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“Background SbQ (a styrylpyridinium salt), similar to surfactants, is an amphiphilic sensitizer of the styrylpyridinium family [1], and it produces a very planar stacked rod-like micelle structure. Such a structure makes it possible to stack the molecules with Thalidomide the hydrophobic regions one above the other, with the aldehyde

and nitrogen-methyl groups alternating, and finally produces an aggregate [2]. SbQ can react with amino groups of Apoptosis inhibitor proteins to improve the protein stabilization [3]. Moreover, it can be dimerized via the [2 + 2]-cycloaddition reaction under ultraviolet (UV) irradiation [4]. According to Tao et al. [5], cross-linking of the hydrophobic core via dimerization reaction of the SbQ molecules induced by UV light ultimately produced cross-linked micelles because of hydrophobic interactions between SbQ molecules. Hence, the cross-linked SbQ-montmorillonite (MMT) has potential applications for hydrophobic drug delivery and can be used as an additive into polymeric composites and improve the stability and mechanical properties of polymers [6–9].