H-acceptor sites, which are able to form intra-molecular reversible hydrogen bonds (globule conformation below UCST) and inter-molecular bonds with water (coil conformation above UCST). [11][12][13][14][15][16][17][18][19][20][21] The non-ionic polymers have attracted a great deal of attention due to their insensitivity to salts, which make them more attractive for applications in physiological environment. [22][23][24] During the last decade, efforts have been focused toward developing novel water-soluble copolymers exhibiting UCST behavior by copolymerizing H-donor monomers (N-acryloyl glycinamide [11][12][13][14][15][16] or acrylamide [15,[17][18][19][20][21]25] ) and H-acceptor monomers (acrylonitrile, [11,15,18,19,21,25,26] styrene, [15,17] and butyl acrylate [15] ). Such (co)polymers have been mainly prepared using free radical polymerization [11,[14][15][16][17]26] and by thermally initiated controlled radical polymerization such as atom transfer radical polymerization [13] and reversible addition fragmentation chain transfer (RAFT) [11,12,[16][17][18][19]25] The impacts of various parameters on the UCST phase transition, including salts, pH, molecular weight, molecular weight distribution, and chemical composition, have been well evaluated. [7][8][9]25,27] However, such studies were carried out at low polymer concentrations (below 5 wt%). This could induce, an unintentional confusion between the UCST and the apparent cloud point temperature (T CP ), which refers to the temperature at which the phase transition occurs depending on the investigated concentration level. The UCST of a given polymer in solution is obtained from an isobaric phase diagram where T CP are plotted versus the polymer concentrations. [7][8][9] T CP should increase with the polymer concentrations up to a maximum temperature, called UCST, before going down again.In this context, we envisioned to use aqueous photo-mediated RAFT (photo-RAFT) polymerization that would be able to prepare well-controlled UCST-type copolymers directly in water at very high concentration. Although photo-RAFT [28][29][30][31][32][33] has grasped great interests due to its versatility, rapidity, and ability to produce well-controlled polymers, it has never been employed for the synthesis of UCST-type polymers. This study provides new insight into UCST-type copolymers and aims to develop facile approach to investigate such kind of thermoresponsive behavior, less described in the literature currently.