Dergiler / Acta Materialia Turcica / 2017 / Volume: 1 Issue: 1

Synthesis, Characterization and Biological Activities of Novel a 1,2,3,4-tetrahydroquinazoline and Its Nickel(II) Complexes

Sayfa
—
Yayın Tarihi
2017-12-28
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Complex 3 exhibited moderate antimicrobial activity against Staphylococcus epidermidis and Candida albicans.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:The 2-methyl-2-(1-hydroxyiminoethyl)-1,2,3,4-tetrahydroquinazoline (HL or 1 ) and its novel Ni(II) complexes, square-planar [Ni(L)(LH)]·(NO 3 ) ( 2 ) and octahedral [NiCl 2 (LH)(H 2 O) 2 ]·(H 2 O) ( 3 ), have been synthesized.
📊
Temel Bulgular & Veri:The ligand and complexes have been characterized by means of elemental, IR, UV-Vis. spectroscopic studies, 1 H-NMR, 13 C-NMR, magnetic susceptibility, thermal analysis, mass spectroscopy and X-ray diffraction technique.
💡
Sonuç & Katkı:Complex 3 exhibited moderate antimicrobial activity against Staphylococcus epidermidis and Candida albicans.
🔬Tür:Research Article
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:antimicrobial activity · nickel complex · oxime

Abstract

The 2-methyl-2-(1-hydroxyiminoethyl)-1,2,3,4-tetrahydroquinazoline (HL or 1 ) and its novel Ni(II) complexes, square-planar [Ni(L)(LH)]·(NO 3 ) ( 2 ) and octahedral [NiCl 2 (LH)(H 2 O) 2 ]·(H 2 O) ( 3 ), have been synthesized. The ligand and complexes have been characterized by means of elemental, IR, UV-Vis. spectroscopic studies, 1 H-NMR, 13 C-NMR, magnetic susceptibility, thermal analysis, mass spectroscopy and X-ray diffraction technique. The HL ligand crystallizes in the P2 1 /c. Antimicrobial activity of ligand ( 1 ) and complexes ( 2 and 3 ) was evaluated by the agar diffusion method. Complex 2 showed weak antimicrobial activity against tested microorganism strains. Complex 3 exhibited moderate antimicrobial activity against Staphylococcus epidermidis and Candida albicans.

🔖

Bu Makaleye Atıf Yap

Çolak, A., Taş, M., İrez, G., Büyükgüngör, O., Çolak, F., Günay, H. (2017). Synthesis, Characterization and Biological Activities of Novel a 1,2,3,4-tetrahydroquinazoline and Its Nickel(II) Complexes. Acta Materialia Turcica, Volume: 1 Issue: 1. https://ajindex.com/articles/1438781

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (26)

  1. W. H.Correa, S. Papadopoulos, P. Radnidge, B. A. Roberts, J. L. Scott, Green Chem. 2002, 4, 245-251
  2. A. Göblöys, L. Lázár, F. Fülöp, Tetrahedron 2002, 58, 1011-1016
  3. J. Sinkkonen, K. N. Zelenin, A. K. A. Potapov, I. V. Lagoda, V. V. Alekseyev, K. Pihlaja, Tetrahedron 2003, 59, 1939-1950
  4. K. Tanaka, R. Shiraishi, Green Chem. 2000, 2, 272-273
  5. A. T. Çolak, M. Taş, G. İrez, O. Z. Yeşilel, O. Büyükgüngör, Z. Anorg. Allg. Chem. 2007, 633, 504-508
  6. National committee for clinical laboratory standards (NCCLS) Performance standards for antimicrobial disk susceptibility tests. Approved standard (M2-A4). National committee for clinical laboratory standards Villanova, PA. 1990a
  7. National committee for clinical laboratory standards. Methods for dilution antimicrobial susceptibility test for bacteria that grow aerobically. Approved standard (M7-A2). National committee for clinical laboratory standards, Villanova, PA. 1990b
  8. Stoe&Cie, X-Area (Version 1.18) and X-Red32 (Version 1.04), Stoe&Cie. Darmstadt, Germany, 2002
  9. M.C. Burla, R. Caliandro, M. Camalli, B. Carrozzini, G. L. Cascarano, L. D. Caro, C. Giacovazzo, G. Polidori, R. Spagna, J. Appl. Crystallogr. 2005, 38, 381-388
  10. Sheldrick G.M. SHELXL-97: Program for the Refinement of Crystal Structures. (Germany University of Göttingen), 1997
  11. C.K. Johnson, M.N. Burnett, ORTEP-III (version 1.0.2), Rep. ORNL-6895, Oak Ridge National Laboratory, Oak Ridge, TN (USA) (1996). Windows version: Farrugia L.J., University of Glasgow, Glasgow, Scotland (U.K.), 1997
  12. L. J. Farrugia, J. Appl. Crystallogr. 1999, 32, 837-838. Reference 13 Á. Somogyi, Medical applications of Mass Spectrometry, K. Vékey, A. Telekes and A. Vertes (editors) Elsevier B.V. 2008
  13. L. Bajpai, M. Varshney, C. N. Seubert, S. M. J. Stevens, J. V. Johnson, R. A. Yost, D. M. Dennis, J. Am. Soc. Mass Spectrom. 2005, 16, 814-824
  14. M. Taş, H. Batı, J. Chem. Res. 2006, 87-92
  15. A. Zülfikaroğlu, M. Taş, H. Batı, B. Batı, Synth. React. Inorg.Met. Org. Chem. 2003, 33, 625-638
  16. H. Batı, M. Taş, B. Batı, Synth. React. Inorg. Met. Org. Chem. 2001, 31, 541-548
  17. H. Batı, M. Taş, M. Macit, Synth. React. Inorg. Met. Org.Chem. 1998, 28, 1371-1380
  18. M. V. Barybin, P. L. Diaconescu, C. C. Cummins, Inorg. Chem. 2001, 40, 2892-2897
  19. S. Sevagapandian, G. Rajagopal, K. Nehru, P. Athappan, Trans. Metal Chem. 2000, 25, 388-393
  20. R. M. Srivastava, I. M. Brinn, J. O. Machura-Herrera, H. B. Faria, G. B. Carpenter, D. Andrade, C.G. Venkatesh, L. P. F. Morais, J. Mol. Struct. 1997, 406, 159-167
  21. F. Karipçin, H. I. Uçan, I. Karataş, Trans. Metal Chem. 2002, 27, 813-817
  22. M. Taş, H. Batı, J. Therm. Anal. Cal. 2006, 85, 295-299
  23. B. K. Singh, U. K., Jetley, R. K., Sharma, B. S. Garg, Spectrochimica Acta Part A 2007, 68, 63-73
  24. N. Tounsi, L. Dupont, A. Mohamadou, E. Guillon, M. Aplincourt, G. Rogez, Polyhedron 2008, 27, 674-3682
  25. M. C. Fernández-Fernández, R. B. Calle, A. Macías, L. V. Matarranz, P. P. Lourido, Polyhedron 2008, 27, 2301-2308
  26. F. Hamurcu, A. B. Gündüzalp, S. Çete S., B. Erk, Tran. Met. Chem. 2008, 33, 137-141.