scholarly journals Electronic Transitions of Molecules: Vibrating Lewis Structures

2019 ◽  
Author(s):  
Yu Liu ◽  
Phil Kilby ◽  
Terry J. Frankcombe ◽  
Timothy Schmidt

In this work we demonstrate a simple and intuitive description of electronic resonances in terms of localized electron vibrations. By partitioning the 3N-dimensional space of a many-electron wavefunction into hyper-regions related by permutation symmetry, chemical structures naturally result which correspond closely to Lewis structures, with identifiable single and double bonds, and lone pairs. Here we demonstrate how this picture of electronic structure develops upon the admixture of electronic wavefunctions, in the spirit of coherent electronic transitions. We show that pi-pi* transitions correspond to double-bonding electrons oscillating along the bond axis, and n-pi* transitions reveal lone-pairs vibrating out of plane. In butadiene and hexatriene, the double-bond oscillations combine with in- and out-of-phase combinations, revealing the correspondence between electronic transitions, molecular normal mode vibrations, and molecular plasmonics. This analysis allows electronic excitations to be described by building upon ground state electronic structures, without the need for molecular orbitals.

2019 ◽  
Author(s):  
Yu Liu ◽  
Phil Kilby ◽  
Terry J. Frankcombe ◽  
Timothy Schmidt

In this work we demonstrate a simple and intuitive description of electronic resonances in terms of localized electron vibrations. By partitioning the 3N-dimensional space of a many-electron wavefunction into hyper-regions related by permutation symmetry, chemical structures naturally result which correspond closely to Lewis structures, with identifiable single and double bonds, and lone pairs. Here we demonstrate how this picture of electronic structure develops upon the admixture of electronic wavefunctions, in the spirit of coherent electronic transitions. We show that pi-pi* transitions correspond to double-bonding electrons oscillating along the bond axis, and n-pi* transitions reveal lone-pairs vibrating out of plane. In butadiene and hexatriene, the double-bond oscillations combine with in- and out-of-phase combinations, revealing the correspondence between electronic transitions, molecular normal mode vibrations, and molecular plasmonics. This analysis allows electronic excitations to be described by building upon ground state electronic structures, without the need for molecular orbitals.


2016 ◽  
Vol 18 (19) ◽  
pp. 13385-13394 ◽  
Author(s):  
Yu Liu ◽  
Terry J. Frankcombe ◽  
Timothy W. Schmidt

A method is presented to partition the 3N-dimensional space of a many-electron wavefunction into hyper-regions related by permutation symmetry.


2019 ◽  
Vol 10 (28) ◽  
pp. 6809-6814 ◽  
Author(s):  
Yu Liu ◽  
Philip Kilby ◽  
Terry J. Frankcombe ◽  
Timothy W. Schmidt

A partitioning of the wavefunction into tiles allows electronic excitations to be viewed as electron vibrations.


2006 ◽  
Vol 59 (3) ◽  
pp. 211 ◽  
Author(s):  
Leonid B. Krivdin ◽  
Lyudmila I. Larina ◽  
Kirill A. Chernyshev ◽  
Natalia A. Keiko

A configurational assignment of the isomeric methylglyoxal bisdimethylhydrazones derived from the 2-ethoxypropenal precursor has been performed based on experimental measurements and high-level ab initio calculations of 1J(C,C) and 1J(C,H) couplings. The results reveal the marked stereochemical dependence upon the orientation of the lone pairs of both nitrogen atoms in different isomers. Methylglyoxal bisdimethylhydrazone is shown to exist in a mixture of the EE and ZE isomers (ca. 75:25), both of which adopt predominant s-trans conformations with minor (up to 8°) out-of-plane deviations.


2020 ◽  
Vol 22 (42) ◽  
pp. 24640-24648
Author(s):  
Adaeze Osonkie ◽  
Veronica Lee ◽  
Adeola Oyelade ◽  
Maximillian Mrozek-McCourt ◽  
Precious Chukwunenye ◽  
...  

