Two-Dimensional Correlation Spectroscopy (2D-COS) of Gas-Phase Pyrrole Clusters in a Supersonic Jet: Treatment of Sharp Bands on a Broad Background

2020 ◽  
Vol 74 (4) ◽  
pp. 408-416
Author(s):  
Yoshiteru Matsumoto ◽  
Souichi Tezuka

Two-dimensional correlation spectroscopy (2D-COS) is a useful technique to analyze any intensity behavior of optical spectra that exhibit a complicated feature with overlapped bands. In this study, we apply 2D-COS to the infrared (IR) spectra of gas-phase pyrrole (Py) clusters. The NH stretching vibrations of the Py clusters are measured by cavity ringdown spectroscopy. The observed IR spectra of the Py clusters consist of sharp bands, full width half-maximum (FWHM) ∼1 cm−1, and a broad background (FWHM >50 cm−1). The 2D asynchronous correlation spectra reveal that the sharp bands and a broad background are assigned to small clusters of dimer to pentamer and large clusters with bulk-like structures, respectively, which support the results of our previous study. The sharp bands are also analyzed using another 2D asynchronous correlation spectrum, which is obtained by decomposing the observed IR spectra into sharp and broad components. Because the asynchronous signals are consistent with those obtained from the IR spectra without decomposition, the result would suggest that we need not to decompose the IR spectra into sharp and broad components before applying 2D-COS. However, our model simulations of 2D-COS showed a counterexample that gives an incorrect result without removing a broad background component from the IR spectra. This study strongly suggests that we need to undertake a careful treatment of the complicated IR spectrum with various widths of bands.

2002 ◽  
Vol 56 (9) ◽  
pp. 1186-1193 ◽  
Author(s):  
Yuqing Wu ◽  
Koichi Murayama ◽  
Boguslawa Czarnik-Matusewicz ◽  
Yukihiro Ozaki

Attenuated total reflection (ATR)/FT-IR spectra were measured for human serum albumin (HSA) in aqueous solutions (pH 6.6) with concentrations of 1.0, 2.0, 3.0, 4.0, and 5.0 wt % over a temperature range of 45–80 °C. Generalized two-dimensional (2D) correlation spectroscopy was employed to explore concentration and heat-induced structural variations of HSA in aqueous solutions. To generate 2D correlation spectra, the raw spectra were subjected to the appropriate pretreatment procedure involving ATR correction, subtraction of the spectrum of an aqueous solution, and smoothing. The synchronous and asynchronous correlation spectra were calculated for the concentration-dependent IR spectral variations in the amide I region at various temperatures. The two-dimensional ATR/IR correlation spectra greatly enhance band separation in the region and provide information about the correlation between the amide bands of HSA arising from the same and different secondary structure components. Based on the correlation investigated and previously proposed relationship between the secondary structure elements and the amide band frequencies, we have proposed the detailed assignments in the amide I region at 45 and 80 °C. The proposed assignments are compared with those based on the results of second derivative and Fourier self-deconvolution (FSD) of the ATR/IR spectra. The asynchronous spectrum generated from the concentration-dependent spectral variations at 45 °C show that side chains, the random coil, and extended chains are more sensitive than the α-helices and β-turns to the concentration change. On the other hand, the corresponding spectrum at 80 °C reveals that the conformation changes in side chains and β-turns (or β-strands) of HSA start before those in extended chain, random coil structures, and α-helices.


Materials ◽  
2021 ◽  
Vol 14 (19) ◽  
pp. 5672
Author(s):  
Xuewen Zheng ◽  
Wenyuan Xu ◽  
Shuangrui Xie

In order to explore the influence mechanism of carbon nanotubes on the ultraviolet (UV) aging properties of the SBS-modified asphalt binder, the changes of functional groups in the one-dimensional infrared spectrum and two-dimensional infrared correlation spectrum are studied in this paper. The results show that the UV aging process of the SBS-modified asphalt binder is the process of alkane chain cleavage and reorganization, the formation of oxygen-containing functional groups and decomposition of SBS. The incorporation of carbon nanotubes can reduce the mutual conversion of methyl and methylene functional groups, inhibit the decomposition of butadiene and the destruction of C = C double bonds in SBS. The degradation of SBS during the process of UV aging leads to the change of many functional groups and acceleration of the aging of the SBS-modified asphalt binder. The addition of carbon nanotubes can effectively alleviate the degradation of SBS and the formation of oxygen-containing functional groups at the early stage of UV aging, and reduce the influence of these two changes on other functional groups; thus, improving the anti-aging performance of the SBS-modified asphalt binder.


