Intermolecular Vibrational Modes Research Articles

Integrated identification and detection of hydration state and its evolution using terahertz technology

The accurate detection of dehydration processes in hydrated drugs can reveal various intermolecular vibration modes mediated by hydrogen bonds between water molecules and other components, which underpin the further development of pharmaceutical science, food safety and biophysics. Herein, terahertz (THz) technology is utilized to investigate the dehydration state of d(+)-Raffinose pentahydrate (Rf·5H2O), in conjunction with imaging-based point by point scanning data acquisition and barcodes methods, to establish an innovative platform integrated identification, trace detection, and application capabilities. Our study demonstrates that the dehydration process of Rf·5H2O can be dynamically monitored through the evolution of its THz absorption peaks, offering more precise results compared to XRD and Raman spectroscopies. Moreover, the absorbance spectra data collected at each individual pixel is utilized to build visualized THz images, achieving an ultralow minimum content required for detection of 0.032 μg/(50 μm)2. Additionally, we introduce a THz spectra-barcode conversion system that not only ensures efficient electronic recordkeeping but also enhances user readability, thereby facilitating the practical applications of THz technology.

Low-Frequency Raman Spectroscopy on Amorphous Poly(Ether Ether Ketone) (PEEK).

Low-frequency peaks in the Raman spectra of amorphous poly(ether ether ketone) (PEEK) were investigated. An amorphous sample with zero crystallinity, as confirmed by wide-angle X-ray diffraction, was used in this study. In a previous study, two peaks were observed in the low-frequency Raman spectra of the crystallized samples. Among these, the peaks at 135 cm-1 disappeared for the amorphous sample. Meanwhile, for the first time, the peak at 50 cm-1 was observed in the crystallized sample. Similar to the peak at 135 cm-1, the peak at 50 cm-1 disappeared in the amorphous state, and its intensity increased with increasing crystallinity. The origins of the two peaks were associated with the Ph-CO-Ph-type intermolecular vibrational modes in the simulation. This suggests that the Ph-CO-Ph vibrational mode observed in the low-frequency region of PEEK was strongly influenced by the intermolecular order.

Label-free detection of inclusion body formation in E. coli with application of terahertz

Extensive production of recombinant protein is essential for use in various fields. Bacterial cells, especially the Escherichia coli (E. coli) expression system, are widely used for the production of recombinant proteins due to their advantages in time and cost. However, the formation of inclusion bodies (IBs) caused by the production of recombinant protein is a significant issue. Therefore, a precise tool for the detection of IBs is in high demand. In this study, we demonstrated a label-free and rapid sensing platform for the detection of IBs formation in E. coli using terahertz-time domain spectroscopy (THz-TDS) system and terahertz metamaterials. The detection was based on the local polarity difference between E. coli samples with induced (positive) and non-induced (negative) protein overexpression. The formation of IBs in positive samples resulted in a decrease in local polarity compared to negative samples. This local polarity difference, strongly related to intermolecular interactions, influenced THz absorption as the THz regime involves weak intermolecular vibrational modes. Experimental results showed that the THz transmittance (ΔT) and resonance frequency shift (Δf) were significantly different between positive and negative samples, confirming the effectiveness of our method. Specifically, positive samples exhibited a ΔT value of 26.57% and a Δf value of 0.12 THz, while negative samples showed a ΔT value of 31.83% and a Δf value of 0.14 THz. These results highlight the capability of our platform to detect IBs rapidly and accurately.

HCl trimer: HCl-stretch excited intramolecular and intermolecular vibrational states from 12D fully coupled quantum calculations employing contracted intra- and inter-molecular bases.

