We examine the effects of compressive external forces on the mechanisms of the parent Diels-Alder (DA) reaction between butadiene and ethylene. Reaction pathways and transition states were calculated using the nudged elastic band method within a mechanochemical framework at the CASSCF(6,6)/6-31G**, as well as the B3LYP/6-311++G** levels of theory. Our results suggest that compressive hydrostatic pressure lowers the energy barrier for the parent DA reaction while suppressing the undesirable side reaction, thereby leading to a direct increase in the yield of cyclohexene. Compressive pressure also increases the exothermicity of the parent DA reaction, which would lead to increased temperatures in a reaction vessel and thereby indirectly increa...
International audienceHigh pressure effects on the Diels-Alder reaction in condensed phase are inves...
Both experiment and first principles calculations unequivocally indicate that properties of elements...
The interactions (including weak interactions) between dienophiles and dienes play an important role...
The effect of a hydrostatic pressure of up to 1000 kg cm-2 on the rate constants of the Diels - Alde...
The rate constants for temperature and pressure range, enthalpy, entropy, and volume of activation a...
The basic chemical and physical factors determining the rate and equilibrium of the Diels-Alder reac...
The pressure effect on the forward and backward rate constants and equilibrium constants of the Diel...
A number of recent studies have shown that mechanical stress can significantly lower or raise the ac...
The kinetics (rate, activation, and volume) of the high-pressure (up to 2500 bar) Diels-Alder reacti...
Mechanochemical activation has created new opportunities for applications such as solvent-free chemi...
AbstractAllosteric control of reaction thermodynamics is well understood, but the mechanisms by whic...
The effect of increased hydrostatic pressure on the rate of the Diels-Alder reaction of tetracyanoet...
Quantum chemical calculations are reported for the thermal dimerizations of 1,3-cyclohexadiene at 1 ...
External pressure was found to similarly affect the rate of a gallium chloride-catalyzed Diels-Alder...
The enthalpy, entropy, and volume of activation and volume of the Diels-Alder reaction of diethyl az...
International audienceHigh pressure effects on the Diels-Alder reaction in condensed phase are inves...
Both experiment and first principles calculations unequivocally indicate that properties of elements...
The interactions (including weak interactions) between dienophiles and dienes play an important role...
The effect of a hydrostatic pressure of up to 1000 kg cm-2 on the rate constants of the Diels - Alde...
The rate constants for temperature and pressure range, enthalpy, entropy, and volume of activation a...
The basic chemical and physical factors determining the rate and equilibrium of the Diels-Alder reac...
The pressure effect on the forward and backward rate constants and equilibrium constants of the Diel...
A number of recent studies have shown that mechanical stress can significantly lower or raise the ac...
The kinetics (rate, activation, and volume) of the high-pressure (up to 2500 bar) Diels-Alder reacti...
Mechanochemical activation has created new opportunities for applications such as solvent-free chemi...
AbstractAllosteric control of reaction thermodynamics is well understood, but the mechanisms by whic...
The effect of increased hydrostatic pressure on the rate of the Diels-Alder reaction of tetracyanoet...
Quantum chemical calculations are reported for the thermal dimerizations of 1,3-cyclohexadiene at 1 ...
External pressure was found to similarly affect the rate of a gallium chloride-catalyzed Diels-Alder...
The enthalpy, entropy, and volume of activation and volume of the Diels-Alder reaction of diethyl az...
International audienceHigh pressure effects on the Diels-Alder reaction in condensed phase are inves...
Both experiment and first principles calculations unequivocally indicate that properties of elements...
The interactions (including weak interactions) between dienophiles and dienes play an important role...