https://www.selleckchem.com/products/ots964.html The 2-vinylbenzoic acids have wide applications in the field of polymer chemistry and are key precursors for the synthesis of important bioactive molecules. Herein, an ortho-halogen-induced deoxygenative approach for the generation of 2-vinylbenzoic acids from alkyl aryl ketones by palladium catalysis is discovered and explored. This approach requires no base or stoichiometric additives and can be carried out through a simple one-step process. Furthermore, the present reaction is scalable up to one-gram scale. The commercially available palladium on carbon (5 wt%) was used as a heterogeneous catalyst and showed excellent recyclability ( less then 5 times) without significant loss in catalytic activity. Pleasingly, under our optimized conditions, the alpha alkyl substituted 2-iodoacetophenones exhibit good diastereoselectivity and predominantly (E)-2-vinylbenzoic acids were obtained with good to excellent yields.Novel crystalline covalent organic polymers (COPs) were constructed by reacting 1,4-diaminoanthraquinone with 1,3,5-triformylphloroglucinol or tris(4-formylphenyl)amine (TPDA or TADA). After they were covalently bonded to amine-functionalized graphene oxides, the resulting mesoporous COPs@graphene composites demonstrated efficient capacitance storage performance in both alkaline and acidic media. In particular, the as-synthesized TPDA@graphene displayed a reversible specific capacitance of 522 F g-1 in a 6.0 mol L-1 aqueous KOH electrolyte, superior to the previously reported COPs with inconspicuous capacitance storage properties in alkaline media. Its specific capacitance also reached 390 F g-1 in 2.0 mol L-1 H2SO4. The impressive capacitance storage properties of this composite can be ascribed to its unique structure with abundant pendulous anthraquinone redox groups and better electrical conductivity enhanced by the coupled graphenes.Transition metal phosphides (TMPs) have received considerable attention owi