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Polarized IR Spectra of p-Nitroaniline-Loaded AlP04-5 Single Crystals

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Marlow,  F.
lnstitut fur Angewandte Chemie, Berlin-Adlershof FRG;
Research Group Marlow, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Demuth,  D.
Institut für Anorganische und Analytische Chemie, Johannes Gutenberg-Universitat Mainz, FRG;
Research Department Schüth, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

/persons/resource/persons58985

Schüth,  F.
Institut für Anorganische und Analytische Chemie, Johannes Gutenberg-Universitat Mainz, FRG;
Research Department Schüth, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Citation

Marlow, F., Demuth, D., Stucky, G., & Schüth, F. (1995). Polarized IR Spectra of p-Nitroaniline-Loaded AlP04-5 Single Crystals. The Journal of Physical Chemistry, 99(4), 1306-1310. doi:10.1021/j100004a034.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0024-2775-7
Abstract
Single crystals of the aluminophosphate AlP04-5 loaded with different amounts of p-nitroaniline (PNA) were investigated by polarized IR microspectroscopy. For a loading of 4 wt % the bands due to PNA were almost totally polarized. From the dicroic ratios a mean deviation of the long molecule axis from the crystal c-axis of around 12° can be inferred. At higher loading levels H bonding between adjacent PNA molecules reduces the symmetry, thus leading to dicroic ratios closer to unity. However, absorption bands related to the aromatic ring are less affected by the H bonding and show dicroic ratios comparable to those of the lowly loaded samples. This means that also in the high-loading situation the orientation of the molecules by the channel system is very high. Heating of the highly loaded sample to up to 573 K leads to a breaking of the H bonds, the spectrum changes from a solid like type to a solution type spectrum