𝔖 Bobbio Scriptorium
✦   LIBER   ✦

1H1H and 1H19F coupling constants of some styrene, benzaldehyde and benzylidene amine derivatives

✍ Scribed by Sirpa Suntioinen; Reino Laatikainen; Vladimir Král


Publisher
John Wiley and Sons
Year
1994
Tongue
English
Weight
372 KB
Volume
32
Category
Article
ISSN
0749-1581

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Five para‐fluorobenzene derivatives having a CHCR~2~ or a CHNR group were prepared and their ^1^H and ^19^F NMR spectra in acetone‐d~6~ were analysed. The ^6^J(H~α~,F) and ^4^J(H^α^,H) couplings of the nitrogen derivatives fall between those of the carbon and oxygen derivatives: the electronegativity of the side‐chain β‐atom seems to have a prominent role in the spin information transmission. The ^6^J(H^α^,F) and ^4^(H^α^,H) couplings indicate that the nitrogen derivatives are rigidly planar whereas the carbon derivatives are non‐planar.


📜 SIMILAR VOLUMES


Solvent effects on the 1H1H, 1H19F and 1
✍ Sirpa Suntioinen; Reino Laatikainen 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 357 KB

## Abstract The ^1^H and ^19^F NMR spectra of fluorobenzene and 1,2‐difluorobenzene were measured in several pure solvents and in binary solvent mixtures to study the solvent dependence of ^1^H^19^F and ^19^F^19^F coupling constants. The solvents are distinctly divided into two groups on the basi

Temperature effects on the 1H1H, 1H19F a
✍ Sirpa Suntioinen; Ursula Weber; Reino Laatikainen 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 276 KB

## Abstract The ^1^H NMR spectra of fluorobenzene and 1,2‐difluorobenzene were measured in acetonitrile‐d~3~ and cyclohexane‐d~12~ at four temperatures to study the temperature dependence of ^1^H^1^H, ^1^H^19^F and ^19^F^19^F coupling constants. In acetonitrile‐d~3~ the ^5^__J__(F,H) coupling co

Signs of 19F1H and 19F13C spin–spin coup
✍ I. D. Rae; J. A. Weigold; R. H. Contreras; G. Yamamoto 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 397 KB

## Abstract The details of two‐dimensional ^13^C^1^H correlated spectra have provided information about the relative signs of __J__(C, F) and __J__(F, H) for several molecules in which C, F and H are mutually coupled. Unlike signs are found for __J__(C, F) and __J__(F, H) when the coupling pathway

A 13C{1H} double resonance study of the
✍ W. S. Brey; L. W. Jaques; H. J. Jakobsen 📂 Article 📅 1979 🏛 John Wiley and Sons 🌐 English ⚖ 397 KB

## Abstract The signs of all ^13^C^19^F and ^1^H–^19^F coupling constants in fluorobenzene, some substituted derivatives, and in 2‐fluoropyridine have been related using single‐frequency ^13^C{^1^H} double resonance techniques. All ^13^C^19^F couplings in these compounds are shown to be positive

19F and 1H NMR spectra of halocarbons
✍ Anthony Foris 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 289 KB

## Abstract ^19^F NMR chemical shifts and coupling constants are reported for 215 compounds. For 77 of these compounds, ^1^H NMR spectral data are also given. Long‐range couplings, including ^8^J(F,F) and ^5^J(F,H), are reported. The complexity of halocarbon spectra owing to the presence of rotatio

Long range phenomena—XIV: 1H-{1H} indor
✍ M. Anteunis; F. Borremans; R. Van Den Bossche; G. Verhegge 📂 Article 📅 1972 🏛 John Wiley and Sons 🌐 English ⚖ 435 KB

## Abstract PMR parameters of some methylene substituted oxiranes are obtained from INDOR experiments on the ABXMN spin systems. Compounds investigated include safrol‐ and bromosafrol epoxide and β‐phenoxypropylene oxide. For the latter compound all the relative signs (except for some long range co