As for CH-C1 xerogel from 1,4-dioxane, due to the flexibility of

As for CH-C1 xerogel from 1,4-dioxane, due to the flexibility of ether band in the molecular skeleton and different intermolecular forces with solvents, after the intermolecular hydrogen bonding and orderly

stacking in different solvents, various repeating units with different lengths were obtained. So selleckchem corresponding d values of 4.07 and 2.84 nm were obtained from 1,4-dioxane and nitrobenzene, respectively, as shown in Figure  7a,b. As for CH-C3 with an additional diphenyl group linked by ether band in the spacer part, the combination of a flexible ether band and a rigid diphenyl segment in the molecular spacer with π-π stacking seemed more suitable to adjust molecular conformation to self-assemble and form organized stacking nanostructures. The obtained experimental value of CH-C3 in nitrobenzene was 2.14 nm, which was near half of the calculated molecular length, suggesting a symmetrical stacking mode, shown in Figure  7c. In addition, for the case of CH-C4 with a five-carbon alkyl substituent chain linked by phenoxy ether band in the molecular spacer, due to the addition of a flexible

alkyl segment and a weak hydrophobic force between alkyl chains, it can also stack and form some belt-like aggregates with a stacking length of 3.23 nm in nitrobenzene, as shown in Figure  7d. Moreover, for CH-C2 and CH-N1, the inefficient or poor gelation behaviors in the present solvents

may be mainly attributed to the too rigid or too flexible spacers in molecular skeletons, which cannot cause enough intermolecular forces to make the molecules align and stack in an organized way to form various nanostructures. Meanwhile, it should be noted that this phenomenon can be compared with the results of our recent works [24, 25, 48]. Therein, functionalized imide derivatives with the substituent groups of cholesteryl, azobenzene, luminol, and benzimidazole/benzothiazole residue can have a profound effect on the gelation abilities and the as-formed nanostructures of the Erastin purchase studied compounds. For the present gelators, the experimental data showed that the spacers in the molecular skeleton have played a crucial role in the gelation behavior of all gelators in various organic solvents. Suitable combination of flexible/rigid segments in molecular spacers in the present cholesteryl gelators is favorable for the gelation of organic solvents. Now, the drug release behaviors generated by the present xerogels in the mixture of Congo red are under investigation to display the relationship between the molecular structures of as-formed nanostructures and their properties. Figure 7 Rational assembly modes of CH- C1, CH- C3, and CH- C4 in gels. Experimental values of (a, b) CH-C1 in 1,4-dioxane and nitrobenzene, (c) CH-C3 in nitrobenzene, and (d) CH-C4 in nitrobenzene.

Comments are closed.