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Articles

Synthesis, complexation and biological effects studies of new thiacrown ethers derived quinoline: part I

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Pages 277-288 | Received 19 Nov 2018, Accepted 30 Jan 2019, Published online: 15 Feb 2019

References

  • Foulkes E. Biological effects of heavy metals. Vols. I and II. Boca Raton (FL): CRC Press; 1990.
  • Izatt RM, Christensen JJ. Synthetic multidentate macrocyclic compounds. New York (NY): Academic Press; 1978.
  • Lamb JD, Izatt RM, Christensen JJ, et al. Thermodynamics and kinetics of cation-macrocycle interaction. In: Melson GA, editor. Coordination chemistry of macrocyclic compounds. New York (NY): Plenum Press; 1979. p. 145–217.
  • Vögtle F. Host-Guest complex chemistry I. New York (NY): Springer-Verlag; 1981.
  • Vögtle F. Host-Guest complex chemistry I. New York (NY): Springer-Verlag; 1982.
  • Christensen JJ, Eatough DJ, Izatt RM. The synthesis and ion bindings of synthetic multidentate macrocyclic compounds. Chem Rev. 1974;74:351–384. doi: 10.1021/cr60289a003
  • Izatt RM, Bradshaw JS, Nielsen SA, et al. Thermodynamic and kinetic data for cation-macrocycle interaction. Chem Rev. 1985;85:271–339. doi: 10.1021/cr00068a003
  • Park TK; Schroeder J, Rebek Jr. J. New molecular complements to imides. Complexation of thymine derivatives. J Am Chem Soc. 1991;113:5125–5127. doi: 10.1021/ja00013a093
  • Vicens J, Asfari S. Calixcrowns and related supramolecular systems. J Inclusion Phenom Macrocycl Chem. 2001;41:95–97. doi: 10.1023/A:1014454622039
  • Konczyk J, Nowik-Zajac A, Kozlowski CA. Calixarene-based extractants for heavy metal ions removal from aqueous solutions. Sep Sci Technol. 2016;51:2394–2410. doi: 10.1080/01496395.2016.1209219
  • Robert DH, Arthur EM. Ligand design for selective complexation of metal ions in aqueous solution. Chem Rev. 1989;89:1875–1914. doi: 10.1021/cr00098a011
  • Yohji N, Tetsuya N, Masayuki Y, et al. Molecular design of the electron-donating sidearm of lariat ethers: effective coordination of the quinoline moiety in complexation toward alkali-metal cations. J Am Chem Soc. 1988;110:531–538. doi: 10.1021/ja00210a037
  • Bradshaw JS, Song H, Xue G, et al. Synthesis of diazadi(and tri)thiacrown ethers containing two 5-substituent(or 2-methyl)-8-hydroxyquinoline side arms. Supramol Chem. 2001;13:499–508. doi: 10.1080/10610270108029465
  • Prodi L, Bargossi C, Montalti M, et al. An effective fluorescent chemosensor for mercury ions. J Am Chem Soc. 2000;122:6769–6770. doi: 10.1021/ja0006292
  • Shahrisa A, Banaei A. Chemistry of pyrones, part 5: new crown ether and podand derivatives of 3,5-bis(bromomethyl)-2,6-diphenyl-4H-pyran-4-one. Molecules. 2001;6:721–727. doi: 10.3390/60900721
  • Sugimoto M, Fujiwara K, Wakita R, et al. Complexation of acyclic ligands having two terminal quinoline units with alkali metal cations. Supramol Chem. 1993;2:145–151. doi: 10.1080/10610279308038309
  • Albrecht M, Fiege M, Osetska O. 8-Hydroxyquinolines in metallosupramolecular chemistry. Coord Chem Rev. 2008;252:812–824. doi: 10.1016/j.ccr.2007.06.003
  • Ashram M. Synthesis of calix[4]crowns containing soft donor atoms and a study of their metal–cation binding properties: highly selective receptors for Cu2+. J Chem Soc, Perkin Trans. 2002;2:1662–1668. doi: 10.1039/B205436A
  • Ashram M. Conductance and thermodynamic study of the complexation of ethyl p-tert-butylcalix[4]arene tetraacetate with alkali metal and silver ions in various solvents. J Inclusion Phenom Macrocycl Chem. 2002;42:25–31. doi: 10.1023/A:1014546214884
  • Ashram M, Mizyed S, Zereini W, et al. Synthesis, metal ion complexation and antibacterial activities of some thiapodands with lipophilic amide and ester end groups. J Sulfur Chem. 2012;33:561–571. doi: 10.1080/17415993.2012.716843
  • Tochtrop GP, Sadhukhan S, Koner RR, et al. The syntheses and applications of β-benzylmercaptoethylamine derivatives. Tetrahedron. 2009;65:10515–10534. doi: 10.1016/j.tet.2009.10.041
  • Fedorova OV, Mordovskoi GG, Rusinov GL, et al. Synthesis andin vitro tuberculostatic activity of podands containing semicarbazide or thiosemicarbazide fragments. Pharm Chem J. 1998;32:64–66. doi: 10.1007/BF02464163
  • Anh LT, Nhung DT, Tuyet LA, et al. Novel podands containing N-arylthiosemicarbazide moiety. Macroheterocycles. 2017;10:243–246. doi: 10.6060/mhc170289l
  • Mistry BM, Jauhari S. Synthesis and in vitro antimicrobial and anti-tubercular evaluation of some quinoline-based azitidinone and thiazolidinone analogues. Med Chem Res. 2013;22:635–646. doi: 10.1007/s00044-012-0060-8
  • Buter J, Kellogg RM. Synthesis of sulfur-containing macrocycles using cesium thiolates. J Org Chem. 1981;46:4481. doi: 10.1021/jo00335a032
  • Al-Zereini WA. Bioactive crude extracts from four bacterial isolates of marine sediments from Red Sea, Gulf of Aqaba, Jordan. Jordan J Biol Sci. 2014;7:133–137. doi: 10.12816/0008227
  • Al-Zereini WA. Ononis natrix and Salvia verbenaca: two Jordanian medicinal plants with cytotoxic and antibacterial activities. J Herbs Spices Med. Plants. 2017;23:18–25. doi: 10.1080/10496475.2016.1241200
  • Brand-Williams W, Cuvelier ME, Berset C. Use of a free radical method to evaluate antioxidant activity. LWT – Food Sci. Technol. 1995;28:25–30. doi: 10.1016/S0023-6438(95)80008-5

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