Effect of Substituents on the Volume and Free Energy Changes for Electron Attachment to Butadienes

1995 ◽  
Vol 99 (39) ◽  
pp. 14528-14530 ◽  
Author(s):  
Pingyun Chen ◽  
Richard A. Holroyd

2014 ◽  
Vol 118 (8) ◽  
pp. 2164-2171 ◽  
Author(s):  
Richard Holroyd ◽  
John R. Miller ◽  
Andrew R. Cook ◽  
Masaru Nishikawa


2018 ◽  
Vol 1 (1) ◽  
pp. 38-44
Author(s):  
Ghassab Al-Mazaideh

In this study, the geometry optimizations, orbital energies (HOMO-LUMO) and relative stabilities of methylene cyclopentane and 1-methylcyclopentene were investigated by DFT calculations. 1-methylcyclopentene was found to be more stable than methylene cyclopentane isomer with enthalpy value H=18.518 kJ/mol. Also, the effect of substituents X (F, OH, CH3, NH2, CN, NO2, CHO and CF3) also studied on the relative stabilities of these two tautomers. The results showed that the stability of both isomers is increased by all substitutes. Gibbs free energy calculations have been used to find the effect of substituents X on the system.



2020 ◽  
Vol 43 ◽  
Author(s):  
Robert Mirski ◽  
Mark H. Bickhard ◽  
David Eck ◽  
Arkadiusz Gut

Abstract There are serious theoretical problems with the free-energy principle model, which are shown in the current article. We discuss the proposed model's inability to account for culturally emergent normativities, and point out the foundational issues that we claim this inability stems from.







1987 ◽  
Vol 48 (2) ◽  
pp. 169-171 ◽  
Author(s):  
G. Aubert ◽  
E. du Tremolet de Lacheisserie
Keyword(s):  


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