Carbon-13/carbon-12 isotope effects on nitrogen-15 chemical shielding in some diamagnetic cyano complexes

1982 ◽  
Vol 60 (17) ◽  
pp. 2194-2197 ◽  
Author(s):  
Roderick E. Wasylishen

Carbon-13/carbon-12 isotope-induced 15N chemical shifts of 0.06 to 0.10 ppm have been observed for the cyanide ion and several transition metal cyanides. In each case, the 15N resonance of the 13C labelled isotopomers is to high field of that in the corresponding carbon-12 species. The sensitivity of the 15N and 13C shielding constants in the cyanide ion to small changes in the CN bond length are evaluated using the theoretical formulation of Jameson: (∂σ(15N)/∂r)e = −872 ± 160 ppm/Å and (∂σ(13C)/∂r)e = −473 ± 90 ppm/Å. Nitrogen-15 chemical shifts in the metal complexes exhibit basically the same behaviour as do the 13C chemical shifts in these same complexes.


1987 ◽  
Vol 65 (7) ◽  
pp. 1469-1473 ◽  
Author(s):  
Kevin L. Leighton ◽  
Roderick E. Wasylishen

Deuterium induced isotope effects on the 119Sn chemical shielding constants have been measured for stannane and the stannonium cation; they are found to be approximately −0.403 ppm/D and −0.05 ppm/D respectively. The 119Sn shifts in the series SnDnH4−n (n ≤ 4) deviate from additivity as predicted by Jameson and Osten. The primary and secondary isotope effects on Sn–H spin–spin coupling for stannane were obtained and are −2.8 Hz and −1.7 Hz respectively. The primary isotope effect for Sn–H spin–spin coupling for the stannonium cation was found to be −11.6 ± 7 Hz; an accurate value for the secondary isotope effect on the spin–spin coupling could not be obtained. The derivative of the 119Sn shielding constant and J (Sn,H) with respect to extensions in the equilibrium bond length have been calculated for stannane.



1980 ◽  
Vol 41 (2) ◽  
pp. 341-342 ◽  
Author(s):  
Roderick E Wasylishen ◽  
Dennis H Muldrew ◽  
Kenneth J Friesen


2011 ◽  
Vol 115 (22) ◽  
pp. 5654-5659 ◽  
Author(s):  
Peter Hrobárik ◽  
Veronika Hrobáriková ◽  
Florian Meier ◽  
Michal Repiský ◽  
Stanislav Komorovský ◽  
...  


Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3763
Author(s):  
Poul Erik Hansen

This review outlines methods to investigate the structure of natural products with emphasis on intramolecular hydrogen bonding, tautomerism and ionic structures using NMR techniques. The focus is on 1H chemical shifts, isotope effects on chemical shifts and diffusion ordered spectroscopy. In addition, density functional theory calculations are performed to support NMR results. The review demonstrates how hydrogen bonding may lead to specific structures and how chemical equilibria, as well as tautomeric equilibria and ionic structures, can be detected. All these features are important for biological activity and a prerequisite for correct docking experiments and future use as drugs.



2000 ◽  
Vol 122 (51) ◽  
pp. 12878-12879 ◽  
Author(s):  
Parwin Schah-Mohammedi ◽  
Ilja G. Shenderovich ◽  
Carsten Detering ◽  
Hans-Heinrich Limbach ◽  
Peter M. Tolstoy ◽  
...  


2009 ◽  
Vol 47 (9) ◽  
pp. 782-790 ◽  
Author(s):  
Alexey N. Egorochkin ◽  
Olga V. Kuznetsova ◽  
Nadiya M. Khamaletdinova ◽  
Yury A. Kurskii ◽  
Lada G. Domratcheva-Lvova ◽  
...  


1969 ◽  
Vol 8 (11) ◽  
pp. 2499-2503 ◽  
Author(s):  
Jesse G. Reinstein ◽  
Ernest Griswold ◽  
Jacob Kleinbert


1987 ◽  
Vol 65 (5) ◽  
pp. 941-946 ◽  
Author(s):  
Ross M. Dickson ◽  
Michael S. McKinnon ◽  
James F. Britten ◽  
Roderick E. Wasylishen

The static 13C nmr powder pattern for solid ammonium thiocyanate is analyzed to obtain the 13C chemical shielding anisotropy, 321 ± 7 ppm, and the 13C–14N dipolar splitting, 1295 ± 25 Hz. Slow magic angle spinning 15N nmr experiments are analyzed to obtain a nitrogen chemical shielding anisotropy of 415 ± 15 ppm. The 13C–14N dipolar splitting leads to an effective C—N bond length of 1.19 ± 0.01 Å, in good agreement with the value of 1.176 Å reported from accurate X-ray and neutron crystallographic studies. In solid NH4NCS absolute values of the average shielding constants [Formula: see text] and ct[Formula: see text] are 52 and 34 ppm, respectively. Comparison of calculated and observed [Formula: see text] values indicates that intermolecular interactions decrease the 13C and 15N shielding constants by approximately 10 and 30 ppm, respectively.



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