Temperature- and Light-Responsive Polyacrylamides Prepared by a Double Polymer Analogous Reaction of Activated Ester Polymers was written by Jochum, Florian D.;Theato, Patrick. And the article was included in Macromolecules (Washington, DC, United States) in 2009.Recommanded Product: Benzyl benzodithioate This article mentions the following:
Two different series of polyacrylamides containing different amounts of salicylideneaniline moieties have been synthesized via a double polymer analogous reaction of poly(pentafluorophenyl acrylate) (PPFPA). All copolymers were designed to exhibit a lower critical solution temperature (LCST) in aqueous solution, which was dependent on (i) the amount of incorporated chromophoric salicylideneaniline groups and (ii) the isomerization state of the resp. salicylideneaniline group. Higher LCST values were measured for UV-irradiated solutions of the copolymers in comparison to the nonirradiated copolymer solutions A maximum difference in the LCST of up to 13 °C was found for poly(N-cyclopropylacrylamide) copolymer containing 15.0 mol % of salicylideneaniline groups. Within this temperature range, a reversible solubility change of the copolymer could be induced by irradiation with light. In the experiment, the researchers used many compounds, for example, Benzyl benzodithioate (cas: 27249-90-7Recommanded Product: Benzyl benzodithioate).
Benzyl benzodithioate (cas: 27249-90-7) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Recommanded Product: Benzyl benzodithioate
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics