102603-45-2Relevant academic research and scientific papers
Synthesis and photoisomerization of 4,4-diphenyl-2,6-di(p-methoxyphenyl)-4H-thiopyran-1,1-dioxide, an approach to the regioselectivity in photorearrangement of 2,4,4,6-tetraaryl-4H-thiopyran-1,1-dioxides
Mouradzadegun, Arash,Pirelahi, Hooshang
, p. 149 - 154 (2000)
Synthesis and photoisomerization of the new sulfone derivative 1c is described. Upon photolysis at 254 nm the sulfone 1c, unlike those of the model compound 1b and the other 2,4,4,6-tetraarylsubstituted sulfone derivatives, undergoes rearrangement in high
PHOTOCHEMICAL TRANSFORMATIONS OF 2,4,4,6-TETRAPHENYL-4H-THIOPYRAN-1,1-DIOXIDE AND SOME ITS para-SUBSTITUTED DERIVATIVES
Sebek, Pavel,Sedmera, Petr,Kuthan, Josef
, p. 869 - 881 (2007/10/02)
1,2,4,5-Tetrasubstituted cyclopentadienes VIa - VIf or phenanthrene derivative VIII, respectively, were obtained as the main photoproducts upon irradiation of sulfones Ia - If and II in acetonitrile, methanol or benzene.Bridged isomers Va - Vd were isolated from the reaction of Ia - Id carried out in acetonitrile.Probable course of the investigated photochemical transformations of 4H-thiopyran-1,1-dioxides is discussed.
SIGMATROPIC ISOMERIZATION OF TETRAPHENYLCYCLOPENTADIENES: REACTION MECHANISM AND QUANTUM CHEMICAL TREATMENT
Sebek, Pavel,Sedmera, Petr,Boehm, Stanislav,Kuthan, Josef
, p. 882 - 892 (2007/10/02)
Thermal isomerizations of 2,3,5,5-tetraphenylcyclopenta-1,3-diene (Ia) or 1,2,4,5-tetraphenylcyclopenta-1,3-diene (IIa) in melts lead to identical equilibrium mixtures of hydrocarbon IIa with prevailing 1,2,3,4-tetraphenylcyclopenta-1,3-diene (IIIa).The isomerization of bis-tert-butyl cyclopentadienes Ib or Ic produces an equilibrium mixture with preponderant 1,2,3,4-tetrasubstituted cyclopentadienes IIIb, IIIc besides minority isomers IIb, IIc.On the contrary, the 1,2,4,5-tetrasubstituted phenanthrene hydrocarbon IXa having forced coplanarity of both benzene rings only partially isomerizes to IXb.Equilibrium constants of the isomerization IIa IIIa in diphenyl ether at 323 to 433 K were measured (K = 5.8 - 2.3).Relative stability of hydrocarbons Ia, IIa, IIIa, and VIIa is interpreted on the basis of quantum chemical AM1 calculations.The time course of isomerization of the hydrocarbon IIc allowed us to propose two reaction mechanisms based on the - and -sigmatropic steps.The preparation of 2,3,5,5-tetrasubstituted cyclopentadienes Ia - Ic by dehydration of cis-1,2-diols IVa - IVc is described.
