C08G2261/19

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.

Multicolored electrochromic polymer compositions and methods of making and using the same
11066513 · 2021-07-20 · ·

Electrochromic polymers include conjugated chromophores in spaced relation with one another, and conjugation-break spacers (CBSs). At least one CBS separates adjacent chromophores. The chromophores may be colored in the neutral state, and multicolored to transmissive in different oxidization states.

NANOHOOP-FUNCTIONALIZED POLYMER EMBODIMENTS AND METHODS OF MAKING AND USING THE SAME
20210095069 · 2021-04-01 · ·

Disclosed herein are embodiments of a nanohoop-functionalized polymer and methods of making and using the same. In particular embodiments, polymer comprises one or more nanohoops that extend from the polymer backbone. Also disclosed herein are polymerizable nanohoop monomer embodiments that can be used to make the polymer embodiments disclosed herein.

MULTICOLORED ELECTROCHROMIC POLYMER COMPOSITIONS AND METHODS OF MAKING AND USING THE SAME
20230416452 · 2023-12-28 ·

This disclosure relates generally to electrochromic polymers that include a plurality of -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.

Enhancing performance stability of electroactive polymers by vapor-deposited organic networks

Disclosed are compositions of electroactive polymers (EAPs) having improved performance stability. In the EAP compositions, a cross-linked polymer is deposited onto the surface of the EAP by vapor-deposition methods. Upon contact with an aqueous solution (e.g., an aqueous electrolyte solution), the vapor-deposited polymeric network becomes a hydrogel that encapsulates the EAPs. By modulating precursors and vapor deposition conditions, the mesh size of the resultant hydrogel coatings can be controlled to accommodate the key species that interact with the EAPs.

TACKIFIER FOR RUBBER COMPOSITIONS

A tackifier comprising a resin with repeating units of formula (I) wherein R.sup.1 is a linear or branched alkylen group with 1 to 10 carbon atoms and R.sup.2 is a linear or branched, saturated or unsaturated aliphatic hydrocarbon group with up to 20 carbon atoms and a non-aromatic compound which consists to at least 50% by weight of one or more linear or branched, saturated or unsaturated aliphatic hydrocarbon groups with at least 4 carbon atoms.

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MULTICOLORED ELECTROCHROMIC POLYMER COMPOSITIONS AND METHODS OF MAKING AND USING THE SAME
20200131304 · 2020-04-30 · ·

This disclosure relates generally to electrochromic polymers that include a plurality of -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
10544257 · 2020-01-28 · ·

Electrochromic polymers that include a plurality of -conjugated chromophores in spaced relation with one another, and a plurality of conjugation-break spacers (CBSs), where at least one CBS separates adjacent chromophores, are provided. The chromophores may be colored in the neutral state, and multicolored to transmissive in different oxidation states.

Small molecule acceptors derived from renewable furan source

Embodiments described herein provide a precursor for synthesizing a number of molecules for use in organic photovoltaics. The precursor is diiodo-furopyran (DFP), such as dibromo-DFP (DBDFP), to be used to synthesize a number of different molecules for use in organic photovoltaics. DFP possesses numerous reactive sites that can be used to simultaneously modify the backbone structure (which can be used to tune electronic and crystalline properties) and the side-chains (affecting the solubility and the solubility of any subsequent copolymers). Each of the molecules has either a biisocoumarin or biisoquinoline core structure and can be easily varied to yield a different functional backbone or different substituents. The molecules can be used in copolymers or small molecules for use in OPVs.

Fluorine atom-containing polymer and use of same

Provided is a fluorine atom-containing polymer which is a condensation polymer of a fluorene derivative that provides a repeating unit represented by formula (1), a fluorene derivative that provides a repeating unit represented by formula (2) and a fluorene derivative that provides a repeating unit represented by formula (3). ##STR00001##