2009 ◽  
Vol 63 (8) ◽  
pp. 920-925 ◽  
Author(s):  
Jianbo Chen ◽  
Qun Zhou ◽  
Isao Noda ◽  
Suqin Sun

Two-dimensional (2D) correlation spectroscopy, which takes advantage of the apparent enhancement of spectral resolution, is known to be useful in qualitative discrimination of seemingly similar samples. The possibility of quantitative classification of 2D correlation spectra is even more desirable. Two useful parameters, namely Euclidian distance and correlation coefficient between 2D correlation spectra, are introduced for this purpose. Dry and sweet red wine samples are used to demonstrate the utility of these parameters. The distances between the 2D infrared (IR) spectra of sweet and dry red wines are roughly proportional to the differences of sugar contents in them. The result shows that the two parameters are useful measures for the quantitative evaluation of the similarity among the samples and their corresponding 2D correlation spectra.


1993 ◽  
Vol 47 (9) ◽  
pp. 1317-1323 ◽  
Author(s):  
I. Noda ◽  
A. E. Dowrey ◽  
C. Marcott

Recent developments in two-dimensional infrared (2D IR) correlation spectroscopy are reviewed. Since the initial introduction of the basic concept seven years ago, the field of 2D IR spectroscopy has evolved considerably. The method for generating 2D IR spectra from perturbation-induced time-dependent fluctuations of IR intensities and the properties of such 2D spectra are summarized first. Applications of 2D IR spectroscopy are then surveyed, and improvements in the instrumentation are reviewed. Different types of external perturbation schemes capable of inducing dynamic fluctuations of IR spectra are listed. Finally, a new 2D correlation method for dynamic spectral data with arbitrary time-dependence is discussed.


2013 ◽  
Vol 9 (S297) ◽  
pp. 237-246 ◽  
Author(s):  
L. N. Zack ◽  
J. P. Maier

AbstractCarriers of the diffuse interstellar bands (DIBs) cannot be definitively identified without laboratory spectra. Several techniques, including matrix isolation, cavity ringdown spectroscopy, resonance enhanced multiphoton ionization, and ion trapping, have been used to measure the electronic spectra of carbon chains and their derivatives. The gas-phase laboratory spectra could then be compared to the astronomical data of known DIBs. The choice of molecules studied in the gas phase depends on the presence of strong electronic transitions at optical wavelengths, the lifetimes of excited electronic states, and chemical feasibility in diffuse astrophysical environments. Collisional-radiative rate models have also be used in conjunction with laboratory spectra to predict absorption profiles under interstellar conditions.


1991 ◽  
Vol 46 (1-2) ◽  
pp. 203-205
Author(s):  
Attila Felinger ◽  
Jänos Liszi

AbstractNon-equilibrium crystallization was simulated on a two dimensional square lattice. Several clusters were grown simultaneously by using the model of diffusion limited aggregation. The growing process was reversible, i.e. dissolution of particles from the boundary of any cluster was made possible. The rate of growth and dissolution was determined by a stochastic method. The simulation resulted in an aggregate pattern having a few large and several small clusters. The fractal dimensions of the large clusters were found in the range of D = 1.62-1.72.


2004 ◽  
Vol 82 (6) ◽  
pp. 848-853 ◽  
Author(s):  
Mitsunori Araki ◽  
Pawel Cias ◽  
Alexey Denisov ◽  
Jan Fulara ◽  
John P Maier

The electronic spectrum of a nonlinear carbon chain radical C4H4+ was observed after mass-selective deposition in a 6 K neon matrix. The corresponding gas-phase spectra of C4H4+ and C4D4+ have been observed in the 512 to 513 nm region and at 710 nm for C8H4+. These were detected in direct absorption by cavity ringdown spectroscopy through a supersonic planar discharge. The electronic transition energies of these nonlinear carbon chain radicals correlate well with those of the polyacetylene cations HCnH+ (n = 4, 6, 8). The observed profiles are reproduced with rotational constants obtained by ab initio geometry optimizations and extrapolation between the ground and excited electronic states. Key words: nonlinear carbon chain, carbon cation, electronic transition, diffuse interstellar bands, molecular structure.


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