Sulfur mononitride

Sulfur mononitride

Wireframe model of sulfur mononitride Spacefill model of sulfur mononitride
Names
Preferred IUPAC name sulfur mononitride
Systematic IUPAC name Azaniumylsulfanidylidyne
Other names Aminiosulfanidylidyne Thionitroso radical Thionitrosyl radical
Identifiers
CAS Number	12033-56-6
3D model (JSmol)	Interactive image
Abbreviations	(NS)(.)
ChEBI	CHEBI:29451
ChemSpider	4576119
Gmelin Reference	660
PubChem CID	5463441
CompTox Dashboard (EPA)	DTXSID50923331
InChI InChI=1S/H3NS/c1-2/h1H3 Key: ZGSDJMADBJCNPN-UHFFFAOYSA-N
SMILES [N+] [S-]
Properties
Chemical formula	NS
Molar mass	46.07 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Sulfur mononitride is an inorganic compound with the molecular formula SN. It is the sulfur analogue of and isoelectronic to the radical nitric oxide, NO. It was initially detected in 1975, in outer space in giant molecular clouds and later the coma of comets. This spurred further laboratory studies of the compound. Synthetically, it is produced by electric discharge in mixtures of nitrogen and sulfur compounds, or combustion in the gas phase and by photolysis in solution.

Synthesis

The NS radical is a highly transient species, with a lifetime on the order of milliseconds, but it can be observed spectroscopically over short periods of time through several methods of generation. NS is too reactive to isolate as a solid or liquid, and has only been prepared as a vapor in low pressure or low-temperature matrices due to its tendency to rapidly oligomerize to more stable, diamagnetic species.

Discharge of nitrogen and sulfur vapor

Transmission of electric discharge through a glass tube with quartz windows containing a mixture of nitrogen and sulfur vapor (rigorously free of oxygen) results in the spectrum of emitted light gaining bands consistent with the formation of NS.

Passing a mixture of gaseous N₂ and S₂Cl₂ through the side arm of an absorption cell undergoing microwave discharge produces NS. Infrared diode laser spectroscopy taken using this method allowed for derivation of the equilibrium rotational constant, and therefore calculation of the equilibrium bond length as 1.4940 Å.

With low pressure microwave discharge of elemental nitrogen and sulfur, followed by low temperature trapping in argon matrices, one obtains a mixture of products including NS, NNS, SNS, and NSS. By adding excess sulfur, SSNS is also produced.

Burning of sulfur and nitrogen doped flames

Methane was premixed with fuel in the form of either O₂, N₂O, or air and burned at ambient pressure. The source of nitrogen was introduced by addition of 1-5 mole% NH₃ gas and sulfur by 0.01-0.5 mol% H₂S or SF₆ gas. A steady state concentration of NS within the flame front is observed by laser-induced fluorescence (LIF) spectrum.

Flash laser photolysis of tetranitrogen tetrasulfide

The NS radical was detected by LIF spectrum as the product of photolysis of tetranitrogen tetrasulfide (N₄S₄) gas by a 248 nm laser.

Flash and continuous photolysis of Cr(CH₃CN)₅(NS)²⁺

Aerated solutions of Cr(CH₃CN)₅(NS)²⁺ are highly photoactive and prone to rapid decomposition. Deaerated solutions of Cr(CH₃CN)₅(NS)²⁺ in acetonitrile are stable as long as they are kept in the dark. Continuous photolysis using 366 nm light is slow, while using a 355 nm pulsed laser results in faster labilization of NS.

Reactivity

Oligomerization

Evidence suggests that NS can react with itself to reach N₂S₂, N₄S₄, and polymers of the form (NS)_x. (NS)_x forms from polymerization of cyclo-N₂S₂.

cyclo-N₂S₂.

N₄S₄.

(NS)_x polymer.

Trans-NSSN results from direct dimerization of NS.

N₃S₃ has been observed through photoelectron spectroscopy of vapors of the (SN)_x, polymer, but has not yet been characterized further. Attempts to produce N₃S₃ by oxidation of [PPN] [S₃N₃] were unsuccessful. Its theorized that rapid dimerization to (N₃S₃)₂ will disproportionate irreversibly to N₄S₄ and N₂S₂.

