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We herein demonstrate the synthesis of a pair of enantiomerically pure Yb complexes by post-functionalisation of the parent Yb complex condensation with an enantiomerically pure chiral amine. The enantiomeric pair is structurally characterised by single crystal and powder X-ray diffraction, showing that it crystalises in the 222 Sohncke space group with Flack parameters close to zero, which confirms their enantiopurity. Circular Dichroism (CD) and absorption spectroscopies in the NIR reveal sharp F → F f-f transitions, with values up to 0.07, indicating a chiral environment for the ytterbium centre. Furthermore, a dynamic mechanism with mixing of ligand states is shown to contribute to the CD intensity. X-band pulse Electron Paramagnetic Resonance spectroscopy, on a magnetically dilute single crystal containing 1% of Yb complexes within the isostructural Y diamagnetic host, reveals a phase memory time, , of the electronic spin of 600 ns and that it can be coherently manipulated by microwave pulses, as evidenced by Rabi nutations.
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http://dx.doi.org/10.1039/d5qi00977d | DOI Listing |
Inorg Chem Front
September 2025
Department of Chemistry, University of Copenhagen Universitetsparken 5 2100 Denmark
We herein demonstrate the synthesis of a pair of enantiomerically pure Yb complexes by post-functionalisation of the parent Yb complex condensation with an enantiomerically pure chiral amine. The enantiomeric pair is structurally characterised by single crystal and powder X-ray diffraction, showing that it crystalises in the 222 Sohncke space group with Flack parameters close to zero, which confirms their enantiopurity. Circular Dichroism (CD) and absorption spectroscopies in the NIR reveal sharp F → F f-f transitions, with values up to 0.
View Article and Find Full Text PDFOrg Lett
September 2025
Department of Organic Chemistry, Faculty of Sciences, Unidad de Excelencia de Química (UEQ), University of Granada, Avda. Fuente Nueva s/n, 18071 Granada, Spain.
Two distorted nanographenes combining helicenes and a fluoranthene unit within their polycyclic scaffolds were synthesized. Their structural and electronic properties were elucidated by various spectroscopic methods, and the experimental data were corroborated computationally. The optical and electrochemical properties of the nanographenes were evaluated.
View Article and Find Full Text PDFPlants (Basel)
August 2025
Departamento de Química, Universidad Técnica Particular de Loja (UTPL), Calle Paris s/n y Praga, Loja 110107, Ecuador.
The present study described, for the first time, the chemical and enantiomeric composition of an essential oil, distilled from the cupules of (Sw.) R. Rohde.
View Article and Find Full Text PDFChem Biodivers
August 2025
Supramolecular and Catalysis Lab, Department of Natural Products Chemistry, School of Chemistry, Madurai Kamaraj University, Madurai, India.
To target epidermal growth factor receptor (EGFR) signaling in breast (MCF-7) and lung (A549) cancers, a library of chirally functionalized 1,3,5-triazine scaffolds was designed by a ligand-based drug design approach. An optimized synthetic protocol employing sequential chlorine replacement on cyanuric chloride delivered enantiomerically pure chiral-1,3,5-triazine derivatives. Through systematic structural modifications, fine-tuned physicochemical properties and optimal ADME profiles are achieved.
View Article and Find Full Text PDFBioorg Chem
August 2025
School of Food Science and Pharmaceutical Engineering, Nanjing Normal University, NO. 1, Wenyuan Road, Nanjing 210023, PR China; State Key Laboratory of Microbial Technology, Nanjing Normal university, PR China. Electronic address:
Optically pure (S)-1-phenylethanol, a crucial synthetic intermediate widely applied in the pharmaceutical and food industries, is currently produced via well-established biological methods primarily relying on ketoreductase-mediated asymmetric synthesis and lipase-catalyzed kinetic resolution. This study presents a biocatalytic approach utilizing haloalkane dehalogenase DbjA for the kinetic resolution of racemic 1-chloro-1-phenylethane in organic solvents to synthesize (S)-1-phenylethanol. Following systematic optimization of reaction conditions, the system achieved an enantiomeric excess (ee) of 97 % for (S)-1-chloro-1-phenylethane and an (S)-1-phenylethanol yield of 46 % (ee > 99 %), demonstrating exceptional enantioselectivity (E = 536).
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