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

Abstract

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.

15N and31P NMR Insights into Lactam–Lactim Tautomerism Activity Usingcyclo-μ-Imidopolyphosphates

“…Hence in this study the product mixture was separated and purified by a pH-controlled recrystallization process by applying the pH dependence of the difference in the solubility of Na 3 cP 3 O 6 (NH) 3 and Na 4 cP 4 O 8 (NH) 4 as illustrated in Scheme S2 (Supporting Information) as well as our previous report. 37 The product mixture (1.59 g) was dissolved in 45 mL of water, adjusted to pH 2.5 with nitric acid, and 18 mL of acetone was added to this solution, and then 15 N-Na 4 cP 4 O 8 (NH) 4 precipitated. The precipitate was collected by suction filtration, and then the filtrate was adjusted to pH 6.7 with sodium hydroxide.…”

Quantitative NMR of quadrupolar nucleus as a novel analytical method: hydrolysis behaviour analysis of aluminum ion

“…As a result, it is possible not only to trace chemical reactions, but also to determine chemical equilibrium constants. [35][36][37][38][39] Furthermore, variable temperature measurements allow analysis of the reaction rate and determination of the activation energy.…”

“…In contrast, the concentration of a specific chemical species or functional group can be directly determined by qNMR from the integrated intensity of the corresponding NMR signal if a known amount of an internal standard is added and a calibration curve is prepared with an external standard. All nuclei can be classified as dipolar or quadrupolar nuclei in terms of magnetic resonance; dipolar nuclei (e.g., 1 H, 13 C, 19 F, 29 Si, and 31 P) have a spin quantum number of 1/2 and quadrupolar nuclei (e.g., 7 Li, 11 B, 23 Na, 27 Al, and 35 Cl) have a spin quantum number that is not 1/2. qNMR analysis has been reported for many dipolar nuclei.…”