Relative Band Intensities Research Articles

Vapor phase GC-IR identification of regioisomeric N-methoxybenzyl-4-substituted-2,5-dimethoxyphenethylamines (NBOMe)

The common NBOMe drugs of abuse, N-(2-methoxybenzyl)-4-iodo-2,5-dimethoxyphenethylamine (25I-NBOMe) and N-(2-methoxybenzyl)-4-bromo-2,5-dimethoxyphenethylamine (25B-NBOMe), can be differentiated from their corresponding 3- and 4-methoxybenzyl isomers by gas chromatography with vapor phase infrared spectroscopy. The mass spectra for these regioisomeric compounds are essentially identical providing only the identity of the halogen but no specific ions to identify the methoxy group position on the benzyl aromatic ring. The bands from single ring model compounds 2C-B, 2C-I, and all three positional methoxy substituted benzylamines were used to assign each vapor phase absorption band to either the halogenated 2,5 dimethoxybenzene ring or the methoxybenzylamine ring.A pair of aromatic ring stretching bands reflect the position of methoxy group substitution on the benzyl aromatic ring. The 1608 cm−1 band is specific for the two regioisomeric 4-methoxy-benzylamine isomers and this band occurs at 1593 cm−1 for the 2-methoxy isomer in both the 25I and 25B series and shifts to1597/1598 cm−1 for 3-methoxybenzyl 25I and 25B. Asymmetric aryl-O stretching frequencies shift with a change in methoxy substitution around the benzyl aromatic ring (Ring 2) and occur at 1237/1238 cm−1 for ortho, 1261 cm−1 for meta, and 1246 cm−1 for the para isomers. The overall shape and relative intensities of numerous bands in the vapor phase spectra provide clear identification for the individual methoxybenzyl isomers for the 25I-NBOMe and 25B-NBOMe series.

Femtosecond Stimulated Raman Scattering from Triplet Electronic States: Experimental and Theoretical Study of Resonance Enhancements.

Femtosecond stimulated Raman scattering (FSRS) is a spectroscopic technique that probes the structural dynamics of molecules. The technique typically relies on an electronic resonance condition to increase signal strength or enhance species selectivity, giving a Raman enhancement that is vibrational-mode-specific and depends on the character of the resonant electronic state. The resonance condition is complicated for molecules already in an excited electronic state and also for systems where multiple electronic states are resonant or nearly resonant with the Raman excitation energy, both of which are often the case for FSRS. This paper examines the excitation wavelength dependence of the FSRS spectrum for the lowest triplet state of 2-phenylthiophene (PT). Except for an overall increase of the signal strength due to the resonance condition, the relative intensities of most Raman bands are relatively insensitive to the excitation wavelength, and the spectrum is remarkably similar to the calculated off-resonance spectrum obtained by neglecting the resonance condition. On the other hand, calculated resonance Raman spectra using a gradient approximation to simulate the resonance condition correctly predict the excitation wavelength dependence for a few modes but overestimate the relative enhancement of others. The weak wavelength dependence of the triplet spectrum of PT contrasts the case of the singlet FSRS spectrum for the same molecule. We attribute this discrepancy to a combination of homogeneous broadening, overlapping TN ← T1 transitions, and possibly vibronic coupling among states in the triplet manifold. This work highlights important limitations in using standard approaches to simulate excited-state resonance Raman spectra.

Seasonal Variations in Femoral Gland Secretions Reveals some Unexpected Correlations Between Protein and Lipid Components in a Lacertid Lizard

Animals modulate intraspecific signal shape and intensity, notably during reproductive periods. Signal variability typically follows a seasonal scheme, traceable through the expression of visual, acoustic, chemical and behavioral patterns. The chemical channel is particularly important in lizards, as demonstrated by well-developed epidermal glands in the cloacal region that secrete lipids and proteins recognized by conspecifics. In males, the seasonal pattern of gland activity is underpinned by variation of circulating androgens. Changes in the composition of lipid secretions convey information about the signaler's quality (e.g., size, immunity). Presumably, individual identity is associated with a protein signature present in the femoral secretions, but this has been poorly investigated. For the first time, we assessed the seasonal variability of the protein signal in relation to plasma testosterone level (T), glandular activity and the concentration of provitamin D3 in the lipid fraction. We sampled 174 male common wall lizards (Podarcis muralis) over the entire activity season. An elevation of T was observed one to two months before the secretion peak of lipids during the mating season; such expected delay between hormonal fluctuation and maximal physiological response fits well with the assumption that provitamin D3 indicates individual quality. One-dimensional electrophoretic analysis of proteins showed that gel bands were preserved over the season with an invariant region; a result in agreement with the hypothesis that proteins are stable identity signals. However, the relative intensity of bands varied markedly, synchronously with that of lipid secretion pattern. These variations of protein secretion suggest additional roles of proteins, an issue that requires further studies.

