Molecular Orbital Approximation to Electron‐Spin Coupled Nuclear Spin‐Spin Interactions in Molecules

1955 ◽  
Vol 23 (4) ◽  
pp. 760-760 ◽  
Author(s):  
Harden McConnell
2005 ◽  
Vol 97 (4) ◽  
pp. 043706 ◽  
Author(s):  
Seungwon Lee ◽  
Paul von Allmen ◽  
Fabiano Oyafuso ◽  
Gerhard Klimeck ◽  
K. Birgitta Whaley

2009 ◽  
Vol 36 (2-4) ◽  
pp. 181-194 ◽  
Author(s):  
Elena G. Bagryanskaya ◽  
David Bardelang ◽  
Sandrine Chenesseau ◽  
Jean-Pierre Finet ◽  
Laszlo Jicsinszky ◽  
...  

2009 ◽  
Vol 24 (2) ◽  
pp. 023001 ◽  
Author(s):  
Y Hirayama ◽  
G Yusa ◽  
K Hashimoto ◽  
N Kumada ◽  
T Ota ◽  
...  

1972 ◽  
Vol 50 (18) ◽  
pp. 2232-2234 ◽  
Author(s):  
Gerald F. Dionne

The argument that Ti3+ ions produce 12 magnetic complexes when substituted for Al3+ in CsAl (SO4)2∙12H2O (Cs alum) is supported neither by experimental evidence nor a realistic physical model. The uniform intensity of the superhyperfine structure in Rb(TiAl) alum disproves the idea that titanium nuclei are involved because the natural abundance of nuclear magnetic isotopes is only 13%. In addition, the magnitudes of the splittings are too small to represent electron–nuclear spin interactions within the Ti3+ ions.


1999 ◽  
Vol 23 (1) ◽  
pp. 52-53
Author(s):  
Mansour Zahedi ◽  
Mohammed Al-Kobaisi (Latif)

A π-orbital axis vector (POAV) analysis used in Hückel molecular orbital approximation calculations indicates that the cutoff in the fullerene mass spectrum at C n ( n = 32) must naturally occur with no need to define a ‘magic’ number.


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