The chemical structures of Co oxynitrides – in particular, interactions among N and O atoms bonded to the same cobalt – are of great importance for an array of catalytic and materials applications.


1965 ◽  
Vol 43 (5) ◽  
pp. 1569-1576 ◽  
Author(s):  
N. Solony ◽  
F. W. Birss ◽  
John B. Greenshields

The semiempirical SCF–LCAO–MO method of Pariser–Parr–Pople is utilized in the study of the π-electronic structures of thiophene, furan, and pyrrole. The core Hamiltonian expansion contains a Uz++ term, the potential due to the ionized hetero-atom contributing two electrons to the π-system. The γzz, one-center coulomb repulsion integral for the hetero-atom is evaluated from the experimental spectroscopic data only. With the resonance integral βczc as the only variable parameter, the calculated π*–π electronic transitions are in a satisfactory agreement with the experimental data.


1970 ◽  
Vol 37 (1) ◽  
pp. 180-185 ◽  
Author(s):  
C. A. Sciammarella ◽  
G. Di Chirico ◽  
T.-Y. Chang

The moire´ method is combined with hologram interferometry to obtain the three displacements of an arbitrarily deformed plane in the three-dimensional space. Double beam interference patterns are utilized. The interfering beams are obtained from the diffraction patterns of a grating printed in the analyzed plane. The in-plane and the out-of-plane displacements are measured in separate steps and yield separate patterns. The patterns are generated by double exposure and observed by a wave front reconstruction process. The experimental results included in the paper show a good agreement with theoretical results, proving the feasibility of the proposed technique.


2010 ◽  
Vol 428-429 ◽  
pp. 317-321
Author(s):  
Bao Gai Zhai ◽  
Yuan Ming Huang

The electronic transitions in a classical banana-shaped liquid crystal 1,3-phenylene-bis [4-(4-octylphenylimino) methyl] benzoate have been investigated by measuring its optical absorption spectra in dilute solutions of ethyl alcohol and by calculating its electronic structures with extended Hückel tight binding program. The banana-shaped compound shows strong absorptions at 240, 280, 350 nm, respectively. On the basis of the calculated electronic structures, the three strong absorptions can be assigned to the *, n*, and nn* electronic transitions in this banana-shaped compound.


2018 ◽  
Vol 42 (15) ◽  
pp. 12621-12631 ◽  
Author(s):  
Amit Rajput ◽  
Akhilesh Kumar ◽  
Arunava Sengupta ◽  
Priyanka Tyagi ◽  
Himanshu Arora

Comparative structural and magnetic studies on the binuclear Cu complexes of 1L(2−)/2L(2−) have been done and their electronic structures and observed electronic transitions (DFT and TD-DFT calculations) rationalized. The dimer complex can be converted into the corresponding monomeric Cu(ii) complex, [1L2CuII2(X)] (X = py), by adding an exogenous ligand such as pyridine (py).


2010 ◽  
Vol 663-665 ◽  
pp. 300-303 ◽  
Author(s):  
Yuan Ming Huang ◽  
Bao Gai Zhai ◽  
Qing Lan Ma

A soluble polypyrrole without any substituent groups was obtained by controlling the oxidation level of polypyrrole in the presence of oxygen. Upon the exposure to the 325 nm ultraviolet excitation from a helium-cadmium laser, thin films of the non-substituted polypyrrole could give off strong photoluminescence with its peak at about 530 nm. To elucidate the origin of the recorded strong photoluminescence, we measured the absorption spectra of the polypyrrole thin films with ultraviolet-visible absorption spectroscopy and our data indicated the appropriately oxidized polypyrrole are free of polarons. With the help of the electronic structures calculated with Hückel tight-binding method, the intense photoluminescence is interpreted in terms of the direct electronic transitions from the conduction band to valence band of the conjugated polymer.


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