Thermal conversions of sodium cyclotriphosphate monohydrate, Na3P3O9 · H2O

Galogaza, V. M.; Prodan, E. A.; Pytlev, S. I.; Skala, Dejan; Ristić, Ivan; Obradović, L.

doi:10.1016/0040-6031(86)87002-2

Cited by 4 publications

(2 citation statements)

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“…A large excess amount of acetone was added to the filtrate and a white precipitate was collected by suction filtration, and then washed with 5 mL of ethanol followed by 10 mL of acetone. Against the past reports by other researchers, 43,52,62,63,[67][68][69][70] acetone is more suitable for the final washing than alcohol for the syntheses of various inorganic phosphates. Since acetone does not readily form hydrogen bonds with inorganic phosphates, the powder is prevented from being strongly adhered mutually, and kept to a better 3− anions, i.e., 1.5 ppm, 39 and that of -O-PO 2 -NH-in cP 3 O 7 (NH) 2 3− anions, i.e., −8.5 ppm, 36 which have been previously reported.…”

Section: Observation Of Thermal Decomposition Behaviormentioning

confidence: 91%

Synthesis, protonation equilibrium and peculiar thermal decomposition behavior of cyclo-tri-μ-imidotetraphosphate

et al. 2014

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The synthesis and isolation of the sodium salt of cyclo-tri-μ-imidotetraphosphate, i.e. Na4cP4O9(NH)3·H2O, were achieved by the hydrolysis of Na4cP4O8(NH)4·2H2O under very weak acidic conditions, i.e. using 0.2 mol L(-1) propionic acid and the pH-controlled recrystallization procedure. The purity of Na4cP4O9(NH)3·H2O was improved from 2% to 95% by the pH-controlled recrystallization only two times. The first protonation constants of a series of cyclo-μ-imidotetraphosphate anions, i.e. cP4O(12-n)(NH)n(4-) (n = 0, 2, 3, 4), were determined by potentiometric titration and (31)P NMR chemical shift measurements in aqueous solution. Regardless of the paucity of the purity of trans-cP4O10(NH)2(4-) anions, the protonation processes of all anions may be evaluated accurately without any previous purification, because the NMR signals corresponding to cP4O(12-n)(NH)n(4-) (n = 0, 2, 3, 4) anions are well resolved. The logarithmic first protonation constants increase with a "linear" increase in the number of imino groups which constitute the ligand molecules. Macroscopic protonation reactions could be divided into three microscopic protonation processes for -O-PO2-O-, -O-PO2-NH-, and -NH-PO2-NH- groups. The basicity of the -NH-PO2-NH- group is especially high, because the delocalization of H(+) ions by lactam-lactim tautomerism on the whole ring molecule of cP3O6(NH)3 and cP4O8(NH)4 enhances the protonation of these ligands. In addition, also the concurrent change observed in the (31)P NMR chemical shift values of the phosphorus nuclei in the -O-PO2-NH- and -NH-PO2-NH- groups of cP4O9(NH)3(4-) anions suggested the effect of the lactam-lactim tautomerism. The intrinsic (31)P NMR chemical shifts for the central phosphorus nuclei for -O-PO2-O-, -O-PO2-NH-, and -NH-PO2-NH- groups show a good proportional relationship with the number of nitrogen atoms bonded to the central phosphorus atoms. Two types of imino groups with mutually dissimilar chemical environments which are present in the Na4cP4O9(NH)3 molecule, that is -O-PO2-NH-PO2-NH- and -NH-PO2-NH-PO2-NH-, brought about a two-stage pyrolytic elimination of imino groups from the initial stage of combustion over a wide temperature range.

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Section: Observation Of Thermal Decomposition Behaviormentioning

confidence: 91%

Synthesis, protonation equilibrium and peculiar thermal decomposition behavior of cyclo-tri-μ-imidotetraphosphate

et al. 2014

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“…This is not so rare a phenomenon as might appear at first sight. As an example, we may take the solid-state decyclization which takes place on the heating of Na3P30 9 "H20 crystals [9,10]. At any site inside the crystal there is one molecule of H20 per anionic cycle, and cycle opening according to the mechanism of intrinsic hydrolysis may occur with approximately equal probability at any point of the crystal volume.…”

mentioning

confidence: 99%

Some kinetic problems of inorganic topochemistry

Prodan¹

1987

Journal of Thermal Analysis

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ChemInform Abstract: Thermal Conversions of Sodium Cyclotriphosphate Monohydrate, Na₃P₃O₉·H₂O.

Galogaza¹,

Prodan²,

Pytlev³

et al. 1986

Chemischer Informationsdienst

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Thermal conversions of sodium cyclotriphosphate monohydrate, Na3P3O9 · H2O

Cited by 4 publications

References 5 publications

Synthesis, protonation equilibrium and peculiar thermal decomposition behavior of cyclo-tri-μ-imidotetraphosphate

Synthesis, protonation equilibrium and peculiar thermal decomposition behavior of cyclo-tri-μ-imidotetraphosphate

Some kinetic problems of inorganic topochemistry

ChemInform Abstract: Thermal Conversions of Sodium Cyclotriphosphate Monohydrate, Na₃P₃O₉·H₂O.

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Thermal conversions of sodium cyclotriphosphate monohydrate, Na3P3O9 · H2O

Cited by 4 publications

References 5 publications

Synthesis, protonation equilibrium and peculiar thermal decomposition behavior of cyclo-tri-μ-imidotetraphosphate

Synthesis, protonation equilibrium and peculiar thermal decomposition behavior of cyclo-tri-μ-imidotetraphosphate

Some kinetic problems of inorganic topochemistry

ChemInform Abstract: Thermal Conversions of Sodium Cyclotriphosphate Monohydrate, Na3P3O9·H2O.

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ChemInform Abstract: Thermal Conversions of Sodium Cyclotriphosphate Monohydrate, Na₃P₃O₉·H₂O.