We present fully coupled, full-dimensional quantum calculations of the inter- and intra-molecular vibrational states of HCl trimer, a paradigmatic hydrogen-bonded molecular trimer. They are performed utilizing the recently developed methodology for the rigorous 12D quantum treatment of the vibrations of the noncovalently bound trimers of flexible diatomic molecules [Felker and Bačić, J. Chem. Phys. 158, 234109 (2023)], which was previously applied to the HF trimer by us. In this work, the many-body 12D potential energy surface (PES) of (HCl)3 [Mancini and Bowman, J. Phys. Chem. A 118, 7367 (2014)] is employed. The calculations extend to the intramolecular HCl-stretch excited vibrational states of the trimer with one- and two-quanta, together with the low-energy intermolecular vibrational states in the two excited v = 1 intramolecular vibrational manifolds. They reveal significant coupling between the intra- and inter-molecular vibrational modes. The 12D calculations also show that the frequencies of the v = 1 HCl stretching states of the HCl trimer are significantly redshifted relative to those of the isolated HCl monomer. Detailed comparison is made between the results of the 12D calculations on the two-body PES, obtained by removing the three-body term from the original 2 + 3-body PES, and those computed on the 2 + 3-body PES. It demonstrates that the three-body interactions have a strong effect on the trimer binding energy as well as on its intra- and inter-molecular vibrational energy levels. Comparison with the available spectroscopic data shows that good agreement with the experiment is achieved only if the three-body interactions are included. Some low-energy vibrational states localized in a secondary minimum of the PES are characterized as well.

Theory and experiment on the terahertz vibrational spectrum of ferulic acid

Ferulic acid (FA, C10H10O4), a type of hydroxycinnamic acid derivative, has beneficial pharmacological effects and biological activities and is known for its high application value in medicine, health care, and cosmetic products. The vibration spectrum of FA ranging from 0.3 THz to 2.0 THz has been investigated by terahertz time-domain spectroscopy. The characteristic absorption peaks located at 0.937, 1.159, 1.464, 1.694, and 1.910 THz are obtained experimentally. To understand the origin of the characteristic absorption peaks of FA, density functional theory calculations based on isolated molecule and crystalline structure are separately performed to differentiate the intramolecular and intermolecular vibrational modes. Combined analysis of the experimental and theoretical results informs that the characteristic absorption peak at 1.464 THz comes from intramolecular interaction, and the ones at 0.937, 1.159, 1.694, and 1.910 THz originate from intermolecular collective vibrational modes.

Research on vibrational features of CL-20/MTNP cocrystal by terahertz spectroscopy

Cocrystals represent an effective method to manipulate the physicochemical properties of materials at a molecular level. However, understanding the relationship between their complex crystal structures and macroscopic properties is a challenge. In this paper, by using terahertz (THz) spectroscopy to characterize non-covalent interactions within crystals, the THz vibrational spectra of the CL-20/MTNP cocrystal are studied. Firstly, the THz spectra of CL-20, MTNP, and the CL-20/MTNP cocrystal are measured at room temperature. Both absorption positions and intensities of the cocrystals differ from those of their original components, confirming the unique advantage of terahertz spectroscopy in cocrystal identification. Secondly, the THz vibrational features of the three materials are calculated based on density functional theory (DFT). Then, the experimental absorptions are matched with the calculated vibrations. Furthermore, a vibrational decomposition method is employed to decompose the molecular vibrations into intermolecular and intramolecular vibrations. The vibrational variations of the cocrystal compared with its original components are analyzed. The results reveal that in the cocrystal, the intermolecular vibrational modes of both CL-20 and MTNP molecules have changed compared with their raw materials. This indicates that the non-covalent interactions in the cocrystal have changed the original intermolecular interactions of these molecules. Consequently, this enhancement promotes the heat transfer between MTNP and CL-20 molecules, thereby improving the thermal stability of the cocrystal. These findings in this study demonstrate that the THz vibrational spectroscopy technology helps establish a relationship between the molecular structure of cocrystal and its macroscopic properties. This research contributes to deepening our understanding of cocrystal systems and opens up a new way for designing and optimizing materials.

