s-Indacenes reveal the limits of the Hückel rules: These 12π systems are formally antiaromatic, but the results of more recent quantum mechanical calculations indicate π-electron delocalization. The synthesis and spectroscopic investigation of the non-electronically stabilized 4-hetero-s-indacenes 1 and 2 have now been achieved for the first time
A comparative study is made of the properties and reactions of the two isomeric hydrocarbons, 7,15-d...
One antiaromatic polycyclic hydrocarbon (PH) with and without solubilizing tert-butyl substituents, ...
Reduction of the formally antiaromatic compound 1,3,5,7-tetra-tert- butyl-s-indacene to the dianion ...
s-Indacenes reveal the limits of the Hückel rules: These 12π systems are formally antiaromatic, but ...
To check the influence of substituents on the bonding of the 12π-perimeter of s-indacene, a tetraalk...
Frontier orbital analysis of two conjugated, cyclic polyenes held face-to-face in close proximity s...
In search of the causes and the nature of "aromaticity" numerous non-benzenoid carbocyclic conjugate...
The first tricyclic [12]annulene with an unsubstituted perimeter, namely the blue hydrocarbon 2, cou...
Acknowledgements We are grateful to the UK EPSRC National Mass Spectrometry Service Centre for mass ...
Cycloaddition reactions of the azulene system 1 with electron-poor and electron-rich alkynes provide...
The question of the nature of bonding in pentalene (1) has motivated numerous experimental and theo...
A completely planar, delocalized 14π-electron system which does not contain cyclically conjugated su...
An den Methyl- und Phenyl-substituierten Allenyl-Kationen 3 - 12 (Tab. 1) wurden ab-initio-MO-Berech...
International audienceA new set of fully-conjugated indenofluorenes has been synthesized and confirm...
A comparative study is made of the properties and reactions of the two isomeric hydrocarbons, 7,15-d...
One antiaromatic polycyclic hydrocarbon (PH) with and without solubilizing tert-butyl substituents, ...
Reduction of the formally antiaromatic compound 1,3,5,7-tetra-tert- butyl-s-indacene to the dianion ...
s-Indacenes reveal the limits of the Hückel rules: These 12π systems are formally antiaromatic, but ...
To check the influence of substituents on the bonding of the 12π-perimeter of s-indacene, a tetraalk...
Frontier orbital analysis of two conjugated, cyclic polyenes held face-to-face in close proximity s...
In search of the causes and the nature of "aromaticity" numerous non-benzenoid carbocyclic conjugate...
The first tricyclic [12]annulene with an unsubstituted perimeter, namely the blue hydrocarbon 2, cou...
Acknowledgements We are grateful to the UK EPSRC National Mass Spectrometry Service Centre for mass ...
Cycloaddition reactions of the azulene system 1 with electron-poor and electron-rich alkynes provide...
The question of the nature of bonding in pentalene (1) has motivated numerous experimental and theo...
A completely planar, delocalized 14π-electron system which does not contain cyclically conjugated su...
An den Methyl- und Phenyl-substituierten Allenyl-Kationen 3 - 12 (Tab. 1) wurden ab-initio-MO-Berech...
International audienceA new set of fully-conjugated indenofluorenes has been synthesized and confirm...
A comparative study is made of the properties and reactions of the two isomeric hydrocarbons, 7,15-d...
One antiaromatic polycyclic hydrocarbon (PH) with and without solubilizing tert-butyl substituents, ...
Reduction of the formally antiaromatic compound 1,3,5,7-tetra-tert- butyl-s-indacene to the dianion ...