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Proton hardness

We can also add inorganic acid to the resin to form the composite membrane. This membrane has a good electrical conductivity at high temperature where the proton hardly carries water molecules. This simplifies the water management. More details can be observed from literatures. [Pg.583]

The tliree protons in PH are identical aud indistinguishable. Therefore the molecular Hamiltonian will conmuite with any operation that pemuites them, where such a pemiutation interchanges the space and spin coordinates of the protons. Although this is a rather obvious syimnetry, and a proof is hardly necessary, it can be proved by fomial algebra as done in chapter 6 of [1]. [Pg.142]

The same reaction performed in ether at 0°C (336) gives the same major adduct, but the structure proposed by Acheson et al. corresponds to 86, although such a structure is hardly compatible with the presence of an isolated low-field proton. Very recently, in a reinvestigation of these cyclo-additions of DMA to azoles (338, 339), Acheson et al. were able to establish the correct structure of the adducts on the base of CNMR spectra and X-ray diffraction studies. The adduct of thiazole is represented by formula 87, and it results from the rearrangement of the... [Pg.95]

The O or S atoms in P=0 and P=S groups may act as electron donors although these groups form relatively weak complexes with electron acceptor compounds such as nonpolarizable, more electropositive (ie, hard) acids, including protons (14). Use is made of this property in the recovery of uranium from wet-process phosphoric acid by extractants such as trioctylphosphine oxide [78-50-2] and di(2-ethylhexyl) hydrogen phosphate [298-07-7]. [Pg.359]

A mercurinium ion has both similarities and differences as compared with the intermediates that have been described for other electrophilic additions. The proton that initiates acid-catalyzed addition processes is a hard acid and has no imshared electrons. It can form either a carbocation or a hydrogen-bridged cation. Either species is electron-deficient and highly reactive. [Pg.370]

Compound 5 was analyzed by NMR spectroscopy to gain information relative to conformation and complexation preferences. When complexation with potassium cations was attempted, the N—CHj signals were affected more than others. When the cation present was Ag , the protons adjacent to sulfur were more strongly affected. This observation may indicate the relative binding sites for soft versus hard cations in this system. ... [Pg.349]

Since one proton separation will hardly occur at pH 2.2, extraction ratios of Fe " with compounds 1-7 are quite low. Yet compound 8, which carries oxime groups, was able to extract a considerable amount of Fe- at pH 2.2. [Pg.344]

Today, the term solid electrolyte or fast ionic conductor or, sometimes, superionic conductor is used to describe solid materials whose conductivity is wholly due to ionic displacement. Mixed conductors exhibit both ionic and electronic conductivity. Solid electrolytes range from hard, refractory materials, such as 8 mol% Y2C>3-stabilized Zr02(YSZ) or sodium fT-AbCb (NaAluOn), to soft proton-exchange polymeric membranes such as Du Pont s Nafion and include compounds that are stoichiometric (Agl), non-stoichiometric (sodium J3"-A12C>3) or doped (YSZ). The preparation, properties, and some applications of solid electrolytes have been discussed in a number of books2 5 and reviews.6,7 The main commercial application of solid electrolytes is in gas sensors.8,9 Another emerging application is in solid oxide fuel cells.4,5,1, n... [Pg.91]

In this equation, r) the absolute hardness, is one-half the difference between /, the ionization potential, and A, the electron affinity. The softness, a, is the reciprocal of T]. Values of t) for some molecules and ions are given in Table 8.4. Note that the proton, which is involved in all Brdnsted acid-base reactions, is the hardest acid listed, with t — c (it has no ionization potential). The above equation cannot be applied to anions, because electron affinities cannot be measured for them. Instead, the assumption is made that t) for an anion X is the same as that for the radical Other methods are also needed to apply the treatment to polyatomic... [Pg.341]

Carboxylic esters are produced by the addition of carboxylic acids to alkenes, a reaction that is usually acid catalyzed (by proton or Lewis acids ) and similar in mechanism to 15-5. Since Markovnikov s rule is followed, hard-to-get esters of... [Pg.997]

From the crystal structure of the complex (Fig. 10) it appears that only minimal conformational changes occur within the MoFe protein on complexation, although it is hard to be dogmatic about these when at 3 A resolution. Nevertheless, ENDOR 116) studies on the FeMoco center demonstrated that at least one class of protons in the vicinity of the FeMoco center is altered in the complex relative to the free protein. [Pg.189]


See other pages where Proton hardness is mentioned: [Pg.105]    [Pg.86]    [Pg.105]    [Pg.86]    [Pg.580]    [Pg.191]    [Pg.146]    [Pg.164]    [Pg.572]    [Pg.42]    [Pg.23]    [Pg.46]    [Pg.491]    [Pg.102]    [Pg.89]    [Pg.164]    [Pg.236]    [Pg.293]    [Pg.159]    [Pg.361]    [Pg.8]    [Pg.106]    [Pg.277]    [Pg.161]    [Pg.3]    [Pg.134]    [Pg.120]    [Pg.561]    [Pg.38]    [Pg.447]    [Pg.185]    [Pg.227]    [Pg.756]    [Pg.154]    [Pg.117]    [Pg.345]    [Pg.443]    [Pg.444]    [Pg.22]    [Pg.149]    [Pg.257]    [Pg.14]   
See also in sourсe #XX -- [ Pg.133 ]




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Hard hydrogen-bonded protons

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