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The ro-vibrationally excited state D2(X1∑g+, v = 1, J = 15) was prepared using stimulated Raman pumping, and its collisional rotational relaxation behavior with D2 and N2 molecules was experimentally investigated at 297 K. The effective lifetime of D2(1,15) was determined by measuring time-resolved CARS signals in both pure D2 and D2-N2 systems. Combining the Stern-Volmer equation, the self-relaxation rate coefficient for D2-D2 collisions in the pure D2 system was calculated to be (2.3 ± 0.1) × 10-14 cm3 s-1. The rotational relaxation rate coefficients for D2(1,15) molecules colliding with D2 and N2 molecules in the D2-N2 system were (0.5 ± 0.1) × 10-14 and (6.0 ± 0.3) × 10-14 cm3 s-1, respectively. The results show that near-resonant rotational-vibrational (R-V) collisions between D2 and N2 accelerate the rotational relaxation of D2(1,15), which is the dominant pathway for rotational energy transfer. Time-resolved CARS spectra of D2(v = 1, J = 15, 13, 11) were recorded at 297 K under varying N2 molar ratios. Kinetic analysis revealed that R-V collisions in D2-D2 interactions primarily induce multi-quantum relaxation (J = 15 → 11). At lower N2 molar ratios, a prominent fast multi-quantum relaxation process was observed. As the N2 molar ratio increased, single-quantum relaxation via D2-N2 collisions became more dominant. The effect of temperature on the rotational relaxation of D2(1,15) was studied over the 297-400 K range. At an N2 molar ratio of 0.3, rising temperatures increased D2-D2 collision frequency, enhancing near-resonant multi-quantum relaxation. Meanwhile, secondary D2-N2 collisions prolonged the time required for single-quantum relaxation to reach its peak population. At an N2 molar ratio of 0.7, elevated temperatures significantly enhanced D2-N2 energy exchange, leading to a marked increase in D2(J = 13) population, with single-quantum relaxation becoming the dominant energy transfer pathway for D2(1,15) molecules.
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http://dx.doi.org/10.1063/5.0273748 | DOI Listing |
Langmuir
September 2025
Biophysical Chemistry Laboratory, Physical Chemistry Section, Department of Chemistry, Jadavpur University, Raja S. C. Mullick Road, Jadavpur, Kolkata 700032, India.
Photophysical studies on the interaction of small molecules with various forms of nucleic acids are attracting attention nowadays in order to delineate the molecular level mechanism of various biological processes occurring in vivo. Herein, we employed vivid steady-state and time-resolved spectroscopic techniques to elucidate the detailed characterization of the binding interaction of a biologically active cationic dye thioflavin T (ThT) with double and triple helical forms of RNA - A.U duplex and U.
View Article and Find Full Text PDFDalton Trans
September 2025
School of Chemistry, University of Glasgow, University Avenue, Glasgow G12 8QQ, UK.
Distortions in the local symmetry around Ln(III) ions in SMMs significantly impacts slow magnetic relaxation by introducing transverse crystal field parameters that enhance quantum tunnelling of the magnetisation (QTM). Minimising these distortions, often using macrocyclic or sterically hindered ligands, or by tuning intermolecular interactions, is essential for suppressing QTM. A less-explored strategy involves aligning the molecular symmetry elements within the crystal lattice to generate a high-symmetry crystal lattice with symmetry enforced bond angles and lengths.
View Article and Find Full Text PDFChemistry
September 2025
Institute of Chemical Sciences, Heriot-Watt University, Riccarton, Edinburgh, EH14 4AS, UK.
BODIPY-functionalized host molecules have been used as effective visible-light photosensitizers in the conversion of α-terpinene to ascaridole in the presence of molecular oxygen. Host-guest interactions enhance the effective local concentration of the substrate and singlet oxygen generated by the photosensitizing host. This results in up to a 28-fold increase in the rate of conversion depending on the host employed.
View Article and Find Full Text PDFSpine J
August 2025
School of Electrical and Mechanical Engineering, The University of Adelaide, Level 7, Adelaide Health and Medical Sciences Building, North Terrace, Adelaide, SA, 5000. Electronic address:
Background Context: Understanding human passive neck range of motion (ROM) and stiffness, and their association with age and sex, can be beneficial for clinical assessment, surrogate and computational modelling.
Purpose: To assess passive head-neck ROM and stiffness, and to investigate association with age and sex, in flexion, extension, left and right lateral bending, and axial rotation.
Study Design/setting: In-vivo human participant testing.
In this Letter, we report phase-dependent excited-state relaxation pathways and fluorescence mechanisms of the 1-NH molecule using quantum chemical simulations. In the liquid phase, the synergistic coupling between excited-state intramolecular proton transfer (ESIPT) and twisted intramolecular charge transfer (TICT) facilitates nonradiative decay through a conical intersection (CI) channel, leading to the quenching of Keto* fluorescence. Conversely, in the solid phase, restricted molecular rotation blocks the CI channel and promotes barrierless ESIPT, yielding strong Keto* emission in the near-infrared (NIR) region.
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