As cosolvent

Note 1. If commercial BuLi in hexane is used with diethyl ether or THF as cosolvent, a dark brown reaction mixture is formed, from which the desired product can be isolated in lower yields. 

NMP are examples of suitable solvents for PES and PPSF polymerizations. Chlorobenzene or toluene are used as cosolvents at low concentrations. These cosolvents form an azeotrope with water as they distill out of the reaction mixture, thereby keeping the polymerization medium dehydrated. Potassium carbonate is a suitable choice for base. The synthesis of PES and PPSE differ from the PSE case in that the reaction is carried out in a single-step process. In other words, the formation of the dipotassium salt of the bisphenol is not completed in a separate first step. Equations 2 and 3 represent polymerizations based on the dipotassium salts of bisphenol S and biphenol to make PES and PPSE, respectively. 

H2NOH-HC1, Pyr, 60°. This is the standard method for the preparation of oximes. Ethanol or methanol can be used as cosolvents. 

Photolysis of aryl azides in amine solution, with a tertiary amine as cosolvent to promote stabilization of the singlet nitrene, has met with some success. For example, the yield of 2-piperidino-3 W-azepme. obtained by the photolysis of phenyl azide in piperidine, is increased from 35 to 58% in the presence of A A /V. /V -tetramethylethylenediamine (TMLDA).180 Also, an improved yield (36 to 60 %) of A,(V-diethyl-3W-azepin-2-amine (38, R = Et) can be obtained by irradiating phenyl azide in triethylamine, rather than in dicthylaminc, solution.181 Photolysis (or thermolysis) of phenyl azide in TMEDA produces, in each case, 38 (R = Et) in 40% yield.181 In contrast, irradiation of phenyl azide in aniline with trimethylamine as cosolvent furnishes jV-phenyl-377-azepin-2-amine (32, R = Ph) in only low yield (2%).35... 

To a stirred, cold (< —90 C) solution of 10 mmol of the nitroalkanc 1 in 60 mL of TltF/cosolvcnt (IIMPA or DMPU) is added dropwisc a solution of 12.8 mL of 1.16 N BuLi (20.5 mmol) in hexane (in the case of DMPU as cosolvent, the internal temperature is maintained below -88"C). The solution is warmed to... 

In the case of a water insoluble quinonc or carboxylic acid, acetonitrile can be used as cosolvent.2... 

Soluble organic solvents have often been used as cosolvents to solubilize miscible organic substrates. Since organic compounds including solvents are possibly incorporated inside of the enzyme, they may affect the stereoselectivity of enzymatic reactions. For example, dimethyl sulfoxide (DMSO) (10%) enhance not only chemical yield but also enantioselectivity of yeast reduction. Thus, the poor yield of 23% with 80% ee was increased to 65% yield with >99% ee (Figure 8.20) [17]. 

An intriguing influence of a cosolvent immiscible with water on the enantioselec-tivity of the enzyme-catalyzed hydrolysis was observed. It was proven that enzyme enantioselectivity is directly correlated with the cosolvent hydrophobicity. In the best example, for ethyl ether as cosolvent, the reaction proceeded with E = 55, and the target compound was obtained in 33% yield with 92.7% ee. This finding may be of great practical importance, particularly in industrial processes [24], since it will enable better optimization of enzyme-catalyzed processes. It is clear that, in future, immobilized enzymes, as heterogeneous catalysts, wiU be widely used in most industrial transformations, especially in the preparation of pharmaceuticals [25]. 

Surfactants. The use of surfactants is greatly restricted in formulating ophthalmic solutions. The order of surfactant toxicity is anionic > cationic >> nonionic. Several nonionic surfactants are used in relatively low concentrations to aid in dispersing steroids in suspensions and to achieve or to improve solution clarity. Those principally used are the sorbitan ether esters of oleic acid (Polysorbate or Tween 20 and 80), polymers of oxyethylated octyl phenol (Tyloxapol), and polyoxyl 40 stearate. The lowest concentration possible is used to perform the desired function. Their effect on preservative efficacy and their possible binding by macromolecules must be taken into account, as well as their effect on ocular irritation. The use of surfactants as cosolvents for an ophthalmic solution of chloramphenicol has been described [271]. This com-... 

