Luminescent chiral molecular glasses by melt-quenching enantiopure BINAP
| dc.contributor.author | Krittametaporn, Nuttaporn | |
| dc.contributor.author | Ralle, Philipp | |
| dc.contributor.author | Dierks, Dorothea | |
| dc.contributor.author | Nelle, Christian | |
| dc.contributor.author | Vasa, Suresh K. | |
| dc.contributor.author | Kolodzeiski, Pascal | |
| dc.contributor.author | Linser, Rasmus | |
| dc.contributor.author | Steffen, Andreas | |
| dc.contributor.author | Henke, Sebastian | |
| dc.date.accessioned | 2026-01-15T06:59:41Z | |
| dc.date.available | 2026-01-15T06:59:41Z | |
| dc.date.issued | 2025-11-23 | |
| dc.description.abstract | Chiral organic glasses combine unique optical properties with the processing advantages of amorphous solids. Here, melt-quenching as a strategy for preparing optically active glasses from enantiopure BINAP (2,2′-bis(diphenylphosphino)-1,1′-binaphthyl), a pivotal ligand in asymmetric catalysis and for luminescent metal complexes is demonstrated. Thermal characterization reveals that only R-BINAP and S-BINAP, not rac-BINAP, form molecular glasses with glass transition temperatures near 100 °C. Pair distribution function analysis and circular dichroism confirm the retention of local structure and homochirality despite the loss of long-range order. Remarkably, the glassy state has a beneficial influence on the molecular optoelectronic properties relative to the crystalline state, resulting in an increase of the radiative rate constant by ≈30%, attributed to more favourable Franck-Condon factors. In addition, a highly unusual simultaneous enhancement of circularly polarized luminescence (CPL) by nearly an order of magnitude is observed, achieving dissymmetry factors |glum| approaching 10−2 that are competitive with the top-performing purely organic molecular chiral emitters reported to date. These findings establish melt-quenched chiral molecular glasses as promising platforms for advanced optoelectronic and photonic materials, combining exceptional chiroptical properties, strong luminescence, and processability without the constraints of crystallinity. | en |
| dc.identifier.uri | http://hdl.handle.net/2003/44674 | |
| dc.language.iso | en | |
| dc.relation.ispartofseries | Advanced science | |
| dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
| dc.subject | amorphous materials | en |
| dc.subject | circularly polarized luminescence | en |
| dc.subject | melt-quenching | en |
| dc.subject | molecular glasses | en |
| dc.subject | optical materials | en |
| dc.subject.ddc | 540 | |
| dc.subject.rswk | Amorpher Festkörper | |
| dc.subject.rswk | Lumineszenz | |
| dc.subject.rswk | Zirkularpolarisation | |
| dc.subject.rswk | Schmelzen | |
| dc.subject.rswk | Quenching | |
| dc.subject.rswk | Optischer Werkstoff | |
| dc.title | Luminescent chiral molecular glasses by melt-quenching enantiopure BINAP | en |
| dc.type | Text | |
| dc.type.publicationtype | ResearchArticle | |
| dcterms.accessRights | open access | |
| eldorado.dnb.deposit | true | |
| eldorado.doi.register | false | |
| eldorado.secondarypublication | true | |
| eldorado.secondarypublication.primarycitation | N. Krittametaporn, P. Ralle, D. Dierks, et al. “ Luminescent Chiral Molecular Glasses by Melt-Quenching Enantiopure BINAP.” Adv. Sci. (2025): e18879. https://doi.org/10.1002/advs.202518879 | |
| eldorado.secondarypublication.primaryidentifier | https://doi.org/10.1002/advs.202518879 |
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