Chiral perovskites have attracted considerable attention as excellent spin-emitting materials for applications in spintronics, quantum optics, and biological. Especially in drug development of biological, weak chirality molecules are frequently selected to reduce the side effects of toxics, and there is a common defect for accurately detecting the weak chirality with common methods at room temperature. In this study, formamidine lead bromide perovskite nanocrystals (FAPbBr NCs) were coated with chiral ligands, whose chirality was too weak to be observed in the visible region at room temperature. Thus, by characterizing the transverse shift of photonic spin Hall effect (SHE), the accurate discrimination of weak chirality in the visible region was achieved successfully. By measuring the shift value and light spot splitting of photonic SHE at the same concentration, NEA-coated FAPbBr NCs can effectively enhance the chirality of naphthalene ethylamine (NEA) ligands when under the mutually reinforcement of chiral molecular and inorganic parts. In addition, we furtherly clearly distinguished the tiny chiral distinction of NEA-coated FAPbBr NCs with different particle sizes, which revealed that the chirality decreases with the increase of particle size. These findings could provide effective solutions for the detection and application of weak chirality in hybrid perovskite nanocrystals in universal environment.
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http://dx.doi.org/10.1515/nanoph-2022-0313 | DOI Listing |
ACS Photonics
January 2025
Laboratory of Nanoscience for Energy Technologies (LNET), Faculty of Engineering (STI), Ecole Polytechnique Federale de Lausanne (EPFL), Lausanne 1015, Switzerland.
Circular dichroism (CD) can distinguish the handedness of the chiral molecules. However, it is typically very weak due to vanishing absorption at low molecular concentrations. Here, we suggest thermal CD (TCD) for chiral detection, leveraging the temperature difference in the chiral sample when subjected to right- and left-circularly polarized excitations.
View Article and Find Full Text PDFNanoscale
January 2025
State Key Laboratory of Low-Dimensional Quantum Physics and Department of Physics, Tsinghua University, Beijing 100084, P.R. China.
Chirality, a pervasive phenomenon in nature, is widely studied across diverse fields including the origins of life, chemical catalysis, drug discovery, and physical optoelectronics. The investigations of natural chiral materials have been constrained by their intrinsically weak chiral effects. Recently, significant progress has been made in the fabrication and assembly of low-dimensional micro and nanoscale chiral materials and their architectures, leading to the discovery of novel optoelectronic phenomena such as circularly polarized light emission, spin and charge flip, advocating great potential for applications in quantum information, quantum computing, and biosensing.
View Article and Find Full Text PDFElectrophoresis
January 2025
Institute for Infectious Diseases, University of Bern, Bern, Switzerland.
Computer simulation was utilized to characterize the electrophoretic processes occurring during the enantioselective capillary electrophoresis-mass spectrometry (CE-MS) analysis of ketamine, norketamine, and hydroxynorketamine in a system with partial filling of the capillary with 19 mM (equals 5%) of highly sulfated γ-cyclodextrin (HS-γ-CD) and analyte detection on the cathodic side. Provided that the sample is applied without or with a small amount of the chiral selector, analytes become quickly focused and separated in the thereby formed HS-γ-CD gradient at the cathodic end of the sample compartment. This gradient broadens with time, remains stationary, and gradually reduces its span from the lower side due to diffusion such that analytes with high affinity to the anionic selector become released onto the other side of the focusing gradient where anionic migration and defocusing occur concomitantly.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Department of Chemistry, Zhejiang University, Hangzhou, 310058, China.
Heck silylation of unactivated alkenes is an efficient strategy for the synthesis of useful organosilicon compounds. However, extensive efforts have been dedicated to only achieving achiral molecules. Herein, a highly regio- and enantioselective cobalt-catalyzed Heck silylation of unactivated alkenes with hydrosilanes is reported for the first time, providing access to axially chiral alkenes in good to excellent yields with 87-98 % ee.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Exploiting novel noncovalent interactions for catalysis design represents a fascinating direction. For the flexible and relatively weak anion-π interactions, manipulation of two or more π-acidic surfaces for cooperative activation is highly desirable. Here, we demonstrate the strategy of cooperative anion-π catalysis based on chiral molecular cages with V-shaped electron-deficient cavities for synergic binding and activation of dicarbonyl electrophiles toward highly enantioselective desymmetrization transformation.
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