What absorbs at 1313 cm⁻¹ in an FTIR spectrum?
Et bånd nær 1313 cm⁻¹ kan peke på flere funksjonelle grupper. Nedenfor er de mest sannsynlige tildelingene, rangert etter hvor mye publiserte bevis som støtter hver — hver enkelt sporbar til litteratur (DOI) og kryssvalidert mot våre 130 000+ referansespektre og kunnskapsgraf.
Backed by 8 cited sources
Raskt svar
A band near 1313 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.
Mulige funksjonelle gruppe-tilordninger
| Funksjonell gruppe | Støttende fakta | Siterte kilder | Toppkonfidens |
|---|---|---|---|
| N h | 5 | 5 | 1.0 |
| Secondary amine | 4 | 3 | 1.0 |
| Amide | 4 | 3 | 1.0 |
| C-O single bond | 3 | 3 | 1.0 |
| C n single bond | 3 | 2 | 1.0 |
| Methoxy (OCH3) | 2 | 2 | 1.0 |
| Methacrylate | 2 | 2 | 1.0 |
| Acetate | 2 | 2 | 1.0 |
| Carboxyl (COOH) | 1 | 1 | 1.0 |
| Ammonium | 1 | 1 | 1.0 |
| Ring structure | 1 | 1 | 1.0 |
| N eq o | 1 | 1 | 1.0 |
| Alkene (C=C) | 1 | 1 | 1.0 |
| Aromatic ring | 1 | 1 | 1.0 |
| Hydroxyl (O-H) | 1 | 1 | 1.0 |
| N c o | 1 | 1 | 1.0 |
| C c single bond | 1 | 1 | 0.8 |
Rangeringen gjenspeiler akkumulert litteraturbevis, ikke en enkelt autoritativ regel. Bekreft alltid mot prøvekonteksten din.
Mulige materialer
| Materiale | Støttetopper | Overlappende grupper | Siterte kilder |
|---|---|---|---|
| saliva | 1313, 1648, 1664 | Amide, C-O single bond | 1 |
| hydrogel | 1313, 1632, 1062 | Amide, N h | 1 |
Materialer vises kun når samme litteraturbase støtter dette båndet og minst en annen karakteristisk topp.
Spektrum-logikk
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 1313 cm⁻¹ is usually not enough for material identification by itself.
Virkelig bruk
Denne typen forespørsel er vanlig i polymeridentifikasjon, screening av ukjent plast, feilsøking i kvalitetskontroll, verifisering av resirkulert materiale og litteraturstøttet gjennomgang av topptilordning.
Vanlige feil
- Behandle ett isolert bånd som bevis på et materiale uten å sjekke minst en eller to støttende topper.
- Ignorerer overlapping: flere funksjonelle grupper kan bidra nær samme bølgetall.
- Hopp over validering når tilsetningsstoffer, blandinger, oksidasjon eller forurensning kan forvrenge spekteret.
Verifiseringsråd
Når tvetydighet gjenstår, valider hypotesen med DSC, GC-MS eller TGA, spesielt for blandinger, nedbrutte prøver og fylte polymerer.
Litteratur bak disse tilordningene
-
konfidens 1.0
“The peak observed at 1313 is due to the presence of N-H vibration.”
Rajendra 等 - 2018 - Luminescence properties of dysprosium doped YVO4 p DOI: 10.1016/j.jre.2018.07.001 -
Amide konfidens 1.0
“amide III band (1313 which contains information C-N C-O N-H Based on this work, however, spectral analysis of the regarding the and stretching and the and cm-1”
Shi 等 - 2018 - Biochemical alterations of Candida albicans during DOI: 10.1039/c8an01452c -
C-O single bond konfidens 1.0
“cm-1 Pure PVA absorption maxima at 1313 and 1410 have been ascribed to C-OH cm-1 Pure PVA absorption maxima at 1313 and 1410 cm-1 have been ascribed to C-OH plane bending and CH wagging, respectively [35].”
Innovative Green Chemistry Approach to Synthesis of Sn2+-Metal Complex and Design of Polymer Composites with Small Optical Band Gaps DOI: 10.3390/molecules27061965 -
Amide konfidens 1.0
“methyl groups of proteins (1452 amide III band components of proteins (1313 cm-1) mannose-6-phosphate and phosphorylated saccharide residue (1120 and C conforma2”
Salivary molecular spectroscopy: A sustainable, rapid and non-invasive monitoring tool for diabetes mellitus during insulin treatment DOI: 10.1371/journal.pone.0223461 -
Aromatic ring konfidens 1.0
“The appearance of characteristic cm-1 tions of sulfanilamide aromatic ring C=C bond, two high intensity, sharp bands at 1313 bands in the spectrum of hydrogel with incorporated sulfanilamide at 1599 and cm-1, and 1154 cm-1, originating from”
Modified Sulfanilamide Release from Intelligent Poly(N-isopropylacrylamide) Hydrogels DOI: 10.3390/pharmaceutics15061749 -
Acetate konfidens 1.0
“FTIR and NMR analysis cm-1 cm-1 2DCTZ showed bands at 3310 (N-H broad stretches), 2531 The FTIR data of H 1710cm-1 1313cm-1(C-O cm-1 (COOH stretch), (C=O stretch), stretch), 1320, 1197 (=C-N), cm-1 [Error! Bookmark not defined.].”
Jaiswal 等 - 2015 - Protective properties of functionalised tetrazine DOI: 10.1016/j.matchemphys.2015.07.029 -
N eq o konfidens 1.0
“The peaks at 1490 and 1313 cm-1 are attributed to the N=O stretching vibrations of the coordinated nican be assigned to Zntrate group and the nitrate ion, respectively.”
Deposition of Zinc Oxide Coatings on Wood Surfaces Using the Solution Precursor Plasma Spraying Process DOI: 10.3390/coatings11020183 -
Ring structure konfidens 1.0
“cm-1 The C-C and C-N ring stretching bands were moved to 1380 and 1308 cm-1 for U(VI) and 1738, 1420, 1378, and 1313 for Th(IV), whereas, the ring bending vibration was shifted to 817 for U(VI) cm-1 1378, and 1313 cm-1 for Th(IV), whereas,”
Salah 等 - 2019 - The Removal of Uranium and Thorium from Their Aque DOI: 10.3390/min9100626
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