Substituent effects on15N NMR chemical shifts in selectedN-alkylthiohydroxamic acids. A comparative study

2004 ◽  
Vol 43 (1) ◽  
pp. 27-30 ◽  
Author(s):  
Witold Przychodze? ◽  
Leszek Doszczak ◽  
Janusz Rachon

ChemInform ◽  
2010 ◽  
Vol 24 (23) ◽  
pp. no-no
Author(s):  
V. BALIAH ◽  
V. PREMASAGAR ◽  
M. UMA ◽  
A. MANGALAMUDAIYAR




2010 ◽  
Vol 185 (4) ◽  
pp. 772-784 ◽  
Author(s):  
Zaira Domínguez ◽  
Javier Hernández ◽  
Lorena Silva-Gutiérrez ◽  
Magali Salas-Reyes ◽  
Mario Sánchez ◽  
...  


1976 ◽  
Vol 31 (12) ◽  
pp. 1641-1645 ◽  
Author(s):  
Walter Grahn

The 13C NMR chemical shifts of fifteen 6 substituted 2,3-dihydro-1,4-diazepinium salts (cis trimethincyanines) (1) and twelve 2 substituted bis(dimethylamino)trimethinium salts (trans trimethincyanines) (2) have been determined. A comparison of the substituentinduced shifts (13C SCS) of 1 and 2 allows no distinction between steric and electronic effects. In the three 6 п-electron systems 1, 2 and monosubstituted benzenes the 13C SCS are similar for the substituent bearing carbon atoms. A surprisingly large 4JFCCNC coupling constant has been observed.





Author(s):  
Frans J. Hoogesteger ◽  
David M. Grove ◽  
Leonardus W. Jenneskens ◽  
Theodorus J. M. de Bruin ◽  
Bart A. J. Jansen


1980 ◽  
Vol 35 (7) ◽  
pp. 934-936 ◽  
Author(s):  
R. Radeglia ◽  
S. L. Spassov ◽  
R. Stefanova ◽  
S. D. Sofia

Carbon-13 chemical shifts have been measured of para-substituted 3-phenyl propanoic acid methyl esters. The substituent-induced 13C shifts of the side chain were related to Hammett substituent effects by the dual substituent parameter method. The transmission of substituent effects and the factors that influence 13C shifts are discussed



Sign in / Sign up

Export Citation Format

Share Document