What absorbs at 434 cm⁻¹ in an FTIR spectrum?
A band near 434 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
クイックアンサー
A band near 434 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.
可能性のある官能基アサイン
| 官能基 | 裏付け事実 | 引用元 | 最高信頼度 |
|---|---|---|---|
| Metal oxygen | 3 | 2 | 1.0 |
| Silicon-oxygen (Si-O) | 2 | 2 | 1.0 |
| Acetate | 2 | 2 | 1.0 |
| Silicon (Si) | 1 | 1 | 1.0 |
| Carbonyl (C=O) | 1 | 1 | 1.0 |
| Methoxy (OCH3) | 1 | 1 | 1.0 |
| Methacrylate | 1 | 1 | 1.0 |
| C-O single bond | 1 | 1 | 1.0 |
| Aromatic ring | 1 | 1 | 1.0 |
ランキングは蓄積された文献証拠を反映しており、単一の権威あるルールではありません。常にサンプルのコンテキストと照合して確認してください。
可能性のある材料
| 素材 | 補助ピーク | 重複グループ | 引用元 |
|---|---|---|---|
| iron oxide nanoparticles | 434, 2972, 528 | Metal oxygen, Acetate | 1 |
| MWCNT | 434, 2876, 1430 | Acetate | 1 |
同じ文献プールがこのバンドと少なくとも1つの追加の特性ピークをサポートする場合にのみ、材料が表示されます。
スペクトルロジック
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 434 cm⁻¹ is usually not enough for material identification by itself.
実使用例
この種のクエリは、ポリマー識別、未知のプラスチックスクリーニング、QCトラブルシューティング、リサイクル材料の検証、および文献に基づいたピーク帰属のレビューで一般的です。
よくある間違い
- 少なくとも1~2つの支持ピークを確認せずに、1つの孤立したバンドを材料の証拠として扱うこと。
- 重複を無視: 複数の官能基が同じ波数付近に寄与することがあります。
- 添加剤、ブレンド、酸化、または汚染がスペクトルを歪める可能性がある場合に検証を省略すること。
検証アドバイス
曖昧さが残る場合は、特にブレンド、劣化サンプル、充填ポリマーについて、DSC、GC-MS、またはTGAで仮説を検証してください。
これらのアサインの根拠となる文献
-
Aromatic ring 信頼度 1.0
“For the degradation of reactive violet (RV) 1 by the ligninolytic enzymes of the strain Ganoderma cupreum AG-1, the peaks at 1,602 and 1,434 cm-1 may be characteristics of C=C aromatic skeletal vibration and azo linkages (-N=N-) on aromatic”
Trichoderma asperellum laccase mediated crystal violet degradation–Optimization of experimental conditions and characterization DOI: 10.1016/j.jece.2016.11.044 -
Acetate 信頼度 1.0
“For degradation ratios lower than 1 for stretching of C-O bonds (phytate 434 content, 0.90 ± 0.05) and stretching vibrations of C-O bonds (polysaccharides, 0.93 ± 0.03) were 435 observed.”
Valorisation of wheat bran to produce natural pigments using selected microorganisms DOI: 10.1016/j.carres.2013.08.015 -
信頼度 1.0
“Therefore, the dehydrogenation peak at 434 C is probably related to the decomposition of the unknown compounds, which can be denoted as "Li-Al-B-H".”
He 等 - 2019 - The Dehydrogenation Mechanism and Reversibility of DOI: 10.3390/met9050559 -
信頼度 1.0
“The peak at 434 cm-1 was assigned to the Zn-O stretching vibration, confirming the presence of ZnO in the composite Polymers2023,15,9”
Effect of Repeated Contact to Food Simulants on the Chemical and Functional Properties of Nano ZnO Composited LDPE Films for Reusable Food Packaging DOI: 10.3390/polym15010009 -
Silicon-oxygen (Si-O) 信頼度 1.0
“The peak, centered 434 (νO-Si-O) identified by some peaks, centered at 520, 651 cm-1 at 1018 cm-1 slightly decreased.”
Radev 等 - 2009 - OrganicInorganic bioactive materials Part II in DOI: 10.2478/s11532-009-0076-1 -
Carbonyl (C=O) 信頼度 1.0
“The carbonyl (C=O) group stretching cm-1 434 vibration appears at 1757 as a sharp peak (Fu et al., 2018;”
Influence of montmorillonite/carbon nanotube hybrid nanofillers on the properties of poly(lactic acid) DOI: 10.1016/j.clay.2020.105925 -
Silicon (Si) 信頼度 1.0
“The band at 434 was attributed cm-1 to the Si-O the bending-rock mode.”
Zaid 等 - 2017 - Effect of Sintering on Crystallization and Structu DOI: 10.2298/SOS1704409Z -
Metal oxygen 信頼度 0.9
“Text: 'two bands at 527 and 434 were observed for Fe-O'”
Khan 等 - 2022 - Biosynthesis and characterization of iron oxide na DOI: 10.3389/fpls.2022.1001499
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