Zerfall der Dimeren des Acenaphtylens als Folge der Alkalimetall-Reduktion
Trans- and cis-dinaphthylene-cyclobutane formed by photodimerisation of acenaphthylene are shown to produce the radical anions of the monomer on sodium reduction. This is explained in terms of the large energy difference between the lowest antibonding MOs of the dimers and of the monomer.
Gespeichert in:
| Autor*in: |
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| Format: |
E-Artikel |
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| Sprache: |
Deutsch |
| Erschienen: |
1966 |
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| Umfang: |
4 Ill. 8 |
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| Reproduktion: |
Wiley InterScience Backfile Collection 1832-2000 |
|---|---|
| Übergeordnetes Werk: |
in: Helvetica Chimica Acta - New York, NY : Wiley-VCH, 49(1966) vom: Juni, Seite 1837-1844 |
| Übergeordnetes Werk: |
volume:49 ; year:1966 ; month:06 ; pages:1837-1844 ; extent:8 |
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| 520 | |a Trans- and cis-dinaphthylene-cyclobutane formed by photodimerisation of acenaphthylene are shown to produce the radical anions of the monomer on sodium reduction. This is explained in terms of the large energy difference between the lowest antibonding MOs of the dimers and of the monomer. | ||
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(DE-627)NLEJ162596715 DE-627 ger DE-627 rakwb ger Zerfall der Dimeren des Acenaphtylens als Folge der Alkalimetall-Reduktion 1966 4 Ill. 8 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Trans- and cis-dinaphthylene-cyclobutane formed by photodimerisation of acenaphthylene are shown to produce the radical anions of the monomer on sodium reduction. This is explained in terms of the large energy difference between the lowest antibonding MOs of the dimers and of the monomer. Wiley InterScience Backfile Collection 1832-2000 Gerson, F. oth Weidmann, B. oth in Helvetica Chimica Acta New York, NY : Wiley-VCH 49(1966) vom: Juni, Seite 1837-1844 (DE-627)NLEJ159071178 (DE-600)1475013-2 0018-019X nnns volume:49 year:1966 month:06 pages:1837-1844 extent:8 http://dx.doi.org/10.1002/hlca.19660490618 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 49 1966 6 1837-1844 8 |
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zerfall der dimeren des acenaphtylens als folge der alkalimetall-reduktion |
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Zerfall der Dimeren des Acenaphtylens als Folge der Alkalimetall-Reduktion |
| abstract |
Trans- and cis-dinaphthylene-cyclobutane formed by photodimerisation of acenaphthylene are shown to produce the radical anions of the monomer on sodium reduction. This is explained in terms of the large energy difference between the lowest antibonding MOs of the dimers and of the monomer. |
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Trans- and cis-dinaphthylene-cyclobutane formed by photodimerisation of acenaphthylene are shown to produce the radical anions of the monomer on sodium reduction. This is explained in terms of the large energy difference between the lowest antibonding MOs of the dimers and of the monomer. |
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Trans- and cis-dinaphthylene-cyclobutane formed by photodimerisation of acenaphthylene are shown to produce the radical anions of the monomer on sodium reduction. This is explained in terms of the large energy difference between the lowest antibonding MOs of the dimers and of the monomer. |
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