4.6 Article

Activation and Inhibition of Isomerization of a Cationic Azobenzene Surfactant in the Large Void Space of Polyglycerol Dendron Micelles

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LANGMUIR
卷 39, 期 11, 页码 4015-4025

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AMER CHEMICAL SOC
DOI: 10.1021/acs.langmuir.2c03373

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Due to the unique geometric structure of dendritic amphiphiles, their micelles can provide a large void space, which offers a new research focus and approach for micellar functionalization. In this study, we used the void space to construct a UV-responsive micelle system of mixed dendritic amphiphile and cationic azobenzene surfactant. The results showed that the micelles can inhibit the UV response of the trans-isomer and activate the thermal relaxation of the cis-isomer, suggesting potential applications in light-controlled smart nanocarriers.
Owing to the unique geometric structure of dendritic amphiphiles with voluminous dendrons, their micelles can harbor a large void space, which provides a new research focus and approach for micellar functionalization. In this work, we used the void space to construct a UV responsive micelle system of the mixed dendritic amphiphile (C-12-(G(3))(2)) and cationic azobenzene surfactant (C4AzoTAB). The synthesized C-12(G(3))(2) that possesses double third generation polyglycerol (PG) dendrons and a single alkyl chain is expected to highlight the large void space within the inside of the micelles. Thus, the aims of this work are to achieve the isomerization of C4AzoTAB in situ and to deeply understand the intermolecular interaction in the mixed micelles. The effect of the large void room with a wall decorated with the ether oxygen atoms on the isomerization of C4AzoTAB was studied by isomerization kinetics, conductivity measurements, isothermal titration calorimetry (ITC), and H-1 NMR and 2D NOESY spectroscopies. The isomerization behavior of C4AzoTAB in C-12-(G(3))(2) micelles was presented in terms of its kinetic constant, counterionic association, interaction enthalpy, and position and orientation of C4AzoTAB. The results of NMR and conductivity show that the quaternary ammonium group of C4AzoTAB situates on the surface of the mixed micelles with C-12-(G(3))(2) both before and after UV-irradiation, while the position of azobenzene group in C-12-(G(3))(2) micelles depends on its conformation. The C-12-(G(3))(2) micelles can inhibit the UV response of the trans-isomer and activate the thermal relaxation of the cis-isomer, which has a potential application in the field of light-controlled smart nanocarriers.

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