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|a 10.1002/mrc.5334
|2 doi
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|a eng
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|a Semenov, Valentin A
|e verfasserin
|4 aut
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|a Computational studies of [1]benzothieno[2,3-c]naphtho[1,2-f]quinoline
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|c 2023
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
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|2 rdacarrier
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|a Date Completed 03.04.2023
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|a Date Revised 03.04.2023
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|a published: Print-Electronic
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|a Citation Status PubMed-not-MEDLINE
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|a © 2023 John Wiley & Sons Ltd.
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|a Early NMR studies of several heterohelicenes containing an annular nitrogen atom and a thiophene ring in their structure suggested the possibility of the lengthening of the carbon-carbon bonds in the interior of the helical turn of the molecule based on the progressive more shielded nature of 13 C resonances toward the center of the helical turn. Computational chemistry capabilities when those NMR studies were performed were primitive in comparison to what is now possible. We now report the optimized geometry and a comparison of the calculated versus observed 1 H and 13 C NMR chemical shift assignments for [1]benzothieno[2,3-c]naphtho[1,2-f]quinoline that confirms these suspicions
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|a Journal Article
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|a 13C NMR
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|a 1H NMR
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|a DFT
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|a heterohelicene
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|a molecular geometry
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|a Martin, Gary E
|e verfasserin
|4 aut
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|a Krivdin, Leonid B
|e verfasserin
|4 aut
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|i Enthalten in
|t Magnetic resonance in chemistry : MRC
|d 1985
|g 61(2023), 5 vom: 19. Mai, Seite 301-305
|w (DE-627)NLM098179667
|x 1097-458X
|7 nnas
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| 773 |
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|g volume:61
|g year:2023
|g number:5
|g day:19
|g month:05
|g pages:301-305
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|u http://dx.doi.org/10.1002/mrc.5334
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