Benzene, 1,1'-(1,2-cyclobutanediyl)bis-, trans-
- Formula: C16H16
- Molecular weight: 208.2982
- IUPAC Standard InChI: InChI=1S/C16H16/c1-3-7-13(8-4-1)15-11-12-16(15)14-9-5-2-6-10-14/h1-10,15-16H,11-12H2/t15-,16-/m1/s1
- IUPAC Standard InChIKey: AERGGMDNGDDGPI-HZPDHXFCSA-N
- CAS Registry Number: 20071-09-4
- 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. - Stereoisomers:
- Other names: trans-1,2-Diphenylcyclobutane; (2-Phenylcyclobutyl)benzene,(E)-; Cyclobutane, 1,2-diphenyl, trans
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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
View reactions leading to C16H16+ (ion structure unspecified)
Ionization energy determinations
| IE (eV) | Method | Reference | Comment |
|---|---|---|---|
| 8.2 ± 0.1 | EI | Groenwold, Chess, et al., 1984 | LBLHLM |
Appearance energy determinations
| Ion | AE (eV) | Other Products | Method | Reference | Comment |
|---|---|---|---|---|---|
| C8H8+ | 9.0 ± 0.1 | C8H8 | EI | Groenwold, Chess, et al., 1984 | LBLHLM |
References
Go To: Top, 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.
Groenwold, Chess, et al., 1984
Groenwold, G.S.; Chess, E.K.; Gross, M.L.,
Structure of the intermediate formed in the reaction of the styrene radical cation and neutral styrene,
J. Am. Chem. Soc., 1984, 106, 539. [all data]
Notes
Go To: Top, Gas phase ion energetics data, References
- Symbols used in this document:
AE Appearance energy - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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