Chiral bis(benzo[1, 2-b:4, 3-b′]dithiophene) atropisomers: experimental and theoretical investigations of the stereochemical and chiroptical properties. (9th August 2021)
- Record Type:
- Journal Article
- Title:
- Chiral bis(benzo[1, 2-b:4, 3-b′]dithiophene) atropisomers: experimental and theoretical investigations of the stereochemical and chiroptical properties. (9th August 2021)
- Main Title:
- Chiral bis(benzo[1, 2-b:4, 3-b′]dithiophene) atropisomers: experimental and theoretical investigations of the stereochemical and chiroptical properties
- Authors:
- Pelliccioli, Valentina
Franzini, Roberta
Mazzeo, Giuseppe
Villani, Claudio
Abbate, Sergio
Longhi, Giovanna
Licandro, Emanuela
Cauteruccio, Silvia - Abstract:
- Abstract : Conformational chirality is a feature that may arise from the presence of a hindered rotation around a single bond that corresponds to a stereogenic axis. Abstract : Conformational chirality is a feature that may arise from the presence of a hindered rotation around a single bond that corresponds to a stereogenic axis. Atropisomers that feature such an element show interesting characteristics suitable for developing chiral systems with applicability in asymmetric synthesis, catalysis and materials chemistry. Here, we report the investigation of the stereochemical and chiroptical properties of a series of axially chiral intermediates useful in the synthesis of helicenes. Racemates of the four studied atropisomeric bisbenzodithiophenes were resolved by enantioselective HPLC and the single enantiomers were investigated by HPLC, ECD, VCD and CPL. Configurational stability was successfully established by dynamic HPLC or by monitoring thermal racemization, allowing the measurement of the free activation energy values for the stereomutation process. Moreover, the absolute configuration was assigned, thanks to a combination of TD-DFT and DFT calculations and experimental data derived by ECD and VCD, and the emissive chiral properties were measured by recording the CPL spectrum. Attention was paid to the importance of considering also aliphatic pendant groups in order to obtain a good calculation–experiment correspondence for both the ECD and VCD spectra. Considering theAbstract : Conformational chirality is a feature that may arise from the presence of a hindered rotation around a single bond that corresponds to a stereogenic axis. Abstract : Conformational chirality is a feature that may arise from the presence of a hindered rotation around a single bond that corresponds to a stereogenic axis. Atropisomers that feature such an element show interesting characteristics suitable for developing chiral systems with applicability in asymmetric synthesis, catalysis and materials chemistry. Here, we report the investigation of the stereochemical and chiroptical properties of a series of axially chiral intermediates useful in the synthesis of helicenes. Racemates of the four studied atropisomeric bisbenzodithiophenes were resolved by enantioselective HPLC and the single enantiomers were investigated by HPLC, ECD, VCD and CPL. Configurational stability was successfully established by dynamic HPLC or by monitoring thermal racemization, allowing the measurement of the free activation energy values for the stereomutation process. Moreover, the absolute configuration was assigned, thanks to a combination of TD-DFT and DFT calculations and experimental data derived by ECD and VCD, and the emissive chiral properties were measured by recording the CPL spectrum. Attention was paid to the importance of considering also aliphatic pendant groups in order to obtain a good calculation–experiment correspondence for both the ECD and VCD spectra. Considering the significant interest for axially chiral biaryl derivatives, this novel class of bisbenzodithiophenes are expected to have broad applications, not only in asymmetric synthesis, but also as potential chiral ligands or CPL emitters. … (more)
- Is Part Of:
- New journal of chemistry. Volume 45:Number 36(2021)
- Journal:
- New journal of chemistry
- Issue:
- Volume 45:Number 36(2021)
- Issue Display:
- Volume 45, Issue 36 (2021)
- Year:
- 2021
- Volume:
- 45
- Issue:
- 36
- Issue Sort Value:
- 2021-0045-0036-0000
- Page Start:
- 16442
- Page End:
- 16451
- Publication Date:
- 2021-08-09
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/d1nj03248h ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 19621.xml