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ELECTRON-PARAMAGNETIC RESONANCE-SPECTRA OF THE RADICAL CATIONS OF SOME BENZOCYCLOBUTENES, BENZOCYCLOPENTENES AND BENZOCYCLOHEXENES
被引:16
作者:
AVILA, DV
[1
]
DAVIES, AG
[1
]
LI, ER
[1
]
NG, KM
[1
]
机构:
[1] UNIV LONDON UNIV COLL,DEPT CHEM,20 GORDON ST,LONDON WC1H 0AJ,ENGLAND
来源:
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2
|
1993年
/
03期
关键词:
D O I:
10.1039/p29930000355
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
1,2,4,5-Tetrahydrobenzo[1,2:4,5]dicyclobutene, 1,2,3,5,6,7-hexahydrobenzo[1,2:4,5]dicyclopentene and 1,2,3,4,6,7,8,9-octahydrobenzo[1,2:4,5]dicyclohexene, and their dimethyl derivatives, and tetramethylbenzocyclo-butene, -pentene and -hexene have been prepared. All except the first compound have been oxidised to their corresponding radical cations, and the EPR spectra have been analysed by assigning McConnell-type Q-values to the substituents in the benzene ring. It is suggested that the ordering of the orbital energy levels (psi(A) above psi(S)) in 3,6-dimethylbenzo[1,2:4,5]biscyclobutene and -pentene is a manifestation of the Mills-Nixon effect, and results from rehybridisation of the strained molecular framework. In the radical cations of 5,10-dimethyl-1,2,3,4,6,7,8,9-octahydrobenzo[1,2:4,5]dicyclohexene and 5,6,7,8-tetramethyl-1,2,3,4-tetrahydrobenzocyclohexene the total unpaired electron density, as implied by the McConnell type of relationship, appears to be less than unity. Various possible causes of this are examined.
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页码:355 / 362
页数:8
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