Chemistry graduates have much scope to use their knowledge in a range of research sectors, including roles within chemical engineering, chemical and related industries, healthcare and more. Application In Synthesis of D-Arabinose10323-20-3, Name is D-Arabinose, SMILES is O=C[C@@H](O)[C@H](O)[C@H](O)CO, belongs to dioxole compound. In a article, author is DesMarteau, DD, introduce new discover of the category.
A series of copolymers of tetrafluoroethylene and 4-trifluormethoxy-1,3-perfluorodioxole (TFETFMD) were prepared as well as a homopolymer of the dioxole (TEMD) using various free-radical initiators. The copolymers were characterized by F-19 NMR, TGA, DSC and VUV measurements. The transparency at 157nm increased with increasing dioxole content reaching an alpha (mum(-1)) = 0.76 for an unoptimized homopolymer of the dioxole prepared with a perfluorinated peroxide initiator. Exposure studies of the dioxole homopolymer at 157 nm indicate rapid formation of carbonyl species and therefore an anticipated short lifetime as a potential polymer pellicle for 157 nm lithography.
But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 10323-20-3, you can contact me at any time and look forward to more communication. Application In Synthesis of D-Arabinose.
Reference:
1,3-Benzodioxole – Wikipedia,
,Dioxole | C3H4O2 – PubChem