2-Butynedinitrile
- Formula: C4N2
- Molecular weight: 76.0562
- IUPAC Standard InChIKey: ZEHZNAXXOOYTJM-UHFFFAOYSA-N
- CAS Registry Number: 1071-98-3
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
The 3d structure may be viewed using Java or Javascript. - Other names: Acetylenedicarbonitrile; Dicyanoacetylene; 1,2-Dicyanoacetylene; NCC≡CCN; Dicyanoethyne; Sous-azote de carbone; C4N2
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Gas phase thermochemistry data
Go To: Top, Condensed phase thermochemistry data, Phase change data, Reaction thermochemistry data, Gas phase ion energetics data, Mass spectrum (electron ionization), References, Notes
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:
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔfH°gas | 533.46 | kJ/mol | Review | Chase, 1998 | Data last reviewed in March, 1961 |
ΔfH°gas | 529.3 | kJ/mol | Ccb | Armstrong and Marantz, 1963 | Correction of Armstrong and Marantz, 1960; ALS |
Quantity | Value | Units | Method | Reference | Comment |
S°gas,1 bar | 290.11 | J/mol*K | Review | Chase, 1998 | Data last reviewed in March, 1961 |
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 | 75.60488 | 129.7793 |
B | 70.61086 | 3.927480 |
C | -29.19311 | -0.764036 |
D | 3.452336 | 0.051342 |
E | -0.734589 | -14.12284 |
F | 505.5695 | 462.7922 |
G | 357.6889 | 404.6660 |
H | 533.4600 | 533.4600 |
Reference | Chase, 1998 | Chase, 1998 |
Comment | Data last reviewed in March, 1961 | Data last reviewed in March, 1961 |
Condensed 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.
Data compiled by: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔfH°liquid | 500.4 | kJ/mol | Ccb | Armstrong and Marantz, 1963 | Correction of Armstrong and Marantz, 1960 |
Quantity | Value | Units | Method | Reference | Comment |
ΔcH°liquid | -2074.4 ± 1.3 | kJ/mol | Ccb | Armstrong and Marantz, 1963 | Reanalyzed by Cox and Pilcher, 1970, Original value = -2073. ± 0.8 kJ/mol; Correction of Armstrong and Marantz, 1960 |
Quantity | Value | Units | Method | Reference | Comment |
ΔcH°solid | -2156. | kJ/mol | Ccb | Moureu and Bongrand, 1920 |
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 as indicated in comments:
BS - Robert L. Brown and Stephen E. Stein
DRB - Donald R. Burgess, Jr.
AC - William E. Acree, Jr., James S. Chickos
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
Tboil | 349.7 | K | N/A | Weast and Grasselli, 1989 | BS |
Quantity | Value | Units | Method | Reference | Comment |
ΔvapH° | 28.9 | kJ/mol | N/A | Armstrong and Marantz, 1963 | DRB |
Quantity | Value | Units | Method | Reference | Comment |
ΔsubH° | 44.246 | kJ/mol | V | Saggiomo, 1957 | Hfusion=3.700 kcal/mol; ALS |
Enthalpy of vaporization
ΔvapH (kJ/mol) | Temperature (K) | Method | Reference | Comment |
---|---|---|---|---|
27.3 | 310. | A | Stephenson and Malanowski, 1987 | Based on data from 295. to 350. K.; AC |
Enthalpy of sublimation
ΔsubH (kJ/mol) | Temperature (K) | Method | Reference | Comment |
---|---|---|---|---|
44.3 | 268. | I | SAGGIOMO, 1957 | Based on data from 263. to 273. K. See also Govers, 1975 and Stephenson and Malanowski, 1987.; AC |
Reaction thermochemistry data
Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Phase change data, Gas phase ion energetics data, Mass spectrum (electron ionization), References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: 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
+ = C24H16N2O
By formula: C4N2 + C20H14O = C24H16N2O
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | -129. | kJ/mol | Kin | Samuilov, Nurullina, et al., 1983 | liquid phase; solvent: Nonaquous |
Gas phase ion energetics 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:
LBLHLM - Sharon G. Lias, John E. Bartmess, Joel F. Liebman, John L. Holmes, Rhoda D. Levin, and W. Gary Mallard
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi
RDSH - Henry M. Rosenstock, Keith Draxl, Bruce W. Steiner, and John T. Herron
Ionization energy determinations
IE (eV) | Method | Reference | Comment |
---|---|---|---|
11.81 ± 0.02 | PIPECO | Maier, Misev, et al., 1982 | LBLHLM |
11.81 ± 0.01 | PI | Baker and Turner, 1968 | RDSH |
11.4 ± 0.2 | EI | Dibeler, Reese, et al., 1961 | RDSH |
11.84 | PE | Asbrink, Von Niessen, et al., 1980 | Vertical value; LLK |
11.84 | PE | Bieri, Heilbronner, et al., 1979 | Vertical value; LLK |
Appearance energy determinations
Ion | AE (eV) | Other Products | Method | Reference | Comment |
---|---|---|---|---|---|
C+ | 24. ± 1.0 | ? | EI | Dibeler, Reese, et al., 1961 | RDSH |
CN+ | 19.2 ± 0.3 | ? | EI | Dibeler, Reese, et al., 1961 | RDSH |
C2+ | 18.5 ± 0.3 | ? | EI | Dibeler, Reese, et al., 1961 | RDSH |
C2N+ | 18.1 ± 0.4 | ? | EI | Dibeler, Reese, et al., 1961 | RDSH |
C3+ | 24.6 | ? | EI | Dibeler, Reese, et al., 1961 | RDSH |
C3N+ | 18.4 ± 0.2 | CN | EI | Dibeler, Reese, et al., 1961 | RDSH |
C4+ | 17.2 ± 0.2 | N2 | EI | Dibeler, Reese, et al., 1961 | RDSH |
C4N+ | 18.8 ± 0.5 | N | EI | Dibeler, Reese, et al., 1961 | RDSH |
N+ | 26.0 ± 1.0 | ? | EI | Dibeler, Reese, et al., 1961 | RDSH |
Mass spectrum (electron ionization)
Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Phase change data, Reaction thermochemistry data, Gas phase ion energetics data, References, Notes
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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Additional Data
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Due to licensing restrictions, this spectrum cannot be downloaded.
