C08G2261/411

Phenyl derivatives substituted with at least two electron acceptors and at least two electron donors for use in organic electronic devices

The present invention relates to a phenyl-derivative compound substituted with at least two electron acceptors and at least two electron donors. Formula (I) R.sup.AaR.sup.DbR.sup.ScC.sub.6 wherein a is 2, 3 or 4; b is 2, 3 or 4; c is 0, 1 or 2; a+b−c=6; R.sup.A is at each occurrence independently a group with −M-effect; R.sup.B is at each occurrence independently a group with +−M-effect; R.sup.S is as defined in claim 1. Said compound is suited for use in organic electronic devices, particularly in organic electroluminescent devices.

BENZOTHIENOTHIOPHENE ISOINDIGO POLYMERS
20180009936 · 2018-01-11 · ·

Polymers comprising at least one unit of formula (1) and their use as semiconducting materials.

##STR00001##

BLUE-EXCITABLE WATER-SOLVATED POLYMERIC DYES
20180009989 · 2018-01-11 ·

Water solvated polymeric dyes and polymeric tandem dyes having a blue excitation spectrum are provided. The polymeric dyes are conjugated polymers that can include a thiophene-containing co-monomer. The polymeric tandem dyes further include a signaling chromophore covalently linked to the conjugated polymer in energy-receiving proximity therewith. Also provided are labelled specific binding members that include the subject polymeric dyes. Methods of evaluating a sample for the presence of a target analyte and methods of labelling a target molecule in which the subject polymeric dyes find use are also provided. Systems and kits for practicing the subject methods are also provided.

ELECTROLUMINESCENT POLYMER BASED ON PHENANTHROIMIDAZOLE UNITS, PREPARATION METHOD THEREFOR, AND USE THEREOF
20230240127 · 2023-07-27 · ·

Disclosed are an electroluminescent polymer based on phenanthroimidazole units, a preparation method therefor, and the use thereof. The electroluminescent polymer based on phenanthroimidazole units has a structure as shown in the formula (I), and the side chain thereof contains phenanthroimidazole units. The electroluminescent polymer (1) has the properties of hybridized local and charge-transfer states, which can improve the utilization of excitons and the electroluminescence properties of devices by means of reverse inter-system crossing to effectively utilize triplet state excitons; (2) the phenanthroimidazole unit has a large degree of conjugation and a strong rigidity, which can not only improve the thermal stability of a material, but can also increase the radiation transition rate of the material and improve the light-emitting efficiency thereof; and (3) the raw materials of the polymer are cheap, the synthetic route is simple, and purification is convenient, which is beneficial for industrial scaled-up production thereof. The polymer has a good solubility, and can be used to prepare large-area flexible display devices by means of a solution processing technology. The polymer has great development potential and prospects in the field of organic electronic display.

##STR00001##

POLYMER COMPOSITIONS FOR VERTICAL CHANNEL ORGANIC ELECTROCHEMICAL TRANSISTORS AND COMPLEMENTARY LOGIC CIRCUITS

Photocurable compositions that combine redox-active semiconducting organic polymers with photocurable organic molecules are provided. Upon exposure to radiation, the photocurable compositions form ion-permeable, electrically conductive crosslinked organic films that can be used as conducting channels in n-channel or p-channel organic electrochemical transistors, including vertical organic electrochemical transistors (vOECTs). The vOECTs can be incorporated in complementary electronic circuits.

Polymer and organic thin film and thin film transistor and electronic device

Disclosed are a polymer including at least one structural unit with a moiety represented by Chemical Formula 1, an organic thin film including the polymer, a thin film transistor, and an electronic device. ##STR00001## In Chemical Formula 1, Ar.sup.1 to Ar.sup.3, L.sup.1, L.sup.2, and R.sup.1 to R.sup.6 are the same as described in the detailed description.

LIGHT-EMITTING COMPOSITION
20220380523 · 2022-12-01 · ·

A light-emitting composition comprising: a light-emitting group and a polymer comprising: a repeat unit of formula Ar.sup.1 wherein Ar.sup.1 is an arylene repeat unit which is unsubstituted or substituted with one or more substituents; and a repeat unit of formula (I): (I) wherein Ar.sup.2 and Ar.sup.3 each independently represent a C.sub.6-20 arylene group or a 5-20 membered heteroarylene group which is unsubstituted or substituted with one or more substituents and CB represents a conjugation-breaking group which does not provide a conjugation path between Ar.sup.2 and Ar.sup.3; wherein the polymer has a solubility in water or a C.sub.1-8 alcohol at 20° C. of at least 0.1 mg/ml. The composition may be a light-emitting polymer in which the polymer contains the light-emitting group. The light-emitting composition may be part of a particle containing the polymer and a matrix material, e.g. silica. The light-emitting composition may be used in an assay for detection of a target analyte.

POLYMER, QUANTUM DOT COMPOSITION AND LIGHT-EMITTING DEVICE EMPLOYING THE SAME

A polymer, a quantum dot composition, and a light-emitting device employing the same are provided. The polymer includes a first repeat unit that has a structure represented by Formula (I):

##STR00001##

wherein the definitions of R.sup.1, R.sup.2, A.sup.1, A.sup.2, A.sup.3, and Z.sup.1 and n are as defined in the specification.

Non-Fullerene Acceptor Polymer

The present disclosure provides a non-fullerene acceptor polymer, which includes a structure represented by formula (I). Formula (I) is defined as in the specification. The non-fullerene acceptor polymer has an electron donating unit and an electron attracting end group. The non-fullerene acceptor polymer uses phenyl or its derivatives as the linker to form the polymer.

POLYMER AND LIGHT-EMITTING DEVICE

A polymer and a light-emitting device employing the same are provided. The polymer includes a first repeat unit with a structure represented by Formula (I):

##STR00001##

wherein the definitions of R.sup.1, R.sup.2, A.sup.1, A.sup.2, A.sup.3, and Z.sup.1 and n are as defined in the specification. At least one of A.sup.1, A.sup.2, and A.sup.3 is not hydrogen.