N₃S₃.

Products of decay with NO₂

The radical decay time of NS alone is on the order of 1-3 ms. As evident by no change to this decay time upon addition of NO or O₂ at ambient temperatures, the NS radical is unreactive with NO and O₂. However, rapid, first-order decay is observed with the addition of NO₂. This reaction is proposed to proceed through various intermediates, ultimately reaching final products of N₂ and SO₂. This rapid reaction occurs with a rate constant of k = (2.54 ± 0.12) × 10⁻¹¹ cm³ molecules⁻¹ s⁻¹ at 295 K. By use of Density Functional Theory based computational calculations, the minima and transition states of the potential energy surface of this reaction have been predicted.

Astronomical reactivity

Within the inner coma of comets, many reactions are theorized to be relevant to the formation and reactivity of the NS radical.

Metal-thionitrosyl complexes

As a ligand, NS acts as a σ-donor and π-acceptor, forming metal-thionitrosyl complexes. Transition-metal thionitrosyl complexes have been prepared by the following procedures:

• Sulfur transfer to metal nitrido complexes
  • Example: Reflux of (Ph₄P)[OsNCl₄] and (Ph₄P)NCS yields green-brown solid [Ph₄P]₂[Os(NS)(NCS)₅]
• Reaction of trithiazyltrichloride with transition metal complexes
  • NSCl₃ + OsCl₃ > [Os(NS)Cl₃]
• Halide abstraction from coordinated thiazyl complexes
  • Abstraction of sulfur-bonded fluorine from [(η⁵_-C₅H₅)Cr(NO)₂(NSF)]-[AsF₆] by AsF₅ > [(η⁵-C₅H₅)Cr(NO)₂(NS)]-[AsF₆]₂
• Reaction of NS⁺ salts with transition metal complexes
  • NS⁺SbF₆⁻ + [M(CO)₅Br] > [M(CO)₅(NS)]²⁺, M=Mn, Re
  • NS⁺AsF₆⁻ + [(η⁵-C₅H₅)Fe(CO)₂(SO₂)]⁺ > [(η⁵-C₅H₅)Fe(CO)₂(NS)] [AsF₆]₂
• Reaction of tetrasulfur tetranitride with metal halides or nitrides

From X-ray crystallography of many of such metal-thionitrosyl complexes, one can observe that the M-N-S bond angle is nearly linear, suggesting sp hybridization about N. Short M-N distances and long N-S distances reflect the resonance structure of M=N=S having greater contribution than M-N≡S.

Typical v(NS) IR stretching frequencies are approximately 1065 cm⁻¹ for low-valent transition metal complexes and around 1390 cm⁻¹ in the high valent cases, whereas the free gas-phase radical exhibits a 1204 cm⁻¹ signal.

Electronic structure of Fe(S₂CNMe₂)₂(NS)

The electronic structures of Fe(S₂CNMe₂)₂(NE), where E=O, S, or Se were calculated using Density Functional Theory methods. It was found that the large Mulliken spin density remained concentrated on the Fe(NE) core and Fe-N distances experienced little change from the chalcogen atom used. The HOMO of both nitrosyl and thionitrosyl complexes retained 1a₁ (d_z²) character. The small changes in the energies of the spin orbitals of the complexes, particularly the decreased energetic gap between 2b₂ and 1b₁ and 2b₁ and 1b₁ orbitals is attributed to NS being a weaker π-acceptor than NO.

Photoinduced NS transfer from chromium to iron

When a spin-trapping agent, such as Fe(S₂CNEt₂)₂ is present during the photolysis of Cr(CH₃CN)₅(NS)²⁺, new S=1/2 EPR bands are observed, attributed to the formation of Fe(S₂CNEt₂)₂(NS), and the signal from Cr(CH₃CN)₅(NS)²⁺ disappears. This suggests that the NS radical has transferred from the chromium complex to the iron complex.

NS in situ transfer from chromium to iron.

This was particularly significant as it was the first controlled and well-characterized reactivity of NS in solution. Further, it showed the potential for similar reactivity in known reactions with NO, such as use of this iron dithiocarbamate complex.

