Theoretical study of electronic transitions using simple and sophisticated methods

In this paper, the use of both simple and sophisticated models in the study of electronic transitions was explored for a set of molecular systems: C2H4, C4H4, C4H6, C6H6, C6H8, C8, C60, and [H2NCHCH(CHCH)kCHNH2]+, where k = 0 to 4. The simple model of the free particle (1D, 2D, and 3D boxes, rings or spherical surfaces), considering the boundary conditions, was found to yield similar results to the sophisticated theoretical methods such as EOM-CCSD/6-311++G** or TD(NStates=5,Root=1)-M06-2X/6-311++G**.593599Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq

The behavior of the electron: an analysis of the compton effect and the de Broglie's relation

The De Broglie's relation was a fundamental step in the development of a wave nature for matter. Therefore, we have examined it from the perspective of the new atomic theory. This relation makes successful predictions of the stable energy levels for electrons orbiting a nucleus. The formulation of the de Broglie's relation is a fundamental application of the theory of wave-particle duality for a material particle. In this work, the direct demonstration employing the equations E = mc² and E = hcλ, was avoided. We provide a complete analysis of this relation considering features of the special theory of relativity.18691874Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq

Theoretical study of thermochemical properties using composite methods adapted to ONIOM

Composite methods adapted to the ONIOM approach were used in the description of proton (PA) and electron (EA) affinities for a group of 50 molecules (alcohols, ketones, radicals and alkenes). The electronic energy was described considering the scaling ZPE (λ) and higher level (HLC) corrections. The optimal value for λ was obtained from the PA data. The EA calculations were used for optimization of the terms in HLC. Different performances of exchange-correlation functionals were considered. The methodology ONIOM2(QCISD(T)/6-311++G(2dF,p):HF/6-31G(d))//ONIOM2(B3LYP/6-31G(d):HF/6-31G(d)) provided the smallest median absolute deviation (MAD) for PA and EA, 5.38 kJ mol-1 and 0.11 eV, respectively, in comparison to the experimental data.Métodos compostos adaptados ao método ONIOM foram utilizados no cálculo teórico de afinidades por próton (PA) e eletrônica (EA) para um grupo de 50 moléculas (álcoois, cetonas, radicais e alcenos). A energia eletrônica foi descrita considerando-se o escalonamento de ZPE (λ) e a correção de alto nível (HLC). O valor ótimo para λ foi obtido através dos dados de PA. Os cálculos de EA foram utilizados na otimização dos termos presentes em HLC. Foram explorados diferentes tipos de funcionais de troca-correlação. A metodologia ONIOM2(QCISD(T)/6-311++G(2dF,p):HF/6-31G(d))//ONIOM2(B3LYP/6-31G(d):HF/6-31G(d)) forneceu os menores desvios absolutos médios para PA e EA, 5,38 kJ mol-1 e 0,11 eV, respectivamente, em comparação com dados experimentais.17411746Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq

Spurious phosphorus pyramidalization induced by some DFT functionals

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)The molecular geometries of boraphosphabenzene (BP-benzene) and boron phosphorus coronene (BP-coronene) can be misinterpreted when they are obtained from density functional theory (DFT) calculations. In this study, we found that some exchange-correlation (XC) functionals yielded a distorted geometry of the above molecules when P atoms are present in their resonance structures. This phosphorus pyramidalization may be due to spurious errors caused by using these functionals. To verify this behavior, the electronic structures of BP-benzene and BP-coronene were studied using sixteen functionals (B3LYP, B97D, BHLYP, BP96, PBE, PBE0, PWLDA, Slater-Dirac-exchange, TPSS, M05, M06, M062X, M08HX, M11, wB97 and wB97X-D) with the SVP or TZVPP basis sets. The calculations were carried out using the TURBOMOLE and GAMESS programs. The geometry optimization calculations were carried out for each functional using both of the basis sets. Two different initial geometries, plane (D-3h symmetry) and distorted (C-1 symmetry) were considered. The optimized geometries of the BP-systems obtained at the MP2/TZVPP and CC2/TZVPP levels of theory exhibited D-3h symmetry. These calculations were used as a reference and compared with those obtained from DFT. The optimized geometries obtained from DFT were found to exhibit C-1 symmetry for the majority of the XC functionals.The molecular geometries of boraphosphabenzene (BP-benzene) and boron phosphorus coronene (BP-coronene) can be misinterpreted when they are obtained from density functional theory (DFT) calculations. In this study, we found that some exchange-correlation26816481655FAPESP - FUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULOCNPQ - CONSELHO NACIONAL DE DESENVOLVIMENTO CIENTÍFICO E TECNOLÓGICOFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)sem informaçãosem informaçãoWe would like to acknowledge the computational facilities of the Chemistry Institute at UNICAMP as well as the financial support from Fundação de Amparo à Pesquisa de São Paulo (FAPESP) and Conselho Nacional de Desenvolvimento Científico e Tecnológico (C

