Sulfides alkylene

Other modifications of the polyamines include limited addition of alkylene oxide to yield the corresponding hydroxyalkyl derivatives (225) and cyanoethylation of DETA or TETA, usuaHy by reaction with acrylonitrile [107-13-1/, to give derivatives providing longer pot Hfe and better wetting of glass (226). Also included are ketimines, made by the reaction of EDA with acetone for example. These derivatives can also be hydrogenated, as in the case of the equimolar adducts of DETA and methyl isobutyl ketone [108-10-1] or methyl isoamyl ketone [110-12-3] (221 or used as is to provide moisture cure performance. Mannich bases prepared from a phenol, formaldehyde and a polyamine are also used, such as the hardener prepared from cresol, DETA, and formaldehyde (228). Other modifications of polyamines for use as epoxy hardeners include reaction with aldehydes (229), epoxidized fatty nitriles (230), aromatic monoisocyanates (231), or propylene sulfide [1072-43-1] (232). 

Anionic polymerization of alkylene sulfides was extensively studied by Sigwalt and collaborators. In contrast to propylene oxide, anionic polymerization of pro-... 

Alkylene sulfide —CH2CH2S—CH2CH2S— Linear polymer converted with some difficulty to ring 3 ... 

Alkylene ether-sulfide —CH2CH20—CH2CH2S— Linear polymer ... 

The reaction of suitable aliphatic dihalogen compounds with alkali or alkaline earth polysulfides results in the formation of linear, rubbery or resinous, po-ly(alkylene sulfide)s ... 

Among the variations in chemical structure of these triblock copolymers developed in our laboratories were the use of poly(a-methyl styrene)(43, 44) as end blocks, and poly(alkylene sulfides) (42, 45 ) 311 d polydimethylsiloxanes (43, 46) as center blocks. The reactions of cyclic sulfides with organolithium is illustrated in Figure 10. Both the propylene sulfide and the methyl thietane can be used for the center block with styrene or a-methylstyrene end blocks, but the chemistry shown in Figure 10... 

Extremely shock-sensitive alkylene bis[5-thiatriazolyl]sulfides were prepared by Pilgram et al.44 45 by treating sodium thiatriazole-5-thiolate with dihaloalkane. Dichloromaleimide reacted analogously.45... 

The structurally ordered poly(ester 0-sulfide)s are designated according to the number n of methylene units in the sulfide segment, or to the number m of methylene units in the fully alkylene segment in their repeat unit. 

The reaction of carbon disulfide with 1,2-alkylene diamines (I) yields N-(2-aminoethyl) dithiocarbamic acids (II) which split off hydrogen sulfide thermally to give imidazolidine-2-thiones (III) (Hofmann-process). The simplest example, the reaction of carbon disulfide with ethylenediamine, is described in Organic Synthesis (5). The reaction is general for N,N -dialkyl-, N,N -diaryI, as well as for N,N -bis-(arylakyl) ethylene diamines. The rate of reaction is determined by the basicity of the diamine. Electron-donor substituents in the para-position of N-aromatically substituted ethylene diamines accelerate dithiocarbamate formation electron-acceptor groups retard it. 

Poly(ethylene oxide) is a linear polymer containing the donor oxygen atoms in the main backbone. Some other similar systems known to function as polymer electrolytes include simple poly ethylene glycol (PEG) [145], end acetylated PEG [146], poly propylene oxide (PPO) [ 147-148], poly(/ -propiolactone) [149], polyethylene succinate) [150-151],poly (ethylene adipate) [152],poly (ethylene imine) [153] and poly (alkylene sulfide) [154], Many of these form metal salt complexes. However, conductivities of the order of 10 s S cm are observed only at high temperatures. Table 5 summarizes this data. 

It is claimed that styrene/butadiene diblock polymers bring about an improvement in the hardness, strength, and processability of polybutadiene elastomers (27), as well as an improvement in the ozone resistance of neoprene rubber (28). Styrene diblock polymers have also been made with isoprene, a-methyIstyrene, methyl methacrylate, vinylpyridine, and a-olefins. Block copolymers of ethylene, propylene, and other a-olefins with each other have been made as well. Heteroatom block copolymers based on styrene or other hydrocarbons and alkylene oxides, phenylene oxides, lactones, amides, imides, sulfides, or slloxanes have been prepared. 

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