• Title/Summary/Keyword: Dichloro ketone

Search Result 3, Processing Time 0.014 seconds

The Study on Organic Hardners for Gelatin of Photographic Emulsion (사진유제용 Gelatin의 유기경화제에 관한 연구 (I))

  • 청진쑹
    • Journal of the Korean Graphic Arts Communication Society
    • /
    • v.1 no.1
    • /
    • pp.69-75
    • /
    • 1983
  • Among the gelatin hardness for photographic emulsion, the formal dehyde , dialdehydes, n-Methylol compounds, ketonea, carbonylic acid and carbamic acid derivatives, and s-Triazine derivatives were studied. The greater purts of hardeners formed cross-link by the reaction with ${\varepsilon}$-Amino group in the lysine and OH group in the hydroxylysine. Glutaraldehyde produced most stable cross-link due to the formation of pyridinum ion. 2.5 hexanedione and 3-hexone-2.5-dione possible to use as the ketone hardner . The sodium salt of 2.4-dichloro-6-hydroxy-S-Triazine was newly developed as the olefinic hardners for emulsion.lsion.

  • PDF

Effect of an Extra Chloro Substituent on Photochemistry of o-Alkylphenacyl Chloride

  • Park, Bong-Ser;Jeong, Seong-Jin
    • Bulletin of the Korean Chemical Society
    • /
    • v.30 no.12
    • /
    • pp.3053-3056
    • /
    • 2009
  • The title compound, ${\alpha},{\alpha}$-dichloro-o-methylacetophenone, was prepared and its photochemical behavior was investigated. Addition of an extra chlorine at alpha position to the carbonyl showed many different features from photochemical reactivities of mono chloro analogue, 2,5-dimethylphenacyl chloride. In benzene, a rearrangement product with a formal 1,5-Cl shift and a reduction product were formed beside indanone. In methanol, solvolysis and cyclization of a common dienol intermediate occurred at comparable reaction rates.

횡서신문과 활자

  • JengGyuPark
    • Journal of the Korean Graphic Arts Communication Society
    • /
    • v.1 no.1
    • /
    • pp.57-60
    • /
    • 1983
  • Among the gelatin hardness for photographic emulaion, the formaldehyde, dialdehydes, n-Methylol compounds, ketones, carbonylic acid and carbamic acid derivatives, and s-Triazine derivatives were studied The greater purts of hardeners formed cross-link by the reaction with E-Amino group in the lysine and OH group in the hydroxylysine. Glutaraldehyde produced most stable cross-link due to the formation of pyridinum ion. 2.5- hexanedione and 3-hexene-2,5-dione possible to use as the ketone hardner. The sodium salt of 2.4-dichloro-6-hydroxy-S-Triazine was newly developed as the olefinic hardners for emulsion.

  • PDF