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Spectroscopy can detect a much wider region of the EM spectrum than the visible wavelength range of 400 nm to 700 nm in a vacuum. A common laboratory spectroscope can detect wavelengths from 2 nm to 2500 nm. [1] Detailed information about the physical properties of objects, gases, or even stars can be obtained from this type of device.
For example, a wavenumber in inverse centimeters can be converted to a frequency expressed in the unit gigahertz by multiplying by 29.979 2458 cm/ns (the speed of light, in centimeters per nanosecond); [5] conversely, an electromagnetic wave at 29.9792458 GHz has a wavelength of 1 cm in free space.
The nanometre is often used to express dimensions on an atomic scale: the diameter of a helium atom, for example, is about 0.06 nm, and that of a ribosome is about 20 nm. The nanometre is also commonly used to specify the wavelength of electromagnetic radiation near the visible part of the spectrum: visible light ranges from around 400 to 700 ...
Spatial frequency is a reciprocal length, which can thus be used as a measure of energy, usually of a particle. For example, the reciprocal centimetre, cm −1, is an energy unit equal to the energy of a photon with a wavelength of 1 cm. That energy amounts to approximately 1.24 × 10 −4 eV or 1.986 × 10 −23 J.
10 cm = 1.0 dm – wavelength of the highest UHF radio frequency, 3 GHz; 12 cm = 1.2 dm – wavelength of the 2.45 GHz ISM radio band; 21 cm = 2.1 dm – wavelength of the 1.4 GHz hydrogen emission line, a hyperfine transition of the hydrogen atom; 100 cm = 10 dm – wavelength of the lowest UHF radio frequency, 300 MHz
In the near-infrared range liquid water has absorption bands around 1950 nm (5128 cm −1), 1450 nm (6896 cm −1), 1200 nm (8333 cm −1) and 970 nm, (10300 cm −1). [ 19 ] [ 20 ] [ 15 ] The regions between these bands can be used in near-infrared spectroscopy to measure the spectra of aqueous solutions, with the advantage that glass is ...
1,1-disub. alkenes 1655 medium cis-1,2-disub. alkenes 1660 medium trans-1,2-disub. alkenes 1675 medium trisub., tetrasub. alkenes 1670 weak conjugated C═C dienes 1600 strong 1650 strong with benzene ring 1625 strong with C═O 1600 strong C═C (both sp 2) any 1640–1680 medium aromatic C═C any 1450 weak to strong (usually 3 or 4) 1500 1580
A striking way this was exhibited is that, while mid-IR spectroscopists use wavenumbers (cm −1) when displaying spectra, NIR spectroscopists used wavelength (nm), as is used in ultraviolet–visible spectroscopy.