Raman Microspectroscopic Imaging of Binder Remnants in Historical Mortars Reveals Processing Conditions

Binder remnants in historical mortars represent a record of the connection between the raw materials that enter the kiln, the process parameters, and the end product of the calcination. Raman microspectroscopy combines high structural sensitivity with micrometre to sub-micrometre spatial resolution and compatibility with conventional thin-sectional samples in an almost unique fashion, making it an interesting complementary extension of the existing methodological arsenal for mortar analysis. Raman spectra are vibrational fingerprints of crystalline and amorphous compounds, and contain marker bands that are specific for minerals and their polymorphic forms. Relative intensities of bands that are related to the same crystalline species change according to crystal orientations, and band shifts can be caused by the incorporation of foreign ions into crystal lattices, as well as stoichiometric changes within solid solution series. Finally, variations in crystallinity affect band widths. These effects are demonstrated based on the analysis of three historical mortar samples: micrometric distribution maps of phases and polymorphs, crystal orientations, and compositional variations of solid solution series of unreacted clinker grains in the Portland cement mortars of two 19th century castings, and the crystallinities of thermal anhydrite clusters in a high-fired medieval gypsum mortar as a measure for the applied burning temperature were successfully acquired.

Characterization of Serpentines from Different Regions by Transmission Electron Microscopy, X-ray Diffraction, BET Specific Surface Area and Vibrational and Electronic Spectroscopy

Serpentinite powdered samples from four different regions were characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), SBET and porosity measurements, UV-Vis and Infrared Spectroscopy of the skeletal region and surface OH groups. SEM micrographs of the samples showed a prismatic morphology when the lizardite was the predominant phase, while if antigorite phase prevailed, the particles had a globular morphology. The few fibrous-shaped particles, only observed by SEM and weakly detected by XRD on MO-9C and MO13 samples, were characteristic of the chrysotile phase. All diffraction XRD patterns showed characteristic peaks of antigorite and lizardite serpentine phases, with crystallite sizes in the range 310–250 A and with different degrees and types of carbonation processes, one derived from the transformation of the serpentine, generating dolomite, and another by direct precipitation of calcite. The SBET reached values between 38–24 m2∙g−1 for the samples less crystalline, in agreement with the XRD patterns, while those with a higher degree of crystallinity gave values close to 8–9 m2∙g−1. In the UV region all electronic spectra were dominated by the absorption edge due to O2− → Si4+ charge transfer transition, with Si4+ in tetrahedral coordination, corresponding to a band gap energy of ca 4.7 eV. In the visible region, 800–350 nm, the spectra of all samples, except Donai, presented at least two weak and broad absorptions centred in the range 650–800 and 550–360 nm, associated with the presence of Fe3+ ions from the oxidation of structural Fe2+ ions in the serpentinites ((MgxFe2+1−x)3Si2O5(OH)4). The relative intensity of the IR bands corresponding to the stretching modes of the OH’s groups indicated the prevalence of one of the two phases, antigorite or lizardite, in the serpentinites. We proposed that the different relative intensity of these bands could be considered as diagnostic to differentiate the predominance of these phases in serpentinites.

Characterization of Serpentines from Different Regions by Transmission Electron Microscopy, X-ray Diffraction, BET Specific Surface Area and Vibrational and Electronic Spectroscopy

