Anthracene
- Formula: C14H10
- Molecular weight: 178.2292
- IUPAC Standard InChIKey: MWPLVEDNUUSJAV-UHFFFAOYSA-N
- CAS Registry Number: 120-12-7
- 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. - Isotopologues:
- Other names: Anthracin; Green Oil; Paranaphthalene; Tetra Olive N2G; Anthracene oil; p-Naphthalene; Anthracen; Coal tar pitch volatiles:anthracene; Sterilite hop defoliant
- Permanent link for this species. Use this link for bookmarking this species for future reference.
- Information on this page:
- Other data available:
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Phase change data
Go To: Top, 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 as indicated in comments:
BS - Robert L. Brown and Stephen E. Stein
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
AC - William E. Acree, Jr., James S. Chickos
DRB - Donald R. Burgess, Jr.
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
DH - Eugene S. Domalski and Elizabeth D. Hearing
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
Tboil | 613.2 | K | N/A | Weast and Grasselli, 1989 | BS |
Tboil | 613.0 | K | N/A | Buckingham and Donaghy, 1982 | BS |
Tboil | 613.1 | K | N/A | Burriel, 1931 | Uncertainty assigned by TRC = 0.3 K; TRC |
Tboil | 613. | K | N/A | Kirby, 1921 | Uncertainty assigned by TRC = 5. K; TRC |
Quantity | Value | Units | Method | Reference | Comment |
Tfus | 490. ± 3. | K | AVG | N/A | Average of 27 values; Individual data points |
Quantity | Value | Units | Method | Reference | Comment |
Ttriple | 488.93 | K | N/A | Goursot, Girdhar, et al., 1970 | Uncertainty assigned by TRC = 0.01 K; TRC |
Quantity | Value | Units | Method | Reference | Comment |
ΔvapH° | 78.5 | kJ/mol | CGC | Zhao, Unhannanant, et al., 2008 | AC |
ΔvapH° | 79.5 ± 1.2 | kJ/mol | GC | Haftka, Parsons, et al., 2006 | Based on data from 413. to 473. K.; AC |
ΔvapH° | 79.1 | kJ/mol | CGC | Puri, Chickos, et al., 2001 | AC |
ΔvapH° | 79.8 | kJ/mol | CGC | Chickos, Hesse, et al., 1998 | AC |
ΔvapH° | 79.6 | kJ/mol | CGC | Chickos, Hosseini, et al., 1995 | Based on data from 453. to 503. K.; AC |
Quantity | Value | Units | Method | Reference | Comment |
ΔsubH° | 98. ± 10. | kJ/mol | AVG | N/A | Average of 12 values; Individual data points |
Enthalpy of vaporization
ΔvapH (kJ/mol) | Temperature (K) | Method | Reference | Comment |
---|---|---|---|---|
66.7 | 498. | N/A | Rojas and Orozco, 2003 | See also Hanshaw, Nutt, et al., 2008.; AC |
72.4 | 398. | GC | Lei, Chankalal, et al., 2002 | Based on data from 323. to 473. K.; AC |
69.7 | 398. | GC | Hinckley, Bidleman, et al., 1990 | Based on data from 343. to 453. K.; AC |
58.6 | 519. | A | Stephenson and Malanowski, 1987 | Based on data from 504. to 615. K.; AC |
62.1 | 500. | N/A | Kudchadker, Kudchadker, et al., 1979 | See also Hanshaw, Nutt, et al., 2008.; AC |
59.2 | 558. | I | Mortimer and Murphy, 1923 | Based on data from 500. to 616. K.; AC |
60.3 | 515. | I | Mortimer and Murphy, 1923 | Based on data from 500. to 616. K. See also Boublik, Fried, et al., 1984.; AC |
59.6 | 555. | I | NELSON and SENSEMAN, 1922 | Based on data from 496. to 614. K.; AC |
60.7 | 511. | I | NELSON and SENSEMAN, 1922 | Based on data from 496. to 614. K. See also Boublik, Fried, et al., 1984.; AC |
Antoine Equation Parameters
log10(P) = A − (B / (T + C))
P = vapor pressure (bar)
T = temperature (K)
View plot Requires a JavaScript / HTML 5 canvas capable browser.
