Ionic protic

The latter appears to be formed as a result of HX generation and is the exclusive product under ionic (protic) conditions <83BCJ3193>. 

Solvent Effects on the Rate of Substitution by the S 2 Mechanism Polar solvents are required m typical bimolecular substitutions because ionic substances such as the sodium and potassium salts cited earlier m Table 8 1 are not sufficiently soluble m nonpolar solvents to give a high enough concentration of the nucleophile to allow the reaction to occur at a rapid rate Other than the requirement that the solvent be polar enough to dis solve ionic compounds however the effect of solvent polarity on the rate of 8 2 reactions IS small What is most important is whether or not the polar solvent is protic or aprotic Water (HOH) alcohols (ROH) and carboxylic acids (RCO2H) are classified as polar protic solvents they all have OH groups that allow them to form hydrogen bonds... 

Eor ionic liquids that do not mix completely with water (and which display sufficient hydrolysis stability), there is an easy test for acidic impurities. The ionic liquid is added to water and a pEf test of the aqueous phase is carried out. If the aqueous phase is acidic, the ionic liquid should be washed with water to the point where the washing water becomes neutral. Eor ionic liquids that mix completely with water we recommend a standardized, highly proton-sensitive test reaction to check for protic impurities. 

Obviously, the check for protic impurities becomes crucial if the ionic liquid is to be used for applications in which protons are known to be active compounds. Eor some organic reactions, one has to be sure that an ionic liquid effect does not turn out to be a protic impurity effect at some later stage of the research ... 

Apart from halide and protic impurities, ionic liquids can also be contaminated with other ionic impurities from the metathesis reaction. This is especially likely if the alkali salt used in the metathesis reaction shows significant solubility in the... 

Water in an ionic liquid may be a problem for some applications, but not for others. However, one should in all cases know the approximate amount of water present in the ionic liquid used. Moreover, one should be aware of the fact that water in the ionic liquid may not be inert and, furthermore, that the presence of water can have significant influence on the physicochemical properties of the ionic liquid, on its stability (some wet ionic liquids may undergo hydrolysis with formation of protic impurities), and on the reactivity of catalysts dissolved in the ionic liquid. 

The influence of the acidity of the relevant protic substrates on the final reaction products is further demonstrated by two examples shown in Scheme 2. Decamethylsilicocene (1) reacts with HBF4 to yield the compound [Cp SiF]4, whereas in the reaction with PyH+BF4 (Py=pyridine) the oxidative addition product Cp 2Si(H)F is formed. Reaction of 1 with two equivalents of F3CS03H leads to an ionic species,... 

Bromination is less stereoselective, and the reactions of cis- and trans-olefins tend to be stereoconvergent. The stereospecific formation of the mixed bromoadducts in protic media, such as methanol or acetic acid, could be interpreted in the light of the recent finding (Ruasse et al., 1991) that these solvents assist the formation of the ionic intermediate nucleophilically. If a solvent molecule is close to the cationic part of the transition state in the rate-limiting step, the intermediate can be trapped by this solvent molecule in a necessarily trans mode with respect to the first bromine, before the two components of the ion-pair diffuse away from each other (15). This would... 

The UV spectra of nitronates, which are not functionalized at the a-C atom, have an intense absorption at 230 to 240 nm, which is very similar in characteristics to UV absorption of salts of nitro compounds and solutions of aci-nitro compounds in protic solvents. Since standard alkyl- or silyl nitronates cannot have ionic structures, the presence of the above mentioned absorption in the UV spectra of nitronates, unambiguously confirms, that these compounds have the structures of O-esters. 

Miscibility is an important consideration when selecting solvents for use in biphasic systems. Table 4.4 shows the miscibility of three ionic liquids with water and some organic solvents. [bmim][PFe] was found to be miscible with organic solvents whose dielectric constant is higher than 7, but was not soluble in less polar solvents or in water. Basic [bmim][AlCl4] was found to react with protic solvents, and the acidic form also reacted with acetone, tetrahydrofuran and toluene. 

The first step is usually the formation of a halogen-olefin charge transfer complex30,70, which rapidly evolves to an ionic intermediate. Protic solvents can electrophilically assist... 

This hl-alkylated heterocycle (2) acts as the actual initiator because it is attacked rapidly under ring-opening by an oxazoline molecule, present in excess. The newly formed dimer (3) contains an ionic ring function, which is subjected to the same attack as the initiator molecule. The molecular weight of the polymers is controlled by the amount of the alkylating agent. Other suitable initiators for the polymerization of oxazolines are Lewis acids, protic acids, and alkyl chloroformates. 

Various methods and reagents have been used to effect the interconversion between meso-ionic isomers 304 305 including (i) heating in protic solvents such as ethanol or ethyl mercaptan, - (ii) treatment with hot ethanolic ammonia or ethanolic sodium hydroxide, - (iii) heating, (iv) heating with aryl isocyanates or isothiocyanates. ... 

Fig. 3. Equilibration of meso-ionic isomers in protic solvents (e.g., EtOH) involving a betaine intermediate.

Reaction between C in methanol and RTCNQ in acetonitrile yielded three kinds of ionic solids (1) insulators composed of methoxy substituted RTCNQ anions such as (CHC )[F4TCNQ-0Me ](H20) (Fig. 6) [136], (2) semiconducting CT solids with fully ionic RTCNQ radical anions such as (CHC )(TCNQ ) [137, 138], and (3) conducting CT solids of partially ionic or mixed valent RTCNQ radical anions such as (CHC"XMeTCNQ° >2 [138], where CHC" is the hemiprotonated cytosine pair (Fig. 6b). Cation units in aU products were found to be protonated cytosine species, most commonly CHC, where comes from methanol. This result suggests that the intrinsic transport properties of DNA should be studied not in protic solvents but under strictly dried conditions. 

Protic impurities have to be taken into account for two groups of ionic Hquids those that have been produced by an exchange reaction involving a strong acid (often the case, for example, for [BMIM][PF ]), and those that are sensitive to hydrolysis. In the latter case, the protons may originate from the hydrolysis of the anion, forming an acid that may be dissolved in the ionic liquid. 

Reactions with Protic, Ionic, Polar Reagents. 250... 

Reactions with Protic, ionic, Poiar Reagents. The reactions of radical anions with proton donors include the reduction of arenes, the well-known Birch reduction, as well as alkynes by alkali metals in liquid ammonia. Both reactions have synthetic utility and belong to the few radical ion reactions included in elementary textbooks. 

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