Probing Dielectric Relaxation of Water at Electrochemical Interfaces with Low-Frequency SERS Spectroscopy

Dynamic and structural properties of hydrogen-bonded water molecules in liquid phase have a significant impact on many chemical and biological processes in aqueous systems. Therefore, the bulk behavior of water is quite actively studied from both experimental and theoretical point of view. In the frequency domain, collective motions of water molecules appear in the terahertz (THz) range. For example, the central frequency of Debye-type dielectric relaxation of water exists at around 1 cm-1, and that of the so-called fast Debye relaxation is found at around 10 cm-1. There are several spectroscopic means to obtain such low-frequency information in the bulk liquid of water. However, for interfacial water molecules interacting with a solid surface, their dynamic behavior of hydrogen-bond networks remains unexplored in the experimental research field, despite of the importance of such behavior to molecular-level understanding of heterogeneous electrochemical processes. The reason for lack of such information is due to lack of adequate surface-selective spectroscopic means. In this talk, in-situ observation of the relaxational and vibrational dynamics of water at electrochemical interfaces is demonstrated using low-frequency surface-enhanced Raman spectroscopy (SERS). In this spectroscopic method, not only intermolecular dynamics but also intramolecular vibrational behaviors of water can be simultaneously monitored due to the intrinsic nature of the inelastic scattering technique accessible in the wide frequency range covering both THz and mid-IR regions, which helps us to understand the relation between microscopic and macroscopic behaviors of water molecules.To obtain low-frequency SERS spectrum, volume Bragg grating filters were used for both monochromatization of He-Ne laser radiation of 632.8 nm and removal of Rayleigh scattered light [1]. SERS-active Au electrodes were prepared by electrochemical surface roughening of Au surface in 0.1M KCl solution. For SERS-active Pt electrodes, monoatomic Pt overlayers were formed on the roughened Au surfaces. SERS spectra for interfacial water were measured on these electrode surfaces under application of electrochemical potentials. The measured spectra were converted to density states of formats by reducing the Purcell factor, Bose-Einstein thermal factor, and frequency factor, which can unveil vibrational features in low-frequency range [2-5].The measured spectra clearly showed potential-dependent features in the THz region. According to the previously reported spectra for bulk water, these features were assigned to the fast Debye relaxation component and two intermolecular vibration modes of interfacial water layer. By analyzing the observed spectral features by the assistance of classical molecular dynamics (MD) simulations, we found that the potential-induced change of water orientation causes formation of local defects in hydrogen-bonded networks of interfacial water layer and the lateral mobility of such defects on negatively charged surface is larger than that on positively charged surface [6]. Figure shows the dynamical behavior of potential-induced defects in hydrogen-bonded networks of interfacial water molecules on negatively and positively charge surfaces. The details will be discussed in the presentation.[1] M. Inagaki, K. Motobayashi, K. Ikeda, J. Phys. Chem. Lett., 8, 4236-4240 (2017).[2] M. Inagaki, T. Isogai, K. Motobayashi, K. -Q. Lin, B. Ren, K. Ikeda, Chem. Sci., 11, 9807-9717 (2020).[3] M. Inagaki, K. Motobayashi, K. Ikeda, Nanoscale, 12, 22988-22994 (2020).[4] R. Kamimura, T. Kondo, K. Motobayashi, K. Ikeda, Phys. Status Solidi B, 259, 2100589 (2022).[5] T. Kondo, M. Inagaki, K. Motobayashi, K. Ikeda, Catal. Sci. Technol., 12, 2670-2676 (2022).[6] T. Isogai, M. Inagaki, M. Uranagase, K. Motobayashi, S. Ogata, K. Ikeda, submitted. Figure 1

Wetting of a Hydrophobic Surface: Far-IR Action Spectroscopy and Dynamics of Microhydrated Naphthalene.

