C08G2261/364

Organic electronic material, ink composition containing same, and organic thin film, organic electronic element, organic electroluminescent element, lighting device, and display device formed therewith

Provided are: an organic electronic material which can be easily multilayered and that can be used in substrates, such as resin, that cannot be processed at high temperatures; an ink composition containing the same; an organic thin film formed using said organic electronic material or said ink composition; and an organic electronic element and an organic EL element that are formed using said organic thin film and that have a superior luminous efficacy and emission lifespan than conventional elements. Specifically, provided are: an organic electronic material that is characterized by containing an oligomer or a polymer having a structure that branches into three or more directions and has at least one polymerizable substituent; an ink composition containing said organic electronic material; and an organic thin film prepared using the aforementioned organic electronic material. Further, provided are an organic electronic element and an organic electroluminescent element containing said organic thin film.

Narrow band gap conjugated polymers employing cross-conjugated donors useful in electronic devices

The invention provides for new polymer compounds and methods for the preparation of modular narrow band gap conjugated compounds and polymers that incorporate exocyclic cross-conjugated donors or substituents, as well as novel monomer components of such polymers and the resulting products which comprise materials and useful electronic devices with novel functionality.

Solution-processable indenofluorenes and methods to generate solution-processable indenofluorenes

In an embodiment, a composition is provided that includes an indenofluorene moiety; an alkyl radical, an aryl radical, or a heteroaryl radical chemically bound to the indenofluorene moiety; and an electron donor moiety bound to the indenofluorene moiety. In another embodiment, a device is provided that includes compositions described herein. In another embodiment, a method of forming a donor-acceptor small molecule or a donor-acceptor copolymer is provided that includes forming an indenofluorene moiety; forming an electron donor moiety; and reacting the indenofluorene moiety with the electron donor moiety in a cross-coupling reaction.

Polymer containing S,S-dioxide-dibenzothiophene in backbone chain with content-adjustable triarylamine end groups and preparation method and application thereof

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.

Copolymer and organic solar cell including same
11225549 · 2022-01-18 · ·

The present specification provides a copolymer including: a repeating unit derived from a compound represented by Formula 1; a first conjugated monomer; and a second conjugated monomer different from the first conjugated monomer, and an organic solar cell including the same.

Electrochromic polymers with amide-containing side chains and methods of fabricating same and electrochromic device containing same
11220573 · 2022-01-11 · ·

The present invention generally relates to electrochromic compounds, the synthesis method and the uses thereof, particularly to a family of conjugated electrochromic polymers containing solubilizing side chains, where at least one side chain contains amide functional groups. The disclosed conjugated electrochromic polymers with amide-containing side chains demonstrated excellent redox switching in not only organic but also aqueous media while maintaining high photo contrast. The presence of the amide groups is also beneficial when it comes to lower the oxidation onset potential of the polymers, making them attractive candidates for electrochromic in aqueous environment.

CONJUGATED POLYMERS INCLUDING AN INDACEN-4-ONE DERIVATIVE, PROCEDURE FOR THEIR PREPARATION AND PHOTOVOLTAIC DEVICES COMPRISING THE SAME
20210351355 · 2021-11-11 · ·

There is a conjugated polymer having a derivative of indacen-4-one having general formula (I):

##STR00001##

wherein: R.sub.1 and R.sub.2, same or different, are selected from C.sub.1-C.sub.30 alkyl groups, linear or branched; optionally substituted cycloalkyl groups; optionally substituted aryl groups; optionally substituted heteroaryl groups; C.sub.1-C.sub.30 alkoxyl groups, linear or branched; R.sub.4—O—[CH.sub.2—CH.sub.2—O].sub.m— polyoxyethylene groups, wherein R.sub.4 is selected from C.sub.1-C.sub.30 alkyl groups, linear or branched, and m is an integer ranging from 1 to 4; —R.sub.5—OR.sub.6 groups, wherein R.sub.5 is selected from C.sub.1-C.sub.30 alkylene groups, linear or branched, and R.sub.6 represents a hydrogen atom or is selected from C.sub.1-C.sub.30 alkyl groups, linear or branched, or is selected from R.sub.4—[—OCH.sub.2—CH.sub.2—].sub.p— polyoxyethylene groups, wherein R.sub.4 has the same meanings as reported above and p is an integer ranging from 1 to 4; —COR.sub.7 groups, wherein R.sub.7 is selected from C.sub.1-C.sub.30 alkyl groups, linear or branched; —COOR.sub.8 groups, wherein R.sub.8 is selected from C.sub.1-C.sub.30 alkyl groups, linear or branched; or they represent a —CHO group or a cyano (—CN) group; R.sub.3 is selected from C.sub.1-C.sub.30 alkyl groups, linear or branched; optionally substituted cycloalkyl groups; optionally substituted aryl groups; and C.sub.1-C.sub.30 alkoxyl groups, linear or branched; n is an integer ranging from 10 to 500. There is also a photovoltaic device (or solar device) having a support having the conjugated polymer having a derivative of indacen-4-one.

UV PATTERNABLE POLYMER BLENDS FOR ORGANIC THIN-FILM TRANSISTORS

A cross-bred organic semiconductor (OSC) polymer, includes a diketopyrrolopyrrole (DPP)-fused thiophene polymeric material, such that: the DPP-fused thiophene polymeric material comprises a first linear alkyl-substituted DPP portion and a second branched alkyl-substituted DPP portion, the cross-bred OSC polymer comprises a repeat unit having both the first linear alkyl-substituted DPP portion and the second branched alkyl-substituted DPP portion, and the fused thiophene is beta-substituted.

MULTICOLORED ELECTROCHROMIC POLYMER COMPOSITIONS AND METHODS OF MAKING AND USING THE SAME
20210340313 · 2021-11-04 · ·

This disclosure relates generally to electrochromic polymers that include a plurality of π-conjugated chromophores in spaced relation with one another, and a plurality of conjugation-break spacers (CBSs), where at least one CBS separates adjacent chromophores. The chromophores may be colored in the neutral state, and multicolored to transmissive in different oxidization states.

Multicolored electrochromic polymer compositions and methods of making and using the same
11773214 · 2023-10-03 · ·

This disclosure relates generally to electrochromic polymers that include a plurality of π-conjugated chromophores in spaced relation with one another, and a plurality of conjugation-break spacers (CBSs), where at least one CBS separates adjacent chromophores. The chromophores may be colored in the neutral state, and multicolored to transmissive in different oxidization states.