What absorbs at 1779 cm⁻¹ in an FTIR spectrum?
Una banda cerca de 1779 cm⁻¹ puede apuntar a varios grupos funcionales. A continuación se muestran las asignaciones más probables, clasificadas por cuánta evidencia publicada respalda cada una — cada una trazable a literatura (DOI) y validada de forma cruzada con nuestros más de 130,000 espectros de referencia y grafo de conocimiento.
Backed by 5 cited sources
Quick answer
A band near 1779 cm⁻¹ is usually interpreted by checking which functional groups repeatedly co-occur there in the literature, then confirming at least one or two additional peaks in the same sample. This page ranks those assignments by accumulated evidence rather than by a single fixed textbook rule.
Posibles asignaciones de grupos funcionales
| Grupo funcional | Hechos de respaldo | Fuentes citadas | Confianza máxima |
|---|---|---|---|
| Carbonyl (C=O) | 5 | 5 | 1,0 |
| Imide | 2 | 2 | 1,0 |
| Ring structure | 1 | 1 | 1,0 |
| Alkyl C-H | 1 | 1 | 1,0 |
La clasificación refleja la evidencia acumulada de la literatura, no una única regla autorizada. Siempre confirme según el contexto de su muestra.
Possible materials
| Material | Supporting peaks | Overlapping groups | Fuentes citadas |
|---|---|---|---|
| polyimide | 1779, 1720, 1778 | Carbonyl (C=O), Imide | 1 |
Materials are shown only when the same literature pool supports this band and at least one additional characteristic peak.
Spectrum logic
This band becomes meaningful only when read with its neighboring peaks. In practice, analysts first look at the assignments above, then check whether the same sample also shows other peaks expected for the same structural motif. A lone band near 1779 cm⁻¹ is usually not enough for material identification by itself.
Real-world usage
This type of query is common in polymer identification, unknown plastic screening, QC troubleshooting, recycled-material verification, and literature-backed peak assignment review.
Common mistakes
- Treating one isolated band as proof of a material without checking at least one or two supporting peaks.
- Ignoring overlap: multiple functional groups can contribute near the same wavenumber.
- Skipping validation when additives, blends, oxidation, or contamination may distort the spectrum.
Verification advice
When ambiguity remains, validate the hypothesis with DSC, GC-MS, or TGA, especially for blends, degraded samples, and filled polymers.
Literatura detrás de estas asignaciones
-
Imide confianza 1,0
“the unaged CBR 320/328 composites reveal three imide carbonyl peaks at 1779, 1728 and 1712 These peaks may be assigned to the symmetric and asymmetric stretches of an unsaturated imide (1779 and 1728 cm(cid:2)1)”
Fox 等 - 2004 - Investigation of failure mechanisms in aged aerosp DOI: 10.1016/j.engfailanal.2003.05.010 -
Carbonyl (C=O) confianza 1,0
“Fourier Transt Copyright: American Scientific Publishers cm-1, form Infrared Spectroscopy (FTIR) spectra shows two new absorbance peaks at 1779 and 1851 which i Delivered by Ingenta c correspond to symmetrical and asymmetrical stretching vi”
Compatibilization effect of EVA-g-MAH on mechanical, morphological and rheological properties of recycled PC/ABS blend DOI: 10.1166/mex.2014.1198 -
Alkyl C-H confianza 1,0
“Peaks that can only be assigned to polyimide in the blend include the methyl group C-H stretching cm-1), cm-1), C=O (symmetric stretching) (1779 C=O (anti-symetric stretching) (2957-2863 cm-1),”
Maab 等 - 2009 - SPEEKPolyimide Blends for Proton Conductive Membr DOI: 10.1002/fuce.200800121 -
Carbonyl (C=O) confianza 1,0
“In the FTIR cm(cid:3)1 spectrum strong absorption bands appeared at 1779 due to the asymmetric vibration of the carbonyl imide ring, at 1719 cm(cid:3)1 attributed to the symmetric vibration of carbonyl imide”
Serbezeanu 等 - 2016 - Phosphorus-containing polyimide fibers and their t DOI: 10.1039/c6ra06497c -
Carbonyl (C=O) confianza 0,95
“Explicit assignment: 'the C=O (of SMA) peak at a wavelength of 1779'”
The effect of Styrene Maleic Anhydride on the microstructure evolution of PSF-based membrane prepared by thermal-induced phase separation method DOI: 10.1016/j.mtcomm.2019.100687
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