What absorbs at 1298 cm⁻¹ in an FTIR spectrum?
A band near 1298 cm⁻¹ can point to several functional groups. Below are the most likely assignments, ranked by how much published evidence supports each — every one traceable to literature (DOI) and cross-validated against our 130,000+ reference spectra and knowledge graph.
Backed by 8 cited sources
Quick answer
A band near 1298 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.
Mogelijke functionele-groeptoewijzingen
| Functionele groep | Ondersteunende feiten | Geciteerde bronnen | Hoogste vertrouwen |
|---|---|---|---|
| Secondary amine | 5 | 5 | 1,0 |
| C n single bond | 5 | 5 | 1,0 |
| Amide | 5 | 5 | 1,0 |
| Methoxy (OCH3) | 3 | 3 | 1,0 |
| Methacrylate | 3 | 3 | 1,0 |
| C-O single bond | 3 | 3 | 1,0 |
| Acetate | 3 | 3 | 1,0 |
| N h | 2 | 2 | 1,0 |
| Aromatic ring | 2 | 2 | 1,0 |
| C c single bond | 1 | 1 | 1,0 |
| Ester | 1 | 1 | 1,0 |
| Boron nitrogen | 1 | 1 | 1,0 |
| S eq o | 1 | 1 | 1,0 |
| Carboxyl (COOH) | 1 | 1 | 1,0 |
| Lewis acid site | 1 | 1 | 1,0 |
| Ring structure | 1 | 1 | 1,0 |
| Sulfonate | 1 | 1 | 0,95 |
Ranglijst weerspiegelt cumulatief literatuurbewijs, niet één gezaghebbende regel. Bevestig altijd aan de hand van uw monsterecontext.
Possible materials
| Materiaal | Ondersteunende pieken | Overlapping groups | Geciteerde bronnen |
|---|---|---|---|
| alginate | 1298, 1100, 1715 | Methoxy (OCH3), Amide | 1 |
| collagen | 1298, 1408, 1660 | Amide, Methoxy (OCH3) | 1 |
| sodium alginate | 1298, 1636, 1080 | Methoxy (OCH3), Amide | 1 |
| chitosan | 1298, 1650, 1655 | Amide, Methoxy (OCH3) | 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 1298 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.
Literatuur achter deze toewijzingen
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Amide vertrouwen 1,0
“to (ii) the band corresponding to the C-N stretching is present at 1298 (iii) the bands to calculate the copolymer composition but reveals that aniline monomer units are present in the”
Bongiovanni Abel 等 - 2019 - Synthesis of a Smart Conductive Block Copolymer Re DOI: 10.3390/polym11111744 -
vertrouwen 1,0
“cm-1 While the peaks at 1297.6 and 1240.8 correspond to the N-H bending and the asymmetric cm-1 C-N stretching of the benzenoid ring, respectively.”
Li 等 - 2013 - Synthesis and Microwave Absorption Characteristics DOI: 10.4028/www.scientific.net/AMM.327.53 -
Lewis acid site vertrouwen 1,0
“After the introduction 3 Lewis acid sites immediately disappeared upon exposure to NO, of NH 3, a broad feature with peaks at 1298, 1387, and 1465 that participates in the suggesting that it is this type of NH cm-1 cm-1 appeared, and the pe”
Pena 等 - 2004 - Identification of surface species on titania-suppo DOI: 10.1021/jp0313122 -
Amide vertrouwen 1,0
“cm-1 cm-1 plan, 802 corresponds to para di-substituted ring, 1119 is due to delocalization of 7 cm-1 cm-1 electrons in aromatic ring, 1298 corresponds to C - N stretching vibration, 1490 due cm-1”
Antistatic and Dielectric properties of one-dimensional Al2+:Nd2O3 nanowire doped polyaniline nanocomposites for electronic application DOI: 10.1016/j.sna.2018.07.018 -
Amide vertrouwen 1,0
“The dotted blue lines crossing the peak at ~1153 is for asymmetric cm-1 stretch of C-O-C, and that at 1298 is for the C-N stretching vibration of type I amine.”
Awadallah-F 和 Al-Muhtaseb - 2019 - Influence of Chitosan Addition on Resorcinol-Forma DOI: 10.3390/app9214582 -
Aromatic ring vertrouwen 1,0
“cm-1/1298 cm-1 cm-1 1323 doublet and 1151 peak were assigned to the asymmetric and 318 symmetric stretching of the aromatic sulfone chromophore, respectively [25].”
Garcia-Ivars 等 - 2014 - Development of fouling-resistant polyethersulfone DOI: 10.1016/j.seppur.2014.07.056. -
Carboxyl (COOH) vertrouwen 1,0
“Figure 1C shows the typical absorption bands of sodium alginate, mainly the O-H stretching at 3424 cm-1, pyranoid ring (six-membered ring) C-H stretching at 2903 and 2932 cm-1, COO asymmetric stretching at 1595 cm-1, COO symmetric stretchin”
Characteristics and Preparation of Designed Alginate-Based Composite Scaffold Membranes with Decellularized Fibrous Micro-Scaffold Structures from Porcine Skin DOI: 10.3390/polym13203464 -
Acetate vertrouwen 1,0
“The band located at 1298 cm-1 3 originates from the asymmetric valence C-O-C vibrations of HEMA and is also present in the polymer spectrum.”
Influence of Dimethacrylate Monomer on the Polymerization Efficacy of Resin-Based Dental Cements—FTIR Analysis DOI: 10.3390/polym14020247
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