Alkyl chain internal motions

Howartht17b)has used the theory of Internal Librational Motion to successfully predict the field dependent relaxation behavior of the 1,2-decanediol (DD), PBMA, and PHMA systems (using our published experimental data). We have utilized together multiple internal rotations (MIR) and distributions of correlation times. These methods individually have been successful in predicting relaxation behavior at one field. However, only the distribution theory predicts the observed field dependence for the carbons at or near sites of motional restriction, yet still having apparent correlation times <10 <-)sec. Our interest in the study of concerted motions along these alkyl chains has led us to combine the two approaches in the treatment of 13C relaxation parameters. 

Nonionics. With selective deuteration in the alkyl chain, the internal gradient of mobility in adsorption layers could be monitored in a 2H-NMR-study of the non-ionic surfactant C12E5 adsorbed to colloidal silica [37, 38]. The surfactant was selectively deuterated in the a, (3, or y-position of the alkyl chain, respectively. Surface aggregate spectra were isotropically averaged with a Lorentzian lineshape, see Fig. 10, consequently the existence of an isotropic motional mode present in surface aggregates was concluded. 

Chachaty and co-workers [8.20, 8.37, 8.38] were first to describe correlated internal motions in alkyl chains of surfactant molecules that form lyotropic liquid crystals. The last section described an extension of the master equation method of Wittebort and Szabo [8.4] to treat spin relaxation of deuterons on a chain undergoing trans-gauche jump rotations in liquid crystals. This method was also followed by Chachaty et al. to deal with spin relaxation of nuclei in surfactants. However, they assumed that the conformational changes occur by trans-gauche isomerization about one bond at a time. In their spectral density calculations (see Section 8.3.1), they used a transition rate matrix that was constructed from the jump rate Wi, W2, and Ws about each bond. Since W3 is much smaller than Wi and W2, the time scale of internal motions was practically governed by Wi and W2 of each C-C bond. Since... 

The calculated Tc can be contributed by additional relaxation processes like fast local motions such as internal rotation around a three symmetrical axis in CH3, segmental motions of alkyl chains, conformational exchange of imidazorium ring or ring inversional motion of pyrrolidinium ring as given in Eq. (4). 

Thus far only processes involving motion of the surfactant as a whole have been mentioned. Other processes may occur in micellar solutions internal motion of the surfactant alkyl chains within the micelles exchange of cormterions between free and micelle-bound states and fast changes of micelle shape, among others. Also in the case of solubilized systems, i.e., micellar solutions that have solubilized compounds that are sparingly soluble in water, the solubilizate may exchange between micelles and the intermicellar solution. The dynamics of the exchange of counterions and of solubilizates are reviewed later. The dynamics of internal motions of the surfactant alkyl chains are not dealt with in this chapter, but some information and references can be found in Chapter 5, Section V. Some information on the fluctuations of micelle shapes can be found in Chapter 1, Section III.B. 

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