Fabrication of imide hybrid nanocomposites using amine modified oligosiloxanes nanoclusters was written by Lee, Tae-Ho;Kim, Jeong Hwan;Bae, Byeong-Soo. And the article was included in PMSE Preprints in 2006.Related Products of 73003-90-4 This article mentions the following:
Fabrication of inorganic-organic hybrid nanocomposites (IOHN) using well-defined nanoclusters has attracted much attention over the last decade. In particular, amine groups have very promising properties for roles as binding sites for DNA, microcrystals, diamond surfaces and photo-functional organic mols. The amine modified oligosiloxanes nanoclusters (AONC) are synthesized as useful and effective well-defined nanoclusters to fabricate IOHN. AONC are easily prepared in a single step by barium hydroxide monohydrate catalyzed condensation reactions between diphenylsilanediol (DPSD) and 3-aminopropyltrimethoxysilane (APTS). AONC are well-defined nanoclusters below 2 nm and their chem. modifications are easily achieved by changing precursors. We report here the synthesis of amine modified oligosiloxane nanoclusters (AONC), methacryl modified AONC and vinyl cinnamate modified AONC. Addnl., we report the fabrication of photo-functional hybrid nanocomposites derived from AONC, methacryl modified AONC and vinyl cinnamate modified AONC. Three different photo-functional hybrid nanocomposites are fabricated using AONC, derivatives of AONC and dianhydrides. (1)colorless imide hybrid nanocomposites, (2) photo-patternable imide hybrid nanocomposites and (3) photo-reactive hybrid nanocomposites for photo-alignment of liquid crystals. In the experiment, the researchers used many compounds, for example, 6-(2,5-Dioxotetrahydrofuran-3-yl)-4-methyl-7,7a-dihydroisobenzofuran-1,3(3aH,6H)-dione (cas: 73003-90-4Related Products of 73003-90-4).
6-(2,5-Dioxotetrahydrofuran-3-yl)-4-methyl-7,7a-dihydroisobenzofuran-1,3(3aH,6H)-dione (cas: 73003-90-4) belongs to tetrahydrofuran derivatives. Tetrahydrofurans and furans are important oxygen-containing heterocycles that often exhibit interesting properties for biological applications or applications in the cosmetic industry. Tetrahydrofuran can also be produced, or synthesised, via catalytic hydrogenation of furan. This process involves converting certain sugars into THF by digesting to furfural. An alternative to this method is the catalytic hydrogenation of furan with a nickel catalyst.Related Products of 73003-90-4
Referemce:
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem