• 제목/요약/키워드: 2-Fluoroaniline

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Physical and Optical Properties of Hydrophilic Tinted Lens Materials with the Fluoro-substituted Aniline Group

  • Park, Se-Young;Lee, Min-Jae;Sung, A-Young
    • 통합자연과학논문집
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    • 제8권1호
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    • pp.60-66
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    • 2015
  • The physical and optical properties of polymers with 2-fluoroaniline and 4-fluoroaniline added, which can be used for hydrophilic ophthalmic lenses, were investigated in this study. The UV-blocking properties of 2- and 4-fluoroaniline were also investigated by measuring their UV transmissibility. 2- and 4-Fluoroaniline were used as additives for the basic combination of HEMA, 5% AA, and 1% MMA, and the materials were copolymerized with EGDMA as the cross-linking agent and AIBN as the initiator. The refractive index, water content, optical transmittance, tensile strength, and contact angle were measured to evaluate the physical properties of the produced hydrogel lens. The measured physical properties of the hydrogel contact lens produced with the copolymerized polymer showed a refractive index of 1.425-1.436; a water content of 36.95-44.65%; a visual light transmittance of 66.0-81.0%; a tensile strength of 0.138-0.281 kgf; and a contact angle of $55.02-57.87^{\circ}$. The UV transmissibility was significantly reduced, which indicates that 2-fluoroaniline and 4-fluoroaniline have UV-blocking properties. This study showed that 2- and 4-fluoroaniline are expected to be used as UV-blocking materials in hydrogel ophthalmic lenses whose physical properties, such as their refractive index and water content, do not change.

항응고성의 3-(N-Arylamino)-1,4-Naphthoquinone 유도체 합성(II) (Synthesis of Anticoagulant 3-(N-Arylamino)-1,4-Naphthoquinones(II))

  • 유충규;오재돈;서명은
    • 약학회지
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    • 제33권5호
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    • pp.273-279
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    • 1989
  • 2,3-Dichloro-1,4-naphthoquinone was reacted with o-fluoroaniline, p-sulfadiazine, p-acetoanline, N,N-dimethyl-1,4-phenylenediamine as a nucleophilic substitution to form 2-chloro-3-(N-arylamino)-1,4-naphthoquinones (1.-6.) in good yield. 2,3-Dibromo-1,4-naphthoquinone was also reacted with o-fluoroaniline, m-aminobenzoic acid, m-chloroaniline, morpholine, p-acetoaniline, N,N-dimethyl-1,4-phenylenediamine as a nucleophilic substitution to give 2-bromo-3-(N-arylamino)-1,4-naphthoquinones (7.-12.). These new compounds are expected to have a biological activities such as anticoagulant, cytotoxic.

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