3-Methoxydiphenylamine-4-diazonium salt (MDDS) and its diazoresin were synthesized. The photo-and thermal decomposition of salt and the resins were investigated. The results show that MDDS exhibits excellent thermostability as well as high photosensitivity. A series of diazoresins with different org
Synthesis of diazoresin and its photocrosslinking reaction
β Scribed by Cao, Shuguang; Zhao, Chao; Cao, Weixiao
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 246 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0959-8103
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β¦ Synopsis
Diazoresins with di β erent speciΓc viscosities were prepared from diphenylamine-4-diazonium salt and paraformaldehyde in concentrated sulphuric acid with di β erent ratios of In order to obtain a diazo-CH 2 O/wN 2 `X~. resin with a speciΓc viscosity in a given time at 0Γ5Β‘C, more than a stoichiometric ratio was necessary.
The photocrosslinking reaction of the diazoresins with various binder resins in solid Γlm was investigated. The results show that the photocrosslinking reaction took place only in a system composed of diazoresin and binder resin containing wOH side-chain groups. The photodecomposition of diphenylamine-4-diazonium salt and its diazoresin in alcohol was studied. It was demonstrated that the diphenylamine aryl cation formed on decomposition is the dominant intermediate. The photocrosslinking mechanism between diazoresin and binder resin is discussed in a preliminary way.
1998 SCI. (
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