Imidogen(Redirected from Nitrogen monohydride)
Imidogen is an inorganic compound with the chemical formula NH. Like other simple radicals, it is highly reactive and consequently short-lived except as a dilute gas. Its behavior depends on its spin multiplicity, i.e. the triplet vs singlet ground state.
3D model (JSmol)
|Molar mass||15.02 g·mol−1|
|21.19 J K−1 mol−1|
|181.22 kJ K−1 mol−1|
Std enthalpy of
|358.43 kJ mol−1|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Production and propertiesEdit
Imidogen has a large rotational splitting and a weak spin-spin interaction, therefore it will be less likely to undergo collision-induced Zeeman transitions. Ground-state imidogen can be magnetically trapped using buffer-gas loading from a molecular beam.
Imidogen is isoelectronic with carbene (CH2) and oxygen (O) atoms, and it exhibits comparable reactivity. The first excited state can be detected by laser-induced fluorescence (LIF). LIF methods allow for detection of depletion, production, and chemical products of NH. It reacts with nitric oxide (NO):
- NH + NO → N2 + OH
- NH + NO → N2O + H
The former reaction is more favorable with a ΔH0 of −408 ± 2 kJ/mol compared to a ΔH0 of −147 ± 2 kJ/mol for the latter reaction.
The trivial name nitrene is the preferred IUPAC name. The systematic names, λ1-azane and hydridonitrogen, valid IUPAC names, are constructed according to the substitutive and additive nomenclatures, respectively.
In appropriate contexts, imidogen can be viewed as ammonia with two hydrogen atoms removed, and as such, azylidene may be used as a context-specific systematic name, according to substitutive nomenclature. By default, this name pays no regard to the radicality of the imidogen molecule. Although, in even more specific context, it can also name the non-radical state, whereas the diradical state is named azanediyl.
Interstellar NH was identified in the diffuse clouds toward Zeta Persei and HD 27778 from high-resolution high S/N spectra of the NH Å 3Pi-X 3Sigma (0,0) absorption band near 3358 Å.A temperature of about 30 K favored an efficient production of CN from NH within the diffuse cloud.
Reactions relevant to astrochemistryEdit
|N + H− → NH + e−||1x10−9||3.5x10−18|
|NH2 + O → NH + OH||2.546x10−13||1.4x10−13|
|NH2+ + e− → NH + H||3.976x10−7||2.19x10−21|
|NH3+ + e− → NH + H + H||8.49x10−7||2.89x10−19|
|NH + N → N2 + H||4.98x10−11||4.36x10−16|
|NH + O → OH + N||1.16x10−11||1.54x10−14|
|NH + C+ → CN+ + H||7.8x10−10||4.9x10−19|
|NH + H3+ → NH2+ + H2||1.3x10−9||3.18x10−19|
|NH + H+ → NH+ + H||2.1x10−9||4.05x10−20|
Within diffuse clouds H− + N → NH + e− is a major formation mechanism. Near chemical equilibrium important NH formation mechanisms are recombinations of NH2+ and NH3+ ions with electrons. Depending on the radiation field in the diffuse cloud, NH2 can also contribute.
NH is destroyed in diffuse clouds by photodissociation and photoionization. In dense clouds NH is destroyed by reactions with atomic oxygen and nitrogen. O+ and N+ form OH and NH in diffuse clouds. NH is involved in creating N2, OH, H, CN+, CH, N, NH2+,NH+ for the interstellar medium.
NH has been reported in the diffuse interstellar medium but not in dense molecular clouds. The purpose of detecting NH is often to get a better estimate of the rotational constants and vibrational levels of NH. It is also needed in order to confirm theoretical data which predicts N and NH abundances in stars which produce N and NH and other stars with left over trace amounts of N and NH. Using current values for rotational constants and vibrations of NH as well as thoxe of OH and CH lets us study the CNO abundances without resorting to a full spectrum synthesis with a 3D model atmosphere.
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