𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A 1H, 13C, and 15N NMR spectral analysis of 15N-nitrobenzene

✍ Scribed by Ludger Ernst; Ernest Lustig; Victor Wray

Publisher
Elsevier Science
Year
1976
Weight
461 KB
Volume
22
Category
Article
ISSN
0022-2364

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

1H, 13C and 15N NMR spectral assignments
1H, 13C and 15N NMR spectral assignments for new triazapentalene derivatives
✍ Pascal Palmas; Coralie Nyffenegger; Eric Pasquinet; Gérald Guillaumet 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 126 KB

## Abstract Mesomeric heteropentalene betaines are conjugated fused polyheterocyclic structures that represent interesting intermediates for organic synthesis. Five such structures, containing at least four nitrogen atoms and various substituents, have been characterized by ^1^H, ^13^C and ^15^N NM

1H, 13C and 15N NMR spectra of [1,2-15N2
1H, 13C and 15N NMR spectra of [1,2-15N2]pyrazole derivatives
✍ Alain Fruchier; Valdo Pellegrin; Rosa Maria Claramunt; Jose Elguero 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 English ⚖ 199 KB

## REFERENCE DATA carbons, for various substituent groups and positions were carried out by gated decoupling with NOE. ## RESULTS AND DISCUSSION The I3C NMR chemical shifts of the compounds are shown in Tables 123; 'J(CH) and long-range coupling constants of 2, 9, 13 and 18, measured by gated d

1H, 13C and 15N NMR spectra of ciproflox
1H, 13C and 15N NMR spectra of ciprofloxacin
✍ Andrzej Ziȩba; Andrzej Maślankiewicz; Jerzy Sitkowski 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 103 KB

## Abstract ^1^H NMR assignment, including the values of δ~H~ and __J__(H,H) for the cyclopropane moiety, and ^13^C NMR and ^15^N NMR spectral data for ciprofloxacin are presented. Copyright © 2004 John Wiley & Sons, Ltd.

1H, 13C and 15N NMR study of N1-alkyl-N2
1H, 13C and 15N NMR study of N1-alkyl-N2-arylthioureas
✍ Iwona Wawer; Vera Koleva 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 407 KB

## Abstract ^13^C and ^15^N NMR chemical shifts were measured for __N__^1^‐alkyl‐__N__^2^‐arylthioureas. The absence of decoalescence of the __N__^1^‐alkyl group carbon signals down to 190 K, the europium‐induced chemical shifts and the molecular mechanics calculations indicate that the preferred c

15N1H and 15N–13C couplings in 15N-enric
15N1H and 15N–13C couplings in 15N-enriched dihydroxamic acids
✍ Jan Schraml; Petr Cigler 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 202 KB

## Abstract ^15^N‐enriched dihydroxamic acids (HONHCO(CH~2~)~__n__~CONHOH, __n__ = 0, 1, and 2) were prepared and their spectra NMR (^1^H, ^13^C, ^15^N) recorded in dimethyl sulfoxide (DMSO) solutions with the aim of determining ^15^N coupling constants (^15^N^1^H and ^15^N^13^C). The results sup