Synthesis and characterization of some antifungal Oalkyl (O-aryl) trithiophosphato derivatives of 1,3,2- dioxaborinanes

Journal of the Iranian Chemical Research

مقاله 3، دوره 5، شماره 4، اسفند 2012، صفحه 223-229   

نویسندگان

Alok Chaturvedi^* ؛ Mukesh Chand Gupta؛ Kiran Sankhala,

Synthetic and Surface Science Laboratory, Dept. of Chemistry, Govt. College, Ajmer (Raj.), India

چکیده

Complexes of the type (OCH2C(CH3)2CH2OB)2S2P(S)OR (where R=Me,Et,Pri,Bui,Ph,CH2Ph) have been
synthesized by the reactions of 2-chloro-1,3,2-dioxaborinanes and potassium salt of O-alkyl (O-aryl)
trithiophosphates in 2:1 molar ratio in refluxing benzene. The product are formed as white or light yellow
coloured monomeric solid, soluble in common organic solvents and exhibit high sensitivity towards
atmospheric moisture. These complexes have been characterized by elemental analysis (C,H,S,B), molecular
weight measurement, IR and NMR (1H,11B,31P) spectral studies. On the basis of above studies it is postulated
that boron is in three coordinated state. The newly synthesized complexes show effectiveness against
powdery mildew disease at a fixed interval of days.

کلیدواژه‌ها

2-chloro-1,3,2-dioxaborinanes؛ O-alkyl(O-aryl)trithiophosphates (1H,11B,31P )spectral studies؛ Antifungal activity

مراجع

[1] O.P.Singh, A.Chaturvedi, D.B. Saxena, R.K. Mehrotra, G.Srivastava, Monatshafte fur Chemie, 125
(1994) 607-613.
[2] A. Chaturvedi, P.N. Nagar, G.Srivastava, Phosphorus Sulfur and Silicon, 90 (1994) 229-233.
[3] G.E.Mc Achran, S.G. Shore, Inorg. Chem, 5 (1966) 2044-2049.
[4] S.K.Mehrotra, G. Srivastava, R.C. Mehrotra, Synth. React Inorg. Met. Org-Chem, 4 (1974) 27-36.
[5] P.N.Bhardwaj, G. Srivastava, J. Indian Chem. Soc. 59 (1982) 300-307.
[6] P.N. Nagar, G. Srivastava, R.C. Mehrotra, Synth. React. Inorg. Met-Org. Chem., 12 (1982) 749-759.
[7] O.P. Singh, R.K. Mehrotra, G. Srivastava, Synth. React. Inorg. Met Org. Chem., 21 (1991) 717-728.
[8] A.S. Kothiwal, A. Singh, A.K. Rai, R.C. Mehrotra, Ind. J. Chem. 24 (1985) 828-834.
[9] Y.P. Singh, P. Rupani, A. Singh, A.K. Rai, R.D. Rogers, J.L. Atwood, Inorg. Chem., 25 (1985) 3076-
3081.
[10] A. Chaturvedi, C.S. Sharma, P.N. Nagar, Phosphorus sulfur and Silicon, 178 (2003) 1923-1929.
[11] L. Chordia, A. Chaturvedi, Phosphorus, Sulfur and Silicon, 182 (2007) 2821-2831.
[12] Y. Kimuva, T. Wakabayashi, K. Okada, T. Wada, H. Nishikawa, Wear, 232 (1999) 199-206.
[13] M. Lovell, C.F. Higgs, P. Deshmukh, A.J. Mobleymat, Pro. Teeh, 177 (2006) 87-90.
[14] C.C. Klepper, J.M. Williams, J.J.J. Truhan, J. Qu, L. Riestev, R.C. Hazelton, J.J. Moshchella, P.J. Blau,
J.P. Anderson, O.O. Popooia, M.D. Keitz, Thin Solid films, 516 (2008) 3070-3080.
[15] J.H.Wu, B.S.Phillips, W.Jiang, J.H.Sanders, J.S. Zabinsk, A.P. Malshe, Wear 261 (2006) 592-599.
[16] B.A. Baldwin, Wear, 45 (1977) 345-353.
[17] Z.S. Hu, Y. Yie, L.G. Wang, G.X. Chen, J.X. Dong, Tribol. Lett. 8 (2000) 45-50.
[18] W. Liu, Z. Jin, Q. Xue, Lubricat. Sci.7 (1994) 49-60.
[19] J.M. Herdan, Lubricat Sci. 2 (2000) 265-276.
[20] W. Liu, Q. Xue, X. Zhang, H. Wang, C. Huang, Tribol. Trans. 48 (1992) 475-479.
[21] G. Shen, Z. Zheng, Y. Wan, X. Xu, L. Cao, Q. Yue, T. Sun, A. Liu, Wear, 246 (2000) 55-58.
[22] L. Chordia, A. Chaturvedi, Main group Met. Chem. 31 (2008) 319-329.
[23] L. Chordia, A. Chaturvedi, J. Chin. Chem. Soc. 56 (2009) 636-641.
[24] P.N. Bhardwaj, G. Srivastava, Bull. Chem. Soc. Japan 51 (1978) 524-531.
[25] A.I. Vogel. A Textbook of Qualitative Inorganic Analysis ELBS, IV Edition 1973.
[26] A.K.Sobti, A.K. Mathur, B.S. Siradhana, India Phytopathology 45 (1992) 200-208.