Preparation of Telechelic Hydroxyl Low Molecular Weight Fluoropolymers

2017 ◽  
Vol 753 ◽  
pp. 93-98
Author(s):  
Dong Han Li ◽  
Ming Yi Liao

Preparation of telechelic hydroxyl low molecular weight fluoropolymers by reduction reaction was presented. The telechelic carboxyl low molecular weight fluoropolymers were chosen as raw materials which were prepared by oxidative degradation method. The molecular weights of telechelic carboxyl low molecular weight fluoropolymers were about 3700. Then, using lithium aluminum hydride reacted with carboxyl groups to prepare the telechelic hydroxyl low molecular weight fluoropolymers. The effects of reaction temperatures, reaction times, contents of solvent and lithium aluminum hydride were investigated in detail. The structures, Mn and dynamic viscosity of low molecular weight fluoropolymers were analyzed by FTIR, 1H-NMR, GPC and viscometer respectively. Finally telechelic hydroxyl low molecular weight fluoropolymers were prepared. The conversion rate of that reduction reaction was about 95%. The product was a viscous fluid with a dynamic viscosity of 48Pa·s at 50°C.

1963 ◽  
Vol 41 (5) ◽  
pp. 1051-1058 ◽  
Author(s):  
F. M. Peters ◽  
B. Bartocha ◽  
A. J. Bilbo

Alkylaluminum hydride trimethylamine complexes have been obtained by several different methods: (a) reduction of an alkylaluminum halide trimethylamine complex with lithium hydride, (b) alkylation of aluminum hydride trimethylamine with dialkylmercury, (c) reaction of trialkylaluminum trimethylamine and aluminum hydride trimethylamine, and (d) reaction of dialkylaluminum chloride with lithium aluminum hydride and trimethylamine. Some physical properties of the compounds are reported, including the infrared and proton magnetic resonance spectra. Cryoscopic molecular weight determinations indicate that the compounds are associated in cyclohexane. Their possible structures are discussed.


1973 ◽  
Vol 51 (13) ◽  
pp. 2102-2104 ◽  
Author(s):  
Donald G. Lee ◽  
James R. Brownridge

The reduction of ethyl phenylpropiolate by lithium aluminum hydride results in partial reduction of the triple bond to give trans-cinnamyl alcohol. If ethyl phenylpropiolate is reduced by LiAlD4 followed by work-up with acetone and H2O the product is the specifically labeled compound, trans-3-phenyl-2-propen-1-ol-1,1,2-d3. If the ester is reduced with LiAlH4 followed by work-up with acetone-d6 and D2O the product is trans-3-phenyl-2-propen-1-ol-O,3-d2. Oxidation of these two products by sodium ruthenate leads to formation of trans-cinnamic acid-α-d and trans-cinnamic acid-β-d, respectively.


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