Synthesis, characterization and biocidal studies of new ferrocenyl thiadiazolp-triazinone complexes

Applied Organometallic Chemistry

Volumn 20, Issue 8, 2006, Pages 505-511

  El shiekh, Said M ^a   Abd Elzaher, Mokhles M ^b   Eweis, Mohamed ^c  

^a CMRDI   (Egypt)

^b NATIONAL RESEARCH CENTRE   (Egypt)

^c CAIRO UNIVERSITY   (Egypt)

Author keywords

Biocidal activity; Diacetylferrocene; Magnetic properties; Thiadiazolo triazinone

Indexed keywords

COMPLEXATION; ESCHERICHIA COLI; MAGNETIC PROPERTIES; MAGNETIC SUSCEPTIBILITY; MOLECULAR STRUCTURE; NUCLEAR MAGNETIC RESONANCE; SYNTHESIS (CHEMICAL);

BIOCIDAL ACTIVITY; DIACETYLFERROCENE; ONE-POT SYNTHESIS; THIADIAZOLO-TRIAZINONE;

ORGANOMETALLICS;

EID: 33747603938     PISSN: 02682605     EISSN: 10990739     Source Type: Journal    
DOI: 10.1002/aoc.1100     Document Type: Article

References (50)

1. Sato Y, Kato D, Niwa O, Mizutani F. Sensors Actuators 2004; 108: 617.
2. Forrow N, Walters S. Biosens. Bioelectron. 2004; 19:763.
3. Hu X, Bai C, Dai H, Chen H, Zheng Z. J. Mol. Catal. A: Chem. 2004; 218:107.
4. Murata M, Buchwald SL. Tetrahedron 2004; 60: 7397.
5. Ojani R, Raoof JB, Alinezhad A. Electroanalysis 2002; 14: 1197.
6. Hudson RDA. J. Organametal. Chem. 2001; 47:637.
7. Ferry-Forgues S, Delaraux-Nicot B. J. Photochem. Photobiol. A. Chem. 2000; 132:137.
8. Mang C, Wu K, Zhang M, Hong T, Wei Y. J. Mol. Struct.: THEOCHEM 2004; 674:77.
9. Tsuboya N, Lamrani M, Hamasaki R, Ito M, Mitsuishi M, Miyashita T, Yamamoto Y. J. Mater. Chem. 2002; 12:2701.
10. Togni A, Hayashi T. Ferrocenes, Homogeneous Catalysis, Organic Synthesis, Material Science. VCH: Weinheim, 1995.
11. Kaifer EA, Mendoza JDE. Comprehensive Supramolecular Chemistry, Vol. 1. Elsevier Oxford, 1996; 701.
12. Tonguchi N, Uemura M. J. Am. Chem. Soc. 2000; 122:8301.
13. Catasus M, Bueno A, Moyano A, Maestro MA. J. Organometal. Chem. 2002; 642:212.
14. Henderson W, Alley SR. Inorg. Chim. Acta 2001; 322:106.
15. Liu R-C, Ma Y-Q, Yu L, LiJ-S, Cui J-R, Wang R-Q. Appl. Organometal. Chem. 2003; 17: 662.
16. Top S, Vessieres A, Cabestaing C, Laios I, Leclercq G, Provot C, Jaouen G.J. Organometal. Chem. 2001; 637-639: 500.
17. Jaouen G, TopS, Vessieres A, Leclercq G, Quivy J, Jin L, Croisy ACR. Acad. Sd. IIC 2000; 3: 89.
18. Allardyce CS, Dorcier A, Scolaro C, Dyson PJ. Appl. Organometal. Chem. 2005; 19:1.
19. Domarle O, Blampain G, Agnanet H, Nzadiyabi T, Lebibi J, Brocard J, Maciejewski L, Biot L, Georges AJ, Millet P. Antimicrob. Agents Chemother. 1998; 42:540.
20. Biot P, Delhaes L, Diaye CMN, Maciejewski LA, Camus D, Dive D, Brocard JS. Bioorg. Med. Chem. 1999; 7:2843.
21. Popova LV, Babin VN, Belousov YA, Nekrasov YS, Snegireva AE, Borodina NP, Shaposhnikova GM, Bychenko OB, Raevskii PM, Morozova NB, Iiyina AI, Shitkov KG. Appl. Organometal. Chem. 1993; 7: 85.
22. Kateritzky A, Caster K, Maren T, Conroy C, Bar-Dan A. J. Med. Chem. 1987; 30:2058.
23. Dhar L, Vaish A, Sharma S. J. Agric. Food Chem. 1994; 42: 811.
24. Dhar L, Sharma S, Vaish A. J. Agric. Food Chem. 1994; 42:1352.
25. Crop L. US patent 4.246.126, 1981;
26. [Chem. Abstr. 94: 142505h, 1981].
27. Kidwai M, Bhushan K, Kumar P. Monatshefte Chem. 1999; 130: 585.
28. Gakhar HK, Prabha U, Gill JK. J. Ind. Chem. Soc. 1984; 61: 552
29. [Chem. Abstr. 102:113436q.].
30. Abd-Elzaher MM. Appl. Organometal. Chem. 2004; 18:149.
31. Abd-Elzaher M, Hegazy W, Gaafar A. Appl. Organometal Chem. 2005; 19:911.
32. Abd-Elzaher M, Ali IAI. Appl. Organometal. Chem. 2006; 20:107.
33. Shawali AS, Elghandour AA, El-Sheikh SM. J. Park.Chem. 2000; 342:96.
34. Rosenblum M, Woodward RB. J. Am. Chem. Soc. 1958; 80:5443.
35. Olurinola PF, Ehinmidu JO and Bonire JJ. Appl. Environ. Microbiol. 1992; 58: 758.
36. Nair MG, Mishra SK and Putnam AR. J. Antibiot. 1992; 45:1738.
37. Park JS, Kim JH, Nho YC and Kwon OH. J. Appl. Polym. Sci. 1998; 69:2213.
38. Csampai A, Abran A, Kudar V, Turos G, Wamhoff H, Sohar P. J. Organometal. Chem. 2005; 690:802.
39. Mohapatra SC, Rao DVR. J. Indian Chem. Soc. 1980; 57:262.
40. Abd-Elzaher MM. J. Chin. Chem. Soc. 2004; 51:499.
41. Osowole AA, Woods JAO, Odunola OA. Synth. React. Inorg. Metal. Org. Chem. 2003; 33:167.
42. Xiaoxian Z, Yongmin L, Fajun N, Yongxiang M. Polyhedron 1992; 11:447.
43. Chohan ZH, Farooq MA. Synth. React. Inorg. Met. Org. Chem. 2001; 31:1853.
44. Patil SR, Kantank UN, Sen DN. Inorg. Chim. Acta 1982; 63:261.
45. Wang G, Chang JC. Synth. React. Inorg. Met. Org. Chem. 1994; 24: 1091.
46. Shah NR. J. Ind. Chem. Soc. 1981; 9:851
47. [Chem. Abstr. 96:96527h.].
48. Singh H, Yadav LSD, Mishra SBS. J. Inorg. Nucl. Chem. 1981; 43: 1701.
49. Jones RP, Greenfield PE. Process. Biochem. 1984; 19:48.
50. Joho M, Imada Y, Murayama T. Microbios 1987; 51:183.