Derivatives coupling constants

Table 7.36 Miscellaneous deuterated derivatives Coupling constants...

Nuclear Overhauser enhancement (NOE) spectroscopy has been used to measure the through-space interaction between protons at and the protons associated with the substituents at N (20). The method is also useful for distinguishing between isomers with different groups at and C. Reference 21 contains the chemical shifts and coupling constants of a considerable number of pyrazoles with substituents at N and C. NOE difference spectroscopy ( H) has been employed to differentiate between the two regioisomers [153076 5-0] (14) and [153076 6-1] (15) (22). N-nmr spectroscopy also has some utility in the field of pyrazoles and derivatives. 

Nuclear Magnetic Resonance Spectroscopy. Nmr is a most valuable technique for stmeture determination in thiophene chemistry, especially because spectral interpretation is much easier in the thiophene series compared to benzene derivatives. Chemical shifts in proton nmr are well documented for thiophene (CDCl ), 6 = 7.12, 7.34, 7.34, and 7.12 ppm. Coupling constants occur in well-defined ranges J2-3 = 4.9-5.8 ... 

Application of NMR spectroscopy to heterocyclic chemistry has developed very rapidly during the past 15 years, and the technique is now used almost as routinely as H NMR spectroscopy. There are four main areas of application of interest to the heterocyclic chemist (i) elucidation of structure, where the method can be particularly valuable for complex natural products such as alkaloids and carbohydrate antibiotics (ii) stereochemical studies, especially conformational analysis of saturated heterocyclic systems (iii) the correlation of various theoretical aspects of structure and electronic distribution with chemical shifts, coupling constants and other NMR derived parameters and (iv) the unravelling of biosynthetic pathways to natural products, where, in contrast to related studies with " C-labelled precursors, stepwise degradation of the secondary metabolite is usually unnecessary. 

Proton-proton coupling constants of benzo rings of benzazoles can illuminate the bonding in such compounds. Thus, comparison of the J values for naphthalene with those for benzotriazoles of different types (Table 13) shows evidence of bond fixation, particularly in the 2-methyl derivative (98) (71PMH(4)l2l). 

The most characteristic coupling constant in indazoles is the cross-ring Vs, present both in indazoles and in isoindazoles unsubstituted in positions 3 and 7. 2-Methyl isomers show an additional Vmc.h coupling which can serve to identify an isoindazole unsubstituted in position 3. In 3-azidoindazole, as in 3-azidopyrazole (56), the prototropic exchange is slowed down sufficiently to allow the measurement of a zig-zag /i,4 coupling constant. The deshielding effects observed in A-acetyl derivatives, e.g. 1-acetyl (60) on H-7 and 2-acetyl (61) on H-3, are related to a preferred E conformation (Section 4.04.1.4.3). 

Scheme 1 H NMR shifts and coupling constants of azetidine derivatives...

Chemical shifts ( H, C) and coupling constants for some thiiranes and thiirenes are given in Table 2. The shifts of substituted derivatives may be calculated by the use of additivity relationships found in textbooks on NMR. 

For the stable conformers 13a-c of a substituted ethane the vicinal HH coupling constants 3Hz for syn-protons and 15 Hz for anti-protons can be derived from Fig. 2.18. If there is rotation around the C-C single bond, the coupling protons pass through the syn configuration twice and the anti configuration once. 

First the trans configuration of the C-2-C-3 double bond is derived from the large coupling constant Jhh = 15 Hz) of the protons at % = 5.10 and 7.11, whereby the middle CH proton (Sh = 5.10) appears as a doublet of doublets on account of the additional coupling ([Pg.189]

The assignment of all of the chemical shift values and coupling constants as derived from the measurements can be checked in structural formula D. 

The EPR spectrum of the ethyl radical presented in Fig. 12.2b is readily interpreted, and the results are relevant to the distribution of unpaired electron density in the molecule. The 12-line spectrum is a triplet of quartets resulting from unequal coupling of the electron spin to the a and P protons. The two coupling constants are = 22.38 G and Op — 26.87 G and imply extensive delocalization of spin density through the a bonds Note that EPR spectra, unlike NMR and IR spectra, are displayed as the derivative of absorption rather than as absorption. 

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