The photochemistry of the 4-methoxyphenacyl moiety is discussed in section 2.3.
In this review, fundamental aspects of construction of PEMs responsive to a variety of external stimuli such as pH, ionic strength, temperature, light, magnetic field or specific biological moieties, and their possible applications are discussed.
Difficulties associated with modelling the Pt moieties and their interactions with biomolecules are discussed.
The results are discussed in terms of the contributions of the disaccharide moieties into the strength of binding.
The effects due to the nature of the β-diketonate moiety as well as of the ancillary ligand on mentioned properties are discussed in detail.
Significance of C6-oxypicolinamide moiety and SAR study for the C2 aliphatic side chain of benzothiazole are discussed in detail.
The results are discussed in terms of the type of substituents on both main moieties and the linker size.
The photoinduced dichroism in the films has been measured, and the results are discussed in relation to the structure of these polymers, whereas the substitution of the azobenzene moiety and the structure of the backbone are varied.
A probable reason for the metabolic stability of the proposed side chain not having the possibility of generating peroxy type radicals or acrylic acid moieties, unlike Romazarit, is discussed.
A possible influence of the dye moiety on affinity is discussed below.
