Amorphous Conjugated Polymers as Efficient Dual-Mode MALDI Matrices for Low-Molecular-Weight Analytes.

Chempluschem

Leibniz-Institut für Polymerforschung Dresden e.V., Hohe Straße 6, 01069, Dresden, Germany.

Published: September 2019

AI Article Synopsis

  • Matrix-assisted laser desorption/ionization mass spectrometry (MALDI MS) typically uses small-molecule matrices, but new research shows semi-crystalline polymers are effective for detecting low-molecular-weight compounds (LMWCs).
  • Two specific fluorene/napthalene diimide co-polymers were tested; both are amorphous, have high absorption rates for the MALDI laser wavelength, and can be processed in solution.
  • These amorphous matrices perform equally or better than traditional semi-crystalline ones in terms of signal intensity, suggesting that LMWCs are effectively incorporated into the amorphous parts of the polymer matrix.

Article Abstract

Matrix-assisted laser desorption/ionization mass spectrometry (MALDI MS) usually employs highly crystalline small-molecule matrices, and the analyte is interpreted as being co-crystallized with the matrix. We recently showed that semi-crystalline polymers are efficient matrices for the detection of low-molecular-weight compounds (LMWCs) in MALDI MS and MALDI MS Imaging, and are dual-mode, i. e., enabling both positive and negative modes. The matrix performances of two fluorene/napthalene diimide co-polymers P(TNDIT-Fl(C C )) and P(TNDIT-Fl(C C )) were investigated and compared. Both are fully amorphous according to XRD measurements, show high relative absorption values at the wavelength of common MALDI lasers (λ =355 nm: C C =73 %; C C =67 %), and are solution processable. As matrices, they are dual-mode, and enable the detection of LMWCs while being mostly MALDI-silent. Compared with semicrystalline polymer matrices, the amorphous matrices give similar or better signal intensities, thus indicating that analyte inclusion takes place in the amorphous part of the polymer matrix.

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Source
http://dx.doi.org/10.1002/cplu.201900203DOI Listing

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