The interaction of water and polycyclic aromatic hydrocarbons is of fundamental importance in areas as diverse as materials science and atmospheric and interstellar chemistry. The interplay between hydrogen bonding and dipole-π interactions results in subtle dynamics that are challenging to describe from first principles. Here, we employ far-IR action vibrational spectroscopy with the infrared free-electron laser FELIX to investigate naphthalene with one to three water molecules. We observe diffuse bands associated with intermolecular vibrational modes that serve as direct probes of the loose binding of water to the naphthalene surface. These signatures are poorly reproduced by static DFT or Møller-Plesset computations. Instead, a rationalization is achieved through Born-Oppenheimer Molecular Dynamics simulations, revealing the active mobility of water over the surface, even at low temperatures. Therefore, our work provides direct insights into the wetting interactions associated with shallow potential energy surfaces while simultaneously demonstrating a solid experimental-computational framework for their investigation.

HF trimer: 12D fully coupled quantum calculations of HF-stretch excited intramolecular and intermolecular vibrational states using contracted bases of intramolecular and intermolecular eigenstates.

We present the computational methodology, which for the first time allows rigorous twelve-dimensional (12D) quantum calculations of the coupled intramolecular and intermolecular vibrational states of hydrogen-bonded trimers of flexible diatomic molecules. Its starting point is the approach that we introduced recently for fully coupled 9D quantum calculations of the intermolecular vibrational states of noncovalently bound trimers comprised of diatomics treated as rigid. In this paper, it is extended to include the intramolecular stretching coordinates of the three diatomic monomers. The cornerstone of our 12D methodology is the partitioning of the full vibrational Hamiltonian of the trimer into two reduced-dimension Hamiltonians, one in 9D for the intermolecular degrees of freedom (DOFs) and another in 3D for the intramolecular vibrations of the trimer, and a remainder term. These two Hamiltonians are diagonalized separately, and a fraction of their respective 9D and 3D eigenstates is included in the 12D product contracted basis for both the intra- and intermolecular DOFs, in which the matrix of the full 12D vibrational Hamiltonian of the trimer is diagonalized. This methodology is implemented in the 12D quantum calculations of the coupled intra- and intermolecular vibrational states of the hydrogen-bonded HF trimer on an abinitio calculated potential energy surface (PES). The calculations encompass the one- and two-quanta intramolecular HF-stretch excited vibrational states of the trimer and low-energy intermolecular vibrational states in the intramolecular vibrational manifolds of interest. They reveal several interesting manifestations of significant coupling between the intra- and intermolecular vibrational modes of (HF)3. The 12D calculations also show that the frequencies of the v = 1, 2 HF stretching states of the HF trimer are strongly redshifted in comparison to those of the isolated HF monomer. Moreover, the magnitudes of these trimer redshifts are much larger than that of the redshift for the stretching fundamental of the donor-HF moiety in (HF)2, most likely due to the cooperative hydrogen bonding in (HF)3. The agreement between the 12D results and the limited spectroscopic data for the HF trimer, while satisfactory, leaves room for improvement and points to the need for a more accurate PES.

Strong coupling of localized surface plasmons and intermolecular vibration mode at terahertz frequencies

Organic molecular vibrations, typically occurring in the terahertz (THz) regime, can resonate with a metastructure. A hallmark Rabi splitting occurs when the coupling strength is sufficiently strong. In this work, we observe the strong coupling of localized surface plasmons (LSPs) and intermolecular vibration mode at THz on a metasurface spin-coated with organic molecule α-lactose monohydrate. Excited by transverse-electric THz waves, dispersive localized surface plasmons interact with nondispersive intermolecular vibrations and form two vibro-polariton modes. The angle-resolved transmission spectra of the coupled system are detected by using a terahertz time-domain spectrometer, demonstrating an anti-crossing effect with a clear Rabi splitting. By retrieving the coupling strength and Hopfield coefficients of polariton bands from the measured data, we further verify that these two bands originate from the strong coupling between LSPs and molecular vibration mode. Moreover, we show that it is possible to implement molecular concentration sensing based on this strong coupling effect. This study demonstrates a unique approach to investigate vibro-polaritons at the terahertz regime and provides a testbed for future applications of strong coupling effects in chemical detection and biosensing.

Nature of the physicochemical process in water photolysis uncovered by a computer simulation.

