We report one-pot synthesis, encapsulation, and solubilization of high-quality quantum dots based on the use of amphiphilic and multidentate polymer ligands. In this "all-in-one" procedure, the resulting QDs are first capped by the multidentate ligand, and are then spontaneously encapsulated and solubilized by a second layer of the same multidentate polymer upon exposure to water. In addition to providing better control of nanocrystal nucleation and growth kinetics (including resistance to Ostwald ripening), this procedure allows for in-situ growth of an inorganic passivating shell on the nanocrystal core, enabling one-pot synthesis of both type-I and type-II core-shell QDs with tunable light emission from visible to near-infrared wavelengths.Semiconductor quantum dots (QDs) are nanometer-sized particles with unique optical and electronic properties, and are currently under intensive research for a broad range of applications such as solar energy conversion and molecular and cellular imaging. 1-3 Significant advances have been made in the chemical synthesis of highly crystalline and monodispersed QDs, especially with the use of organometallic and chelated cadmium precursors, 4,5 noncoordinating solvents, 6 and inorganic passivating shells. 7 However, the resulting nanocrystals are often hydrophobic and must be encapsulated and solubilized for many important applications. Aqueous synthetic procedures have been used as alternative approaches to prepare water soluble QDs, using small thiol-containing molecules or polymers with carboxylic acid functional groups as stabilizing agents. 8-10 But these methods do not yield QDs with the fluorescence brightness or size monodispersity that are often achieved with the high-temperature organic procedures.Here we report an "all-in-one" strategy for simultaneous synthesis, encapsulation, and solubilization of high-quality quantum dots. This one-pot method is based on the use of amphiphilic multidentate ligands and noncoordinaging solvents such as low-molecular weight polyethylene glycols (PEG) (MW = 350 Daltons). The multidentate polymer ligands contain aliphatic chains and carboxylic acid functional groups, and are found to act as both a cadmium precursor ligand and a nanoparticle surface stabilizer, leading to improved control of chemical reaction kinetics and increased resistance to Ostwald ripening. When exposed to water, excess polymer molecules spontaneously encapsulate and solubilize the QDs without any additional materials or steps. Furthermore, this synthetic procedure allows for in-situ growth of an inorganic passivating shell on the nanocrystal core, enabling one-pot synthesis of both type-I and type-II core-shell QDs. 11 E-mail: E-mail: snie@emory.edu. Supporting Information Available: Detailed procedures for one-pot synthesis of core and core-shell QDs. This material is available free of charge via the Internet at http://pubs.acs.org. Figure 1 shows schematic structures of the multidentate polymer ligands for one-pot QD synthesis and the self-encapsulated...