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An infrared spectroscopy correlation table (or table of infrared absorption frequencies) is a list of absorption peaks and frequencies, typically reported in wavenumber, for common types of molecular bonds and functional groups.
The two isomers can be distinguished by UV-Vis spectroscopy. Absorbance maxima for the nitro isomer occur at 457.5, 325, and 239 nm. The nitrito has maxima at 486, 330, and 220 nm. [3] Their IR spectra also differ. The nitrito isomer absorbs at 1460 and 1065 cm −1. The nitro isomer absorbs at 1430 and 825 cm −1. [4]
The nitro group is one of the most common explosophores (functional group that makes a compound explosive) used globally. The nitro group is also strongly electron-withdrawing. Because of this property, C−H bonds alpha (adjacent) to the nitro group can be acidic. For similar reasons, the presence of nitro groups in aromatic compounds retards ...
In some complexes, however, especially when back-bonding is less important, the M-N-O angle can strongly deviate from 180°. Linear and bent NO ligands can be distinguished using infrared spectroscopy. Linear M-N-O groups absorb in the range 1650–1900 cm −1, whereas bent nitrosyls absorb in the range 1525–1690 cm −1.
The FT-IR spectra were recorded using a Nicolet 170SX or a JASCO FT/IR-410 spectrometer. For spectra recorded in the Nicolet spectrometer, the data were stored at intervals of 0.5 cm −1 in the 4,000 – 2,000 cm −1 region and of 0.25 cm −1 in the 2,000 – 400 cm −1 region and the spectral resolution was 0.25 cm −1.
Spectrochemistry is the application of spectroscopy in several fields of chemistry. It includes analysis of spectra in chemical terms, and use of spectra to derive the structure of chemical compounds, and also to qualitatively and quantitively analyze their presence in the sample.
It is an unstable nitrogen oxide consisting of a covalent nitrogen–nitrogen bond between a nitro group and an azide group. It has been detected by infrared spectroscopy as a short-lived product of the reaction between sodium azide and nitronium hexafluoroantimonate: [1] The compound quickly decomposes to form nitrous oxide.
An auxochrome is known as a functional group that produces a bathochromic shift, also known as red shift because it increases the wavelength of absorption, therefore moving closer to infrared light. Woodward−Fieser rules estimate the shift in wavelength of maximum absorption for several auxochromes attached to a conjugated system in an ...