Validação computacional de métodos compostos no estudo de propriedades moleculares

Composite methods using ONIOM and different basis sets have been used to calculate proton and electron affinities for a set of alcohols at QCISD(T)/6-311++G(2df,p) level of theory. The study was carried out considering HF, MP2 and DFT (25 exchange correlation functional) methods. The calculation performed at ONIOM2(QCISD(T)/6-311++G(2df,p):HF/6-31G(d))//ONIOM2(O3LYP/6-31G(d):HF/6-31G(d)) resulted in the smallest average absolute deviation for AP and AE, 4,75 kJ/mol e 0,43 eV, respectively

Computational validation of composite methods in the study of molecular properties

Composite methods using ONIOM and different basis sets have been used to calculate proton and electron affinities for a set of alcohols at QCISD(T)/6-311++G(2df,p) level of theory. The study was carried out considering HF, MP2 and DFT (25 exchange correlation functional) methods. The calculation performed at ONIOM2(QCISD(T)/6-311++G(2df,p):HF/6-31G(d))//ONIOM2(O3LYP/6-31G(d):HF/6-31G(d)) resulted in the smallest average absolute deviation for AP and AE, 4,75 kJ/mol e 0,43 eV, respectively.868873Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES

The physical chemistry division and the forty years of the brazilian chemical society (SBQ)

One of the goals of this manuscript is to celebrate the forty years of the SBQ (Sociedade Brasileira de Química). We believe using historical analysis could benefit our researchers to overcome the challenges ahead, look into the future, to the scientific progress and the way science increases its problem-solving ability. There are several topics covered by the challenges in Physical Chemistry: nanoscience and nanotechnology, single molecule studies, gas phase photochemistry and photophysics, molecular structure, spectroscopy, reaction dynamics, interfacial phenomena, energy, and so on. However, the critical challenge for our Division still is to create a desired link between experimental approaches and theoretical knowledge.

Theoretical calculations of the proton affinities of n-alkylamines using the ONIOM method

The ONIOM method was used to calculate the proton affinities (PA) of n-alkylamines (CnH2n+1NH2, n = 3 to 6, 8, 10, 12, 14, 16 and 18). The calculations were carried out at several levels (HF, MP2, B3LYP, QCISD(T), ...) using Pople basis sets and at the QCISD(T) level using basis sets developed by the generator coordinate method (GCM) and adapted to effective core potentials. PAs were also obtained through the GCM and high level methods, like ONIOM[QCISD(T)/6-31+G(2df,p):MP2/6-31G+G(d,p))//ONIOM[MP2/6-31+G(d,p):HF/6-31G]. The average error using the GCM, with respect to experimental data, was 3.4 kJ mol-1.187193Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq

«Et rikholdig ordtilfang uten å ville øve press i noen retning» – om Tanums store rettskrivningsordbok

Boye Wangensteen (red.): Tanums store rettskrivningsordbok. 10. utgave. Oslo: Kunnskapsforlaget 2015. s. ix–xi og 1–1576. Pris: 598 NOK. Elektronisk utgåve på <https://www.ordnett.no/>