The 298 K Raman and reflection spectra of the polydiacetylene THD, a close structural variant of DCHD, are presented. The polymer double-and triple-bond stretch frequencies are 1485 and 21 I 1 cm-', respectively, and the lowest electronic transition peaks at 17600 cm-'. The reflection spectrum is mo
Raman and reflection spectra of a polymorph of the polydiacetylene TCDU
โ Scribed by M.E. Morrow; R.C. Dye; C.J. Eckhardt
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 417 KB
- Volume
- 158
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
The 298 K Raman and reflection spectra of a single crystal TCDU polydiacetylene polymorph (TCDU-A') are presented. The lowest energy reflection maximum in TCDU-A* is seen at 15900 cm-'. Raman and reflection spectra ofTCDU-A* are similar to those for TCDU-A and thin film TCDU samples and significantly different from TCDU-B spectra. It is suggested that TCDU-A* is a stable form of TCDU-A at ambient conditions and may also be the corresponding bulk form of the thin film TCDU.
๐ SIMILAR VOLUMES
Analysis of vibronic structure in the 300 K piezomodulated reflection (PMR) spectra of DCHD and THD indicates the presence of a single allowed electronic state accompanied by significant hot band activity. Observed vibronic progressions and hot bands are consistent with corresponding Raman spectra.
Raman spectra of the black polydiacetylene single crystals TS6 and TS/FBS were recorded by means of a conventional Raman spectrometer with excitation in the near-infrared spectral region. We observed several sidegroup vibrations below 900 cm-' additional to the four strong vibrational modes which mo
Raman spectroscopy is a useful tool for identifying polymorphs of pharmaceutical compounds. One limitation of the technique is that the small differences in Raman spectra require confirmation of polymorphs by other methods. Fourteen compounds, both commercial and proprietary pharmaceutical compounds