Organic lithium phosphates

Molecular structures of some organic lithium phosphates. In (a) R1-R12 may be H halogen, or alkyl groups containing 1 to 3 carbon atoms. 

The step-growth polymerization of dibasic lithium phosphate is discussed next as an example of a polymerization reaction followed by immediate crystalhzation to the polymer, studied largely by thermal analysis [14,15]. It illustrates that not only organic molecules can be flexible macromolecules, but also inorganic ones. The two major techniques used for the analysis are differential scanning calorimetry (DSC, see Sect. 4.3) and thermogravimetry (TGA, see Sect. 4.6). The reaction equation is ... 

A suspension of lithium methoxide (prepared from 1.00 g (31.2 mmol) of methanol in 50 mL of THF and 17.7 mL (27.2 mmol) of 1.54 M butyllithium in hexane) is transferred via a cannula into a — 78 C sol ution of 5.86 g (27.1 mmol) of 2-[(/ )-(/T)-1-chloro-2-butenyl]-4,4,5,5-tctramethyl-l,3,2-dioxaborolane in 100 mL of THF. The solution is warmed, becoming homogeneous at 0 JC, and stirred for 1 h. Solvents arc removed in vacuo and the residue dissolved in 150 mL of petroleum ether (bp 40 -60 °C). This solution is washed with a citric acid/boric acid/phosphate buffer (pH 3) until the aqueous phase shows a pH of 4. The aqueous phase is extracted with 50 mL of petroleum ether (bp 40 - 60 rC). The combined organic extracts are dried over MgS04 and concentrated in vacuo to give a slightly tan oil yield 5.34 g (90%) ca. 90% ee. 

Cabon tetrachloride, n-hexane, chloroform, ACN, acetone, THF, pyridine, acetic acid, and their various mixtures were applied as mobile phases for adsorption TLC. Methanol, 1-propanol, ACN, acetone, THF, pyridine and dioxane served as organic modifiers for RP-TLC. Distilled water, buffers at various pH (solutions of and dipotassium hydrogen phosphate or potassium dihydrogen phosphate) and solutions of lithium chloride formed the aqueous phase. Carotenoids were extracted from a commercial paprika sample by acetone (lg paprika shaken with 3 ml of acetone for 30 min), the solution was spotted onto the plates. Development was carried out in a sandwich chamber in the dark and at ambient temperature. After development (15 cm for normal and 7cm for HPTLC plates) the plates were evaluated by a TLC scanner. The best separations were realized on impregnated diatomaceous earth stationary phases using water-acetone and water-THF-acetone mixtures as mobile phases. Some densitograms are shown in Fig.2.1. Calculations indicated that the selectivity of acetone and THF as organic modifiers in RP-TLC is different [14],... 

The early patent disclosures have claimed the application of a wide spectrum of gas-evolving ingredients and phosphorus-based organic molecules as flame retarding additives in the electrolytes. Pyrocarbonates and phosphate esters were typical examples of such compounds. The former have a strong tendency to release CO2, which hopefully could serve as both flame suppressant and SEI formation additive, while the latter represent the major candidates that have been well-known to the polymer material and fireproofing industries.The electrochemical properties of these flame retardants in lithium ion environments were not described in these disclosures, but a close correlation was established between the low flammability and low reactivity toward metallic lithium electrodes for some of these compounds. Further research published later confirmed that any reduction of flammability almost always leads to an improvement in thermal stability on a graphitic anode or metal oxide cathode. 

Sodium chloride, Sodium carbonate, Sodium sulphate, Calcium sulphate, Mono- and Di-basic potassium phosphate, Magnesium chloride, Magnesium sulphate, Lithium chloride Organic osmotic agents... 

Sodium chloride Sodium bromide Sodium iodide Sodium sulphate Sodium silicate Potassium sulphate Lithium chloride Calcium carbonate Calcium sulphate Magnesium sulphate Manganous carbonate Ferrous carbonate. Aluminium phosphate Ammonium nitrate Organic matter... 

Syn 3-(Ethylthiomethyl)-4-hydroxy-6-phenyl-2-hexanone (3) and (4).3 To ethane thiol (10 mg, 0.17 mmol) in THF (2 mL) was added 1.54 M n-butyl-lithium in hexane (0.11 mL) at 0°C under Ar. Stannous triflate (69.0 mg, 0.17 mmol) was added and after 20 min the mixture was cooled to 45°C. Methyl vinyl ketone 1 (118 mg, 1.98 mmol) in THF (1.5 mL) was added followed by 3-phenylpropanal 3 (350 mg, 2.61 mmol) in THF (1.5 mL). After 12 h aq. citric acid was added and the organic material extracted with CH2CI2. The residue after evaporation was dissolved in MeOH and treated with citric acid. After 30 min stirring, the mixture was quenched with pH 7 phosphate buffer, extracted with CH2CI2, the solvent evaporated and the residue chromatographed to afford 336 mg of 3 and 4 (75%), symanti = 90 10. 

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