본문 바로가기
KERD
논문KCI 등재

Anthraquinone을 포함하는 신규 Phthaloperinone 색소의 합성과 특성에 대한 연구

Synthesis and Properties of New Phthaloperinone Dyes containing Anthraquinone Moiety

1

조회

0

다운로드

0

인용

0

참고문헌

키워드

초록

We have synthesized five novel phthaloperinone dyes via a condensation reaction to be applied as yellow colorants for liquid crystal display(LCD) color filters. The reaction between 1,8-naphthalic anhydride(1a), 4-chloro-1,8-naphthalic anhydride(1b), 4-bromo-1,8-naphthalic anhydride(1c), 3-nitro-1,8-naphthalic anhydride(1d), 4-nitro- 1,8-naphthalic anhydride(1e) and 1,2-diaminoanthraquinone(2) proceeded readily giving a product in 72-88% yields. The synthesized dyes were characterized by Uv-Vis, mass spectrometry and elemental analysis. The spectral properties and thermal stability of the dyes were examined. The dyes absorb at around 400-450nm. All five dyes showed satisfactory thermal stability: the dyes retain 99-100% of its original weight at 300℃, 98- 100% at 350℃, 92-98% at 400℃, and 84-92% at 450℃. We have quantitatively evaluated the reaction mechanism and reactivity of dye molecules by means of Pariser- Parr-Pople Molecular Orbital Method(PPP-MO).

Abstract

We have synthesized five novel phthaloperinone dyes via a condensation reaction to be applied as yellow colorants for liquid crystal display(LCD) color filters. The reaction between 1,8-naphthalic anhydride(1a), 4-chloro-1,8-naphthalic anhydride(1b), 4-bromo-1,8-naphthalic anhydride(1c), 3-nitro-1,8-naphthalic anhydride(1d), 4-nitro- 1,8-naphthalic anhydride(1e) and 1,2-diaminoanthraquinone(2) proceeded readily giving a product in 72-88% yields. The synthesized dyes were characterized by Uv-Vis, mass spectrometry and elemental analysis. The spectral properties and thermal stability of the dyes were examined. The dyes absorb at around 400-450nm. All five dyes showed satisfactory thermal stability: the dyes retain 99-100% of its original weight at 300℃, 98- 100% at 350℃, 92-98% at 400℃, and 84-92% at 450℃. We have quantitatively evaluated the reaction mechanism and reactivity of dye molecules by means of Pariser- Parr-Pople Molecular Orbital Method(PPP-MO).

참고문헌 (16)

  1. W. Herbst, "IndustrialOrganic Pigment" (2004), Wiley-VCH
  2. A. Bistrzycki, "Uber die Einwirkung verschiedener Diamine auf Naphtalsaure-anhydride", Helv. Chim. Acta, 8, pp.810~ (1925)
  3. E. Merian, "Process for the Dyeing of Polyester Fibers", US Patent 2955902, ~ (1960)
  4. D. Buffalo, "Phthaloperinone Compounds", US Patent 3299065, ~ (1963)
  5. S. Mitsutoshi, "Photosensitive Member containing PhthaloperinoneorNaphthalimede", USPatent 4988592, ~ (1991)
  6. S. Ernest, "Disperse Dyes of the Phthaloperinone Series", US Patent 3342818, ~ (1967)
  7. P. Buecheler, "PhthaloperinoneDyes and theUse Thereof forMore Dyeing Plastics", US Patent 4417012A, ~ (1983)
  8. W. D. Graham, "New Colouring Matters", US Patent 2889327A, ~ (1959)
  9. R. W. Sabnis, "Color Filter Technology for LiquidCrystal Display", Display, 20, pp.119~ (1999)
  10. K. Tsudaya, "ColorFilters forLCDs", Display, 14, pp.115~ (1993)
  11. P. Yeh, "Optics of Liquid CrystalDisplays" (1999), JohnWiley and Son
  12. 전근, "신규 Phthaloperinone 색소의 합성과 특성에 대한 연구", 한국염색가공학회지, 27(4), pp.275~280 (2015), 한국염색가공학회
  13. B. Delley, "An All -electronNumericalMethod for Solving the Local Density Functional for Polyatomic Polecules", J. Chem. Phys., 92(1), pp.508~ (1990)
  14. B. Delley, "FromMolecules to Solidswith theDMol3Approach", J. Chem. Phys, 113(18), pp.7756~ (2000)
  15. A. D. Boese, "A New Parametrization of Exchange-Correlation Generalized Gradient Approximation Functionals", J. Chem. Phys., 114(13), pp.5497~ (2001)
  16. 전근, "유기색소의 흡수대 형태와 분자구조와의 상관성", 한국염색가공학회지, 27(4), pp.270~274 (2015), 한국염색가공학회

관련 논문AI추천

이 간행물의 다른 논문 (7건)