2-Sulphonic diphenylamine-4-diazonium salt (SDDS) and its diazoresin were synthesized and their thermal stability and photosensitivity were investigated. The results show that the thermal stability of SDDS is better than that of diphenylamine-4-diazonium salt (DDS), and is close to that of 3-methoxy
Synthesis and characterization of N-methyl-2-nitrodiphenylamine-4-diazonium salt and its diazoresin
โ Scribed by Renxian Wang; Jinyu Chen; Weixiao Cao
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 123 KB
- Volume
- 74
- Category
- Article
- ISSN
- 0021-8995
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โฆ Synopsis
A new substituted diphenylamine diazonium salt, N-methyl-2-nitrodiphenylamine-4-diazonium salt (MNDDS) and its diazoresin (MNDDS-resin) were synthesized and their thermostability as well as photosensitivity were investigated. The results show that MNDDS and resin exhibit much higher thermostability than that of the parent compound, diphenylamine-4-diazonium salt (DDS) and resin (DDS resin) in solid state or in coating but the photosensitivities of them are confirmed to be in same level. The excellent thermostability of MNDDS and its diazoresin is very important because the storage life of a negative presensitized plate is mainly dependent on it.
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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
Poly-โค-amides (nylons 3) were synthesized via the anionic polymerization of a series of 4-alkyl-4-methyl-2-azetidinones where the alkyl group is a methyl, ethyl, propyl, butyl, or pentyl. The "non-assisted" polymerization was conducted under vacuum, in the bulk, at 160ยฐC, using potassium 2-pyrrolido
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