C08G2261/72

n-Doped electrically conductive polymeric material

There is provided a material comprising a n-doped electrically conductive polymer comprising at least one electron-deficient aromatic moiety, each electron-deficient aromatic moiety having a gas-phase electron affinity (E.sub.A) of 1-3 eV; and at least one counter-cation covalently bonded to the polymer or to a further polymer comprised in the material, the polymer being n-doped to a charge density of 0.1-1 electron per electron-deficient aromatic moiety, the polymer being capable of forming a layer having a vacuum workfunction (WF) of 2.5-4.5 eV, and wherein all the counter-cations comprised in the material are immobilised such that any electron in the polymer cannot significantly diffuse or migrate out of the polymer. There is also provided a method of preparing the material.

LIQUID HYDROCARBON-BASED COPOLYMERS BEARING TWO CYCLOCARBONATE ESTER END GROUPS

1) Hydrocarbon-based copolymer comprising two end groups preceded by an ester function and chosen from a 2-oxo-1,3-dioxolan-4-yl (or cyclocarbonate), a dithiocyclocarbonate, an exo-vinylene cyclocarbonate and a 2-oxo-1,3-dioxolen-4-yl, the main chain of which comprises units (I) and (II)

##STR00001##

in which R.sup.0 is notably a methyl radical;

and the number-average molecular mass Mn of which is between 400 and 100 000 g/mol.

2) Process for preparing said copolymer, comprising:

(i) a step of heating a statistical bipolymer A chosen from a poly(butadiene-isoprene), a poly(butadiene-myrcene) and a poly(butadiene-farnesene); and then

(ii) a step of heating the product formed, in the presence of a chain-transfer agent.

3) Use as adhesive, as a mixture with an amine compound comprising at least two amine groups.

LIQUID HYDROCARBON COPOLYMERS HAVING TWO CYCLOCARBONATE ETHER END GROUPS

1) Hydrocarbon-based copolymer comprising two end groups preceded by an ether function and chosen from a 2-oxo-1,3-dioxolan-4-yl (or cyclocarbonate), a dithiocyclocarbonate, and a 2-oxo-1,3-dioxolen-4-yl, the main chain of which comprises units (I) and (II)

##STR00001##

in which R.sup.0 is notably a methyl radical;

and the number-average molecular mass Mn of which is between 400 and 100 000 g/mol.

2) Process for preparing said copolymer, comprising: (i) a step of heating a statistical bipolymer A chosen from a poly(butadiene-isoprene), a poly(butadiene-myrcene) and a poly(butadiene-farnesene); and then (ii) a step of heating the product formed, in the presence of a chain-transfer agent.

3) Use as adhesive, as a mixture with an amine compound comprising at least two amine groups.

Chromophoric polymer dots

The present invention provides, among other aspects, stabilized chromophoric nanoparticles. In certain embodiments, the chromophoric nanoparticles provided herein are rationally functionalized with a pre-determined number of functional groups. In certain embodiments, the stable chromophoric nanoparticles provided herein are modified with a low density of functional groups. In yet other embodiments, the chromophoric nanoparticles provided herein are conjugated to one or more molecules. Also provided herein are methods for making rationally functionalized chromophoric nanoparticles.

CONDUCTIVE POLYMER DISPERSION AND METHOD FOR PREPARING SAME, AND METHOD FOR MANUFACTURING CONDUCTIVE FILM
20200181431 · 2020-06-11 ·

A conductive polymer dispersion of this disclosure includes: a conductive composite containing a n-conjugated conductive polymer and a polyanion; an isocyanurate-based compound; and a dispersion medium for dispersing the conductive composite.

MODIFIED CONDUCTIVE STRUCTURE AND METHOD FOR PRODUCING THE SAME

A modified conductive structure includes a conductive substrate and a polymer film disposed over a surface of the polymer film. A chemical bond exists between the polymer film and the conductive substrate, and the polymer film includes repeating units as shown below:

##STR00001##

wherein A is an antifouling molecule group; B is a sulfur-containing group or a nitrogen-containing group; R is a single bond or a first linking group; C is -L-E, wherein L is a second linking group, E is an enzyme unit; x and z are each independently 0 or an integer from 1 to 10000, and y is an integer from 1 to 10000; o is 0 or an integer from 1 to 50, and when o is an integer from 1 to 50, m and n are each independently 0 or an integer from 1 to 50.

Conductive polymer dispersion and method for preparing same, and method for manufacturing conductive film
10647858 · 2020-05-12 · ·

A conductive polymer dispersion of this disclosure includes: a conductive composite containing a -conjugated conductive polymer and a polyanion; an isocyanurate-based compound; and a dispersion medium for dispersing the conductive composite.

Compound, compound fabrication method, and graphene nanoribbon fabrication method
10636539 · 2020-04-28 · ·

A compound represented by the following general formula (1) is used as a precursor of a graphene nanoribbon: ##STR00001##
where X's are independent of each other and are leaving groups, R's are independent of one another and are hydrogen atoms, fluorine atoms, chlorine atoms, or 1-12C straight-chain, branched-chain, or cyclic alkyl groups, and each of p, q, r, and s is an integer in the range of 0 to 5.

Surface treatments for wearable devices
10619022 · 2020-04-14 · ·

A wearable device including a body made of an elastic material having a polymeric backbone where a portion of the polymeric backbone is unsaturated. The body has an outer surface that is oxidized on at least one part with at least one functional group where the at least one part of the outer surface is more oleophobic than the body.

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.