Serpentinite powdered samples from four different regions were characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), SBET and porosity measurements, UV-Vis and Infrared Spectroscopy of the skeletal region and surface OH groups. SEM micrographs of the samples showed a prismatic morphology when the lizardite was the predominant phase, while if antigorite phase prevailed, the particles had a globular morphology. The few fibrous-shaped particles, only observed by SEM and weakly detected by XRD on MO-9C and MO13 samples, were characteristic of the chrysotile phase. All diffraction XRD patterns showed characteristic peaks of antigorite and lizardite serpentine phases, with crystallite sizes in the range 310–250 Å and with different degrees and types of carbonation processes, one derived from the transformation of the serpentine, generating dolomite, and another by direct precipitation of calcite. The SBET reached values between 38–24 m2∙g−1 for the samples less crystalline, in agreement with the XRD patterns, while those with a higher degree of crystallinity gave values close to 8–9 m2∙g−1. In the UV region all electronic spectra were dominated by the absorption edge due to O2− → Si4+ charge transfer transition, with Si4+ in tetrahedral coordination, corresponding to a band gap energy of ca 4.7 eV. In the visible region, 800–350 nm, the spectra of all samples, except Donai, presented at least two weak and broad absorptions centred in the range 650–800 and 550–360 nm, associated with the presence of Fe3+ ions from the oxidation of structural Fe2+ ions in the serpentinites ((MgxFe2+1−x)3Si2O5(OH)4). The relative intensity of the IR bands corresponding to the stretching modes of the OH’s groups indicated the prevalence of one of the two phases, antigorite or lizardite, in the serpentinites. We proposed that the different relative intensity of these bands could be considered as diagnostic to differentiate the predominance of these phases in serpentinites.

Overtones of νC≡N Vibration as a Probe of Structure of Liquid CH3CN, CD3CN, and CCl3CN: Combined Infrared, Near-Infrared, and Raman Spectroscopic Studies with Anharmonic Density Functional Theory Calculations.

The νCN band (νC≡N) is a sensitive probe of the state of molecules with nitrile groups. Hence, physicochemical properties of acetonitrile and its derivatives have been frequently investigated by means of vibrational (IR and Raman) spectroscopy. Near-infrared (NIR) spectroscopy combined with high-level quantum mechanical calculations offers deeper physical insight into the structure of liquid nitriles not available from the fundamental region. This results from unique information provided by the overtones of νCN. Here, we report an application of anharmonic vibrational calculations coupled with IR, NIR, and Raman spectroscopy for investigation of the structure of CH3CN, CD3CN, and CCl3CN in the liquid phase. The computational part was based on generalized vibrational second-order perturbation theory (GVPT2) applied on the density function theory (B3LYP, M06-2X, and B2PLYP) level to monomers as well as linear and cyclic dimers. The obtained data were refined by counterpoise-corrected MP2 calculations to mimic the aggregation in the liquid state. Our results evidence that the intensity variations between the fundamental, first and second overtones of the νCN band depend on the symmetry of aggregated species. The symmetry of the cyclic dimers in liquid nitriles was elucidated from the relative intensity of the 2νCN band. This work advances our understanding of the vibrational spectra of acetonitrile and its derivatives by providing detailed band assignment of IR, NIR, and Raman spectra. For the first time, we reported the position of the first and second overtones of the nitrile group.

Reference Raman Spectral Database of Commercial Pesticides

Among several techniques used to study pesticides, Raman spectroscopy stands out for providing fast and reliable results. The objective of this work is to construct a database with Raman spectra of the main commercial pesticides currently used and make it available to the scientific community. With this aim, liquid and solid samples from 78 pesticides were collected. For the Raman spectroscopy analysis of pesticides, a portable Delta Nu Raman spectrometer with a 785-nm laser wavelength and 8-cm–1 resolution was used. The results obtained from the different pesticides were grouped into tables showing the action class, chemical class, active ingredient, and relative intensities of the characteristic Raman bands.

Vibrational and photoluminescence properties of polydiphenylamine doped with silicotungstic acid heteropolyanions and their composites with reduced graphene oxide

In this work, the influence of silicotungstic acid concentration on the diphenylamine (DPA) electropolymerization in the absence and the presence of reduced graphene oxide (RGO) is studied. The optical properties of the composites based on polydiphenylamine (PDPA) doped with the H4SiW12O40 heteropolyanions and RGO are investigated by Raman scattering, IR absorption spectroscopy and photoluminescence (PL). The presence of RGO induces an up-shift of the oxidation maximum of the DPA, as a result of a covalent functionalization process of graphene sheets with the polymer in the doped state. The deposition of PDPA onto RGO sheets surface is confirmed by the Raman scattering studies. Regardless of the H4SiW12O40 concentration, an up-shift of the IR bands from 910 to 1014 cm−1 to ∼920 and 1022 cm−1 is reported as a consequence of the compensation of positive charges of PDPA macromolecular chains with of the H4SiW12O40 heteropolyanions. An enhancement in the absorbance of the IR bands situated in the spectral range 750–1050 cm−1 accompanied of a decrease in the relative intensity of the PL bands of PDPA and their composites with RGO, as increasing the H4SiW12O40 concentration, is reported. In the presence of RGO, a change in the PDPA PL spectra profile is also highlighted.

