammetric experiments of

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Cited by 36 publications
(16 citation statements)
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“…Result evaluated through the comparative IR spectra of organophosphates with its corresponding metal complexes depicted, 20–30 cm −1 down shift of P = O band (comes originally in between 1,250 and 1,050 cm −1 ), along with, remarkable decrease in intensity and broadening in the peaks (Heineke et al, 1994 ; Murugavel et al, 2008 ). P-NMR up field shift up from a range of 25–65 to 0–10 ppm was observed (Sala et al, 2004 ). Such changes occurred near the P = O bonds in case of organophosphate pesticides, representing the active involvement of this group in complex formation with metal ions.…”
Section: Resultsmentioning
confidence: 99%
“…Result evaluated through the comparative IR spectra of organophosphates with its corresponding metal complexes depicted, 20–30 cm −1 down shift of P = O band (comes originally in between 1,250 and 1,050 cm −1 ), along with, remarkable decrease in intensity and broadening in the peaks (Heineke et al, 1994 ; Murugavel et al, 2008 ). P-NMR up field shift up from a range of 25–65 to 0–10 ppm was observed (Sala et al, 2004 ). Such changes occurred near the P = O bonds in case of organophosphate pesticides, representing the active involvement of this group in complex formation with metal ions.…”
Section: Resultsmentioning
confidence: 99%
“…The capability of [9]aneS 3 to coordinate to transition metal centers (and to ruthenium in particular) as a robust, face-capping, six-electron donor ligand, in analogy to the η 6 -arene and η 5 -cyclopentadienyl fragments (Figure 2), is well known. [22][23][24][25][26][27] Figure 2. Schematic structural comparison of three half-sandwich Ru II fragments with different face-capping ligands.…”
Section: Introductionmentioning
confidence: 99%
“…For related compounds, see: Sala et al (2004); ;; Marques et al (2008). For compounds with the same cation as the title compound, see: Serli et al (2005); Goodfellow et al (1997).…”
Section: Related Literaturementioning
confidence: 98%
“…Some members of this family of compounds have been tested as cytotoxic ) and antimicrobial agents, or as catalysts (Sala et al, 2004). We have also studied the solid-state properties of the inclusion compounds of a number of these ruthenium compounds in cyclodextrins (Marques et al, 2008).…”
Section: Commentmentioning
confidence: 99%