Thermal analyses data and antimicrobial screening of some new nano-structure five coordinated cadmium complexes

Morteza Montazerozohori; Sajjad Mojahedi Jahromi; Asghar Naghiha

Journal of Industrial and Engineering Chemistry, Vol.22, 248-257, February, 2015

DOI10.1016/j.jiec.2014.07.017 Export Citation

Thermal analyses data and antimicrobial screening of some new nano-structure five coordinated cadmium complexes

Morteza Montazerozohori^†, Sajjad Mojahedi Jahromi, and Asghar Naghiha¹

Department of Chemistry, Yasouj University, Yasouj 75918-74831, Iran
¹Department of Animal Sciences, Yasouj University, Yasouj, Iran

E-mail:

In this work, synthesis of some nano-structure five coordinated cadmium complexes of a new tridentate Schiff base ligand (L) under ultrasonic conditions is presented. The ligand and its cadmium complexes were characterized by various analyses such as FT-IR, UV?visible, 1H and 13C NMR spectra, XRD, SEM and TEM. According to applied techniques, the general formula of CdLX2 (X = Cl?, Br?, I?, SCN? and N3?) was suggested for the complexes. SEM, TEM and XRD analyses indicated that all complexes have nano-structure size in the range of 20?60 nm. In the next step, ligand and its cadmium complexes were subjected for in vitro antibacterial activities against two Gram-positive bacteria (Staphylococcus aureus and Bacillus subtilis) and two Gram-negative bacteria (Escherichia coli and Pseudomonas aeruginosa). Moreover in vitro antifungal properties of the compounds against Candida albicans and Aspergillus niger were investigated. The results indicated that all compounds show acceptable antibacterial and antifungal activities. Furthermore, the interaction of these complexes with DNA indicated that both ligand and its complexes can destruct the DNA structure. In final, thermal behaviors of all compounds were studied by TG/DTG/DTA analysis data. The thermo-diagrams showed that the compounds are decomposed via 2?3 temperature stages. Some thermo-kinetic activation data including Arrhenius constant, ΔE*, ΔH*, ΔS* and ΔG* of each thermal decomposition step were estimated graphically by use of experimental TGA data based on the Coats?Redfern equation.

Keywords:Thermal;Antimicrobial;Nano-structure;Complex;Cadmium

[References]

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[1] Ronconi L, Sadler PJ, Coord. Chem. Rev., 251, 1633 (2007)

[2] Bruijnincx PCA, Sadler PJ, Curr. Opin. Chem. Biol., 12, 197 (2008)

[3] Guo Z, Sadler PJ, Adv. Inorg. Chem., 49, 183 (2000)

[4] Desoize B, Anticancer Res., 24, 1529 (2004)

[5] Khan A, Nicholson G, Greenman J, Madden L, McRobbie G, Pannecouque C, De Clercq E, Ullom R, Maples DL, Maples RD, Silversides JD, Hubin TJ, Archibald SJ, J. Am. Chem. Soc., 131(10), 3416 (2009)

[6] Creaven BS, Duff B, Egan DA, Kavanagh K, Rosair G, Thangella VR, Walsh M, Inorg. Chim. Acta, 363, 4048 (2010)

[7] Imran M, Mitu L, Latif S, Mahmood Z, Naimat I, Zaman SS, Fatima S, J. Serb. Chem. Soc., 78(8), 1075 (2010)

[8] Hambley TW, J. Chem. Soc.-Dalton Trans., 4929 (2007)

[9] Scozzafava A, Supuran CT, J. Med. Chem., 43, 3677 (2000)

[10] Brown DH, Smith WE, Teape JW, Lewis AJ, J. Med. Chem., 23, 729 (1980)

[11] Scozzafava A, Menabuoni L, Mincione F, Mincione G, Supuran CT, Bioorg. Med. Chem. Lett., 11(4), 575 (2001)

[12] Al-Mogren MM, Alaghaz ANMA, Int. J. Electrochem. Sci., 8, 8669 (2013)

[13] Badea M, Olar R, Marinescu D, Lazar V, Chifiriuc C, Vasile G, J. Therm. Anal. Calorim., 97, 781 (2009)

[14] Hakimi M, Moeini K, Mardani Z, Khorrami F, J. Korean Chem. Soc., 57, 352 (2013)

[15] Pawar RP, Andurkar NM, Vibhute YB, J. Ind. Chem. Soc., 76, 271 (1999)

[16] Chavan S, Sivappa R, Tetrahedron Lett., 45, 3941 (2004)

[17] Bain GA, West DX, Krejci J, Valdes J, Simon HA, Toscano RA, Polyhedron, 16, 855 (1997)

[18] Chohan ZH, Sumrra SH, Youssoufi MH, Hadda TB, Eur. J. Med. Chem., 45, 2739 (2010)

