Aromatic compounds proton magnetic resonance spectra

Annulene was the first macrocyclic annulene containing (4n -j- 2) zr-electrons to be synthesized. The compound is of considerable interest, since it is the type of annulene that was predicted to be aromatic by Hiickel.10 It proved to be aromatic in practice, as evidenced from the proton magnetic resonance spectrum,8-11 the X-ray crystallographic analysis,18 and the fact that electrophilic substitution reactions could be effected.13... 

Since the product slowly darkens on exposure to air, it should be stored under nitrogen in a refrigerator. The compound solidifies on cooling m.p. 16.0-16.5°. Nuclear magnetic resonance spectrum (neat, tetramethylsilane internal standard) singlets at d 7.00 (aromatic protons), 3.93 (CH2), and 2.24 p.p.m. (NH). 

The NMR spectrum of pyridazine shows two symmetrical quartets of A2X2 type and t values and coupling constants are as follows Te = 0.76, T4 = T5 = 2.45 t/3 4 = /5,e = 4.9 (5.05 ),. Ig 5 = 7 4,6 = 2.0, Jg g = 3.5 (1.4 ), J4 5 = 8.4. The C satellites in natural abundance in the liquid state have been examined in order to obtain a complete set of proton magnetic resonance parameters for pyridazine. It has been found that chemical shifts are strongly concentration-dependent in a sense opposite to that normally found with aromatic compounds. Coupling constants are, however, virtually invariant. From the NMR spectrum, a deshielding effect on the hydrogen atoms at positions 3 and 6 is revealed. ... 

The structures of vanicosides A (1) and B (2) and hydropiperoside (3) were established primarily by one- and two-dimensional nuclear magnetic resonance (NMR) spectroscopy techniques and fast atom bombardment (FAB) mass spectrometry (MS).22 The presence of two different types of phenylpropanoid esters in 1 and 2 was established first through the proton (4H) NMR spectra which showed resonances for two different aromatic substitution patterns in the spectrum of each compound. Integration of the aromatic region defined these as three symmetrically substituted phenyl rings, due to three p-coumaryl moieties, and one 1,3,4-trisubstituted phenyl ring, due to a feruloyl ester. The presence of a sucrose backbone was established by two series of coupled protons between 3.2 and 5.7 ppm in the HNMR spectra, particularly the characteristic C-l (anomeric) and C-3 proton doublets... 

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