Temperature (K) | A | B | C | Reference | Comment |
---|---|---|---|---|---|
496.4 to 613.8 | 4.72997 | 2759.53 | -30.753 | Mortimer and Murphy, 1923 | Coefficents calculated by NIST from author's data. |
Enthalpy of sublimation
ΔsubH (kJ/mol) | Temperature (K) | Method | Reference | Comment |
---|---|---|---|---|
97.9 ± 0.6 | 320. to 355. | ME | Oja, Chen, et al., 2009 | AC |
98.4 ± 0.7 | 320. to 350. | ME | Oja, Chen, et al., 2009 | AC |
97.6 ± 1.3 | 369. | ME | Siddiqi, Siddiqui, et al., 2009 | Based on data from 339. to 399. K.; AC |
95.6 ± 1.2 | 337. | N/A | Chen, Oja, et al., 2006 | Based on data from 320. to 354. K.; AC |
91.2 | 338. | GS | Grayson and Fosbraey, 2006 | Based on data from 323. to 353. K.; AC |
98.8 ± 0.4 | 350. | ME | Ribeiro da Silva, Monte, et al., 2006 | Based on data from 340. to 360. K.; AC |
102.5 ± 1.9 | 358. | ME | Verevkin, 2004 | Based on data from 348. to 368. K.; AC |
96. ± 6. | 283. to 323. | LE | McEachern and Sandoval, 2001 | AC |
94.5 | 423. to 488. | MEM | Emmenegger and Piccand, 1999 | AC |
102.5 | 338. to 353. | ME | Kloc and Laudise, 1998 | AC |
100.0 ± 2.8 | 341. | ME | Oja and Suuberg, 1998 | Based on data from 318. to 363. K.; AC |
99.7 | 383. | GS | Nass, Lenoir, et al., 1995 | Based on data from 313. to 453. K.; AC |
102.6 | 338. | GS | Hansen and Eckert, 1986 | Based on data from 313. to 363. K.; AC |
98.7 | 346. | GS | Rordorf, 1986 | Based on data from 318. to 373. K.; AC |
94.3 | 353. to 399. | GS | Bender, Bieling, et al., 1983 | AC |
91.8 ± 0.9 | 303. | GS | Sonnefeld, Zoller, et al., 1983 | Based on data from 283. to 323. K.; AC |
94.8 | 376. | GS | Macknick and Prausnitz, 1979 | Based on data from 358. to 393. K.; AC |
98.8 ± 0.4 | 363. to 448. | HSA | Dygdala, Stefanski, et al., 1977 | AC |
97.2 | 328. to 372. | ME | Taylor and Crookes, 1976 | AC |
101.0 ± 0.5 | 353. to 432. | ME | Malaspina, 1973 | AC |
99.7 | 393. | C | Malaspina, 1973 | AC |
84.1 | 290. to 358. | ME,C | Wiedemann, 1972 | See also Beech and Lintonbon, 1971.; AC |
98.49 | 342. | V | Kelley and Rice, 1964 | ALS |
98.3 ± 2.1 | 342. to 359. | N/A | Kelley and Rice, 1964, 2 | See also Cox and Pilcher, 1970.; AC |
90. ± 1.3 | 337. | TE | Budurov, 1960 | Based on data from 327. to 346. K.; AC |
103.4 ± 2.9 | 303. to 373. | N/A | Hoyer and Peperle, 1958 | See also Cox and Pilcher, 1970.; AC |
103.3 ± 2.9 | 303. | V | Hoyer and Peperle, 1958, 2 | Reanalyzed by Pedley, Naylor, et al., 1986, Original value = 102. kJ/mol; ALS |
102.1 ± 2.1 | 338. to 353. | N/A | Bradley and Cleasby, 1953 | See also Cox and Pilcher, 1970.; AC |
102.1 | 346. | N/A | Bradley and Cleasby, 1953, 2 | Based on data from 339. to 353. K.; AC |
102.09 | 338.7 | V | Bradley and Cleasby, 1953, 3 | ALS |
98. ± 2. | 396. to 421. | HSA | Stevens, 1953 | AC |
97. ± 2. | 396. | V | Stevens, 1953, 2 | ALS |
92.0 ± 2.1 | 364. | ME | Inokuchi, Shiba, et al., 1952 | AC |
90.4 | 353. | ME | Inokuchi, 1951 | AC |
97.3 ± 1.2 | 378. to 398. | RG | Sears and Hopke, 1949 | AC |
93.3 ± 4.2 | 353. | N/A | Wolf and Weghofer, 1938 | AC |
93.3 ± 0.8 | 353. | V | Wolf and Weghofer, 1938, 2 | ALS |
Enthalpy of fusion
ΔfusH (kJ/mol) | Temperature (K) | Method | Reference | Comment |
---|---|---|---|---|
29.372 | 488.93 | N/A | Goursot, Girdhar, et al., 1970, 2 | Note that table of smoothed values indicates Hm = 6485 J/mol and Sm = 251 J/mol*K.; DH |
29.8 | 492. | DSC | Rojas and Orozco, 2003 | Based on data from 463. to 503. K.; AC |
31.5 | 491. | DSC | Storoniak, Krzyminski, et al., 2003 | AC |
28.8 | 489.4 | DSC | Lisicki and Jamróz, 2000 | AC |
29.37 | 488.9 | N/A | Domalski and Hearing, 1996 | AC |
28.830 | 490. | N/A | Ueberreiter and Orthmann, 1950 | DH |
28.870 | 489.7 | N/A | Hildebrand, Duschak, et al., 1917 | DH |
Entropy of fusion
ΔfusS (J/mol*K) | Temperature (K) | Reference | Comment |
---|---|---|---|
60.07 | 488.93 | Goursot, Girdhar, et al., 1970, 2 | Note; DH |
58.0 | 490. | Ueberreiter and Orthmann, 1950 | DH |
59.0 | 489.7 | Hildebrand, Duschak, et al., 1917 | DH |
Enthalpy of phase transition