Photoelectrons Are Not Always Quite Free.

The photoelectron spectra of Sm2O- obtained over a range of photon energies exhibit anomalous changes in relative excited-state band intensities. Specifically, the excited-state transition intensities increase relative to the transition to the neutral ground state with decreasing photon energy, the opposite of what is expected from threshold effects. This phenomenon was previously observed in studies on several Sm-rich homo- and heterolanthanide oxides collected with two different harmonic outputs of a Nd:YAG (2.330 and 3.495 eV) [ J. Chem. Phys. 2017, 146, 194310]. We relate these anomalous intensities to populations of ground and excited anionic and neutrals states through the inspection of time-dependent perturbation theory within the adiabatic and sudden limits and for the first time show that transition intensities in photoelectron spectroscopy have a deep significance in gauging participation from excited states. We believe our results will have significance in the study of other electron-rich systems that have especially high density of accessible spin states.

Raman Micro-Spectroscopy of Dental Pulp Stem Cells: An Approach to Monitor the Effects of Cone Beam Computed Tomography Low-Dose Ionizing Radiation

The objective of this study was to determine the molecular and biochemical changes in dental pulp stem cells (DPSCs) due to consecutive low-dose ionizing radiation exposures using label-free Raman micro-spectroscopy (RMS). Ionizing radiation produces biological damage leading to health effects of varying severity. The effects and subsequent health implications caused by exposure to low-dose radiation, such as diagnostic exposure, remain ambiguous. We identified Raman biomarkers characteristic to low-dose cone beam computed tomography (CBCT) irradiation of the DPSCs. The biomarkers were monitored inside the cells using the relative intensity distribution of the 785 and 1734 cm−1 bands. The control cells presented a higher relative intensity of the nucleic acid specific Raman bands, whereas the irradiated cells revealed an increased intensity of the lipid-induced bands. The results obtained in this study demonstrate the capability of RMS for the detection of cell response to diagnostic radiation dose levels. This may indicate the potential of the technique for future applications such as monitoring the radiation responses in pediatric patients suffering repeated radiological exposures.

Anharmonicity and the infrared emission spectrum of highly excited polycyclic aromatic hydrocarbons

Aims. Infrared (IR) spectroscopy is a powerful tool to study molecules in space. A key issue in such analyses is understanding the effect that temperature and anharmonicity have on different vibrational bands, and thus interpreting the IR spectra for molecules under various conditions. Methods. We combined second order vibrational perturbation theory and the Wang-Landau random walk technique to produce accurate IR spectra of highly excited polycyclic aromatic hydrocarbons. We fully incorporated anharmonic effects, such as resonances, overtones, combination bands, and temperature effects. Results. The results are validated against experimental results for the pyrene molecule (C16H10). In terms of positions, widths, and relative intensities of the vibrational bands, our calculated spectra are in excellent agreement with gas-phase experimental data.

Tissue degeneration in ALS affected spinal cord evaluated by Raman spectroscopy

The Raman spectral features from spinal cord tissue sections of transgenic, ALS model mice and non-transgenic mice were compared using 457 nm excitation line, profiting from the favourable signal intensity obtained in the molecular fingerprint region at this wavelength. Transverse sections from four SOD1G93A mice at 75 days and from two at 90 days after birth were analysed and compared with sections of similarly aged control mice. The spectra acquired within the grey matter of tissue sections from the diseased mice is markedly different from the grey matter signature of healthy mice. In particular, we observe an intensity increase in the spectral windows 450–650 cm−1 and 1050–1200 cm−1, accompanied by an intensity decrease in the lipid contributions at ~1660 cm−1, ~1440 cm−1 and ~1300 cm−1. Axons demyelination, loss of lipid structural order and the proliferation and aggregation of branched proteoglycans are related to the observed spectral modifications. Furthermore, the grey and white matter components of the spinal cord sections could also be spectrally distinguished, based on the relative intensity of characteristic lipid and protein bands. Raman spectra acquired from the white matter regions of the SOD1G93A mice closely resembles those from control mice.

Explicit Aqueous Solvation Treatment of Epinephrine from Car-Parrinello Molecular Dynamics: Effect of Hydrogen Bonding on the Electronic Absorption Spectrum.

