ChemInform Abstract: STRUCTURAL EFFECTS ON THE REACTIVITY OF CARBON RADICALS IN HOMOLYTIC AROMATIC SUBSTITUTIONS. PART III. REACTION OF THE 1-ADAMANTYL RADICAL WITH BENZENE DERIVATIVES

1976 ◽  
Vol 7 (32) ◽  
pp. no-no
Author(s):  
LORENZO TESTAFERRI ◽  
MARCELLO TIECCO ◽  
PIERO SPAGNOLO ◽  
PAOLO ZANIRATO ◽  
GIORGIO MARTELLI
Keyword(s):  
Benzene Derivatives ◽  
Structural Effects ◽  
Carbon Radicals

the effects of resonance with Jupiter in the system of short-period comets

1974 ◽  
Vol 22 ◽  
pp. 193-203
Author(s):  
L̆ubor Kresák
Keyword(s):  
Structural Effects ◽  
Order Resonance ◽  
Mean Motion ◽  
Short Period ◽  
The Mean ◽  
Compound Effect ◽  
Low Order

AbstractStructural effects of the resonance with the mean motion of Jupiter on the system of short-period comets are discussed. The distribution of mean motions, determined from sets of consecutive perihelion passages of all known periodic comets, reveals a number of gaps associated with low-order resonance; most pronounced are those corresponding to the simplest commensurabilities of 5/2, 2/1, 5/3, 3/2, 1/1 and 1/2. The formation of the gaps is explained by a compound effect of five possible types of behaviour of the comets set into an approximate resonance, ranging from quick passages through the gap to temporary librations avoiding closer approaches to Jupiter. In addition to the comets of almost asteroidal appearance, librating with small amplitudes around the lower resonance ratios (Marsden, 1970b), there is an interesting group of faint diffuse comets librating in characteristic periods of about 200 years, with large amplitudes of about±8% in μ and almost±180° in σ, around the 2/1 resonance gap. This transient type of motion appears to be nearly as frequent as a circulating motion with period of revolution of less than one half that of Jupiter. The temporary members of this group are characteristic not only by their appearance but also by rather peculiar discovery conditions.

Coefficients of molecular homeomorphism and crystalline isomorphism in the series of para-disubstituted benzene derivatives

1991 ◽  
Vol 88 ◽  
pp. 509-514 ◽  
Author(s):  
MA Cuevas Diarte ◽  
T Calvet ◽  
M Labrador ◽  
E Estop ◽  
HAJ Oonk ◽  
...  
Keyword(s):  
Benzene Derivatives ◽  
Disubstituted Benzene

Arene Dearomatization via Radical Hydroarylation

2019 ◽  
Author(s):  
Autumn Flynn ◽  
Kelly McDaniel ◽  
Meredith Hughes ◽  
David Vogt ◽  
Nathan Jui
Keyword(s):  
Precious Metal ◽  
Room Temperature ◽  
Aryl Halide ◽  
Solvent System ◽  
Benzene Derivatives ◽  
Green Solvent ◽  
Photocatalytic System

A photocatalytic system for the dearomative hydroarylation of benzene derivatives has been developed. Using a combination of an organic photoredox catalyst and an amine reductant, this process operates through a reductive radical-polar crossover mechanism where aryl halide reduction triggers a regioselective cyclization event, giving rise to a range of complex spirocyclic cyclohexadienes. This light-driven protocol functions at room temperature in a green solvent system (aq. MeCN), without the need for precious metal-based catalysts or reagents, or the generation of stoichiometric metal byproducts.

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