Fourier transform infrared spectroscopy

Abstract: This review discusses the application of infrared spectroscopy to the study of proteins. The focus is on the mid-infrared spectral region and the study of protein reactions by reaction-induced infrared difference spectroscopy.

Abstract: Infrared spectroscopy is one of the oldest and well established experimental techniques for the analysis of secondary structure of polypeptides and proteins. It is convenient, non-destructive, requires less sample preparation, and can be used under a wide variety of conditions. This review introduces the recent developments in Fourier transform infrared (FTIR) spectroscopy technique and its applications to protein structural studies. The experimental skills, data analysis, and correlations between the FTIR spectroscopic bands and protein secondary structure components are discussed. The applications of FTIR to the secondary structure analysis, conformational changes, structural dynamics and stability studies of proteins are also discussed.

Abstract: The application of a new Fourier transform technique to magnetic resonance spectroscopy is explored. The method consists of applying a sequence of short rf pulses to the sample to be investigated and Fourier‐transforming the response of the system. The main advantages of this technique compared with the usual spectral sweep method are the much shorter time required to record a spectrum and the higher inherent sensitivity. It is shown theoretically and experimentally that it is possible to enhance the sensitivity of high resolution proton magnetic resonance spectroscopy in a restricted time up to a factor of ten or more. The time necessary to achieve the same sensitivity is a factor of 100 shorter than with conventional methods. The enhancement of the sensitivity is essentially given by the square root of the ratio of line width to total width of the spectrum. The method is of particular advantage for complicated high resolution spectra with much fine structure.

Abstract: Graphene and graphitic carbon nitride (g-C3N4) composite photocatalysts were prepared by a combined impregnation−chemical reduction strategy involving polymerization of melamine in the presence of graphene oxide (precursors) and hydrazine hydrate (reducing agent), followed by thermal treatment at 550 °C under flowing nitrogen. The resulting graphene/g-C3N4 composite photocatalysts were characterized by X-ray diffraction, transmission electron microscopy, UV−visible spectrophotometry, nitrogen adsorption, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, Raman spectroscopy, and photoluminescence spectroscopy. The transient photocurrent response was measured for several on−off cycles of intermittent irradiation. The effect of graphene content on the rate of visible-light photocatalytic hydrogen production was studied for a series of graphene−graphitic carbon nitride composite samples containing Pt as a cocatalyst in methanol aqueous solutions. This study shows that graphene sheets a...