Synthesis, characterization, and biological evaluation of new oxime-phosphazenes

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Koran K., Ozkaya A., Ozen F., Cil E., ARSLAN M.

RESEARCH ON CHEMICAL INTERMEDIATES, cilt.39, sa.3, ss.1109-1124, 2013 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Derleme
  • Cilt numarası: 39 Sayı: 3
  • Basım Tarihi: 2013
  • Doi Numarası: 10.1007/s11164-012-0670-2
  • Dergi Adı: RESEARCH ON CHEMICAL INTERMEDIATES
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.1109-1124
  • Anahtar Kelimeler: Hexachlorocyclotriphosphazene, Phosphazene, Oxime-phosphazenes, Antibacterial, Antifungal, DICHLOROPHOSPHORYL-P-TRICHLOROPHOSPHAZENE, CYCLOTRIPHOSPHAZENE DERIVATIVES, LINEAR PHOSPHAZENES, CRYSTAL-STRUCTURE, YEAST-CELLS, SCHIFF-BASE, COMPLEXES, BACTERIAL, ALKYL, CYCLOPHOSPHAZENES
  • Akdeniz Üniversitesi Adresli: Hayır

Özet

Hexachlorocylotriphosphazene (1) was reacted with 4-hydroxy-3-methoxybenzaldehyde to give hexakis[(4-formyl-2-methoxy)phenoxy]cyclotriphosphazene (2). Hexakis[(4-(hydroxyimino)2-methoxy)phenoxy]cyclotriphosphazene (3) was synthesized by reaction of 2 with hydroxlamine hydrochloride in pyridine. Compound 3 was reacted with benzyl chloride, acetyl chloride, allyl bromide, benzoyl chloride, propanoyl chloride, 4-methoxybenzoyl chloride, 2-chlorobenzoyl chloride, chloroacetyl chloride, methyl iodide, and thiophene-2-carbonyl chloride. From these reactions, full or partially substituted compounds were obtained, usually in high yields. Pure or defined products could not be obtained from reaction of 3 with methacryloyl chloride and O-acetylsalicyloyl chloride. The structures of the compounds were determined by elemental analysis, and IR, H-1, C-13, and P-31 NMR spectroscopy. The synthesized compounds were screened for in-vitro antimicrobial activity against two Gram-positive bacteria (Staphylococcus aureus and Enterococcus faecalis), two gram-negative bacteria (Escherichia coli and Klebsiella pneumonia), and fungal strains (Aspergillus niger, and Candida albicans) by the agar well diffusion method. Few compounds had significant activity against both Gram-positive and Gram-negative bacteria. None of the compounds had antifungal activity except compounds 7 and 9, which had moderate activity.