The electronic absorption spectrum of the neurotransmitter epinephrine (EPN) in water solution is studied, combining ab initio Car-Parrinello molecular dynamics (CPMD) with a quantum mechanical approach within the framework of the time-dependent density functional theory (TDDFT) scheme. By selecting 52 uncorrelated snapshots, the excitation modes were calculated at the LC-ωPBE/6-31+G(d) level of theory, using an optimal range-separation parameter ω, determined by means of the gap-tuning scheme in the presence of the solvent molecules. By comparing with static approaches (vacuum and implicit solvation), we show here that explicit solvation treatment dramatically enhances the photophysical properties of the EPN, especially because of the more realistic dynamic description of the molecular geometry. The agreement between the simulated and experimental spectra is demonstrated when TDDFT calculations are performed with the optimally tuned version of the DFT hybrid, not only improving the relative intensities of the absorption bands but also the λmax position. These results highlight that accounting for the nuclear motions, that is, thermal effects (of both chromophore and solvent molecules), is imperative to predict experimental absorption spectra. In this paper, we have addressed the critical importance of explicit solvation effects on the photophysics of the EPN, raking in performance when the simulation is performed based on first-principles molecular dynamics such as CPMD.

Nitrate addition inhibited methanogenesis in paddy soils under long-term managements

Rice fields are a major source of atmospheric methane (CH<sub>4</sub>). Nitrate has been approved to inhibit CH<sub>4</sub> production from paddy soils, while fertilization as well as water management can also affect the methanogenesis. It is unknown whether nitrate addition might result in shifts in the methanogenesis and methanogens in paddy soils influenced by different practices. Six paddy soils of different fertilizer types and groundwater tables were collected from a long-term experiment site. CH<sub>4</sub> production rate and methanogenic archaeal abundance were determined with and without nitrate addition in the microcosm incubation. The structure of methanogenic archaeal community was analysed using the PCR-DGGE (polymerase chain reaction denaturing gradient gel electrophoresis) and pyrosequencing. The results showed that nitrate addition significantly decreased the CH<sub>4</sub> production rate and methanogenic archaeal abundance in all six paddy soils by 70–100% and 54–88%, respectively. The quantity, position and relative intensity of DGGE bands exhibited differences when nitrate was added. Nitrate suppressed the growth of methanogenic archaeal species affiliated to Methanosaetaceae, unidentified Euryarchaeota, Thaumarchaeota and Methanosarinaceae. The universal inhibition of nitrate addition on the methanogenesis and methanogens can be adopted as a practice of mitigating CH<sub>4</sub> emission in paddy soils under different fertilization and water managements.

Molten and glassy tellurium(IV) oxosulfato complexes in the TeO2 –K2S2O7 system studied by Raman spectroscopy: Stoichiometry, vibrational properties and molecular structure

Tellurium(IV) oxide dissolves in molten potassium pyrosulfate following a reaction that leads to TeIV oxosulfato complexes. High temperature Raman spectroscopy is used under static equilibrium conditions at temperatures of 550 – 740oC for inferring the structural properties of the complex(es) formed in TeO2-K2S2O7 molten mixtures (XTeO20 = 0 – 0.70) under O2 atmosphere. The composition effects on the Raman spectra together with the outcome of a quantitative exploitation of the relative Raman band intensities point to a 3:1 TeO2:K2S2O7 stoichiometry, which combined with the observed vibrational properties is suggestive of a (Te=O)3O2(SO4)22- structural formula for the simplest building unit formed. A 3-fold coordination around Te becomes evident comprising an oxide ligand and two oxygen atoms bridging to adjacent Te or S atoms. A gradual association of building units takes place with increasing XTeO20. Cooling results in formation of stable glasses with a concomitant change in the coordination number of TeIV from 3 to 4 by means of a structural mechanism suggestively involving a TeO2/2(=O)→ TeO4/2 transformation. Totally ten bands are attributed to the TeIV oxosulfato complex; the most characteristic ones pertain to the 1040 cm-1 band assigned to symmetric stretching unidentate sulphate and to the 850 cm-1 band assigned to Te=O terminal stretching, the latter band being attenuated on going from the molten to the glassy state due to the TeO2/2(=O)→ TeO4/2 interconversion.

