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NMR Spectral correlations in some Tröger’s bases

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Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Some Tröger’s bases have been synthesised from substituted anilines and paraformaldehyde in presence of Lewis acid catalyst such as anhydrous AlCl3, through electrophilic substitution reaction. The purities of these Tröger’s bases have been checked by their physical constants and spectroscopic data published earlier in the literature. The NMR chemical shift (δ, ppm) of methylene protons and carbon were assigned. The assigned methylene protons and carbon chemical shifts (δ, ppm) of synthesised Tröger’s bases have been correlated with Hammett substituent constants, F and R parameters using single and multi-regression analyses. From the results of statistical analyses, the effects of substituent on methylene protons and carbon were discussed.
Rocznik
Tom
Strony
1--11
Opis fizyczny
Bibliogr. 44 poz., rys., tab.
Twórcy
  • Department of Chemistry, Annamalai University, Annamalainagar 608002, India
autor
  • Department of Chemistry, Annamalai University, Annamalainagar 608002, India
Bibliografia
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  • 36. Sakthinathan S. P., Suresh R., Mala V., Sathiyamoorthi K., Kamalakkannan D., Ranganathan K., Arulkumaran R., Vijayakumar S., Sundararajan R., Vanangamudi G., Thirunarayanan G., International Letters of Chemistry, Physics and Astronomy 6 (2013) 77-90.
  • 37. Sathiyamoorthi K., Mala V., Suresh R., Sakthinathan S. P., Kamalakkannan D., Ranganathan K., Arulkumaran R., Sundararajan R., Vijayakumar S., Vanangamudi G., Thirunarayanan G., International Letters of Chemistry, Physics and Astronomy 7(2) (2013) 102-119.
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Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-dbb015a8-15b0-4305-b9a5-6fe80ed1981a
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