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Stimulated Raman scattering (SRS) spectromicroscopy is a powerful technique that enables label-free detection of chemical bonds with high specificity. However, the low Raman cross section due to typical far-electronic resonance excitation seriously restricts the sensitivity and undermines its application to bio-imaging. To address this bottleneck, the electronic preresonance (EPR) SRS technique has been developed to enhance the Raman signals by shifting the excitation frequency toward the molecular absorption. A fundamental weakness of the previous demonstration is the lack of dual-wavelength tunability, making EPR-SRS only applicable to a limited number of species in the proof-of-concept experiment. Here, we demonstrate the EPR-SRS spectromicroscopy using a multiple-plate continuum (MPC) light source able to examine a single vibration mode with independently adjustable pump and Stokes wavelengths. In our experiments, the C═C vibration mode of Alexa 635 is interrogated by continuously scanning the pump-to-absorption frequency detuning throughout the entire EPR region enabled by MPC. The results exhibit 150-fold SRS signal enhancement and good agreement with the Albrecht A-term preresonance model. Signal enhancement is also observed in EPR-SRS images of the whole brain stained with Alexa 635. With the improved sensitivity and potential to implement hyperspectral measurement, we envision that MPC-EPR-SRS spectromicroscopy can bring the Raman techniques closer to a routine in bio-imaging.
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http://dx.doi.org/10.1021/acs.jpcb.3c02629 | DOI Listing |
Anal Chem
August 2025
School of Physics and Astronomy, University of Exeter, Exeter EX4 4QL, U.K.
Plants are inherently complex systems dynamically interacting at different size scale levels. Spontaneous Raman microscopy links the molecular with the cellular structural level; however, as Raman scattering is a low-probability phenomenon, pixel dwell times for biological applications are not compatible with high-resolution imaging. Due to absorption and autofluorescence interferences, Raman methods are often restricted to pigment-poor regions in plant samples.
View Article and Find Full Text PDFJ Chem Phys
July 2025
Institute of Organic Chemistry and Biochemistry, Academy of Sciences, Flemingovo náměstí 2, 16610 Prague, Czech Republic.
Within the Born-Oppenheimer approximation, differences of the vibrational energies are often neglected compared to the electronic ones. This leads to the Placzek approximation and the coupled-perturbed methodology, where the transition polarizabilities needed to simulate Raman spectra are calculated at an incident frequency. Within this approximation, the frequency change of the outgoing radiation is neglected, which has a little effect on the simulation of Raman and Raman optical activity spectra in the far from resonance limit.
View Article and Find Full Text PDFJ Am Chem Soc
March 2025
Department of Biomedical Engineering and Center for Biomolecular Condensates, Washington University in St. Louis, Saint Louis, Missouri 63130, United States.
Amyloid-β (Aβ) peptides exhibit distinct biological activities across multiple physical length scales, including monomers, oligomers, and fibrils. The transition from Aβ monomers to pathological aggregates correlates with the emergence of chemical toxicity, which plays a critical role in the progression of neurodegenerative disorders. However, the relationship between the physical state of Aβ assemblies and their chemical toxicity remains poorly understood.
View Article and Find Full Text PDFJ Phys Chem Lett
February 2025
School of Biological and Environmental Sciences, Kwansei Gakuin University, 1 Gakuen-Uegahara, Sanda, Hyogo 669-1330, Japan.
We investigate resonance (true resonance and pre-resonance) Raman (RR) effects in glucose, galactose, -acetylglucosamine, and -acetylgalactosamine with ultraviolet resonance Raman (UVRR) and far-ultraviolet (FUV) spectroscopies. Electronic transitions in the FUV region are attributed to electronic orbitals due to σ and π electrons. Their geometric orientations that participate in the resonance effect have not yet been well studied, unlike those for visible and near-infrared RR spectroscopies.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
May 2025
Center of Advanced Research in Bionanocojugates and Biopolymers, Petru Poni Institute of Macromolecular Chemistry, 41A Grigore Ghica Voda Alley 700487 Iasi, Romania; Energy Engineering, Division of Energy Science, Luleå University of Technology 97187 Luleå, Sweden; Department of Materials and Envi
Raman spectroscopy can provide highly sensitive and detailed information about the structural fingerprint of molecules, enabling their identification. In this study, our aim is to understand the enhanced intensity observed in experimental Raman measurements. Five azobenzene derivatives were selected, each substituted with different functional groups, for both experimental and theoretical investigations.
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