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Results20260211032335139761447 ir_****.pdf HK

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FTIR Spectrum Interpretation Summary

Comparative Analysis Conclusion

AI-assisted Interpretation Conclusion

**Data → Analysis → Conclusions/Inferences**

**Data:**
The provided FTIR spectrum exhibits numerous absorption peaks across the fingerprint region (660-1900 cm⁻¹), the C-H stretching region (~2872-2968 cm⁻¹), and the high-frequency region (~3726-3992 cm⁻¹). The most prominent feature is a very strong, sharp peak at 1767 cm⁻¹. Other notable peaks include a medium broad peak at 903 cm⁻¹, a medium broad peak at 951 cm⁻¹, and a cluster of weak, sharp peaks between 1712-1900 cm⁻¹. Several weak, sharp peaks are present in the 3726-3817 cm⁻¹ range.

**Analysis:**
* **Peak at 1767 cm⁻¹ (Strong, Sharp):** This is the dominant feature. Its position and sharpness are characteristic of a carbonyl (C=O) stretching vibration. The high intensity suggests a high concentration or a strongly absorbing carbonyl group. The specific position is typical for a five-membered cyclic anhydride (succinic anhydride-type, ~1840 & ~1780 cm⁻¹ for asymmetric/symmetric stretches) or a saturated aliphatic ester (~1740-1750 cm⁻¹). The exact value of 1767 cm⁻¹ is slightly high for a simple ester but aligns well with the higher-frequency component (symmetric stretch) of a cyclic anhydride.
* **Peaks between 1712-1900 cm⁻¹ (Weak, Sharp/Broad):** This cluster includes peaks at 1712, 1820, 1836 (broad), 1867, and 1900 cm⁻¹. The peak at 1712 cm⁻¹ could be attributed to a second, possibly conjugated or carboxylic acid carbonyl. The series of peaks above 1800 cm⁻¹ is highly indicative of the characteristic pattern for **cyclic anhydrides**, which typically show two C=O stretches: an asymmetric stretch at higher wavenumber (~1820-1850 cm⁻¹) and a symmetric stretch at lower wavenumber (~1750-1780 cm⁻¹). The presence of multiple weak peaks in this region may suggest a mixture, Fermi resonance, or the presence of different anhydride environments.
* **Peaks in 3726-3817 cm⁻¹ region (Weak, Sharp):** These are characteristic of free, non-hydrogen-bonded O-H stretching vibrations. In the context of other peaks, these likely indicate isolated silanol (Si-OH) groups or possibly very dilute, free alcohol/phenol O-H, though the former is more common in this precise wavenumber range for surface species.
* **Peaks at 2872, 2891, 2951 (broad), 2968 (broad) cm⁻¹:** These correspond to C-H stretching vibrations: ~2872-2891 cm⁻¹ (symmetric CH₃/CH₂), ~2951-2968 cm⁻¹ (asymmetric CH₃).
* **Peaks at 1627, 1637, 1649 (broad) cm⁻¹:** These could be attributed to C=C stretching (alkene, possibly conjugated) and/or adsorbed water (H-O-H bending ~1640 cm⁻¹). The weak, sharp nature leans more towards C=C.
* **Peak at 1562 cm⁻¹ (Weak, Sharp):** Possibly C=C stretching in an aromatic ring or C=O of a carboxylate anion (asymmetric stretch).
* **Peaks at 1387, 1395, 1407 cm⁻¹:** Often associated with O-H in-plane bending (of carboxylic acids) or CH deformation vibrations.
* **Peaks in 1000-1300 cm⁻¹ region:** A complex fingerprint region with multiple weak peaks (e.g., 1044, 1076, 1126, 1214, 1228, 1279 cm⁻¹). These are consistent with C-O stretching vibrations (esters, anhydrides, alcohols) and C-C skeletal vibrations.
* **Peaks below 1000 cm⁻¹ (660-968 cm⁻¹):** Several weak, broad peaks. These are in the region for C-H out-of-plane bending (for alkenes/aromatics) and possibly Si-O or M-O (metal-oxygen) vibrations if inorganic components are present.

**Conclusions/Inferences:**
1. **Primary Component:** The spectrum is **dominated by a cyclic aliphatic anhydride** functional group. This is conclusively indicated by the very strong carbonyl stretch at 1767 cm⁻¹ coupled with the characteristic weaker peaks in the 1820-1867 cm⁻¹ region, which form the classic doublet for cyclic anhydrides.
2. **Other Functional Groups Present:**
* **Aliphatic Hydrocarbons:** Confirmed by C-H stretches (~2872-2968 cm⁻¹).
* **Isolated Silanol (Si-OH) Groups or Free O-H:** Indicated by sharp peaks in the 3726-3817 cm⁻¹ range. **[Inference:** The precise wavenumbers are highly typical for surface silanols on silica or silicate materials.**]**
* **C=C Bonds:** Likely present (peaks ~1627-1649 cm⁻¹), possibly in an alkene or as part of an unsaturated anhydride derivative.
* **C-O Bonds:** Multiple absorptions in the 1000-1300 cm⁻¹ region confirm C-O-C linkages from the anhydride and possibly other esters/ethers.
3. **[Inference on Sample Nature:** Based on the co-existence of a strong cyclic anhydride pattern and

This discussion presents an infrared spectral analysis combining automated interpretation with reference comparison to support functional group identification and structural assessment.

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