What absorbs at 1313 cm⁻¹ in an FTIR spectrum?
A band near 1313 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
Ugawaji unaowezekana wa vikundi vya kazi
| Kikundi cha kazi | Ukweli unaounga mkono | Vyanzo vilivyotajwa | Uaminifu wa juu |
|---|---|---|---|
| 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 |
Cheo kinaonyesha ushahidi wa fasihi uliokusanywa, si sheria moja yenye mamlaka. Thibitisha kila mara dhidi ya mazingira ya sampuli yako.
Fasihi nyuma ya ugawaji huu
-
uaminifu 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 uaminifu 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 uaminifu 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 uaminifu 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 uaminifu 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 uaminifu 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 uaminifu 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 uaminifu 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
Una wigo wenye bendi hii?
Pakia wigo wako wa FTIR na upate ripoti kamili ya tafsiri — ugawaji wa vilele na marejeleo ya fasihi, ulinganishaji wa maktaba, na mlolongo wa ushahidi wenye kiwango cha uaminifu — kwa sekunde.
Tafsiri wigo wangu