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Theoretical Investigations of Mechanisms of Thermal Cleavage of E=E Bonds in Heavy Butadiene Systems (E = C, Si, Ge, Sn, and Pb)
Author(s) -
Sheu JengHorng,
Su MingDer
Publication year - 2012
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.201100939
Subject(s) - intramolecular force , chemistry , steric effects , cycloaddition , tin , 1,3 butadiene , germanium , molecule , enthalpy , computational chemistry , pairing , silicon , cleavage (geology) , double bond , bond cleavage , photochemistry , crystallography , stereochemistry , polymer chemistry , organic chemistry , catalysis , thermodynamics , physics , superconductivity , fracture (geology) , engineering , geotechnical engineering , quantum mechanics
The potential energy surfaces for the intramolecular reactions of heavy 1,3‐butadiene have been explored using DFT. All the stationary points, which include the heavy 1,3‐butadienes (R 2 E=ER–ER=ER 2 , E = group 14 element), intramolecular fragments, transition states, and the products, were completely optimized at the B3LYP/LANL2DZ level of theory. Five 1,3‐butadiene species, which include carbon, silicon, germanium, tin, and lead, were chosen as model reactants. Our theoretical findings suggest the following: (1) both sterically bulky substituents attached to the heavy butadiene and the weakness of the E=E double bond lead to the easy cleavage of one E=E double bond in heavy 1,3‐butadiene and (2) for two intramolecular reactions (cycloaddition and 1,2‐migration) of the heavy 1,3‐butadienes with sterically overcrowded substituents, the lighter the E atoms involved in the 1,3‐butadiene molecule, the smaller the intramolecular barrier, the lower the reaction enthalpy, and the more facile its intramolecular reaction at room temperature. Furthermore, a configuration‐mixing model has been used to rationalize the computational results, and the results obtained allow a number of predictions to be made.