What absorbs at 486 cm⁻¹ in an FTIR spectrum?
A band near 486 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
快速回答
A band near 486 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.
可能的官能基指派
| 官能基 | 支持事實 | 引用來源 | 最高信心 |
|---|---|---|---|
| Metal oxygen | 2 | 2 | 1.0 |
| Methoxy (OCH3) | 2 | 2 | 1.0 |
| Methacrylate | 2 | 2 | 1.0 |
| C-O single bond | 2 | 2 | 1.0 |
| Acetate | 2 | 2 | 1.0 |
| Borate | 1 | 1 | 1.0 |
| Alkyl C-H | 1 | 1 | 1.0 |
| N n bond | 1 | 1 | 1.0 |
排名反映累積的文獻證據,而非單一權威規則。請務必根據您的樣品背景進行確認。
可能的材料
| 材料 | 支持峰 | 重疊基團 | 引用來源 |
|---|---|---|---|
| PVA | 486, 1660, 2930 | Methacrylate, C-O single bond, Methoxy (OCH3) | 1 |
僅當同一文獻庫支援此波段以及至少一個額外特徵峰時,才會顯示材料。
光譜邏輯
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 486 cm⁻¹ is usually not enough for material identification by itself.
實際使用
此類查詢常見於聚合物鑑別、未知塑膠篩選、品管故障排除、再生材料驗證,以及基於文獻的峰值歸屬審查。
常見錯誤
- 將一個孤立的譜帶視為材料的證據,而未檢查至少一兩個支持峰。
- 忽略重疊:多個官能團可能在相同波數附近貢獻。
- 當添加劑、混合物、氧化或污染物可能扭曲譜圖時,跳過驗證。
驗證建議
當仍然存在歧義時,使用DSC、GC-MS或TGA驗證假設,特別是對於混合物、降解樣品和填充聚合物。
這些指派背後的文獻
-
N n bond 信心 1.0
“(n n cm-1 845 and 971 and are due to stretching vibrations of SiO and 3) and bands at 486 and N 4 1 A (n n cm-1 682 are due to bending vibrations of O-Si-O and 4) [30, 31].”
Driving the photoluminescent and structural properties of X2-Y2SiO5 by varying the dopant Dy3+ concentration towards cool wLED applications DOI: 10.1016/j.solidstatesciences.2017.05.008 -
Alkyl C-H 信心 1.0
“stretching and the N-H amines group was observed in peak assigned at 1516-1616 The 485 presence of cell wall polysaccharide (C-H) due to aliphatic stretching was observed at peak 1442 486 cm-1.”
Singh 等 - 2017 - Comprehensive characterization of lignocellulosic DOI: 10.1016/j.renene.2016.11.039 -
信心 1.0
“The two peaks located at 486 and 592 may be The absorbance (A) of the various PVA-ZnO nanocomascribed to the defects of the oxygen atom for ZnO NPs or posites versus the incident wavelength is shown in Fig.”
Improvement of Optical Properties of Functionalized Polyvinyl Alcohol-Zinc Oxide Hybrid Nanocomposites for Wide UV Optoelectronic Applications DOI: 10.1007/s10904-023-02616-w -
信心 1.0
“Prominent Raman shifts of norfloxacin 1500-1450 O-C-O group of acid υ stretching vibration of s 485.6 Strong δ aliphatic chain and C-N the O-C-O group”
Sahoo 等 - 2012 - FTIR and Raman Spectroscopic Investigations of a N DOI: 10.4103/0975-1483.100017 -
信心 1.0
“The Raman band at 486 and 498 are the 3, s(O-C-O) mode in the lead oxalate, the 854 cm-1 cm-1 cm-1 ν ν(C-C), ν ν and 891 band are assigned to the 2, 1436 and 1478 are assigned to the 1, s(C-O), and”
Removal mechanism of Pb(II) by Penicillium polonicum: immobilization, adsorption, and bioaccumulation DOI: 10.1038/s41598-020-66025-6 -
信心 1.0
“The band at 486 corresponds to the Cu-O stretching vibration.”
Ultrahigh-Pressure Preparation and Catalytic Activity of MOF-Derived Cu Nanoparticles DOI: 10.3390/nano11041040 -
信心 1.0
“cm-1, cm-1, cm-1 cm-1 While, Ag NPs showed peaks at 486 1,309 2,340 and 3,714 and matched well with the published literature (Rashmi et al., 2020).”
Augmented anticancer effect and antibacterial activity of silver nanoparticles synthesized by using Taxus wallichiana leaf extract DOI: 10.7717/peerj.14391 -
Borate 信心 1.0
“3 cm-1 877, 1012, and 1274 cm-1, where peaks at 258, 271, 391, 408, 425, 648, 854, 877 cm-1 are assigned to BO3 peaks at 486, 1012, 1274 are assigned to BO [24-28].”
Development of FTIR Spectroscopy Methodology for Characterization of Boron Species in FCC Catalysts DOI: 10.3390/catal10111327
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