2005
DOI: 10.1107/s1600536805003855
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2,2′:6′,2′′-Terpyridine 1,1′′-dioxide dihydrate

Abstract: The title compound, C15H11N3O3·2H2O, crystallizes with ter­pyridine dioxide mol­ecules positioned on mirror planes in the space group Pnma. Catemeric assemblages of ter­pyridine mol­ecules [C—H⋯−O—+N = 3.386 (4) Å] are linked by bridging water mol­ecules [C—H⋯O = 3.288 (4) and 3.386 (4) Å; O—H⋯−O—+N = 2.837 (3) and 2.878 (4) Å], giving stacks of two‐dimensional undulating motifs.

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Cited by 3 publications
(6 citation statements)
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“…Colourless, X-ray quality crystals of 3 were obtained by slow evaporation of a CHCl 3 / MeOH solution of the crude product in the presence of excess of 1,3-diaminopropane. The IR and 1 H and 13 C NMR spectroscopic data agreed with those reported. 3,5 FAB-MS 698.0 [M + H] + (calc.…”
Section: Experimental Generalsupporting
confidence: 87%
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“…Colourless, X-ray quality crystals of 3 were obtained by slow evaporation of a CHCl 3 / MeOH solution of the crude product in the presence of excess of 1,3-diaminopropane. The IR and 1 H and 13 C NMR spectroscopic data agreed with those reported. 3,5 FAB-MS 698.0 [M + H] + (calc.…”
Section: Experimental Generalsupporting
confidence: 87%
“…Commercially available chemicals were reagent grade and were used without further purification. 1 H and 13 C NMR spectra were recorded at room temperature on a Bruker Avance DRX 500 MHz spectrometer; chemical shifts are relative to residual solvent peaks with TMS d ¼ 0 ppm. Infrared spectra were recorded on a Shimadzu FTIR-8400S spectrophotometer with solid samples on a Golden Gate diamond ATR accessory.…”
Section: Experimental Generalmentioning
confidence: 99%
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“…We have prepared the title compound as a continuing effort to understand the intermolecular contact preferences of the N-oxide group in molecular crystals [1][2][3][4]. 2,2':6',2"-Terpyridine l,l"-dioxide was prepared using a modification of the procedure for direct oxidation of pyridine and pyrazine moieties [5].…”
Section: Source Of Materialsmentioning
confidence: 99%
“…
Source of materialWe have prepared the title compound as a continuing effort to understand the intermolecular contact preferences of the N-oxide group in molecular crystals [1][2][3][4]. 2,2¢:6¢,2²-Terpyridine 1,1²-dioxide was prepared using a modification of the procedure for direct oxidation of pyridine and pyrazine moieties [5].
…”
mentioning
confidence: 99%