In this work, we investigate the physicochemical process of water photolysis to bridge physical and chemical processes by a newly developed first-principles calculation code. The deceleration, thermalization, delocalization, and initial hydration of the extremely low-energy electrons ejected by water photolysis are sequentially tracked in the condensed phase. We show herein the calculated results for these sequential phenomena during 300fs. Our results indicate that the mechanisms heavily depend on the intermolecular vibration and rotation modes peculiar to water and the momentum transfer between the electrons and the water medium. We suggest that using our results for the delocalized electron distribution will reproduce successive chemical reactions measured by photolysis experiments using a chemical reaction code. We expect our approach to become a powerful technique for various scientific fields related to water photolysis and radiolysis.

Intermolecular energy transfer-enhanced super-broadband stimulated Raman scattering in cyclohexane-benzene mixtures.

Supercontinuum radiation has found numerous applications in diverse fields encompassing spectroscopy, pulse compression, and tunable laser sources. Anomalous enhanced stimulated Raman scattering (SRS) of cyclohexane-benzene mixtures was obtained in this study. SRS of the pure solvent, the multi-order Stokes of the strongest fundamental vibration modes, and energy transfer in intra-molecular modes were observed. SRS of the mixture revealed that the cross-pumping effect was generated between the C-H stretching (v2) mode of cyclohexane and the C=C ring skeleton (v1) mode of benzene, thereby producing the intermolecular secondary stimulated Raman emission and the appearance of two super-broadband radiations at 664.36-673.9nm and 704.62-729.22nm. The results suggest that the energy transfer of intermolecular vibrational modes, where the strongest vibrational mode excites other vibrational modes, is a simple approach for generating supercontinuum coherent radiation.

Terahertz Vibrational Modes of Sodium Magnesium Chlorophyllin and Chlorophyll in Plant Leaves

The low-frequency (terahertz) vibrational spectroscopy has been investigated experimentally for two chlorophyll species, Chl-a and one of its magnesium derivatives (Chl-Mg-Na). The combination of terahertz time-domain spectroscopy and Fourier transform infrared spectroscopy has enabled a broad frequency range to be covered (0.2 to 18 THz). For Chl-Mg-Na, the terahertz spectra show clear and well-marked features at 1.44, 1.64, and 1.83 THz dominated by intermolecular interactions. The frequency dependent refractive index and absorption coefficient of Chl-Mg-Na were both determined using the Fit@TDS software. Below 1.0 THz, a refractive index of 2.09 was measured. In order to acquire further understanding of the observed vibrational modes, a detailed study of the temperature dependence of the line positions of the lowest modes in Chl-Mg-Na was performed. As the temperature was increased from 88 K to 298 K, the feature at 1.83 THz experienced a notable red shift of frequency and line shape broadening, whereas the feature at 1.44 THz showed little change. These results suggest that the 1.83 THz feature is dominated by intermolecular motions occurring over the crystalline unit cell of the Chl-Mg-Na molecular crystal. Finally, terahertz time-domain spectroscopy was used to acquire the spectra of an ornamental plant bearing yellow-green variegated leaves (ivy, Aureomarginata variety), the yellow sectors having lower chlorophyll content compared to the green sectors. In dehydrated green tissue, the chlorophyll molecules showed well-marked intermolecular vibrational modes at 1.86 THz, indicating that chlorophyll molecules are prone to packing with an ordered molecular arrangement. These results demonstrate the potential application of THz spectroscopy in the field of agronomy.

