Polar substituent effects on NMR chemical shifts of group 14 elements: synthesis and NMR (carbon-13, silicon-29, tin-119, and lead-207) substituent chemical shifts (SCS) of 4-substituted bicyclo[2.2.2]oct-1-ylbutanes, -trimethylsilanes, -trimethylstannanes, and -trimethyl plumbanes (M(CH3)3, M = carbon, silicon, tin, and lead) and 4-substituted bicyclo[2.2.1]hept-1-yltrimethylstannanes

1987 ◽  
Vol 6 (1) ◽  
pp. 156-166 ◽  
Author(s):  
William. Adcock ◽  
Hemakanthi. Gangodawila ◽  
Gaik B. Kok ◽  
V. Sankar. Iyer ◽  
William. Kitching ◽  
...  
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.


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