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 | 367 |
References
Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Phase change data, Reaction thermochemistry data, Gas phase ion energetics data, 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]
Armstrong and Marantz, 1963
Armstrong, G.T.; Marantz, S.,
The heat of combustion of dicyanoacetylene [Correction Ref. 60ARM/MAR],
J. Phys. Chem., 1963, 67, 2888. [all data]
Armstrong and Marantz, 1960
Armstrong, G.T.; Marantz, S.,
The heat of combustion of dicyanoacetylene,
J. Phys. Chem., 1960, 64, 1776-1778. [all data]
Cox and Pilcher, 1970
Cox, J.D.; Pilcher, G.,
Thermochemistry of Organic and Organometallic Compounds, Academic Press, New York, 1970, 1-636. [all data]
Moureu and Bongrand, 1920
Moureu, M.C.; Bongrand, J.Ch.,
Thermochimie. - Nouvelles recherches sur le sous-azolure de carbone. Action des halogenes, des acides halohydriques et des alcools,
Compt. Rend., 1920, 170, 1025-1028. [all data]
Weast and Grasselli, 1989
CRC Handbook of Data on Organic Compounds, 2nd Editon, Weast,R.C and Grasselli, J.G., ed(s)., CRC Press, Inc., Boca Raton, FL, 1989, 1. [all data]
Saggiomo, 1957
Saggiomo, A.J.,
The dinitriles of acetylenedicarboxylic and polyacetylenedicarboxylic acids. I. Dicyanoacetylene and dicycanodiacetylene,
J. Org. Chem., 1957, 22, 1171. [all data]
Stephenson and Malanowski, 1987
Stephenson, Richard M.; Malanowski, Stanislaw,
Handbook of the Thermodynamics of Organic Compounds, 1987, https://doi.org/10.1007/978-94-009-3173-2
. [all data]
SAGGIOMO, 1957
SAGGIOMO, ANDREW J.,
The Dinitriles of Acetylenedicarboxylic and Polyacetylenedicarboxylic Acids. 1 I. 2 Dicyanoacetylene and Dicyanodiacetylene,
J. Org. Chem., 1957, 22, 10, 1171-1175, https://doi.org/10.1021/jo01361a009
. [all data]
Govers, 1975
Govers, H.A.J.,
Derivation of carbon--nitrogen, hydrogen--nitrogen and nitrogen--nitrogen non-bonded potential parameters in molecular crystals,
Acta Crystallogr Sect A Cryst Phys Diffr Theor Gen Crystallogr', 1975, 31, 3, 380-385, https://doi.org/10.1107/S0567739475000800
. [all data]
Samuilov, Nurullina, et al., 1983
Samuilov, Ya.D.; Nurullina, R.L.; Konovalov, A.I.,
Thermochemical and kinetic study of the Diels-Alder reaction with ethylene and acetylene dienophiles,
Zh. Org. Khim., 1983, 19, 1431-1435. [all data]
Maier, Misev, et al., 1982
Maier, J.P.; Misev, L.; Thommen, F.,
Dicyanoacetylene cation. Laser-induced fluorescence and photoelectron-photon coincidence studies,
J. Phys. Chem., 1982, 86, 514. [all data]
Baker and Turner, 1968
Baker, C.; Turner, D.W.,
High resolution molecular photoelectron spectroscopy. III.Acetylenes and azaacetylenes,
Proc. Roy. Soc. (London), 1968, A308, 19. [all data]
Dibeler, Reese, et al., 1961
Dibeler, V.H.; Reese, R.M.; Franklin, J.L.,
Mass spectrometric study of cyanogen and cyanoacetylenes,
J. Am. Chem. Soc., 1961, 83, 1813. [all data]
Asbrink, Von Niessen, et al., 1980
Asbrink, L.; Von Niessen, W.; Bieri, G.,
30.4-nm He(II) photoelectron spectra of organic molecules,
J. Electron Spectrosc. Relat. Phenom., 1980, 21, 93. [all data]
Bieri, Heilbronner, et al., 1979
Bieri, G.; Heilbronner, E.; Hornung, V.; Kloster-Jensen, E.; Maier, J.P.; Thommen, F.; von Niessen, W.,
Electronic states of substituted haloacetylene and cyanoacetylene radical cations,
Chem. Phys., 1979, 36, 1. [all data]
Notes
Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Phase change data, Reaction thermochemistry data, Gas phase ion energetics data, Mass spectrum (electron ionization), References
- Symbols used in this document:
AE Appearance energy S°gas,1 bar Entropy of gas at standard conditions (1 bar) Tboil Boiling point ΔcH°liquid Enthalpy of combustion of liquid at standard conditions ΔcH°solid Enthalpy of combustion of solid at standard conditions ΔfH°gas Enthalpy of formation of gas at standard conditions ΔfH°liquid Enthalpy of formation of liquid at standard conditions ΔrH° Enthalpy of reaction at standard conditions ΔsubH Enthalpy of sublimation ΔsubH° Enthalpy of sublimation at standard conditions ΔvapH Enthalpy of vaporization ΔvapH° Enthalpy of vaporization at standard conditions - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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