Described herein are compositions and methods for processing photopolymers based on olefin metathesis. The compositions and methods comprise latent ruthenium complexes and photoacids and/or photoacid generators.

The invention relates to novel organic semiconducting compounds containing a polycyclic unit, to methods for their preparation and educts or intermediates used therein, to compositions, polymer blends and formulations containing them, to the use of the compounds, compositions and polymer blends as organic semiconductors in, or for the preparation of, organic electronic (OE) devices, especially organic photovoltaic (OPV) devices, perovskite-based solar cell (PSC) devices, organic photodetectors (OPD), organic field effect transistors (OFET) and organic light emitting diodes (OLED), and to OE, OPV, PSC, OPD, OFET and OLED devices comprising these compounds, compositions or polymer blends.

The present invention provides an organic nano-grid, a nano-polymer thereof and a preparation method therefor. The organic nano-grid has a general formula (I), and the nano-polymer has a general formula (II), wherein R.sub.1 is an alkyl chain, R.sub.2 is halogen or an electroactive group, and X may comprise a heteroatom such as N, O and S, and n is a natural number from 1 to 10. A nano-connection strategy is applied to the construction of a one-dimensional nano-polymer. The polymer starts from a monomer A.sub.2B.sub.2 to form a corresponding nano-polymer by a Friedel-Crafts polymerization cyclization reaction.

This is to provide a non-halogen containing compound excellent in proton conductivity and capable of suitably being used for a polymer electrolytic fuel cell The compound of the present invention has a structure represented by the following general formula (I). ##STR00001## (In the above-mentioned general formula (I), “l” and “n” are molar fractions when l+n=1.0, and 0≤l<1.0 and 0<n≤1.0, A represents a structure represented by the following general formula (II) or (III), B represents a structure represented by the following general formula (VII), the respective structural units are random copolymerized, and at least one benzene ring in the formula (I) has at least one sulfo group.) ##STR00002## (In the above-mentioned general formula (II) or (III), R.sup.1 to R.sup.4 are each independently selected from hydrogen and an alkyl group having 1 to 3 carbon atoms, le and R.sup.2 form together with the carbon atom, they are attached to, an aromatic ring or a fused aromatic ring and R.sup.3 and R.sup.4 form together with the carbon atom, they are attached to, an aromatic ring or a fused aromatic ring, or R.sup.1, R.sup.3 and R.sup.4 are hydrogens and R.sup.2 is a single bond and bonded to the carbon of “c”, X is a single bond, or a structure represented by the following formula (IV), the following formula (V) or the following formula (VI), when X is a single bond, bonds “a”s are both bonded at ortho positions or both bonded at meta positions relative to the carbons bonded to X, when X is a structure represented by the following formula (IV), bonds “a”s are both bonded at para positions relative to the carbons bonded to X, and when it is a structure represented by the following formula (V), bonds “a”s are both bonded at para positions or both bonded at meta positions relative to the carbons bonded to x, when X is a structure represented by the following formula (VI), the bonds “a”s in the above-mentioned general formula (II) or (III) exist only one of these, and A binds to other structure or a structural unit by one of the bonds “a”s and the bond “b”.) ##STR00003##

A composition for forming an organic film, containing: a material for forming an organic film shown by the following general formula; and an organic solvent, where R.sub.1 represents a hydrogen atom, an allyl group, or a propargyl group, R.sub.2 represents a nitro group, a halogen atom, a hydroxy group, an alkyloxy group having 1 to 4 carbon atoms, an alkynyloxy group having 2 to 4 carbon atoms, an alkenyloxy group having 2 to 4 carbon atoms, a linear, branched, or cyclic alkyl group having 1 to 6 carbon atoms, a trifluoromethyl group, or a trifluoromethyloxy group, m = 0 or 1, n = 1 or 2, 1 = 0 or 1, k represents an integer of 0 to 2, W represents a divalent organic group having 1 to 40 carbon atoms, and each V independently represents a hydrogen atom or a linking moiety.

##STR00001##

A method, includes: reacting at least one donor group with at least one protected acceptor group to form a plurality of protecting group-containing OSC polymers; removing the protecting group from the plurality of protecting group-containing OSC polymers to form H-bonding sites; and fusing the H-bonding sites of a first OSC polymer backbone with H-bonding sites of a second OSC polymer backbone to form π-π interactions between conjugated OSC polymers.

An electrochromic polymer is comprised of a repeat unit comprising one or more meta-conjugated linkers (MCLs) and one or more aromatic moieties (Ars). Each of the one or more MCLs is partially conjugated with the one or more Ars at meta positions of the MCLs to form a polymer backbone of the electrochromic polymer. The electrochromic polymer undergoes an optical switching and a color change in an electrochromic device, which shows a high transparency and a high optical contrast.

Provided are a polymer containing S,S-dioxide-dibenzothiophene in backbone chain with content-adjustable triarylamine end groups, and a preparation method and an application thereof. Triarylamines hole-transport small molecules are introduced into the polymer end group, and a content of the triarylamine end groups can be adjusted by controlling a polymer molecular weight, so that the polymer has better electron-transport and hole-transport capabilities, and charge carrier transport can be balanced, so that more exciton recombination takes place effectively, thus improving the luminous efficiency and stability of the polymer. The polymer is prepared by a Suzuki polymerization reaction and does not require synthesis of new monomers. The polymer material is used for preparing highly effective and stable monolayer devices, and is dissolved directly in an organic solvent, then spin-coated, ink-jet printed, or printed to form a film.

A polymer blend, including at least one organic semiconductor (OSC) polymer and at least one photosensitizer, such that the at least one OSC polymer is a diketopyrrolopyrrole-fused thiophene polymeric material, wherein the fused thiophene is beta-substituted.

A light emitting device with excellent light emission efficiency is provided. The light emitting device has an anode, a cathode, a first layer disposed between the anode and the cathode, and a second layer disposed between the anode and the first layer. The second layer is a layer containing a crosslinked product of a compound having a crosslinkable group selected from Group A, and at least one of the first layer and the second layers contains a compound represented by the formula (T-1). The compound having a crosslinkable group is a polymer compound having a crosslinkable group selected from Group A:

##STR00001## ##STR00002##