ΔHtrs (kJ/mol) | Temperature (K) | Initial Phase | Final Phase | Reference | Comment |
---|---|---|---|---|---|
29.000 | 490.6 | crystaline, I | liquid | Radomska and Radomski, 1980 | DH |
Entropy of phase transition
ΔStrs (J/mol*K) | Temperature (K) | Initial Phase | Final Phase | Reference | Comment |
---|---|---|---|---|---|
59.1 | 490.6 | crystaline, I | liquid | Radomska and Radomski, 1980 | DH |
Reaction thermochemistry data
Go To: Top, Phase change 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 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
By formula: C14H11+ + C14H10 = (C14H11+ • C14H10)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 66.9 | kJ/mol | PHPMS | Meot-Ner (Mautner), 1980 | gas phase; Entropy change calculated or estimated; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 120. | J/mol*K | N/A | Meot-Ner (Mautner), 1980 | gas phase; Entropy change calculated or estimated; M |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
26. | 352. | PHPMS | Meot-Ner (Mautner), 1980 | gas phase; Entropy change calculated or estimated; M |
By formula: C28H20 = 2C14H10
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | -67.0 | kJ/mol | Cm | Bendig, Buchwitz, et al., 1981 | liquid phase; solvent: Cyclohexane; Dimerization, see Bendig and Kreysig, 1981; ALS |
ΔrH° | 28.9 ± 6.1 | kJ/mol | Cm | Donati, Guarini, et al., 1981 | solid phase; ALS |
By formula: C14H10+ + C14H10 = (C14H10+ • C14H10)
Bond type: Charge transfer bond (positive ion)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 68.6 | kJ/mol | PHPMS | Meot-Ner (Mautner), 1980 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 110. | J/mol*K | PHPMS | Meot-Ner (Mautner), 1980 | gas phase; M |
By formula: C4H2O3 + C14H10 = C18H12O3
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | -93. ± 2. | kJ/mol | Cm | Kiselev, Mavrin, et al., 1982 | liquid phase; solvent: Benzene; ALS |
ΔrH° | -93.7 | kJ/mol | Eqk | Lenz, Hegedus, et al., 1982 | liquid phase; solvent: 1,2,4-C6H3Cl3; ALS |
By formula: C14H10 = C14H10
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | -324. ± 1. | kJ/mol | Eqk | Dreeskamp, Kapahnke, et al., 1988 | liquid phase; solvent: Heptane; Isomerization; ALS |
+ = C21H18O3
By formula: C14H10 + C7H8O3 = C21H18O3
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | -87.5 | kJ/mol | Eqk | Lenz, Hegedus, et al., 1982 | liquid phase; solvent: 1,2,4-C6H3Cl3; ALS |
By formula: C20H10N4 = C14H10 + C6N4
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 40.5 ± 2.1 | kJ/mol | Cm | Rogers, 1972 | solid phase; ALS |
Gas phase ion energetics data
Go To: Top, Phase change data, Reaction thermochemistry data, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data evaluated as indicated in comments:
HL - Edward P. Hunter and Sharon G. Lias
L - Sharon G. Lias
Data compiled as indicated in comments:
MM - Michael M. Meot-Ner (Mautner)
LL - Sharon G. Lias and Joel F. Liebman
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
B - John E. Bartmess
View reactions leading to C14H10+ (ion structure unspecified)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
IE (evaluated) | 7.439 ± 0.006 | eV | N/A | N/A | L |
Quantity | Value | Units | Method | Reference | Comment |
Proton affinity (review) | 877.3 | kJ/mol | N/A | Hunter and Lias, 1998 | HL |
Quantity | Value | Units | Method | Reference | Comment |
Gas basicity | 846.6 | kJ/mol | N/A | Hunter and Lias, 1998 | HL |
Electron affinity determinations
EA (eV) | Method | Reference | Comment |
---|---|---|---|
0.530 ± 0.020 | LPES | Ando, Mitsui, et al., 2007 | B |
0.5300 ± 0.0050 | LPES | Scheidt and Weinkauf, 1997 | B |
0.60 ± 0.10 | TDEq | Heinis, Chowdhury, et al., 1993 | ΔGea(343 K) = -13.2 kcal/mol; ΔSea = -1.1 eu.; B |
0.660 ± 0.060 | ECD | Ruoff, Kadish, et al., 1995 | Revised data, work of Becker and Chen, 1966; B |
0.570 ± 0.020 | ECD | Lyons, Morris, et al., 1968 | B |
0.5560 ± 0.0080 | ECD | Becker and Chen, 1966 | B |
<0.481 ± 0.039 | ECD | Wojnarovits and Foldiak, 1981 | EA is an upper limit: Chen and Wentworth, 1989.; B |
