4,12-Bis(2,2-dibromovinyl)[2.2]paracyclophane
نویسندگان
چکیده
In the title compound, C(20)H(16)Br(4), both vinylic substituents were introduced by a Corey-Fuchs reaction using 4,12-diform-yl[2.2]paracyclo-phane as starting material. The title compound may be used as a valuable precursor for the synthesis of diethyn-yl[2.2]paracyclo-phane. The title mol-ecule is centrosymmetric with a crystallographic center of inversion between the centers of the two phenyl rings. A strong tilting is observed with an inter-planar angle between the best aromatic plane and the vinyl plane of 49.4 (5)°. No significant inter-molecular inter-actions are found in the crystal.
منابع مشابه
12,12′-[2,2′-Oxybis(ethane-2,1-diyl)bis(oxy)]bis[(R p)-4-bromo[2.2]paracyclophane]
The title compound, C(36)H(36)Br(2)O(3), was synthesized from (R(p))-4-bromo-12-hy-droxy[2.2]paracyclo-phane and oxydiethane-2,1-diyl bis-(4-methyl-benzene-sulfonate). The crystal packing exhibits a short O⋯Br inter-action [Br⋯O = 3.185 (3) Å] and a weak inter-molecular C-H⋯O contact.
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The urinary metabolites of 1,1,1-trichloro-2,2-bis(p-chlorophenyl)ethane (DDT), 1,1-dichloro-2,2-bis(p-chlorophenyl)ethane (DDD), and 1-chloro-2,2-bis(p-chlorophenyl)ethene in female hamsters are reported. The principal metabolite of both DDT and DDD is 2,2-bis(p-chlorophenyl) acetic acid. DDT- and DDD-treated animals also excreted small amounts of DDD, 1-chloro-2,2-bis(p-chlorophenyl)ethene, 1...
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