Reactivity of (E)-4-aryl-4-oxo-2-butenoic acid phenylamides with piperidine and benzylamine: kinetic and theoretical study

Cvijetić, Ilija N.; Vitorović-Todorović, Maja D.; Juranić, Ivan O.; Nakarada, Đura; Milosavljević, Milica D.; Drakulić, Branko J.

doi:10.1007/s00706-014-1223-8

Cited by 4 publications

(1 citation statement)

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“…Partial atomic charges find application in the molecular modeling of several chemically relevant areas, such as explaining structural and reactivity differences between various molecules and their conformers [15][16][17], investigating charge transfers within a single molecule and between several molecules [18][19][20], and predicting pK a variations in series of molecules [21,22]. Since the definition of partial atomic charges is not strict, various models of partial atomic charges can, however, differ significantly in the reliability of their predictions.…”

Section: Introductionmentioning

confidence: 99%

A Test of Various Partial Atomic Charge Models for Computations on Diheteroaryl Ketones and Thioketones

Matczak

2016

Computation

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Abstract:The effective use of partial atomic charge models is essential for such purposes in molecular computations as a simplified representation of global charge distribution in a molecule and predicting its conformational behavior. In this work, ten of the most popular models of partial atomic charge are taken into consideration, and these models operate on the molecular wave functions/electron densities of five diheteroaryl ketones and their thiocarbonyl analogs. The ten models are tested in order to assess their usefulness in achieving the aforementioned purposes for the compounds in title. Therefore, the following criteria are used in the test: (1) how accurately these models reproduce the molecular dipole moments of the conformers of the investigated compounds; (2) whether these models are able to correctly determine the preferred conformer as well as the ordering of higher-energy conformers for each compound. The results of the test indicate that the Merz-Kollman-Singh (MKS) and Hu-Lu-Yang (HLY) models approximate the magnitude of the molecular dipole moments with the greatest accuracy. The natural partial atomic charges perform best in determining the conformational behavior of the investigated compounds. These findings may constitute important support for the effective computations of electrostatic effects occurring within and between the molecules of the compounds in question as well as similar compounds.

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