C07C47/546

Method for the preparation of a partially hydrogenated polyacene and an intermediate thereof

The present invention relates to a process for preparing a partially hydrogenated polyacene, and a novel intermediate used in such process; also the present invention relates to a process for preparing the corresponding conjugated polyacenes.

Method for the preparation of a partially hydrogenated polyacene and an intermediate thereof

The present invention relates to a process for preparing a partially hydrogenated polyacene, and a novel intermediate used in such process; also the present invention relates to a process for preparing the corresponding conjugated polyacenes.

Condensed-cyclic compound, electroluminescent device and method for manufacturing thereof

A method for manufacturing a condensed-cyclic compound and an electroluminescent device is provided, the condensed-cyclic compound is represented by the following formula: ##STR00001## wherein R1, R2 and CHO are connected to any one of an unsaturated carbon atom of a naphthalene ring; R1, R2 are respectively a hydrogen and any one of an alkane group or a condensed-cyclic aromatic hydrocarbon group. The embodiments provided by the present invention using the above-described manner is able to reduce ACQ phenomenon of the condensed-cyclic compound in aggregate state or solid state.

Condensed-cyclic compound, electroluminescent device and method for manufacturing thereof

A method for manufacturing a condensed-cyclic compound and an electroluminescent device is provided, the condensed-cyclic compound is represented by the following formula: ##STR00001## wherein R1, R2 and CHO are connected to any one of an unsaturated carbon atom of a naphthalene ring; R1, R2 are respectively a hydrogen and any one of an alkane group or a condensed-cyclic aromatic hydrocarbon group. The embodiments provided by the present invention using the above-described manner is able to reduce ACQ phenomenon of the condensed-cyclic compound in aggregate state or solid state.

Solid-supported catalyst for cross-coupling

A solid-supported catalyst ligand which chelates palladium (II) species to form a complex that functions as a heterogeneous catalyst that is stable and can be recycled without significantly losing any catalytic activity in a variety of chemical transformations, a method for producing the solid-supported catalyst ligand and a method for catalyzing a palladium cross-coupling reaction, such as the Suzuki-Miyaura, Mizoroki-Heck, and Sonagashira reactions.

Solid-supported catalyst for cross-coupling

A solid-supported catalyst ligand which chelates palladium (II) species to form a complex that functions as a heterogeneous catalyst that is stable and can be recycled without significantly losing any catalytic activity in a variety of chemical transformations, a method for producing the solid-supported catalyst ligand and a method for catalyzing a palladium cross-coupling reaction, such as the Suzuki-Miyaura, Mizoroki-Heck, and Sonagashira reactions.

Aryl halide cross-coupling method and product made therefrom

A solid-supported catalyst ligand which chelates palladium (II) species to form a complex that functions as a heterogeneous catalyst that is stable and can be recycled without significantly losing any catalytic activity in a variety of chemical transformations, a method for producing the solid-supported catalyst ligand and a method for catalyzing a palladium cross-coupling reaction, such as the Suzuki-Miyaura, Mizoroki-Heck, and Sonagashira reactions.

Aryl halide cross-coupling method and product made therefrom

A solid-supported catalyst ligand which chelates palladium (II) species to form a complex that functions as a heterogeneous catalyst that is stable and can be recycled without significantly losing any catalytic activity in a variety of chemical transformations, a method for producing the solid-supported catalyst ligand and a method for catalyzing a palladium cross-coupling reaction, such as the Suzuki-Miyaura, Mizoroki-Heck, and Sonagashira reactions.

Method of forming paracyclophane containing functional group with disulfide bond

The present invention provides a method of forming paracyclyophane containing disulfide functional group. The paracyclophane is prepared by adding 3,3-dithiodipropionic acid (DPDPA) and N-ethyl-N-(3-(dimethylamino)propyl)carbodiimide (EDC) into 4-aminomethyl [2,2] paracyclophane. The present invention further provides a chemical film and a method of forming the same. The chemical film contains poly-p-xylylene with disulfide functional group and is formed on a substrate by a chemical vapor deposition process.

Method of forming paracyclophane containing functional group with disulfide bond

The present invention provides a method of forming paracyclyophane containing disulfide functional group. The paracyclophane is prepared by adding 3,3-dithiodipropionic acid (DPDPA) and N-ethyl-N-(3-(dimethylamino)propyl)carbodiimide (EDC) into 4-aminomethyl [2,2] paracyclophane. The present invention further provides a chemical film and a method of forming the same. The chemical film contains poly-p-xylylene with disulfide functional group and is formed on a substrate by a chemical vapor deposition process.