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Isocorroles as Homoaromatic NIR-Absorbing Chromophores: A First Quantum Chemical Study

Isocorroles as Homoaromatic NIR-Absorbing Chromophores: A First Quantum Chemical Study

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Isocorroles as Homoaromatic NIR-Absorbing Chromophores: A First Quantum Chemical Study

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article publié dans la revue scientifique Scientific Reports

@fr

im August 2018 veröffentlichter wissenschaftlicher Artikel

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scientific article published in Scientific Reports

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wetenschappelijk artikel

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наукова стаття, опублікована в серпні 2018

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Isocorroles as Homoaromatic NIR-Absorbing Chromophores: A First Quantum Chemical Study

@en

Isocorroles as Homoaromatic NIR-Absorbing Chromophores: A First Quantum Chemical Study

@nl

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Isocorroles as Homoaromatic NIR-Absorbing Chromophores: A First Quantum Chemical Study

@en

Isocorroles as Homoaromatic NIR-Absorbing Chromophores: A First Quantum Chemical Study

@nl

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Isocorroles as Homoaromatic NIR-Absorbing Chromophores: A First Quantum Chemical Study

@en

Isocorroles as Homoaromatic NIR-Absorbing Chromophores: A First Quantum Chemical Study

@nl

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S41598-018-29819-3

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Scientific Reports

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Isocorroles as Homoaromatic NIR-Absorbing Chromophores: A First Quantum Chemical Study

@en

P2093

Cina Foroutan-Nejad

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P2860

Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density

Density-functional exchange-energy approximation with correct asymptotic behavior

β-Octabromo- and β-Octakis(trifluoromethyl)isocorroles: New Sterically Constrained Macrocyclic Ligands

Synthesis and characterization of free-base, copper, and nickel isocorroles.

Electronic Structure of Corrole Derivatives: Insights from Molecular Structures, Spectroscopy, Electrochemistry, and Quantum Chemical Calculations.

Spiroconjugation in spirodicorrolato-dinickel(II).

Relation between the substituent effect and aromaticity.

10-Silacorroles Exhibiting Near-Infrared Absorption and Emission.

Balanced basis sets of split valence, triple zeta valence and quadruple zeta valence quality for H to Rn: Design and assessment of accuracy.

Antiaromatic character of 16 π electron octaethylporphyrins: magnetically induced ring currents from DFT-GIMIC calculations.

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11952

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scholarly article

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10.1038/S41598-018-29819-3

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1

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8

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Jeanet Conradie

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2018-08-10T00:00:00Z

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30097587

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6086901

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