• Title/Summary/Keyword: chemical shift

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Extracting Frequency-Frequency Correlation Function from Two-Dimensional Infrared Spectroscopy: Peak Shift Measurement

  • Kwak, Kyung-Won
    • Bulletin of the Korean Chemical Society
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    • v.33 no.10
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    • pp.3391-3396
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    • 2012
  • Two-dimensional infrared (2D-IR) spectroscopy can probe the fast structural evolution of molecules under thermal equilibrium. Vibrational frequency fluctuation caused by structural evolution produced the time-dependent line shape change in 2D-IR spectrum. A variety of methods has been used to connect the evolution of 2D-IR spectrum with Frequency-Frequency Correlation Function (FFCF), which connects the experimental observables to a molecular level description. Here, a new method to extract FFCF from 2D-IR spectra is described. The experimental observable is the time-dependent frequency shift of maximum peak position in the slice spectrum of 2D-IR, which is taken along the excitation frequency axis. The direct relation between the 2D-IR peak shift and FFCF is proved analytically. Observing the 2D-IR peak shift does not need the full 2D-IR spectrum which covers 0-1 and 1-2 bands. Thus data collection time to determine FFCF can be reduced significantly, which helps the detection of transient species.

Identifuication of College Student's And Teacher's Conceptions for Chemical Equilibrium and Equilibrium Shift (화학평형과 평형이동에 대한 대학생과 교사들의 개념조사)

  • Park, Jong Yun;Park, Hyeon Ju
    • Journal of the Korean Chemical Society
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    • v.46 no.3
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    • pp.265-278
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    • 2002
  • A concept test was administered to college students and teachers to identify their understanding of chemical equilibrium and equilibrium shift. The subjects were 53 freshmen in the General Chemistry class, 28 juniors in the Physical Chemistry class and 26 seniors from a university and 10 high school teachers in Seoul. Test items include the calculations of partial pressure and concentration of the gas in the mixture, the equilibrium constant cal-culation and the prediction of equilibrium shift when an inert gas is added to the gaseous reaction system, and the equilibrium concentration calculation and the prediction of equilibrium shift when water or common ion is added to the weak acid solution. The test was focused to identify whether the subjects can predict equilibrium shift using the reaction quotient change for the situations in which Le Chatelier principle is difficult to apply. The results showed that the achievements of teachers and juniors were significantly higher than those of freshmen and seniors. Many stu-dents had difficulties in predicting equilibrium shift using the reaction quotient while they could calculate partial pres-sure and concentration for the same situation. It means they are lack of conceptual understanding of chemical equilibrium shift.

NMR Chemical Shift for 4d$^n$ System (Ⅱ). Calculation of the Pseudo Contact Shift for a 4d$^1$ System in a Strong Crystal Field Environment of Octahedral Symmetry

  • Sang-woon Ahn;Se-Woong Oh;Eui-suh Park
    • Bulletin of the Korean Chemical Society
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    • v.4 no.2
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    • pp.64-67
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    • 1983
  • NMR shift arising from the electron orbital angular momentum and the electron spin dipolar-nuclear spin angular momentum interactions has been investigated for a $4d^{1}$ system in a strong crystal field of octahedral symmetry. To examine the NMR shif for a $4d^{1}$ system in a strong crystal field of octahedral symmetry, we derive a general expression for ${\Delta}$B/B using a nonmultipole expansion technique. From this expression all the multipolar terms are determined. For the $4d^{1}$ system in a strong crystal field of octahedral symmetry the exact solution for NMR shift, ${\Delta}$B, is compared with the multipolar results. ${\Delta}$B/B for the $4d^{1}$ system is also compared with that for the $3d^{1}$ system. It is found that the $1/R^{7}$ term contributes dominantly to the NMR shift. However, there is good agreement between the nonmultipole and multipolar results for R-values larger than 0.2 nm for the $4d^{1}$ system but for R-values larger than 0.4 nm for the $3d^{1}$ system.

Experimental Study of Chemical Shift Artifacts at 1.5T and 3.0T MRI using Gradient Echo Pulse Sequence (GE 펄스시퀀스을 이용한 1.5T와 3.0T MRI의 화학적 이동 인공물의 실험적 연구)

  • Cheol, Kweon Dae
    • Journal of the Korean Society of Radiology
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    • v.10 no.7
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    • pp.531-537
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    • 2016
  • An experimental study was to use the parameter to determine the MRI artifact of chemical shift that occurs in water and fats. Scanning the image according to the encoding parameter and the bandwidth and change in 1.5T and 3.0T MRI to the SNR, we compared the CNR. In the image was confirmed that the occurrence of artefacts in the chemical shift of the water and oil. 3.0T more image artifacts in the 1.5T was confirmed that the relatively reduced. The width of the bandwidth it could be confirmed that according to the honeycombs artifacts decrease. Therefore, in order to reduce the artifacts in the MRI scan of the chemical shift runners weak field strength, is thought to be appropriate to widen the width of the bandwidth.

Surface Plasmon Resonances of Metal Colloidal Particles Synthesized by a Photo-Chemical Process (광화학적 방법을 이용한 금속입자의 합성과 광학적 특성 연구)

  • Ko, Min-Jin;Plawsky, Joel
    • Journal of the Korean Chemical Society
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    • v.43 no.1
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    • pp.1-7
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    • 1999
  • Metal colloidal particles have been prepared by a photo-chemical process in an aqueous solution containing semiconductor nanocrystallites. Metal colloidal particles produced in CdS and AgBr exhibit different absorption spectra. Au particles produced in solution with CdS show typical Au plasmon resonance absorption spectra. On the other hand Ag particles in solution with AgBr shows surface plasmon resonance absorption spectra which are red-shifted, as compared to that of a dispersion of homogeneous Ag colloidal particles in the same host. The extent of red-shift depends on the UV illumination time. This phenomenon is interpreted within the context of effective medium theory for small volume fractions. From the theory, a metal coated particle predicts Ag plasmon resonance, red shifted with respect to 400 nm that would be associated with a silver particle in solution. The absorption peak position is very sensitive to the coating thickness.

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