A Study of the Proton Nuclear Magnetic Resonance Spectra of Aryl and Mono- and Disubstituted N-Methylazoles

1973 ◽  
Vol 51 (14) ◽  
pp. 2315-2322 ◽  
Author(s):  
Richard Noel Butler
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Chemical Shifts ◽  
Structural Characteristics ◽  
Proton Nuclear Magnetic Resonance ◽  
Methyl Group ◽  
Nuclear Magnetic Resonance Spectra ◽  
Azole Ring ◽  
Magnetic Resonance Spectra ◽  
Nuclear Magnetic

Proton n.m.r. spectra of 111 substituted azoles are compared. The influence of the azole ring on the chemical shifts of substituent phenyl protons is discussed. A correlation between N-methyl chemical shifts and the structural characteristics of the N-methyl group in mono- and disubstituted azoles is noted.

Fluorine and Proton Nuclear Magnetic Resonance Spectra of N-Dialkylaminosulfur Trifluorides

1972 ◽  
Vol 50 (15) ◽  
pp. 2428-2431 ◽  
Author(s):  
D. G. Ibbott ◽  
A. F. Janzen
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Chemical Shifts ◽  
Coupling Constants ◽  
Proton Nuclear Magnetic Resonance ◽  
Nuclear Magnetic Resonance Spectra ◽  
Magnetic Resonance Spectra ◽  
Nuclear Magnetic

The fluorine and proton n.m.r. spectra of N-dimethylaminosulfur trifluoride and N-diethylaminosulfur trifluoride have been recorded under anhydrous conditions at −68 and +22°. Chemical shifts and coupling constants of axial and equatorial fluorines are reported.

The metal nuclear magnetic resonance spectra of some tin(II) and lead(II) complexes with polydentate phosphines

1983 ◽  
Vol 61 (8) ◽  
pp. 1795-1799 ◽  
Author(s):  
Philip A. W. Dean
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Nmr Spectra ◽  
Narrow Range ◽  
Chemical Shifts ◽  
Nuclear Magnetic Resonance Spectra ◽  
Magnetic Resonance Spectra ◽  
Nuclear Magnetic

The previously reported 1:1 complexes formed in MeNO2, between M(SbF6)2 (M = Sn or Pb) and Ph2P(CH2)2PPh2, PhP[(CH2)2PPh2]2, MeC(CH2PPh2)3, P[(CH2)2PPh2]3, and [Formula: see text] have been studied by metal (119Sn or 207Pb) nmr. The metal chemical shifts span the comparatively narrow range of −586 to −792 ppm and 60 to −269 ppm, relative to the resonance of MMe4, for 119Sn and 207Pb nmr, respectively. The implications of these data regarding the denticity of the ligand in M(P[(CH2)2PPh2]3)2+ are discussed, and a comparison with the metal nmr spectra of related stannous and plumbous complexes is made.

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