An organic semiconducting compound and an organic photoelectric component containing the same are provided. The organic semiconducting compound has a novel chemical structure to make the organic semiconducting compound have good response to the infrared light. The organic semiconducting compound can be applied to the organic photoelectric components such as organic photodetector (OPD), organic photovoltaic (OPV) cell, and organic field-effect transistor (OFET). Thus, the organic photoelectric components have better light absorption range and photoelectric response while in use.

A polymer comprising: ##STR00001## In this embodiment, R′ and R″, can be independently selected from the group consisting of: a halogen, a substituted alkyl, an unsubstituted alkyl, a substituted aryl, and an unsubstituted aryl. Additionally, X.sub.1 and X.sub.2 can be independently selected from the group consisting of: O, S, Se, N—R, and Si—R—R. Lastly, Ar and Ar′ can be identical or different and can be independently selected from the group consisting of: a substituted aryl, and an unsubstituted aryl.

Methods of forming a porphene polymeric material are provided. The resulting material can be a porphene or a metalloporphene polymeric material. The structure of the polymer can be selected based on a material provided in the monomer material. Methods of using the polymeric material are also provided.

Described herein are anionic phenylene oligomers and polymers, and devices including these materials. The oligomers and polymers can be prepared in a convenient and well-controlled manner, and can be used in cation exchange membranes. Also described is the controlled synthesis of anionic phenylene monomers and their use in synthesizing anionic oligomers and polymers, with precise control of the position and number of anionic groups.

An organic film forming composition, containing: a material shown by formula (I) and/or (II); and an organic solvent, where R.sub.1 and R.sub.4 each represent a hydrogen atom, an allyl or propargyl group, R.sub.2 and R.sub.5 each represent a substituent, R.sub.3 and R.sub.6 represents a hydrogen atom, an alkyl group having 1 to 4 carbon atoms, an alkynyl group having 2 to 4 carbon atoms, or an alkenyl group having 2 to 4 carbon atoms. “m” and “i” represent 0 or 1, “k” and “q” represent an integer of 0 to 2, “n” represent 1 or 2, “h”, and “j” represent an integer of 0 to 2 and satisfy the relationship 1≤h+j≤4, and “1” and “r” represent 0 or 1. W represents a single bond or divalent group shown by formulae (3). Each V independently represents a hydrogen atom or linking moiety.

##STR00001##

A method of reacting

##STR00001##

with

##STR00002##

to produce

##STR00003##

In this method Y.sub.1 and Y.sub.2 are independently selected from the group consisting of: H, Cl, Br, I, and combinations thereof. Additionally in this method M is selected from the group consisting of H, trialkylstannane, boronate, or ZnX, wherein X is Cl, Br, or I. Furthermore in this method Z is a divalent linking group selected from the group consisting of:

##STR00004##

Lastly, in this method R.sub.1 is selected from: H, unsubstituted or substituted branched alkyls with 1 to 60 carbon atoms or unsubstituted or substituted linear alkyls with 1 to 60 carbon atoms.

A novel dopant according to the present disclosure includes an anion represented by the following Formula (1) and a counter cation. In Formula (1), R.sup.1 and R.sup.2 may be each at least one group selected from a nitro group, a cyano group, an acyl group, a carboxyl group, an alkoxycarbonyl group, a haloalkyl group, a sulfo group, an alkylsulfonyl group, an halosulfonyl group, and a haloalkylsulfonyl group, or may be a group formed by R.sup.1 and R.sup.2 bonded to each other [—SO.sub.2-L-SO.sub.2—] (where L represents a haloalkylene group). The counter cation may be a radical cation represented by Formula (2), where R.sup.1 and R.sup.2 represent electron-withdrawing groups that may be bonded to each other to form a heterocycle, and R.sup.3 to R.sup.5 represent a hydrogen atom, a hydrocarbon group that may have a substituent, or a heterocyclic group that may have a substituent. The dopant is capable of forming an electroconductive composition that shows a high conductivity.

A hard mask-forming composition which forms a hard mask used in lithography, including: a resin containing an aromatic ring and a polar group; and a compound containing at least one of an oxazine ring fused to an aromatic ring, and a fluorene ring.

Described are conjugated polymers and conjugated polymer nanoparticles formed therefrom. The conjugated polymers and conjugated polymer nanoparticles have a maximum emission of light that occurs within a tissue transparent window of the electromagnetic spectrum. These emission properties are particle-size independent. The sizes of the conjugated nanoparticles are controlled by altering the concentration of the conjugated polymer used to make conjugated polymer nanoparticles. Also described are methods of making conjugated polymer nanoparticles that have larger sizes than have been traditionally reported, involving a modified reprecipitation approach. The conjugated polymers and/or conjugated polymer nanoparticles can be used as fluorescent probes in biological imaging.

A polymer compound has a repeating unit represented by general formula (1): ##STR00001##
wherein R.sup.1a represents an alkyl group, an aryl group, a monovalent aromatic heterocyclic group or an aralkyl group, each possibly substituted and the same or different; and X.sup.1a represents a group selected from formulae (1a) to (1c).] ##STR00002##
wherein R.sup.1c represents an aryl group or a monovalent aromatic heterocyclic group, possibly substituted; and R.sup.1d to R.sup.1f represent each independently an alkyl group, an aryl group, a monovalent aromatic heterocyclic group, an alkoxy group, an aryloxy group, an aralkyl group, an arylalkoxy group, a substituted amino group, a substituted carbonyl group, a substituted carboxyl group, a fluorine atom or a cyano group; and the pairs R.sup.1d and R.sup.1e, R.sup.1f and R.sup.1g, R.sup.1d and R.sup.1f, and R.sup.1e and R.sup.1g may be mutually linked to form a ring together with a carbon atom to which they are linked.