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The spectrum is most consistent with a material that combines aromatic rings and methacrylate/ester functionalities, together with amide, hydroxyl, and amine/ammonium groups. The overall pattern points to an organic substance containing phenyl or aromatic moieties linked via ester-type C–O bonds and hydrogen‑bonded O–H/N–H environments, rather than a single well‑defined library compound FTIR In-Depth Interpretation was not selected for this task, so this section shows the library-search result only and no deep AI interpretation was run.
Recommended next steps: Acquire a higher‑resolution spectrum and, if possible, an attenuated total reflectance (ATR) or transmission spectrum with extended signal averaging to detect weak carbonyl bands and to resolve C–H stretching patterns characteristic of aromatic vs. aliphatic substitution. Perform complementary analyses such as NMR (¹H, ¹³C), Raman spectroscopy, or pyrolysis‑GC‑MS to identify the specific monomer units and confirm the aromatic/methacrylate composition. If ozone is suspected from the library match, rule out the presence of ozone gas by headspace analysis or by noting that the sample was condensed‑phase, making the ozone assignment spurious. Compare the spectrum against reference spectra of known methacrylate copolymers (e.g., poly(methyl methacrylate‑C-O‑styrene), aromatic polyesters, or aromatic amide‑containing polymers) to narrow the structural possibilities.
| Rank | Match % | Compound | SMILES | Spectrum No. | Action |
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FTIR.fun
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tem.csv
en&2