0.41998 | ECD | Wentworth and Becker, 1962 | B |
Proton affinity at 298K
Proton affinity (kJ/mol) | Reference | Comment |
---|---|---|
869.4 | Aue, Guidoni, et al., 2000 | Experimental literature data re-evaluated by the authors using ab initio protonation entropies; MM |
Gas basicity at 298K
Gas basicity (review) (kJ/mol) | Reference | Comment |
---|---|---|
842.7 | Aue, Guidoni, et al., 2000 | Experimental literature data re-evaluated by the authors using ab initio protonation entropies; MM |
Ionization energy determinations
References
Go To: Top, Phase change data, Reaction thermochemistry data, Gas phase ion energetics data, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
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]
Buckingham and Donaghy, 1982
Buckingham, J.; Donaghy, S.M.,
Dictionary of Organic Compounds: Fifth Edition, Chapman and Hall, New York, 1982, 1. [all data]
Burriel, 1931
Burriel, F.,
Physico-Chemical Study of Some Solid Organic Compounds at Ordinary Temperatures, and Their COrrelationo with Temperature,
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Kirby, 1921
Kirby, W.,
Determination of the Melting and Boiling Points of Anthracene, Phenanthrene and Carbazole,
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Goursot, Girdhar, et al., 1970
Goursot, P.; Girdhar, H.L.; Westrum, E.F.,
Thermodynamics of Polynuclear Aromatic Molecules III. Heat Capacities and Enthalpies of Fusion of Anthracene,
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Zhao, Unhannanant, et al., 2008
Zhao, Hui; Unhannanant, Patamaporn; Hanshaw, William; Chickos, James S.,
Enthalpies of Vaporization and Vapor Pressures of Some Deuterated Hydrocarbons. Liquid-Vapor Pressure Isotope Effects,
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Supercooled liquid vapour pressures and related thermodynamic properties of polycyclic aromatic hydrocarbons determined by gas chromatography,
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Puri, Chickos, et al., 2001
Puri, Swati; Chickos, James S.; Welsh, William J.,
Determination of Vaporization Enthalpies of Polychlorinated Biphenyls by Correlation Gas Chromatography,
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Chickos, Hesse, et al., 1998
Chickos, James; Hesse, Donald; Hosseini, Sarah; Nichols, Gary; Webb, Paul,
Sublimation enthalpies at 298.15K using correlation gas chromatography and differential scanning calorimetry measurements,
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Chickos, Hosseini, et al., 1995
Chickos, James S.; Hosseini, Sarah; Hesse, Donald G.,
Determination of vaporization enthalpies of simple organic molecules by correlations of changes in gas chromatographic net retention times,
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Rojas and Orozco, 2003
Rojas, Aarón; Orozco, Eulogio,
Measurement of the enthalpies of vaporization and sublimation of solids aromatic hydrocarbons by differential scanning calorimetry,
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Hanshaw, William; Nutt, Marjorie; Chickos, James S.,
Hypothetical Thermodynamic Properties. Subcooled Vaporization Enthalpies and Vapor Pressures of Polyaromatic Hydrocarbons,
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Lei, Ying Duan; Chankalal, Raymond; Chan, Anita; Wania, Frank,
Supercooled Liquid Vapor Pressures of the Polycyclic Aromatic Hydrocarbons,
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Hinckley, Bidleman, et al., 1990
Hinckley, Daniel A.; Bidleman, Terry F.; Foreman, William T.; Tuschall, Jack R.,
Determination of vapor pressures for nonpolar and semipolar organic compounds from gas chromatograhic retention data,
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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
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Kudchadker, Kudchadker, et al., 1979
Kudchadker, Shanti A.; Kudchadker, Arvind P.; Zwolinski, Bruno J.,
Chemical thermodynamic properties of anthracene and phenanthrene,
