One-bond and long-range coupling constants of substituted 2-cyanopyridines. GIAO/DFT calculations of proton and carbon chemical shifts and coupling constants-Reference-Cited by-同舟云学术

One-bond and long-range coupling constants of substituted 2-cyanopyridines. GIAO/DFT calculations of proton and carbon chemical shifts and coupling constants

Published:2006-02 Issue:1-3 Volume:783 Page:191-203
ISSN:0022-2860
Container-title:Journal of Molecular Structure
language:en
Short-container-title:Journal of Molecular Structure

Author:

Katritzky Alan R.,Akhmedov Novruz G.,Güven Alâattin,Scriven Eric F.V.,Majumder Suman,Akhmedova Rena G.,Hall C. Dennis

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry

Reference63 articles.

1. THE ANALYSIS OF NUCLEAR MAGNETIC RESONANCE SPECTRA: III. PYRIDINE AND DEUTERATED PYRIDINES

2. Carbon-13 Proton Spin Coupling Constants in Heteroaromatic Molecules

3. Carbon-13 magnetic resonance. X. Six-membered nitrogen heterocycles and their cations

4. Carbon-13 nuclear magnetic resonance studies of 2-substituted pyridines

5. Studies on the Proton Magnetic Resonance Spectra in Aromatic Systems. XII. Heterocyclic Series. (4). 4-Substituted Pyridines

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The Intramolecular Spin-Spin Interactions in Ruthenium Complexes of Pyrazole Derivatives;SPECTROSC SPECT ANAL;2016

2. The qualitative and quantitative accuracy of DFT methods in computing 1 J(C–F), 1 J(C–N) and n J(F–F) spin–spin coupling of fluorobenzene and fluoropyridine molecules;Journal of Quantitative Spectroscopy and Radiative Transfer;2015-01

3. Long-range proton–carbon coupling constants: NMR methods and applications;Progress in Nuclear Magnetic Resonance Spectroscopy;2013-08

4. Structure of 2,3-dicarboxy-1-methylpyridinium chloride studied by X-ray diffraction, DFT calculation, NMR, FTIR and Raman spectra;Journal of Molecular Structure;2012-06

5. Structure of methyl 3-(trimethylammonium)benzoate iodide studied by X-ray diffraction, DFT calculations, NMR and FTIR spectra;Journal of Molecular Structure;2012-06