Low Frequency Raman Spectroscopy
Technické články | 2015 | MetrohmInstrumentace
Low frequency Raman spectroscopy extends the conventional fingerprint region down to 65 cm-1, unlocking information on weak intermolecular interactions, lattice vibrations and structural changes that are inaccessible with standard probes. This capability is crucial for characterizing protein conformations, detecting polymorphs in pharmaceuticals and monitoring material phases.
This study demonstrates the performance of a portable Raman system equipped with an E grade low frequency probe. The goals include evaluating spectral access from 65 to 3200 cm-1 and illustrating applications in polymorph detection, phase transition monitoring and molecular fingerprinting of model compounds.
The measurements employed a B W Tek i Raman Plus spectrometer with a CleanLaze 785 nm laser (linewidth < 0.2 nm, 300 mW) and a TE cooled back thinned CCD detector. The BAC 102 E grade probe covers a range of 65 to 3200 cm-1 at 4.5 cm-1 resolution. Integration times varied between 100 ms and 10 s at room temperature.
Analysis of L asparagine revealed three prominent low frequency bands below 200 cm-1 alongside the conventional fingerprint region, highlighting intermolecular lattice modes. In polymorph studies, the spectra of alpha D glucose and its monohydrate form showed distinct features in the 65 to 200 cm-1 range, demonstrating enhanced sensitivity to pseudo polymorphic differences. Phase change monitoring of sulfur indicated broadening and shift of the 83.6 cm-1 band upon melting, with no significant changes in the higher frequency region.
The extended spectral range facilitates precise identification of active pharmaceutical ingredient structures, improving quality control in drug development and manufacturing. Additionally, it enables real time monitoring of crystallization processes, analysis of protein dynamics, and characterization of semiconductors, carbon nanotubes, solar cell materials, minerals, pigments and gemstones.
Advancements may include integration of low frequency Raman probes into in situ production lines, coupling with chemometric algorithms for automated analysis, and development of compact handheld devices. Emerging fields such as continuous pharmaceutical manufacturing, real time polymorph screening and advanced material synthesis will particularly benefit from rapid low frequency measurements.
The combination of the i Raman Plus spectrometer and the BAC 102 E grade probe delivers cost effective access to low frequency Raman modes down to 65 cm-1. This capability broadens the range of applications in pharmaceutical analysis, material science and beyond, offering a versatile tool for research and industry.
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Souhrn
Significance of the Topic
Low frequency Raman spectroscopy extends the conventional fingerprint region down to 65 cm-1, unlocking information on weak intermolecular interactions, lattice vibrations and structural changes that are inaccessible with standard probes. This capability is crucial for characterizing protein conformations, detecting polymorphs in pharmaceuticals and monitoring material phases.
Objectives and Study Overview
This study demonstrates the performance of a portable Raman system equipped with an E grade low frequency probe. The goals include evaluating spectral access from 65 to 3200 cm-1 and illustrating applications in polymorph detection, phase transition monitoring and molecular fingerprinting of model compounds.
Instrumentation
The measurements employed a B W Tek i Raman Plus spectrometer with a CleanLaze 785 nm laser (linewidth < 0.2 nm, 300 mW) and a TE cooled back thinned CCD detector. The BAC 102 E grade probe covers a range of 65 to 3200 cm-1 at 4.5 cm-1 resolution. Integration times varied between 100 ms and 10 s at room temperature.
Main Results and Discussion
Analysis of L asparagine revealed three prominent low frequency bands below 200 cm-1 alongside the conventional fingerprint region, highlighting intermolecular lattice modes. In polymorph studies, the spectra of alpha D glucose and its monohydrate form showed distinct features in the 65 to 200 cm-1 range, demonstrating enhanced sensitivity to pseudo polymorphic differences. Phase change monitoring of sulfur indicated broadening and shift of the 83.6 cm-1 band upon melting, with no significant changes in the higher frequency region.
Practical Benefits and Applications
The extended spectral range facilitates precise identification of active pharmaceutical ingredient structures, improving quality control in drug development and manufacturing. Additionally, it enables real time monitoring of crystallization processes, analysis of protein dynamics, and characterization of semiconductors, carbon nanotubes, solar cell materials, minerals, pigments and gemstones.
Future Trends and Applications
Advancements may include integration of low frequency Raman probes into in situ production lines, coupling with chemometric algorithms for automated analysis, and development of compact handheld devices. Emerging fields such as continuous pharmaceutical manufacturing, real time polymorph screening and advanced material synthesis will particularly benefit from rapid low frequency measurements.
Conclusion
The combination of the i Raman Plus spectrometer and the BAC 102 E grade probe delivers cost effective access to low frequency Raman modes down to 65 cm-1. This capability broadens the range of applications in pharmaceutical analysis, material science and beyond, offering a versatile tool for research and industry.
References
- A M R Teixeira P T C Freire A J D Moreno J M Sasaki A P Ayala J Mendes Filho F E A Melo High pressure Raman study of L Alanine Crystal Solid State Communications 2000 116 405 409
- P J Larkin P J et al Polymorph Characterization of Active Pharmaceutical Ingredients Using Low Frequency Raman Spectroscopy Applied Spectroscopy 2014 68 758 776
- E Smith G Dent Modern Raman Spectroscopy A Practical Approach John Wiley and Sons 2005
- M J Pelletier Analytical Applications of Raman Spectroscopy Blackwell Science Ltd 1999
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