Selenophene
- Formula: C4H4Se
- Molecular weight: 131.03
- IUPAC Standard InChIKey: MABNMNVCOAICNO-UHFFFAOYSA-N
- CAS Registry Number: 288-05-1
- Chemical structure:
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Gas phase ion energetics data
Go To: Top, Mass spectrum (electron ionization), UV/Visible spectrum, 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:
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 |
---|---|---|---|
8.955 | PE | Reineck, Nohre, et al., 1983 | LBLHLM |
8.776 | S | Bavia, Zauli, et al., 1975 | LLK |
8.96 | CTS | Aloisi, Santini, et al., 1975 | LLK |
9.01 ± 0.05 | EI | Linda, Marino, et al., 1971 | LLK |
9.01 ± 0.05 | EI | Linda, Marino, et al., 1969 | RDSH |
8.92 | PE | Fringuelli, Marino, et al., 1976 | Vertical value; LLK |
8.80 | PE | Schafer, Schweig, et al., 1973 | Vertical value; LLK |
≤8.92 | PE | Distefano, Pignataro, et al., 1973 | Vertical value; LLK |
Mass spectrum (electron ionization)
Go To: Top, Gas phase ion energetics data, UV/Visible spectrum, 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. |
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Origin | F.Fringuelli ET AL.J.Heterocycl.Chem.,15,137(1978) |
NIST MS number | 281119 |
UV/Visible spectrum
Go To: Top, 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.
Spectrum
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Additional Data
View image of digitized spectrum (can be printed in landscape orientation).
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Download spectrum in JCAMP-DX format.
Source | Churnaevskii, 1959 |
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Owner | INEP CP RAS, NIST OSRD Collection (C) 2007 copyright by the U.S. Secretary of Commerce on behalf of the United States of America. All rights reserved. |
Origin | INSTITUTE OF ENERGY PROBLEMS OF CHEMICAL PHYSICS, RAS |
Source reference | RAS UV No. 12911 |
Instrument | Spectrophotometer SF-4 |
Boiling point | 110/ 752 mm |
References
Go To: Top, Gas phase ion energetics data, Mass spectrum (electron ionization), UV/Visible spectrum, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Reineck, Nohre, et al., 1983
Reineck, I.; Nohre, C.; Lodin, P.; Maripuu, R.; Lindberg, B.; Karlsson, L.; Siegbahn, K.; Hornfeldt, A.-B.; Gronowitz, S.,
Electronic and vibrational structure of 2-substituted selenophenes studied by He(I) photoelectron spectroscopy,
Chem. Scr., 1983, 22, 209. [all data]
Bavia, Zauli, et al., 1975
Bavia, M.; Zauli, C.; Fusina, L.,
Rydberg states in selenophen,
Mol. Phys., 1975, 30, 1289. [all data]
Aloisi, Santini, et al., 1975
Aloisi, G.; Santini, S.; Savelli, G.,
Molecular complexes of heteroaromatic five membered ring compounds with tetracyanoethylene. Charge transfer spectra, equilibrium constants and ionization potentials of the donors,
J. Chem. Soc. Faraday Trans. 1, 1975, 70, 2045. [all data]
Linda, Marino, et al., 1971
Linda, P.; Marino, G.; Pignataro, S.,
A comparison of sensitivities to substituent effects of five- membered heteroaromatic rings in gas phase ionization,
J. Chem. Soc. B, 1971, 1585. [all data]
Linda, Marino, et al., 1969
Linda, P.; Marino, G.; Pignataro, S.,
Ionization potentials and relative rates of electrophilic substitution in five-membered heteroaromatic rings,
Ric. Sci., 1969, 39, 666. [all data]
Fringuelli, Marino, et al., 1976
Fringuelli, F.; Marino, G.; Taticchi, A.; Distefano, G.; Colonna, F.P.; Pignataro, S.,
Photoelectron spectra of the α-substituted derivatives of furan, thiophen, selenophen, and tellurophen. A comparative study of the molecular orbital energies,
J. Chem. Soc. Perkin Trans. 2, 1976, 276. [all data]
Schafer, Schweig, et al., 1973
Schafer, W.; Schweig, A.; Gronowitz, S.; Taticchi, A.; Fringuelli, F.,
Reversal in the sequence of two highest occupied molecular orbitals in the series thiophen, selenophen, and tellurophen,
J. Chem. Soc. Chem. Commun., 1973, 541. [all data]
Distefano, Pignataro, et al., 1973
Distefano, G.; Pignataro, S.; Innorta, G.; Fringuelli, F.; Marino, G.; Taticchi, A.,
Ionization energies of selenophen, tellurophen and some of their derivatives,
Chem. Phys. Lett., 1973, 22, 132. [all data]
Churnaevskii, 1959
Churnaevskii, N.A.,
Optika i Spektrokopya (English translation), 1959, 6, 25. [all data]
Notes
Go To: Top, Gas phase ion energetics data, Mass spectrum (electron ionization), UV/Visible spectrum, References
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