A copolymer includes a repeating unit represented by Formula (I); and a repeating unit represented by Formula (II), in Formula (I), R.sup.1 represents a hydrogen atom or an alkyl group having 1 to 20 carbon atoms; R.sup.2 represents an alkyl group having 1 to 20 carbon atoms and having at least one fluorine atom as a substituent, or a group including Si(R.sup.a3)(R.sup.a4)O; L represents a divalent linking group as defined herein; and R.sup.a3 and R.sup.a4 each independently represent an alkyl group as defined herein, in Formula (II), R.sup.10 represents a hydrogen atom or an alkyl group having 1 to 20 carbon atoms; R.sup.11 and R.sup.12 each independently represent a hydrogen atom, a substituted or unsubstituted aliphatic hydrocarbon group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heteroaryl group; R.sup.11 and R.sup.12 may be linked to each other; and X.sup.1 represents a divalent linking group.

A composition having excellent dischargeability by an ink jet method and reduced clogging of an ink jet apparatus is provided. The composition contains a fluorinated alcohol A represented by the formula (1) and having a boiling point of 50 C. or more and less than 150 C., a fluorinated alcohol B represented by the formula (1) and having a boiling point of 150 C. or more and less than 300 C., and a charge transportable compound, in which the ratio rate of the fluorinated alcohol B with respect to 100 parts by mass of the sum of the fluorinated alcohol A and the fluorinated alcohol B is 10 parts by mass to 90 parts by mass:
C.sub.nFH.sub.2nF+1-mFF.sub.nFOH (1)
In formula (1), nF is an integer of 1 to 12 and mF is an integer of 1 to 25, provided that 2nF+1mF.

A light emitting device contains an anode, cathode, and two organic layers provided therebetween. One organic layer contains a phosphorescent compound, the second organic layer contains a block copolymer containing an end group, a block that binds to the end group and/or a block that does not bind to the end group, and a crosslinked product of the block copolymer. The non-terminal block contains a non-crosslinkable unit represented by the formula (X) and/or a non-crosslinkable unit represented by the formula (Z). At least one of X.sub.I>X.sub.II; Z.sub.I>Z.sub.II; X.sub.I+Z.sub.I>X.sub.II+Z.sub.II is satisfied when the total number of units having formula (X) and the total number of units having formula (Z) in the non-terminal block are X.sub.I and Z.sub.I, respectively, and the total number of units having formula (X) and the total number of units having formula (Z) in the terminal block are X.sub.II and Z.sub.II, respectively.

A block copolymer includes an end group, a block that binds to the end group, and a block that does not bind to the end group. The block that does not bind to the end group contains at least one non-crosslinkable constitutional unit represented by the formula (X) and/or at least one non-crosslinkable constitutional unit represented by the formula (Z). At least one of formulas (i) X.sub.I>X.sub.II, (ii) Z.sub.I>Z.sub.II and (iii) X.sub.I+Z.sub.I>X.sub.II+Z.sub.II is satisfied when the total number of non-crosslinkable constitutional units represented by formulas (X) and (Z) in the block that does not bind to the end group are represented by X.sub.I and Z.sub.I, respectively, and the total number of non-crosslinkable constitutional units represented by formulas (X) and (Z) in the block that binds to the end group are represented by X.sub.II and Z.sub.II, respectively.

A method of reacting bis(R.sub.1) 5,5-dibromo-3,4-difluoro-[2,2:5,2:5,2-quaterthiophene]-3,3-dicarboxylate and bis(R.sub.2) 5,5-dibromo-3,4-difluoro-[2,2:5,2:5,2-quaterthiophene]-3,3-dicarboxylate to form the polymer:

##STR00001##

In this polymer R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5 and R.sub.6 are independently selected from the group consisting of: a halogen, a substituted alkyl, an unsubstituted alkyl, a substituted aryl, an unsubstituted aryl, a substituted heteroaryl and an unsubstituted heteroaryl.

An organic photovoltaic device comprising a polymer:

##STR00001##

and an acceptor. In this organic photovoltaic device, R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5 and R.sub.6 are independently selected from the group consisting of: a halogen, a substituted alkyl, an unsubstituted alkyl, a substituted aryl, an unsubstituted aryl, a substituted heteroaryl and an unsubstituted heteroaryl.

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, NR, and SiRR. 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.

Embodiments in accordance with the present invention encompass a two component composition containing in one component a latent organo-ruthenium carbide catalyst, and in another component a photoactive acid generator or a thermally active acid generator, and either of the components containing a mixture of photoactive compound along with one or more monomers which undergo ring open metathesis polymerization (ROMP) when said components are mixed together and exposed to a suitable radiation (or heat) to form a three-dimensional (3D) object. The three-dimensional objects so formed exhibits improved mechanical properties, particularly, high heat distortion temperature, impact strength, elongation to break, among others. Accordingly, compositions of this invention are useful as 3D inkjet materials for forming high impact strength objects of various sizes with microscale features lower than 100 microns, among various other uses.

A conductive polymer that can be formed by removing or separating a side chain, or alkyl or aryl side chain from an unmodified polymer by heating or exposure to light (hv).

A two-component system can be used for the chemical fastening of an anchor in a borehole by dual cure curing. The dual cure curing used is a combination of radical polymerization and ring-opening olefin metathesis polymerization (ROMP).