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The homochirality of life remains one of the most enigmatic issues in the study of the origin of life. A proposed mechanism for symmetry breaking involves irradiation by circularly polarized light (CPL). To investigate the photoreaction of amino acids under CPL irradiation, a vacuum ultraviolet (VUV) CPL irradiation system was developed at the synchrotron light source UVSOR-III. Hydrogen Lyman-α CPL (121.6 nm) is considered a potential asymmetric source in space. Therefore, racemic alanine film samples were irradiated with Lyman-α CPL to explore the photoreaction of biomolecules. Circular dichroism (CD) spectra measurements revealed that irradiation with right- (left-) handed CPL induced a positive (negative) anisotropy factor g in the wavelength range of 180-240 nm. However, the spectra differed from those of enantiopure alanine, exhibiting broad wavelength ranges and no sign change. Liquid chromatography-mass spectrometry (LC-MS) measurements indicate formation of larger molecules, such as oligomeric alanine adducts or modified oligomers after the Lyman-α CPL irradiation. Additionally, CPL irradiation considerably changes the microstructure of the alanine film surface, leading to the formation of circular network aggregates on the scale of 100 nm. The morphology changes in the alanine film and/or the formation of the larger molecules could be possible causes of the modified anisotropy factor spectra compared to those of enantiopure alanine. These findings highlight the need for further research on the photoreaction of biomolecules in solid states under VUV CPL irradiation, particularly in the photoionization energy range, to validate the cosmic scenario of homochirality.
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http://dx.doi.org/10.1002/chir.70004 | DOI Listing |
Materials (Basel)
June 2025
Institute of Molecular Plus, Tianjin University, Tianjin 300072, China.
The integration of chirality into nanomaterials holds significant potential for improving molecular recognition and biomedical technologies. In this work, we fabricated novel chiral horned gold nanostructures (HNS) by controlling the concentration of chiral ligands L-/D-cysteine (Cys). The unique three-dimensional morphology with horns-rotational arrangement enables synergistic optimization of chiral optical responses and surface-enhanced Raman scattering (SERS) performance.
View Article and Find Full Text PDFACS Appl Mater Interfaces
June 2025
State Key Laboratory of Advanced Materials for Intelligent Sensing, Ministry of Science and Technology & Key Laboratory of Organic Integrated Circuit, Ministry·of Education & Tianjin Key Laboratory of Molecular Optoelectronic Sciences, Department of Chemistry, School of Science, Tianjin University,
Circularly polarized luminescence (CPL) switches have received considerable attention for their potential applications in next-generation information technologies. Nevertheless, the development of solid-state multiresponse CPL switches remains a challenge. Herein, the chiral coassembled material MAPbX@L/d-Phe-LnMOF was synthesized by self-assembly using lanthanide metal-organic frameworks (MOFs) as the host and perovskite quantum dots (QDs) as the guest, using the host-guest space-confined strategy (Ln = Eu, Tb, MA = CHNH, X = Cl, Br, I, l-Phe = l-phenylalanine).
View Article and Find Full Text PDFAdv Sci (Weinh)
July 2025
Colloidal Physics Group, Key Laboratory of Materials Physics, Ministry of Education, School of Physics and Laboratory of Zhongyuan Light, Zhengzhou University, Zhengzhou, 450001, P. R. China.
Seed-mediated growth provides an efficient way to produce chiral hybrid nanocrystals, mainly benefitting from the recent successful synthesis of discrete chiral metal nanocrystals. However, the chiroptical response of chiral core-shell nanostructures decreases rapidly when the functional layer is grown on the discrete chiral metal nanocrystals. Herein, a synthetic methodology is demonstrated for the formation of chiral Au@Pd super-heterostructures, in which Pd nanoarrays are epitaxially and densely grown with a twisted lattice on discrete chiral Au nanorods (Pd-on-cAuNRs).
View Article and Find Full Text PDFChemistry
May 2025
Key Laboratory of Eco-Environment-Related Polymer Materials, Ministry of Education of China, Key Laboratory of Polymer Materials of Gansu Province, College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou, Gansu, People's Republic of China.
Photoinduced organic radicals with unique luminescent properties are highly sought-after due to their important prospects in synthetic chemistry and materials science. However, the current development of organic free radicals, including photoinduced ones, is significantly limited and faces challenges related to stability and poor luminescence behavior. Taking advantage of the photoelectric activity of triarylamine, we herein describe an unusual luminescent radical, which can be rapidly generated by UV irradiation of a solid-state triarylamine-functionalized π-conjugated pillar[5]arene (EtP5NN) in air, accompanied by luminescent color switching from bluish-violet to sky-blue.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
June 2025
Shaanxi Key Laboratory of Chemical Additives for Industry, College of Chemistry and Chemical Engineering, Shaanxi University of Science and Technology, Xi'an, 710021, China.
Multi-response encryption materials with temperature control and time resolution have attracted widespread attention due to their unique response characteristics and higher application security. The design and development of photochromic crystalline materials with multiple stimulus responses remain challenging. In this study, we report a pair of responsive photochromic chiral ionic hydrogen-bonded organic framework (iHOF) R/S-iHOF-19, controlled by both temperature and solvent through charge-assisted synthesis.
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