Nitric oxide

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Gas phase thermochemistry data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Quantity Value Units Method Reference Comment
Δfgas90.29kJ/molReviewChase, 1998Data last reviewed in June, 1963
Quantity Value Units Method Reference Comment
gas,1 bar210.76J/mol*KReviewChase, 1998Data last reviewed in June, 1963

Gas Phase Heat Capacity (Shomate Equation)

Cp° = A + B*t + C*t2 + D*t3 + E/t2
H° − H°298.15= A*t + B*t2/2 + C*t3/3 + D*t4/4 − E/t + F − H
S° = A*ln(t) + B*t + C*t2/2 + D*t3/3 − E/(2*t2) + G
    Cp = heat capacity (J/mol*K)
    H° = standard enthalpy (kJ/mol)
    S° = standard entropy (J/mol*K)
    t = temperature (K) / 1000.

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Temperature (K) 298. to 1200.1200. to 6000.
A 23.8349135.99169
B 12.588780.957170
C -1.139011-0.148032
D -1.4974590.009974
E 0.214194-3.004088
F 83.3578373.10787
G 237.1219246.1619
H 90.2911490.29114
ReferenceChase, 1998Chase, 1998
Comment Data last reviewed in June, 1963 Data last reviewed in June, 1963

Phase change data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: William E. Acree, Jr., James S. Chickos

Enthalpy of vaporization

ΔvapH (kJ/mol) Temperature (K) Method Reference
13.8212.CJohnston and Giauque, 1929

Reaction thermochemistry data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled as indicated in comments:
M - Michael M. Meot-Ner (Mautner) and Sharon G. Lias
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. A general reaction search form is also available. Future versions of this site may rely on reaction search pages in place of the enumerated reaction displays seen below.

Individual Reactions

Nitric oxide anion + Nitric oxide = (Nitric oxide anion • Nitric oxide)

By formula: NO- + NO = (NO- • NO)

Quantity Value Units Method Reference Comment
Δr57.7kJ/molPILinn, Ono, et al., 1981gas phase; M
Δr56.9kJ/molPINg, Tiedemann, et al., 1977gas phase; M

Free energy of reaction

ΔrG° (kJ/mol) T (K) Method Reference Comment
29.296.SAMSPuckett and Teague, 1971gas phase; M

(Nitric oxide anion • Nitric oxide) + Nitric oxide = (Nitric oxide anion • 2Nitric oxide)

By formula: (NO- • NO) + NO = (NO- • 2NO)

Quantity Value Units Method Reference Comment
Δr31.kJ/molPILinn, Ono, et al., 1981gas phase; M

Free energy of reaction

ΔrG° (kJ/mol) T (K) Method Reference Comment
7.9296.SAMSPuckett and Teague, 1971gas phase; M

(Nickel ion (1+) • Nitric oxide) + Nitric oxide = (Nickel ion (1+) • 2Nitric oxide)

By formula: (Ni+ • NO) + NO = (Ni+ • 2NO)

Enthalpy of reaction

ΔrH° (kJ/mol) T (K) Method Reference Comment
115. (+5.0,-0.) CIDKhan, Steele, et al., 1995gas phase; guided ion beam CID; M

Nickel ion (1+) + Nitric oxide = (Nickel ion (1+) • Nitric oxide)

By formula: Ni+ + NO = (Ni+ • NO)

Enthalpy of reaction

ΔrH° (kJ/mol) T (K) Method Reference Comment
123. (+6.7,-0.) CIDKhan, Steele, et al., 1995gas phase; guided ion beam CID; M

(Nitric oxide anion • 2Nitric oxide) + Nitric oxide = (Nitric oxide anion • 3Nitric oxide)

By formula: (NO- • 2NO) + NO = (NO- • 3NO)

Quantity Value Units Method Reference Comment
Δr15.kJ/molPILinn, Ono, et al., 1981gas phase; M

(Nitric oxide anion • 3Nitric oxide) + Nitric oxide = (Nitric oxide anion • 4Nitric oxide)

By formula: (NO- • 3NO) + NO = (NO- • 4NO)

Quantity Value Units Method Reference Comment
Δr15.kJ/molPILinn, Ono, et al., 1981gas phase; M

(Nitric oxide anion • 4Nitric oxide) + Nitric oxide = (Nitric oxide anion • 5Nitric oxide)

By formula: (NO- • 4NO) + NO = (NO- • 5NO)

Quantity Value Units Method Reference Comment
Δr9.6kJ/molPILinn, Ono, et al., 1981gas phase; M

Ethyl-nitrite- = Nitric oxide + Ethoxy radical

By formula: C2H5NO2 = NO + C2H5O

Quantity Value Units Method Reference Comment
Δr158.kJ/molKinRebbert and Laidler, 1952gas phase; ALS

IR Spectrum

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Coblentz Society, Inc.

