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Infrared and ¹³C NMR spectral studies of some aryl hydrazides: Assessment of substituent effects

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A series of some aryl hydrazides have been synthesized. These hydrazides purities were analyzed by physical constants and spectral data. The assigned spectral group frequencies were correlated with Hammett substituent constants and Swain-Lupton parameters using single and multi-linear regression analysis. From the results of statistical analysis, the effect of substituents on the spectral group frequencies has been discussed.
Rocznik
Strony
88--94
Opis fizyczny
Bibliogr. 18 poz., rys., tab., wz.
Twórcy
  • Department of Chemistry, Annamalai University, Annamalainagar - 608 002, India
autor
  • Department of Chemistry, National College, Tiruchirappalli - 620 001, India
  • Department of Chemistry, Shivani College of Engineering and Technology, Navalurkottapattu, Tiruchirappalli - 620 009, India
Bibliografia
  • [1] L. Harer Sunil, G. Rajurkar Vikas, P. Pravin, S. Harer Priyanka, D. Navale Sampat, T. Awuti Sandip, A. Sonawane Anand, Int. J. Pharm. Sci. Drug. Discover 2 (2010) 134-136.
  • [2] A. M. El Masri, J. N. Smith, R. T. Williams, Studies in Detoxication 68 (1957) 587-193.
  • [3] M. Somashekhar, A. R. Mahesh, B. Sonnad, World J. Pharm. Pharm. Sci. 2 (2012) 2011-2020.
  • [4] P. Kumar, B. Narasimhan, D. Sharma, Arkivoc. 13 (2008)159-178.
  • [5] S. S. Tajudeen, G. Kannappan. J. Pharm. Res. 7(2013) 534-539.
  • [6] W. S. El-Hamouly, K. M. Amin, S. A. El-Assaly, E. A. A. El-Meguid, Der Pharma Chemica 3 (2011) 293-306.
  • [7] M. Ahmed, F. B. Bux, R. Huque, J. Environ. Res. Dev. 3 (2008) 203-207.
  • [8] A. Bajracharya, W. Li, Y.E. Dong-Mei, C. Da-Peng, D. Yun-Peng, L. Yuan, Chinese J. Struct. Chem. 31 (2008) 1105-1110.
  • [9] G. Thirunarayanan, M. Gopalakrishnan, G. Vanangamudi, Spectrochim. Acta 67A (2007) 1106-1117.
  • [10] S. John Joseph, et al., International Letters of Chemistry, Physics and Astronomy 4 (2014) 48-65.
  • [11] R. Arulkumaran, R. Sundararajan, G. Vanangamudi, M. Subramanian, K. Ravi, V. Sathiyendiran, S. Srinivasan, G. Thirunarayanan, IUP J. Chem. 3(1) (2010) 82-98.
  • [12] G. Thirunarayanan, G. Vanangamudi, V. Sathiyendiran, K. Ravi, Indian J. Chem. 50B (2011) 593-604.
  • [13] G. Thirunarayanan, P. Mayavel, K. Thirumurthy, S. Dineshkumar, R. Sasikala, P. Nisha, A. Nithyaranjani, European Chem. Bull 2 (9013) 598-605.
  • [14] N. Kalyanasundaram, S. P. Sakthinathan, R. Suresh, D. Kamalakkannan, S. John Joseph, G. Vanangamudi, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 9 (2014) 23-47.
  • [15] G. Thirunarayanan, S. Pazhamalai, K. G. Sekar, International Letters of Chemistry, Physics and Astronomy 8 (2014) 38-46.
  • [16] G. Thirunarayanan, K. G. Sekar, Solvent-free one-pot cyclization and acetylation of chalcones: Synthesis of some 1-acetyl pyrazoles and spectral correlations of 1-(3-(3,4-dimethylphenyl)-5-(substituted phenyl)-4,5-dihydro-1H-pyrazole-1-yl) ethanones, J. Saudi Chem. Soc. (2014).
  • [17] G. Thirunarayanan, K. G. Sekar, International Letters of Chemistry, Physics and Astronomy 10(1) (2013) 18-34.
  • [18] Swain C. G., Lupton Jr. E. C., J. Am. Chem. Soc. 90 (1968) 4328-4337.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-66019cd6-e2c6-4836-b544-8cfefb0bc279
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