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231225s2020 xx |||||o 00| ||eng c |
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|a 10.1002/mrc.4967
|2 doi
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|a eng
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|a Gajda, Magdalena
|e verfasserin
|4 aut
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|a Local aromaticity in polyacenes manifested by individual proton and carbon shieldings
|b DFT mapping of aromaticity
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|c 2020
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
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|2 rdamedia
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|a ƒa Online-Ressource
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|a Date Completed 27.01.2020
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|a Date Revised 27.01.2020
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|a published: Print-Electronic
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|a Citation Status PubMed-not-MEDLINE
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|a © 2019 John Wiley & Sons, Ltd.
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|a Exponential dependencies between locally calculated geometric and magnetic indexes of aromaticity, harmonic oscillator model of aromaticity (HOMA) and nucleus independent chemical shifts (NICS)(0), NICS(1) and NICS(1)zz, and the number of conjugated benzene rings in linear acenes, from benzene to decacene were observed at B3LYP/6-311+G** level of theory. Correlations between HOMA and NICS indexes showed exponential dependencies and were fitted with simple three-parameter function. Similar correlations between both indexes of aromaticity and proton and carbon nuclear isotropic shieldings of individual acene rings were observed. Contrary to proton data, the predicted 13 C nuclear isotropic shieldings of carbon atoms belonging to inner rings in polyacenes were less shielded, indicating lower aromaticity and therefore, higher reactivity
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|a Journal Article
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|a HOMA
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|a NICS
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|a aromaticity
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|a molecular modeling
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| 650 |
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|a nuclear shielding
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| 650 |
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|a polyacenes
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1 |
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|a Gajda, Łukasz
|e verfasserin
|4 aut
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|a Kupka, Teobald
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Kar, Tapas
|e verfasserin
|4 aut
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|i Enthalten in
|t Magnetic resonance in chemistry : MRC
|d 1985
|g 58(2020), 2 vom: 12. Feb., Seite 145-153
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|x 1097-458X
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|g volume:58
|g year:2020
|g number:2
|g day:12
|g month:02
|g pages:145-153
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|u http://dx.doi.org/10.1002/mrc.4967
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