2005
DOI: 10.1021/ja043577f
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Phosphine Oxide Polymer for Water-Soluble Nanoparticles

Abstract: A phosphine oxide polymer was developed using bis(dichlorophosphino)ethane and poly(ethylene glycol). This polymer system was used to transfer various nanoparticles from organic solvents to water, retaining their physical properties and reactivities.

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Cited by 206 publications
(146 citation statements)
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“…[16,17] For biomedical applications, it is indispensable to transfer these nanoparticles to an aqueous phase. Several studies have dealt with a variety of methodological improvements including ligand exchange with tetramethylammonium hydroxide (TMAOH), [18] dimercaptosuccinic acid (DMSA), [19] phosphine oxide polymers, [20] and dendrons [21] to enhance stability of nanoparticles in aqueous solution. Alternatively, a layer of amphiphilic molecules such as poly(maleic anhydride-alt-1-tetradecene), [22] surfactant/lipid, [23] and a-cyclodextrin [24] have been used to form an intercalating structure with the hydrophobic capping molecules on the particle surface.…”
mentioning
confidence: 99%
“…[16,17] For biomedical applications, it is indispensable to transfer these nanoparticles to an aqueous phase. Several studies have dealt with a variety of methodological improvements including ligand exchange with tetramethylammonium hydroxide (TMAOH), [18] dimercaptosuccinic acid (DMSA), [19] phosphine oxide polymers, [20] and dendrons [21] to enhance stability of nanoparticles in aqueous solution. Alternatively, a layer of amphiphilic molecules such as poly(maleic anhydride-alt-1-tetradecene), [22] surfactant/lipid, [23] and a-cyclodextrin [24] have been used to form an intercalating structure with the hydrophobic capping molecules on the particle surface.…”
mentioning
confidence: 99%
“…One of the easiest ways is the attachment of thiolated poly(ethylene glycol) polymers, which renders the water solubility and reduced unspecific cellular uptake of QDs. [9][10][11][12] Other polymers with varying chain lengths and number of binding dentates, such as PEGylated dihydrolipoic acid, [13][14][15] dendrimers, 16,17 and multidentate phosphine polymers, 18 are also used to stabilize QDs in aqueous solution. An alternative protocol for a solubilization and stabilization is ligand capping by various amphiphilic polymers such as poly(maleic anhydride alt-1-tetradecene), 19 triblock copolymer, 5 and alkyl-modified poly (acrylic acid) [20][21][22] to form highly stable polymer linking or micelle-like structures.…”
Section: Surface Stabilization Chemistrymentioning
confidence: 99%
“…Therefore, the substitution of Zn 2+ atoms by Ni 2+ atoms in the lattice is possible. Frequently, QDs are synthesized in organic phase under refluxing, using coordinating solvents like trioctylphosphine oxide (TOPO), trioctylphosphine (TOP), and hexadecylamine [14][15][16][17][18][19][20]. Although, the reflux technique is highly reproducible and able to produce nanocrystals of narrow size distribution; the long time period required for the synthesis; the limited temperatures that can be achieved by this technique; and the generation of QDs stable in organic media limit its application.…”
Section: Introductionmentioning
confidence: 99%
“…The possibility to produce water-stable nanoparticles using thiols agents under microwave irradiation is desirable to biomedical applications [19][20][21][22][23][24]. In this study, we have produced water-stable Nidoped Zn(Se,S) nanocrystals of high-optical quality using 3-mercaptopropionic acid (MPA) under microwave irradiation.…”
Section: Introductionmentioning
confidence: 99%