98%
921
2 minutes
20
Circularly polarized luminescence (CPL) with tunable chirality is currently a challenging issue in the development of supramolecular nanomaterials. We herein report the formation of helical nanoribbons which grow into helical tubes through dynamic helicity inversion. For this, chiral Pt complexes of terpyridine derivatives, namely S-trans-1 and R-trans-1, with respective S- and R-alanine subunits and incorporating trans-double bonds in the alkyl chain were prepared. In DMSO/H O (5 : 1 v/v), S-trans-1 initially forms a fibrous self-assembled product, which then undergoes dynamic transformation into helical tubes (left-handed or M-type) through helical ribbons (right-handed or P-type). Interestingly, both helical supramolecular architectures are capable of emitting CPL signals. The metastable helical ribbons show CPL signals (g =±4.7×10 ) at 570 nm. Meanwhile, the nanotubes, which are the thermodynamic products, show intense CPL signals (g =±5.6×10 ) at 610 nm accompanied by helicity inversion. This study provides an efficient way to develop highly dissymmetric CPL nanomaterials by regulating the morphology of metallosupramolecular architectures.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/anie.202207310 | DOI Listing |
ACS Appl Mater Interfaces
September 2025
State Key Laboratory of Chemical Resource Engineering, Beijing 100029, China.
Circularly polarized luminescence (CPL) has emerged as a critical technology for anticounterfeiting and optical display applications due to its unique chiroptical properties. We report a multicolor CPL-emitting elastomeric film (P37/PSK@SiO-PDMS) that synergistically combines chiral helical polyacetylene (P37) and a surface-engineered perovskite (PSK@SiO) through hydrogen-bond-directed assembly. Confinement within the PDMS matrix drives P37 to self-assemble into a chiral supramolecular structure through hydrogen bonding, inducing a chiroptical inversion.
View Article and Find Full Text PDFChemistry
September 2025
Department of Chemistry, School of Science, Institute of Science Tokyo, 2-12-1 Ookayama, Meguro-ku, Tokyo, 152-8551, Japan.
Expanded helicenes are interesting compounds created by modifying the original helicene structure through the incorporation of linearly fused benzene rings, enlarging the helical diameter. Motivated by Tilley et al.'s report of a key expanded helicene structure in 2017, several research groups have synthesized such nonplanar aromatic compounds, aiming to explore their impressive structures, properties, and chiroptical performance.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Departament de Química Inorgànica i Orgànica, Universitat de Barcelona, Diagonal 645, Barcelona, 08028, Spain.
Spins within molecules benefit from the atomistic control of synthetic chemistry for the realization of qubits. One advantage is that the quantum superpositions of the spin states encoding the qubit can be coherently manipulated using electromagnetic radiation. The main challenge is the fragility of these superpositions when qubits are to partake of solid-state devices.
View Article and Find Full Text PDFChem Sci
August 2025
Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education, Yunnan Research & Development Center for Natural Products, School of Chemical Science and Technology, Yunnan University Kunming 650091 P.R. China
Polycatenar columnar liquid crystals T ( = 1-6) of π-conjugated oligothiophenes end-capped with bulky -tris(hexadecyloxy)benzyl carbazole groups exhibit unusual molecular tilted and parallel assemblies, realizing the reversal of birefringence within the columnar liquid crystalline (LC) phases depending on core length and temperature. In the parallel arrangement of short core compounds 2T and 3T, molecules align perpendicular to the column axis. The stacking of these molecules involves a rotational component, resulting in local helical assembly, and this specific packing motif collectively stabilizes the Col/6 phase with negative birefringence.
View Article and Find Full Text PDFACS Appl Mater Interfaces
July 2025
School of Electronic Science and Engineering (School of Microelectronics), Guangdong Province Key Lab of Chip and Integration Technology, South China Normal University, Foshan 528225, P.R. China.
Research on quantum geometric-related effects in antiferromagnetic van der Waals heterostructures has predominantly focused on separating the contributions of Berry curvature and quantum metric through the manipulation of Parity-Time (PT) symmetry. However, the critical role of interfacial symmetry-breaking mechanisms, particularly those emerging from parity inversion symmetry manipulation, has remained underexplored. This study advances the field by investigating the hBN/CrPS heterojunction, where the mirror symmetry at the interface is systematically controlled.
View Article and Find Full Text PDF