Nitrogen compounds ethers

The key initiation step in cationic polymerization of alkenes is the formation of a carbocationic intermediate, which can then interact with excess monomer to start propagation. We studied in some detail the initiation of cationic polymerization under superacidic, stable ion conditions. Carbocations also play a key role, as I found not only in the acid-catalyzed polymerization of alkenes but also in the polycondensation of arenes as well as in the ring opening polymerization of cyclic ethers, sulfides, and nitrogen compounds. Superacidic oxidative condensation of alkanes can even be achieved, including that of methane, as can the co-condensation of alkanes and alkenes. 

Chlorine Ammonia, acetylene, alcohols, alkanes, benzene, butadiene, carbon disulflde, dibutyl phthalate, ethers, fluorine, glycerol, hydrocarbons, hydrogen, sodium carbide, flnely divided metals, metal acetylides and carbides, nitrogen compounds, nonmetals, nonmetal hydrides, phosphorus compounds, polychlorobi-phenyl, silicones, steel, sulfldes, synthetic rubber, turpentine... 

Cyanuric acid is only slightly soluble (<0.1%) at room temperature ia common organic solvents such as acetone, benzene, diethyl ether, ethanol, and hexane (13). SolubiUty is significant ia basic nitrogen compounds (eg, dimethylformamide 7.2%) or unusual solvents such as DMSO (17.4%). SolubiUty ia... 

Oxidative reactions frequently represent a convenient preparative route to synthetic intermediates and end products This chapter includes oxidations of alkanes and cycloalkanes, alkenes and cycloalkenes, dienes, aromatic fluorocarbons, alcohols, phenols, ethers, aldehydes and ketones, carboxylic acids, nitrogen compounds, and organophosphorus, -sulfur, -selenium, -iodine, and -boron compounds... 

Damascenine, CjqHj3N03, is a nitrogenous compound of an alkaloidal nature, which is present in the oil of Nigella damascena to the extent of about 9 per cent. It can be extracted from the oil by shaking it with dilute hydrochloric acid, rendering the aqueous liquid alkaline and extracting the alkaline liquid with petroleum ether. 

Many GTL-derived fuels are being considered for blending with gasoline and diesel to achieve emission reductions of particulate matter (PM), carbon monoxide (CO), nitrogen compounds (NOx) and nonmethane hydrocarbons (NMHC). The most promising fuels converted from natural gas are methanol and ethers such as dimethyl ether (DME) and mcthyl-t-bntyl ether (MTBE). 

Nitrogen compounds are also effective as nucleophiles in the anodic oxidation of silyl-substituted ethers. The electrochemical oxidation in the presence of a carbamate or a sulfonamide in dry THF or dichloromethane results in the selective cleavage of the C-Si bond and the introduction of the nitrogen nucleophile at the carbon (Scheme 21) [55]. Since a-methoxycarbamates are useful intermediates in the synthesis of nitrogen-containing compounds [44], this reaction provides useful access to such compounds. Cyclic silyl-substkuted ethers such as 2-silyltetrahydrofurans are also effective for the introduction of nitrogen nucleophiles. The anodic oxidation in the presence of a carbamate or a... 

Oxygen is so electronegative that inductive effects from substituents have rather less influence on basicity than they would in similar nitrogen compounds. Alcohols are somewhat less basic than water, with ethers weaker still. 

The chemistry of saturated heterocyclic compounds is characteristic of their functional group. For example, nitrogen compounds are amines, oxygen compounds arc ethers, sulfur compounds are sulfides. Differences in chemical reactivity are observed for three-membered rings, e.g., epoxides, whose enhanced reactivity is driven by the relief of their severe ring strain. This chapter discusses heterocycles that are aromatic and have unique chemical properties. 

Ethyl ether therefore gives off twice as much hydrogen and absorbs twice as much nitrogen as methyl ether, which seems to point to a fixed ratio between the nitrogen compounds formed and the molecular weight of the compounds started with. 

The vapor pressure of /i-[(CH3)2N]B2H5 obeys the relationship log P = 2158.56/T + 1.75 log T - 0.008061T + 7.518831 (101 torr at 0°). The gas-phase infrared spectrum has been reported in detail.5 The compound is a useful intermediate in the synthesis of other boron nitrogen compounds, including those containing NBNB6 and PBNB7 chains, and Na[(CH3)2-N(BH3)2].8 The compound can be stored at 25° for months in sealed, evacuated Pyrex tubes. It is soluble in ethers and aromatic hydrocarbons, but is attacked by protic solvents. 

As shown by Schlesinger et treatment of an ethereal solution of aluminum chloride with excess lithium aluminum hydride leads to the formation of aluminum hydride which may be used in situ in reductions of a variety of nitrogen compounds.74,76 In these reductions, aluminum hydride shows a similar reductive ability as lithium aluminum hydride. 

Many variations " have been used in the preparation of borazines and boranes. The first convenient syntheses utilized lithium tetrahydroborate and an amine hydrochloride in ether. An attempt was made to modify these procedures so that the above boron-nitrogen compounds... 

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