Gas Phase Spectrum

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IR spectrum
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Notice: Except where noted, spectra from this collection were measured on dispersive instruments, often in carefully selected solvents, and hence may differ in detail from measurements on FTIR instruments or in other chemical environments. More information on the manner in which spectra in this collection were collected can be found here.

Notice: Concentration information is not available for this spectrum and, therefore, molar absorptivity values cannot be derived.

Additional Data

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Owner COBLENTZ SOCIETY
Collection (C) 2018 copyright by the U.S. Secretary of Commerce
on behalf of the United States of America. All rights reserved.
Origin WYANDOTTE CHEMICALS CORP., WYANDOTTE, MICHIGAN, USA
Source reference COBLENTZ NO. 1000
Date 1960
State GAS; $$ MATHESON CO. 99% PURE
Instrument Not specified, most likely a prism, grating, or hybrid spectrometer.
Path length 500 CM
Resolution 4
Sampling procedure TRANSMISSION
Data processing DIGITIZED BY NIST FROM HARD COPY

This IR spectrum is from the Coblentz Society's evaluated infrared reference spectra collection.


Mass spectrum (electron ionization)

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Spectrum

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Mass spectrum
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Additional Data

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Owner NIST Mass Spectrometry Data Center
Collection (C) 2014 copyright by the U.S. Secretary of Commerce
on behalf of the United States of America. All rights reserved.
NIST MS number 31

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References

Go To: Top, Gas phase thermochemistry data, Phase change data, Reaction thermochemistry data, IR Spectrum, Mass spectrum (electron ionization), Notes

Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Chase, 1998
Chase, M.W., Jr., NIST-JANAF Themochemical Tables, Fourth Edition, J. Phys. Chem. Ref. Data, Monograph 9, 1998, 1-1951. [all data]

Johnston and Giauque, 1929
Johnston, H.L.; Giauque, W.F., THE HEAT CAPACITY OF NITRIC OXIDE FROM 14°K. TO THE BOILING POINT AND THE HEAT OF VAPORIZATION. VAPOR PRESSURES OF SOLID AND LIQUID PHASES. THE ENTROPY FROM SPECTROSCOPIC DATA, J. Am. Chem. Soc., 1929, 51, 11, 3194-3214, https://doi.org/10.1021/ja01386a004 . [all data]

Linn, Ono, et al., 1981
Linn, S.H.; Ono, Y.; Ng, C.Y., Molecular Beam Photoionization Study of CO, N2, and NO Dimers and Clusters, J. Chem. Phys., 1981, 74, 6, 3342, https://doi.org/10.1063/1.441486 . [all data]

Ng, Tiedemann, et al., 1977
Ng, C.Y.; Tiedemann, P.W.; Mahan, B.H.; Lee, Y.T., The Binding Energy between NO and NO+, J. Chem. Phys., 1977, 66, 9, 3985, https://doi.org/10.1063/1.434450 . [all data]

Puckett and Teague, 1971
Puckett, L.J.; Teague, A.W., Production of H3O+.nH2O from NO+ Precursor in NO - H2O Gas Mixtures, J. Chem. Phys., 1971, 54, 6, 2564, https://doi.org/10.1063/1.1675213 . [all data]

Khan, Steele, et al., 1995
Khan, F.A.; Steele, D.L.; Armentrout, P.B., Ligand effects in organometallic thermochemistry: The sequential bond energies of Ni(CO)x+ and Ni(N2)x+ (x = 1-4) and Ni(NO)x+ (x = 1-3) [Data derived from reported bond energies taking value of 8.273±0.046 eV for IE[Ni(CO)4]], J. Phys. Chem., 1995, 99, 7819. [all data]

Rebbert and Laidler, 1952
Rebbert, R.E.; Laidler, K.J., Kinetics of the decomposition of diethyl peroxide, J. Chem. Phys., 1952, 20, 574-577. [all data]


Notes

Go To: Top, Gas phase thermochemistry data, Phase change data, Reaction thermochemistry data, IR Spectrum, Mass spectrum (electron ionization), References