Bonding

Model of bonding in the NS radical

The valence electrons of this compound match those of nitric oxide. Sulfur mononitride can be described as some average of a set of resonance structures. The singly bonded structure (first resonance structure shown) has little contribution. The formal bond order is considered to be 2.5.

Resonance structures of NS.

Molecular orbital diagram of NS.

Versus NO

The decreasing electronegativity with increasingly heavy chalcogenides leads to a reversal of the dipole. In NO, oxygen is the more electronegative element. In NS, nitrogen is more electronegative. The NS radical is significantly more unstable and prone to catenation than NO.

Comparison of physical properties of nitrogen chalcogenide radicals

	NO	NS	NSe
△fH°, kJ·mol−1	+90.24	+283.4	-
△fG°, kJ·mol−1	+86.57	+217.2	-
S° 273, J/deg	+207.5/273 K	+222.093/298 K	-
B.D.E.	627.6	463±24	370 Cal
d(N-E), Å	1.1517	1.4938	1.6634
Bond order	2.5	2.5	2.5

In astronomy

Molecules in distant astronomical regions can be identified based on their unique rotational transitions, of which the corresponding microwave frequencies are detectable by antennae on Earth. The presence of interstellar sulfur mononitride was first reported in 1975 by back to back letters published in the Astrophysical Journal.

Interstellar NS was first identified in the giant molecular cloud Sagittarius B2 (Sgr B2). Its presence was reported in two concurrent articles. Measurements conducted with the National Radio Astronomy Observatory telescope at Kitt Peak, Arizona, picked up millimeter-wavelength radiation in Sgr B2 attributed to c-state transitions of NS in the ²Π_1/2 state from J=5/2 to J=3/2 at 115.16 GHz. This assignment was confirmed by measurements conducted at University of Texas Millimeter Wave Observatory on Mount Locke as well, demonstrating J=5/2 to J=3/2 c-state and d-state transitions at 115.16 GHz and 115.6 GHz, respectively. Hyperfine interactions arise from ¹⁴N magnetic and electric-quadrupole moments.

NS has been detected in regions responsible for forming massive stars, such as giant molecular clouds like Sg B2 and cold, dark clouds such as L134N and TMC-1. One survey found NS in 12 out of 14 GMC studied, additionally observing the J=7/2 to J=5/2 and J=3/2 to J=1/2 transitions at 161 and 69 GHz, respectively. The abundance of NS in these regions was approximated based on the ratio of observed to intrinsic hyperfine line strengths as well as modeling using a statistical equilibrium program, finding low abundance in all except the Orion molecular cloud.

NS was also observed in the coma of the comets Hyakutake and Hale-Bopp. It's believed that the observed abundance is higher than gas-phase, ion-molecule models due to an unidentified species X-NS photo-dissociating to release NS.

Industrial applications

Detection of NS at steady state concentration in the reaction zone of the combustion of methane doped with ammonia and a fuel sulfur such as H₂S suggests that NS may be an important reactive intermediate in burning of hydrocarbon flames in a reducing atmosphere, which is relevant to coal pyrolysis and combustion.

Fossil fuels contain bound nitrogen, which releases elevated levels of nitric oxide emissions during combustion. NO_x emissions can be controlled by denitrification of the fuel source, combustion chamber modification, or both. One developing technique is the reburning of NO_x, which is reduced to N₂. These fuels also contain variable amounts of sulfur, which is oxidized to SO₂. Therefore, understanding the reactivity of NO and SO₂ is crucial to the process of reburning. The experimental apparatus to test this involved a primary flame for producing combustion products, which were mixed with NO and SO₂ to mimic coal burning byproducts. This mixture was fed into the burner at atmospheric pressure. 1-2% decrease in NO_x concentration is observed at various percentages of total fuel inlet (reburn ratio) in the presence of 0.1% SO₂, which is attributed to the formation of H₂S, HS, and the resulting reaction with NO, giving rise to NS. Reaction: HS + NO > NS + OH.

Related compounds

• Trithiazyl trichloride (NSCl)₃
• Sulfur nitride