The Journal of Chemical Thermodynamics, 1979, 11, 11, 1051-1059, https://doi.org/10.1016/0021-9614(79)90135-6
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Mortimer and Murphy, 1923
Mortimer, F. Spencer.; Murphy, Ray v.,
The Vapor Pressures of Some Substances Found in Coal Tar.,
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Boublik, Fried, et al., 1984
Boublik, T.; Fried, V.; Hala, E.,
The Vapour Pressures of Pure Substances: Selected Values of the Temperature Dependence of the Vapour Pressures of Some Pure Substances in the Normal and Low Pressure Region, 2nd ed., Elsevier, New York, 1984, 972. [all data]
NELSON and SENSEMAN, 1922
NELSON, O.A.; SENSEMAN, C.E.,
Vapor Pressure Determinations on Naphthalene, Anthracene, Phecanthrene, and Anthraquinone between Their Melting and Boiling Points,
J. Ind. Eng. Chem., 1922, 14, 1, 58-62, https://doi.org/10.1021/ie50145a028
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Oja, Chen, et al., 2009
Oja, Vahur; Chen, Xu; Hajaligol, Mohammad R.; Chan, W. Geoffrey,
Sublimation Thermodynamic Parameters for Cholesterol, Ergosterol, β-Sitosterol, and Stigmasterol,
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Siddiqi, Siddiqui, et al., 2009
Siddiqi, M. Aslam; Siddiqui, Rehan A.; Atakan, Burak,
Thermal Stability, Sublimation Pressures, and Diffusion Coefficients of Anthracene, Pyrene, and Some Metal β-Diketonates,
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Chen, Oja, et al., 2006
Chen, Xu; Oja, Vahur; Chan, W. Geoffrey; Hajaligol, Mohammad R.,
Vapor Pressure Characterization of Several Phenolics and Polyhydric Compounds by Knudsen Effusion Method,
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Grayson and Fosbraey, 2006
Grayson, B. Terence; Fosbraey, Lynda A.,
Determination of the vapour pressure of pesticides,
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Ribeiro da Silva, Monte, et al., 2006
Ribeiro da Silva, Manuel A.V.; Monte, Manuel J.S.; Santos, Luís M.N.B.F.,
The design, construction, and testing of a new Knudsen effusion apparatus,
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Verevkin, 2004
Verevkin, Sergey P.,
Vapor pressure measurements on fluorene and methyl-fluorenes,
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McEachern and Sandoval, 2001
McEachern, D.M.; Sandoval, O.,
A molecular flow evaporation apparatus for measuring vapour pressures and heats of sublimation of organic compounds,
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Emmenegger and Piccand, 1999
Emmenegger, F.; Piccand, M.,
Organometallics, 1999, 57, 1, 235-240, https://doi.org/10.1023/A:1010100531350
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Kloc and Laudise, 1998
Kloc, Ch.; Laudise, R.A.,
Vapor pressures of organic semiconductors:,
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Oja and Suuberg, 1998
Oja, Vahur; Suuberg, Eric M.,
Vapor Pressures and Enthalpies of Sublimation of Polycyclic Aromatic Hydrocarbons and Their Derivatives,
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Nass, Lenoir, et al., 1995
Nass, Karen; Lenoir, Dieter; Kettrup, Antonius,
Calculation of the Thermodynamic Properties of Polycyclic Aromatic Hydrocarbons by an Incremental Procedure,
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Hansen and Eckert, 1986
Hansen, Philip C.; Eckert, Charles A.,
An improved transpiration method for the measurement of very low vapor pressures,
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Notes
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- Symbols used in this document:
EA Electron affinity IE (evaluated) Recommended ionization energy T Temperature Tboil Boiling point Tfus Fusion (melting) point Ttriple Triple point temperature ΔHtrs Enthalpy of phase transition ΔStrs Entropy of phase transition ΔfusH Enthalpy of fusion ΔfusS Entropy of fusion ΔrG° Free energy of reaction at standard conditions ΔrH° Enthalpy of reaction at standard conditions ΔrS° Entropy 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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