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We developed a synthetic strategy to form cyclodextrin-based intrananogap particles (CIPs) with a well-defined ∼1 nm interior gap in a high yield (∼97%), and were able to incorporate 10 different Raman dyes inside the gap using the cyclodextrin-based host-guest chemistry, leading to strong, reproducible, and highly multiplexable surface-enhanced Raman scattering (SERS) signals. The average SERS enhancement factor (EF) for CIPs was 3.0 × 10 with a very narrow distribution of the EFs that range from 9.5 × 10 to 9.5 × 10 for ∼95% of the measured particles. Remarkably, 10 different Raman dyes can be loaded within the nanogap of CIPs, and 6 different Raman dye-loaded CIPs with little spectral overlaps were distinctly detected for cancer cell imaging applications with a single excitation source. Our synthetic strategy provides new platforms in precisely forming plasmonic nanogap structures with all key features for widespread use of SERS including strong signal intensity, reliability in quantification of signal and multiplexing capability.
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http://dx.doi.org/10.1021/acs.jpclett.0c02624 | DOI Listing |
J Am Chem Soc
September 2025
Melville Laboratory for Polymer Synthesis, Yusuf Hamied Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, U.K.
Achieving sensitive and reversible responsivity over physiologically relevant pH ranges (4.5-7.5) remains of great interest for the design of next-generation autonomous drug delivery devices.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Soochow University, Suzhou 215123, Jiangsu P. R. China.
Advances in molecular analysis and characterization techniques should revolutionize the methods for scientific exploration across physics, chemistry, and biology, fundamentally overturning our understanding of interactions and processes that govern molecular behavior at the microscopic level. Currently, the absence of a molecular analysis method that can both quantify molecules and achieve single-molecule spatial resolution hinders our study of complex molecular systems in sorption and catalysis. Here, we propose a quantitative analysis strategy for small molecules confined in ZSM-5, a zeolite material extensively used in catalysis and gas separation, based on low-dose transmission electron microscopy.
View Article and Find Full Text PDFChem Sci
September 2025
State Key Laboratory of Chemical Engineering, Center for Chemistry of High-Performance & Novel Materials, Department of Chemistry, Zhejiang University Hangzhou 310027 P. R. China +86-571-8795-3189 +86-571-8795-3189.
[This corrects the article DOI: 10.1039/C6SC00531D.].
View Article and Find Full Text PDFChem Sci
August 2025
Department of Chemistry and Biochemistry, University of South Carolina Columbia SC 29208 USA
Solvent attenuation of dispersion interactions was quantified using a new class of rigid intramolecular CH-π molecular balances. These balances incorporate small, two-carbon CH donors that minimize solvophobic effects and isolate the dispersion component. Folding energies (Δ ) were measured across eight solvents: cyclohexane, toluene, chloroform, ethyl acetate, acetone, acetonitrile, DMSO, and methanol.
View Article and Find Full Text PDFNatl Sci Rev
September 2025
Key Laboratory of Synthetic and Natural Functional Molecule of the Ministry of Education, College of Chemistry and Materials Science, Northwest University, Xi'an 710127, China.
Precision in controlling the microenvironment of nanospaces is a potent strategy for exploring architecture‒function relationships. Herein, a face-capped tetrahedral cage, featuring Pd‒Pd-bonded vertices, with a tailored nanospace surrounded by 12 ethyl units, was facilitated to adaptively accommodate a library of guests with different sizes and shapes, including C6 cyclic hydrocarbons, adamantane derivatives, S and P. This nanocavity can achieve strong binding with cyclohexane in non-aqueous media in contrast to reported structurally similar non--functionalized cages by an increase of four orders of magnitude.
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