Ammonia thermal stability

The organotin amine compounds, with a few exceptions, are liquids. They are extremely sensitive toward moisture when exposed to the air they immediately liberate amine or ammonia. Thermal stability on the other hand is good. Most compounds can be distilled without decomposition. From NMR studies it has been concluded 86) that the tin-nitrogen bond in diethylaminotin compounds is purely covalent. 

The oxide is soluble in ammonia to give the complex [AglNHjlj] (linear). On heating, silver(I) oxide loses oxygen to give the metal (all the coinage metal oxides have low thermal stability and this falls in the order Cu > Ag > Au). 

Thionyl imide, HNSO, is a thermally unstable gas, which polymerizes readily. It can be prepared by the reaction of thionyl chloride with ammonia in the gas phase. Organic derivatives RNSO have higher thermal stability, especially when R = Ar. The typical synthesis involves the reaction of a primary amine or, preferably, a silylated amine with thionyl chloride. A recent example is the preparation of FcNSO (Fc = ferrocenyl) shown in Eq. 9.8. In common with other thionylimines, FcNSO readily undergoes SO2 elimination in the presence of a base, e.g., KO Bu, to give the corresponding sulfur diimide FcNSNFc. 

Herrmann et al. reported for the first time in 1996 the use of chiral NHC complexes in asymmetric hydrosilylation [12]. An achiral version of this reaction with diaminocarbene rhodium complexes was previously reported by Lappert et al. in 1984 [40]. The Rh(I) complexes 53a-b were obtained in 71-79% yield by reaction of the free chiral carbene with 0.5 equiv of [Rh(cod)Cl]2 in THF (Scheme 30). The carbene was not isolated but generated in solution by deprotonation of the corresponding imidazolium salt by sodium hydride in liquid ammonia and THF at - 33 °C. The rhodium complexes 53 are stable in air both as a solid and in solution, and their thermal stability is also remarkable. The hydrosilylation of acetophenone in the presence of 1% mol of catalyst 53b gave almost quantitative conversions and optical inductions up to 32%. These complexes are active in hydrosilylation without an induction period even at low temperatures (- 34 °C). The optical induction is clearly temperature-dependent it decreases at higher temperatures. No significant solvent dependence could be observed. In spite of moderate ee values, this first report on asymmetric hydrosilylation demonstrated the advantage of such rhodium carbene complexes in terms of stability. No dissociation of the ligand was observed in the course of the reaction. 

A,A -Bis(3-aminopicryl)-l,2-ethanediamine (108) (m.p. 275 °C) is prepared from the reaction of ethylenediamine with two equivalents of 3-chloro-2,4,6-trinitroaniline. " The same chemists reported 3,3 -diamino-2,2 4,4, 6,6 -hexanitrodiphenylamine (109), a heat resistant explosive (m.p. 232-237 °C) prepared from the reaction of l,3-dichloro-4,6-dinitrobenzene with 3-chloroaniline followed by mixed acid nitration and subsequent chloro group displacement with ammonia. The potassium salt of 3,3 -diamino-2,2, 4,4, 6,6 -hexanitrodiphenylamine shows very high thermal stability. " ... 

The conjugation in 2,2, 4,4, 6,6 -hexanitroazobenzene (HNAB) (90) is also reflected in its thermal stability (m.p. 220 °C). The synthesis of HNAB from picryl chloride and 2,4-dinitrochlorobenzene is discussed in Sections 4.8.1.2 and 4.8.1.3 respectively. 3,3, 5,5 -Tetraamino-2,2, 4,4, 6,6 -hexanitroazobenzene (149) has been synthesized by an unusual but efficient route which involves the nitration-oxidative coupling of 3,5-dichloroaniline (147) on treatment with nitric acid, followed by reaction of the resulting product, 3,3, 5,5 -tetrachloro-2,2, 4,4, 6,6 -hexanitroazobenzene (148), with ammonia. Both the tetrachloro (148) and tetraamino (149) derivatives exhibit high thermal stability. 

The surface nethoxyl groups on the modified catalyst were measured by i.r. spectroscopy and their thermal stabilities were studied by Temperature-Programmed Decomposition (TPDE) in Ar. The surface acidity was measured by TPD of irreversibly adsorbed ammonia and by pyridine adsorption by dynamic method and i.r. spectroscopy. 0.10 g pretreated catalyst was used to measure the amount of irreversibly adsorbed pyridine. The irreversibly adsorbed ammonia was... 

The product is rather volatile, with an estimated b.p. between 100 and 110 C at 760 mmHg. If the ethylation was carried out at the b.p. of ammonia and this solvent allowed to evaporate, 5-10% of the product would be lost. For this reason and also in view of the limited thermal stability of 1,3-hexadiyne (danger of explosive decomposition at elevated temperatures) we propose a work-up procedure similar to that used in exp. 3. 

The 1-nitro-2-nitramino-A -imidazoline is an explosive comparable in brisance and power to RDX, but it, is much more sensitive to impact. Its thermal stability is low, since 97% is destroyed by 5 minutes of boiling in water. When 1-nitro-2-nitroaminoimidazoline is dissolved in cold aq ammonia and then acidified a stable product corresponding to the formula CH2.NH nh2... 

Derivatives of alkaline, alkaline earth metals and phenols, naphtols, an-troles, etc. (pK> 10). These compounds are salts in their nature and, as the salts of strong bases and moderately weak acids, can exist in water solutions. They are soluble only in polar solvents (water, liquid ammonia), are prone to form adducts with phenols, water, etc., have high thermal stability and cannot be transferred into the gas phase. 

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