[19] Bekhit AA, Hesham TY, Sherif AF, Baraka AM, Eur. J. Med. Chem., 38, 27 (2003)

[20] Pandeya S, Sriram D, Nath G, DeClercq E, Eur. J. Pharm. Sci., 9, 25 (1999)

[21] Shi HT, Qi LM, Ma JM, Cheng HM, J. Am. Chem. Soc., 125(12), 3450 (2003)

[22] Zhang H, Yang DR, Li DS, Ma XY, Li SZ, Que DL, Cryst. Growth Des., 5, 547 (2005)

[23] Kuang DB, Xu AW, Fang YP, Liu HQ, Frommen C, Fenske D, Adv. Mater., 15(20), 1747 (2003)

[24] Kim F, Connor S, Song H, Kuykendall T, Yang PD, Angew. Chem.-Int. Edit., 43, 3673 (2004)

[25] Chen W, Peng Q, Li Y, Cryst. Growth Des., 8, 564 (2008)

[26] Ranjbar ZR, Sheikhshoaie I, Bagheri Z, Int. J. Nano Dimens., 5(4), 409 (2014)

[27] Montazerozohori M, Yadegari S, Naghiha A, Veyseh S, J. Ind. Eng. Chem., 20(1), 118 (2014)

[28] Montazerozohori M, Zahedi S, Naghiha A, Zohour MM, Mater. Sci. Eng. C-Biomimetic Supramol. Syst., 35, 195 (2014)

[29] Montazerozohori M, Musavi SA, Naghiha A, Zohour MM, Spectroc. Acta Pt. A-Molec. Biomolec. Spectr., 129, 382 (2014)

[30] Montazerozohori M, Musavi SA, Naghiha A, Veyseh S, J. Chem. Sci., 126, 227 (2014)

[31] Montazerozohori M, Musavi SAR, J. Coord. Chem., 61, 3934 (2008)

[32] Bauer AW, Kirby WM, Sherris JC, Turck M, Am. J. Clin. Pathol., 45, 493 (1966)

[33] Rois JJ, Reico MC, Villar A, J. Ethnopharmacol., 23, 127 (1988)

[34] Iqbal A, Siddiqui HL, Ashraf CM, Ahmad M, Weaver GW, Molecules, 12, 245 (2007)

[35] Sambrook J, Fritsch EF, Maniatis T, Molecular Cloning: A Laboratory Manual, 2nd ed., Cold Spring Harbor Laboratory, Cold Spring Harbor, New York, 1989.

[36] Saleh AA, J. Coord. Chem., 58, 255 (2005)

[37] Yilmaz I, Cukurovali A, Transit. Met. Chem., 28, 399 (2003)

[38] Sonmez M, Levent A, Sekerci M, Synth. React. Inorg. Met. Org. Chem., 33(10), 1747 (2003)

[39] Samanta B, Chakraborty J, Choudhury CR, Dey SK, Dey DK, Batten SR, Jensen P, Yap GPA, Mitra S, Struct. Chem., 18, 33 (2007)

[40] Bhowmik P, Chattopadhyay S, Drew MGB, Diaz C, Ghosh A, Polyhedron, 29, 2637 (2010)

[41] Das D, Chand BG, Sarker KK, Dinda J, Sinha C, Polyhedron, 25, 2333 (2006)

[42] Amirnasr M, Schenk KJ, Salavati M, Dehghanpour S, Taeb A, Tadjarodi T, J. Coord. Chem., 56, 231 (2003)

[43] Chohan ZH, Transit. Met. Chem., 34, 153 (2009)

[44] Majumder A, Rosair GM, Mallick A, Chattopadhyay N, Mitra S, Polyhedron, 25, 1753 (2006)

[45] Dharmaraj N, Viswanathamurthi P, Natarajan K, Transit.Met. Chem., 26, 105 (2001)

[46] Malhota L, Kumar S, Dhindsa KS, Indian J. Chem., 32A, 457 (1993)

[47] Tweedy BG, Phytopathology, 55, 910 (1964)

[48] Kralova K, Kissova K, Svajlenova O, Vanco J, Chem. Pap., 58(5), 357 (2004)

[49] Vaghasia YK, Nair R, Soni M, Baluja S, Chanda S, J. Serb. Chem. Soc., 69, 991 (2004)

[50] Raman N, Res. J. Chem. Environ., 9(4), 79 (2005)

[51] Zelenak V, Gyoryova K, Mlynarcik D, Met. Based Drugs, 8, 269 (2002)

[52] Soliman AA, J. Therm. Anal. Calorim., 63, 221 (2001)

[53] Sharma N, Thakur AM, Bhatt SS, Chaudhry SC, J. Chem. Sci., 119, 311 (2007)