Study of Correlation Between Hp α1 Expression of Haptoglobin 2-1 and Clinical Course in Aneurysmal Subarachnoid Hemorrhage

Haptoglobin (Hp) comprising 2 light (α) and 2 heavy (β) chains has an antioxidant effect following free hemoglobin binding. Among 3 phenotypes-Hp1-1 (two α1), Hp2-1 (α1 and α2), and Hp2-2 (two α2)-a greater protective effect for toxic-free hemoglobin was reported for Hp2-2 compared with Hp1-1. However, few studies have focused on the association of Hp2-1 with outcomes. This study examined α1 and α2 expression, and evaluated thecorrelation of Hp2-1 with outcomes of subarachnoid hemorrhage (SAH). Eighty-seven patients were enrolled prospectively, including 12 in the Hp1-1 group (13.8%), 36 in the Hp2-1 group (41.4%), and 39 in the Hp2-2 group (44.8%). Phenotypes were confirmed by Western blot analysis. The relative band intensities were measured as α subunit intensities normalized to albumin intensities and expressed as median (interquartile range). The differences in α intensities according to delayed cerebral ischemia (DCI), angiographic vasospasm (AV), and outcome were analyzed. DCI and AV were more frequently associated with Hp2-2 than with Hp1-1 (DCI: 21 [53.8%] vs. 3 [25.0%]; AV: 22 [56.4%] vs. 3 [25.0%]). The α1 intensities of Hp2-1 without DCI and AV were significantly higher than those with DCI and AV (without DCI: 0.70 [interquartile range (IQR), 0.54-0.89]; with DCI: 0.24 [IQR, 0.14-0.32]; P < 0.001; without AV: 0.65 [IQR, 0.32-0.88]; with AV: 0.32 [IQR, 0.17-0.67]; P= 0.046). No significant difference was noted with α2 intensities. The α1 (P= 0.359) and α2 (P= 0.233) intensities did not differ significantly according to outcome. Higher α1 intensities in Hp2-1 are associated with a lower risk of DCI and AV. The degree of α1 intensity may provide additional information about the individual risk of secondary injury following SAH in patients with Hp2-1.

Photochromic Properties and Surface Enhanced Raman Scattering Spectra of Indoline Spiropyran in Silver-Based Nanocomposite Films

The structure and photochromic transformations of composite organometallic nanosystems composed of Ag nanoparticles covered with a layer of indoline-spiropyran (ISP) molecules from solutions were studied by spectrophotometry, surface Raman scattering spectroscopy (SERS) and quantum chemistry. Analysis of experimental data showed that studied nanostructured systems have photochromic properties, manifested in the reversible photo-induced changes both of the electronic-absorption spectra and of the relative intensity of the SERS bands. The open form of ISP, formed in the organometallic nanostructured film as a result of photochromic transformations, has an adsorption geometry, and, possibly, a conformation different from that formed as a result of chemisorption of ISP molecules on silver colloids.

Endogenous Membrane Receptor Labeling by Reactive Cytokines and Growth Factors to Chase Their Dynamics in Live Cells

Summary Cytokine and growth factor receptors localized on cell membranes play key roles in many biological events. Because the dynamic behaviors of receptors are deeply involved in cytokine- and growth-factor-dependent signaling pathways, reliable techniques for real-time imaging of receptors in live cells are strongly desired. Here, we describe a method of covalently labeling and imaging membrane receptors in live cells by using chemically reactive cytokines and growth factors coupled with 4-dimethylaminopyridine (DMAP), an organocatalyst that facilitates acyl transfer. Construction of the DMAP cytokines and growth factors relies on non-covalent coordination chemistry between an oligo-histidine tag and dimeric Ni(II)-nitrilotriacetate in an in situ manner. This supramolecular approach is relatively simple and flexible and can be applied to labeling not only transiently but also endogenously expressed receptors. Moreover, given the benefit of this traceless labeling of the receptors, our technique allows real-time imaging of the ligand-induced dynamics of endogenously expressed receptors in live cells.

Optical Characteristics of Pyrolytic Carbon in the Vicinity of the E 1u Vibrational Mode Calculated within the Framework of the Effective-Medium Model

Spectral optical constants of pyrolytic carbon in the region of activity of the E1u vibrational mode are calculated within the framework of the effective-medium approach in the Bruggeman approximation. It is demonstrated that the number, position, half-width, and relative intensity of the selective-absorption bands in the IR absorption spectrum of pyrolytic carbon are the independent of porosity of the original absorbing object.