Along another line of work in our group (S,S)-l,4-bis(dimethylamino)-2,3-dimethoxy butane (DDB), which had been used as cosolvent in asymmetric synthesis [113], was tested as a core moiety for a dendritic amine catalyst. The conformationally flexible DDB-core, which has been synthesized in five steps from diethyl tartrate was coupled with different branches to give dendritically expanded diamines 90-92 (molecular weight 3800 Da) [114] (Fig. 32). 

Addition of ethylene glycol as cosolvent, as in Eq. (11.16), resulted in efficient formation of the corresponding benzoic acid, instead of the amide [29]. 

Use of cosolvent. Various cosolvents, such as acetone, ethanol, methanol, hexane, dichloromethane, and water, have been used for the removal of carotenoids using SC-CO2 extraction (Ollanketo and others 2001). All these cosolvents except water (only 2% of recovery) increased the carotenoid recovery. The use of vegetable oils such as hazelnut and canola oil as a cosolvent for the recovery of carotenoids from carrots and tomatoes have been reported (Sun and Temelli, 2006 Shi, 2001 Vasapollo and others 2004). For the extraction without cosolvent addition, the lycopene yield was below 10% for 2- to 5-hr extraction time, whereas in the presence of hazelnut oil, the lycopene yield increased to about 20% and 30% in 5 and 8 hr, respectively. The advantages of using vegetable oils as cosolvents are the higher extraction yield the elimination of organic solvent addition, which needs to be removed later and the enrichment of the oil with carotenoids that can be potentially used in a variety of product applications. 

Adapted from Bhaumik et al. 244). Reaction conditions reaction time, 12 h reactant H202 = 1 1 catalyst (TS-1, Si/Ti = 29), 20 wt% with respect to reactant temperature, 353 K. a Tri solid catalyst + two immisible liquid phases (organic reactant + H202 in water) bi solid catalyst + one homogeneous liquid phase (organic reactant + aqueous H202 + CH3CN as cosolvent). 

DMF), /V,/V-dimethylacetamide (DMAc), DMSO, hexamethylphosphoric triamide (HMPA), and AT-methyl-2-pyrrolidone (NMP) may be used as cosolvents. 

Thus, any change in the independent variables P, T, j8p, j3w, and 8 would produce a change in the volume and surface area of the protein substrates which either bind on the surface of the protein or bind within the protein and change j3p, as well as cosolvents which have an effect on Py, can be included in this treatment. 

After more than a decade of exploration, the skeletal components of the electrolyte for the commercialized lithium ion devices have been identified. Within the various brands of lithium ion cells, the exact electrolyte composition differs from manufacturer to manufacturer, and the formulas remain proprietary information however, the overwhelming majority of these are apparently based on two indispensable components EC as the solvent and LiPFe as the solute. In most cases, one or more linear carbonates, selected from DMC, DEC, or EMC, are also used as cosolvents to increase the fluidity and reduce the melting point of the electrolyte, thus forming the popular composition consisting of LiPFe/ EC/linear carbonate (s). 

Like linear carbonates, none of these linear esters were used as single solvents but rather as cosolvents... 

Like all the phosphates investigated as cosolvents, TBP and TPP showed higher anodic stability, as confirmed by their cycling in lithium ion cells based on a LiNio.8Coo.2O2 cathode up to 4.2 V, and separate cyclic voltammetry tests also showed that they would not decompose anodically below 5.0 V on an inert working electrode. Little capacity fading was detected during the extended tests of TPP or TBP in full lithium ion cells up to 150 cycles. 

For this reason ClEC and FEC were treated as cosolvents in this review, instead of as additives as they were in most literature sources. 

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