Terahertz virus-sized gold nanogap sensor

Abstract We demonstrated an ultra-sensitive terahertz virus detection method combined with virus-sized gold nanogaps filled with Al2O3. Large-area high-density 20 nm-gap rectangular loop structures, containing a resonant frequency in the terahertz range, were fabricated on a 4-inch wafer using atomic layer lithography. When target viruses with a 60 nm diameter were located on the nanogaps, we observed a significant redshift of the resonant peak already with an average number of about 100 viruses per unit loop due to the strong field confinement and enhancement near the gap. Furthermore, when the virus was tightly attached to an etched gap like a bridge connecting metals, its sensitivity is doubled compared to the unetched gap, which resulted in 400% more resonance frequency shift per single virus particle than our previous work. Full-wave simulations and theoretical calculations based on modal expansions were in good agreement with the experiments, revealing that the resonant transmission spectrum was mostly determined by the change in refractive index in a two-dimensional-like optical hotspot near the nanogap. A further step could be taken to increase sensitivity by tuning nanogap-loops to the absorption frequencies associated with the intermolecular vibrational modes of the viruses and fingerprinting them as well.

Spectroscopic analysis of vibrational coupling in multi-molecular excited states.

Multi-molecular excited states accompanied by intra- and inter-molecular geometric relaxation are commonly encountered in optical and electrooptical studies and applications of organic semiconductors as, for example, excimers or charge transfer states. Understanding the dynamics of these states is crucial to improve organic devices such as light emitting diodes and solar cells. Their full microscopic description, however, demands sophisticated tools such as ab initio quantum chemical calculations which come at the expense of high computational costs and are prone to errors by assumptions as well as iterative algorithmic procedures. Hence, the analysis of spectroscopic data is often conducted at a phenomenological level only. Here, we present a toolkit to analyze temperature dependent luminescence data and gain first insights into the relevant microscopic parameters of the molecular system at hand. By means of a Franck-Condon based approach considering a single effective inter-molecular vibrational mode and different potentials for the ground and excited state we are able to explain the luminescence spectra of such multi-molecular states. We demonstrate that by applying certain reasonable simplifications the luminescence of charge transfer states as well as excimers can be satisfactorily reproduced for temperatures ranging from cryogenics to above room temperature. We present a semi-classical and a quantum-mechanical description of our model and, for both cases, demonstrate its applicability by analyzing the temperature dependent luminescence of the amorphous donor-acceptor heterojunction tetraphenyldibenzoperiflanthene:C60 as well as polycrystalline zinc-phthalocyanine to reproduce the luminescence spectra and extract relevant system parameters such as the excimer binding energy.

Molecular Dynamics Simulation of Poly(Ether Ether Ketone) (PEEK) Polymer to Analyze Intermolecular Ordering by Low Wavenumber Raman Spectroscopy and X-ray Diffraction.

Poly(ether ether ketone) (PEEK) is an important engineering plastic and evaluation of its local crystallinity in composites is critical for producing strong and reliable mechanical parts. Low wavenumber Raman spectroscopy and X-ray diffraction are promising techniques for the analysis of crystal ordering but a detailed understanding of the spectra has not been established. Here, we use molecular dynamics combined with a newly developed approximation to simulate local vibrational features to understand the effect of intermolecular ordering in the Raman spectra. We found that intermolecular ordering does affect the low wavenumber Raman spectra and the X-ray diffraction as observed in the experiment. Raman spectroscopy of intermolecular vibration modes is a promising technique to evaluate the local crystallinity of PEEK and other engineering plastics, and the present technique offers an estimation without requiring heavy computational resources.

Spectra of CO2-Rg2 and CO2-Rg-He trimers (Rg = Ne, Ar, Kr, and Xe): Intermolecular CO2 rock, vibrational shifts and three-body effects.

Weakly bound CO2-Rg2 trimers are studied by high-resolution (0.002cm-1) infrared spectroscopy in the region of the CO2 ν3 fundamental band (≈2350cm-1), using a tunable optical parametric oscillator to probe a pulsed supersonic slit jet expansion with an effective rotational temperature of about 2K. CO2-Ar2 spectra have been reported previously, but they are extended here to include Rg = Ne, Kr, and Xe as well as new combination and hot bands. For Kr and Xe, a unified scaled parameter scheme is used to account for the many possible isotopic species. Vibrational shifts of CO2-Rg2 trimers are compared to those of CO2-Rg dimers, and in all cases the trimer shifts are slightly more positive (blue-shifted) than expected on the basis of linear extrapolation from the dimer. Combination bands directly measure an intermolecular vibrational mode (the CO2 rock) and give values of about 32.2, 33.8, and 34.7cm-1 for CO2-Ar2, -Kr2, and -Xe2. Structural parameters derived for CO2-Rg2 trimers are compared with those of CO2-Rg and Rg2 dimers. Spectra of the mixed trimers CO2-Rg-He are also reported.

