Poly-Schiff base containing bisthiazole rings (TAPDA) has been prepared from terephthalaldehyde and 2,2 -diamino-4,4-bisthiazole. It was found that the TAPDA polymer film is permeable to H 2 , O 2 , and N 2 and can be converted into an electrical conductor by pyrolysis at high temperature in nitroge
Synthesis and properties of germanium-containing poly(diphenylacetylenes)
β Scribed by Hidehiro Ito; Toshio Masuda; Toshinobu Higashimura
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 344 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0887-624X
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β¦ Synopsis
SYNOPSIS
l-Phenyl-2-[rn-(trimethylgermyl)phenyl]acetylene (m-Me,GeDPA) and 1-phenyl-2-[p-(trimethylgermyl)phenyl]acetylene @-Me,GeDPA) polymerized with TaC1,-cocatalyst systems t o provide in high yields new polymers having weight-average molecular weights over 1 X lo6. Poly(m-Me3GeDPA) was a yellow solid, which completely dissolved in toluene, chloroform, etc., t o form a tough film by solution casting. Poly@-Me,GeDPA) was also a yellow solid and partly insoluble in any solvents. T h e onset temperatures of weight loss for these polymers in the thermogravimetric analysis in air were a s high as ca. 40OoC. T h e oxygen permeability coefficient of poly(rn-Me,GeDPA) was 1100 barrers (25"C), which is about twice t h a t of poly(dimethylsi1oxane).
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New conjugated oligomers were synthesized by reacting diphenylacetylene under high pressure of 0.13-0.76 GPa at 250 and 300ΠC for 1-10 h. The numberaverage molecular weight M V n , and the weight-average molecular weight M V w increased with pressure, but those values were independent of temperature
A series of aromatic polyamides incorporating silicon together with phenylquinoxaline or with hexafluoroisopropylidene groups has been synthesized by solution polycondensation of a silicon-containing diacid chloride with aromatic diamines having phenylquinoxaline rings or hexafluoroisopropylidene gr
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## Polymerization of o-, m-, and p-(dimethylsilyl) phenylacetylene by chloroplatinic acid-catalyzed hydrosilylation gave the corresponding poly(dimethylsilylenephenylenevinylene)s. The monomer reactivity and polymer structure were very much dependent upon the substituent position. Interesting opti