Tri n octylphosphine top
Tri-n-octylphosphine (TOP) is a colorless, viscous liquid organic compound used as a reagent and ligand in various laboratory applications. It is a neutral, trivalent phosphorus compound with three n-octyl substituents. TOP is commonly used in the synthesis and stabilization of semiconductor nanoparticles, such as quantum dots, due to its ability to coordinate with metal ions.
Lab products found in correlation
4 protocols using tri n octylphosphine top
Synthesis of Cadmium Selenide Nanocrystals
Synthesis of Chalcogenide Nanocrystals
Synthesis of Quantum Dot Composites
methacrylate were purchased from Sigma-Aldrich. Octadecene (ODE, Acros),
oleic acid (OA, Showa), selenium (Se, Alfa Aesar), zinc acetate (Riedel-de
Haën), and sulfur (purity >99%, Riedel-de Haën) were
of reagent grade. Analytic-grade solvents of toluene and ethanol were
purchased from Echo. A sample of commercially available acrylic acrylate
oligomer (trade mark, B2) was kindly provided by Hopax Company in
Taiwan to prepare the QD composites. Diphenyl(2,4,6-trimethylbenzoyl)-phosphine
oxide (TPO, Darocur), 1-hydroxy-cyclohexyl-phenyl-ketone (Irgacure
184, Ciba), and 2-methyl-1-[4-(methylthio)phenyl]-2-(4-morpholinyl)-1-propanone
(Irgacure 907, Ciba) were used as photoinitiators. All chemicals were
used as received without further purification.
Synthesis of Semiconductor Nanocrystals
(99%), di-n-propylamine (99%), diethylamine (>99.5%),
phenethylamine
(≥99%), n-dodecylamine (≥99%), n-octylamine (+99%), n-pentylamine (+99%), n-propylamine (+98%), Cd(OAc)2·2H2O (>98%), trin-octylphosphine (TOP) (97%), and
oleylamine
(or cis-9-octadecenylamine, technical grade, 70%) were obtained from
Sigma-Aldrich. Selenourea (99.9%, metal basis) was obtained from Alpha
Aesar. All were used as received and stored under N2. Toluene
was obtained from Sigma-Aldrich (CHROMASOLV for HPLC, ≥99.9%).
Transmission electron microscopy (TEM) sample grids (Cu with holey
carbon film) were obtained from Ted Pella, Inc.
All synthetic
procedures were conducted under dry N2, except the final
washing steps, which were conducted in the ambient atmosphere. The
reaction mixtures were not stirred. The synthetic products were generally
stored as reaction mixtures, after addition of TOP (see below).
About PubCompare
Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.
We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.
However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.
Ready to get started?
Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required
Revolutionizing how scientists
search and build protocols!