A high molecular weight compound according to the present invention includes a substituted triarylamine structural unit represented by a general formula (1) below,

##STR00001## where Ar.sup.1 and Ar.sup.2 are a divalent aromatic hydrocarbon group or a divalent aromatic heterocyclic group, R.sup.1 and R.sup.2 represent a hydrogen atom, a heavy hydrogen atom, a fluorine atom, a chlorine atom, a cyano group, a nitro group, an alkyl group, a cycloalkyl group, an alkenyl group, an alkyloxy group, or a cycloalkyloxy group, X, Y and Z are, on the condition that at least one of them is an aryl group or a heteroaryl group, an aryl group, a heteroaryl group, or a group similar to the groups represented by R.sup.1 and R.sup.2 above.

Aspects of the present disclosure generally describe polyarylether ketones and methods of use. In some aspects, a composition includes one or more polymers of formulae (I), (II), or (III): ##STR00001## ##STR00002##

A hole transport copolymer having the following Formula III is disclosed herein:

##STR00001##

In some embodiments, A is a monomeric unit having Formula Ia or Formula IIa, B is a B is a monomeric unit having at least three points of attachment in the copolymer, E is the same or different at each occurrence and is selected from the group consisting of H, D, halide, alkyl, aryl, arylamino, siloxane, crosslinkable groups, deuterated alkyl, deuterated aryl, deuterated arylamino, deuterated siloxane, and deuterated crosslinkable groups, and x, y, and z are the same or different and are mole fractions, such that x+y+z=1, and x and y are non-zero.

A high-molecular-weight compound having at least one substituted triarylamine structural unit represented by the following general formula (1), further including a structural unit having at least one aromatic hydrocarbon ring or a structural unit having a triarylamine skeleton in addition to the at least one substituted triarylamine structural unit, and having a weight average molecular weight of 10,000 or more and 1,000,000 or less in terms of polystyrene and no a crosslinker, wherein the high-molecular-weight compound is used in an organic EL device as a constituent material of at least one organic layer. A polymer material having excellent hole injection/transport performance, electron blocking capability, high heat resistance, and high stability in a thin-film state for use in a polymer organic EL device, and an organic EL device having a low drive voltage, high light emission efficiency, and a long lifetime using this polymer material. ##STR00001##

An organic electronic material containing a charge transport polymer for which, in a molecular weight distribution chart measured by GPC, the area ratio accounted for by components having a molecular weight of less than 20,000 is not more than 40%, and the area ratio accounted for by components having a molecular weight of 500 or less is not more than 1%.

1) Hydrocarbon polymer of formula (I):

##STR00001##

F.sup.1 and F.sup.2 are exo-vinylene cyclocarbonate monovalent radicals of formulas (IIa) and (IIb):

##STR00002## g and d 0, 1, 2 or 3; A C1-C6 alkyl; X an oxygen atom or NR.sup.17 with R.sup.17 C1-C6 alkyl; R.sup.14, R.sup.15 and R.sup.16 a hydrogen atom or C1-C6 alkyl; R.sup.1 to R.sup.12 H or C1-C14 alkyl; R.sup.13 O or CH.sub.2; x 1 and y 1; n1 and n2 an integer or zero; m an integer or zero; p1 and p2 an integer or zero of non-zero sum; n1, n2, m, p1 and p2 such that the molecular weight of said polymer is 400 to 100,000 g/mol; process of preparation by ring-opening metathesis polymerization; and use as an adhesive in a mixture with an amine compound having at least 2 amine groups.

Hydrocarbon polymer having two 2-oxo-1,3-dioxolane-4-carboxylate end groups of formula (I):

##STR00001## F.sup.1 has formula (IIa) and F.sup.2 has formula (IIb):

##STR00002## in which g and d, which are identical or different, represent an integer equal to 1, 2 or 3; R.sup.1 to R.sup.12 represent a hydrogen atom or an alkyl radical of 1 to 22 carbon atoms; x and y are integers such that the sum x+y is 0 to 2; R.sup.13 is an oxygen or sulphur atom or a divalent CH.sub.2 radical; n1, n2, m, p1 and p2 are an integer or equal to 0 and such that the molecular weight Mn of the polymer of formula (I) is between 400 and 100 000 g/mol, a process for the preparation of the polymer by ring-opening metathesis polymerization, and use as adhesive in mixture with an amino compound having at least two amine groups.

The invention relates to a blend containing an electron acceptor and an electron donor, the acceptor being an n-type semiconductor which is a small molecule that does not contain a fullerene moiety, the electron donor being a p-type semiconductor which is a conjugated polymer comprising donor and acceptor units in random sequence, to a formulation containing such a blend, to the use of the blend in organic electronic (OE) devices, especially organic photovoltaic (OPV) devices, perovskite-based solar cell (PSC) devices, organic photodetectors (OPD) and organic light emitting diodes (OLED), and to OE, OPV, PSC, OPD and OLED devices comprising the blend.

An exemplary embodiment of the present disclosure provides a method of designing a polymer. The method can include: providing a set of polymer data; generating a set of polymer structures; providing one or more target properties for the polymer, predicting properties of each polymer structure of the set of polymer structures, and design considerations for the set of polymer structures; and selecting one or more polymer structures from the set of polymer structures, based at least in part, on the predicted properties of the polymer structures. The polymer data can include a set of monomer structures.

A reversible crosslinking reactant composition is provided. The composition includes at least one furan-group-containing oligomer having a structure represented by Formula (I) and a bismaleimide compound having a structure represented by

##STR00001##

Formula (II), wherein the equivalent ratio of the furan group of the furan-group-containing oligomer having a structure represented by Formula (I) to the maleimide group of the bismaleimide compound having a structure represented by Formula (II) is from 0.5:1 to 1:0.5.