scholarly journals Noble Gases Encaged by the C60 Increase Their Chemical Reactivity

Author(s):  
Avelino Cortés-Santiago ◽  
Rubicelia Vargas ◽  
Jorge Garza

In this work, we use a spherical shell with an attractive potential to simulate the C<sub>60</sub> and its effects on, He, Ne, Ar and Kr when each atom is in the center of the sphere. Within the Kohn-Sham model, two exchange-correlation functionals were used; the main difference between these two functionals is that one incorporates explicitly the self-interaction correction and the correct asymptotic behavior of the exchange-correlation potential, and the other one does not contain such corrections. We found that the considered atoms are softer inside of the cage than when they are free. By using several chemical reactivity predictors as the electrodonating and electroaccepting powers, defined by Professor Gázquez <em>et al</em>. (<em>J. Phys. Chem. A</em> 2007, <em>111</em>, 1966), it is proved that the noble gases increase their chemical reactivity when they are immersed in the C<sub>60</sub>. Naturally, this conjecture must be confirmed by more realistic models, but at first glance this is a very interesting conclusion and opens a new possibility to obtain reactions with encaged inert gases.

2018 ◽  
Vol 96 (10) ◽  
pp. 934-938
Author(s):  
Delano P. Chong

The dipole polarizabilities (α) and polarizability anisotropies (Δα) of over 20 molecules are calculated to search for negative Δα. The geometry of each molecule is first optimized at the level of CCSD(T)/cc-pVQZ. Then, the α tensors are computed both with CCSD(T)/daug-cc-pVTZ in Gaussian 09 and with the exchange-correlation potential Vxc known as SAOP in the Amsterdam density functional theory program called ADF and a large basis set called QZ3P-3DIFFUSE. In addition to the popular formula of the ΔαRaman connected with Raman spectroscopy, we also present values of an alternative definition of the polarizability anisotropy ΔαKerr connected with Kerr spectroscopy, recently proposed by Kampfrath and colleagues (2018. Chem. Phys. Lett. 692: 319). On one hand, the signs of many ΔαRaman are undetermined; on the other hand, we obtain negative ΔαKerr for more than one-half of the small molecules studied. Of the 24 molecules studied, 18 have negative ΔαKerr.


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