Computational investigation of the conformer selective complexes of 1,2,3,4-tetrahydroisoquinoline: Ammonia (THIQ: NH3) in S0

Three low-energy conformations are identified in 1,2,3,4-tetrahydroisoquinoline (THIQ): NH3 complexes. The lone pairs on N atoms strongly affects the conformational landscape. Both density functional theory (DFT) and MP2 levels of computations yield consistent results. Multiple PESs corresponding to different types of hydrogen bonds are drawn to account for all possible complexes. Ten complexes are identified. The global minimum contains a strong N-H⋅⋅⋅N and a weak N-H⋅⋅⋅π hydrogen bonds where NH3 is an H bond acceptor. In the remaining two complexes ammonia acts as a donor. All the low-energy complexes which can show intermolecular proton transfer were studied in detail although none shows PT with a single NH3 molecule. The intermolecular vibrational modes are critically analyzed and the relative shifts in the characteristic modes of ammonia are explained. Types and sites for H-bonding can be ascertained from the vibrational analyses. Changes in molecular electrostatic potentials (MEP) on complex formation are explained and confirm our computational results. We suggest further experiments to confirm our key observations.

Infrared and Terahertz Spectroscopic Investigation of Imidazolium, Pyridinium, and Tetraalkylammonium Tetrafluoroborate Ionic Liquids.

We performed terahertz time-domain spectroscopy and infrared spectroscopy of imidazolium-based, pyridinium-based, and tetraalkylammonium-based tetrafluoroborate ionic liquids to study their characteristic intermolecular and intramolecular vibrational modes to clarify interactions between various cations and the tetrafluoroborate anion. It was found that the central frequency of the intermolecular vibrational band for these ionic liquids has a relatively high frequency, ranging from 90 to 100 cm–1. In the 900–1150 cm–1 range, the intramolecular vibrational absorption band of the 3-fold degenerate mode of tetrafluoroborate anions in the ionic liquids was observed. Although the tetrafluoroborate anion is attributable to one of the weakly coordinated anions, the spectroscopic splitting behavior of the 3-fold degenerate mode differs depending on the cation species. It was revealed that the degenerate mode is very sensitive to local interactions between the tetrafluoroborate anion and each cation.

Terahertz time-domain spectroscopy, imaging and density functional theory based studies of 3, 4, 5 Trinitro 1 H Pyrazole

The paper reports the terahertz time-domain spectroscopy (THz-TDS) and imaging on 3, 4, 5 -Trinitro 1-H Pyrazole (explosive) in solid form between 0.1 and 3.5 THz range, including Density Functional Theory was implemented in this study. We have employed a commercially available fiber-coupled THz reflection mode system. We have experimentally ascertained the optical and dielectric properties such as refractive index, absorption coefficients, and dielectric constants in the THz domain. The refractive index values varies between 1.5 and 2.0 range, and absorption coefficients varies between 10 and 400 cm−1 in the stated THz range. In addition, Density Functional Theory was used to assign some important vibrational modes obtained experimentally. In the next step, the Dimer and Trimer configurations of the molecule were also incorporated in the existing theoretical model for developing a clear-cut understanding the role of the intermolecular vibrational modes in the molecule. The simulated results were compared in the IR region (4000–400 cm−1) and the THz region (0.1–3.5 THz). Finally, an improvised version of the imaging system was used to record the THz time and frequency domain images of pure pyrazole and mixed in a teflon matrix with different concentrations. The spatial distributions of pyrazole in the pure and teflon matrix at different absorption frequencies have been analysed.