An organic semiconducting donor-acceptor (D-A) small molecule, as well as a semiconductor device that can incorporate the D-A small molecule, are disclosed. The D-A small molecule can have electron deficient substituents and R group substituents that can be C.sub.1-C.sub.20 linear alkyl chains, C.sub.2-C.sub.24 branched alkyl chains, hydrogen atoms, etc. The D-A small molecule can be can be synthesized in a reaction between a dithienofuran (DTF) core monomer and an electron deficient monomer. Additionally, the D-A small molecule can be part of an organic semiconducting copolymer. A semiconductor device that can incorporate the D-A small molecule in a photoactive layer is also disclosed herein. Additionally, 3,4-dibrominated furan compound that can, in some embodiments, be a precursor for the D-A small molecule is disclosed. The 3,4-dibrominated furan compound can be synthesized in a reaction involving a furan-2,5-dicarboxylic dimethyl ester (FDME), which can have a bio-renewable precursor.

A polybenzodifuran ladder polymer is disclosed.

A method for forming an electrochromic device includes: forming a first conducting layer on a first substrate; forming a first electrolyte layer on the first conducting layer; forming a second conducting layer on a second substrate; forming an electrochromic layer on the second conducting layer; forming a second electrolyte layer on the electrochromic layer; and laminating the first substrate and the second substrate such that the first electrolyte layer is in contact with the second electrolyte layer.

An organic semiconducting donor-acceptor (D-A) small molecule, as well as a semiconductor device that can incorporate the D-A small molecule, are disclosed. The D-A small molecule can have electron deficient substituents and R group substituents that can be C.sub.1-C.sub.20 linear alkyl chains, C.sub.2-C.sub.24 branched alkyl chains, hydrogen atoms, etc. The D-A small molecule can be can be synthesized in a reaction between a dithienofuran (DTF) core monomer and an electron deficient monomer. Additionally, the D-A small molecule can be part of an organic semiconducting copolymer. A semiconductor device that can incorporate the D-A small molecule in a photoactive layer is also disclosed herein. Additionally, 3,4-dibrominated furan compound that can, in some embodiments, be a precursor for the D-A small molecule is disclosed. The 3,4-dibrominated furan compound can be synthesized in a reaction involving a furan-2,5-dicarboxylic dimethyl ester (FDME), which can have a bio-renewable precursor.

Hydrocarbon polymer having two 2-oxo-1,3-dioxolane-4-carboxylate end groups of formula (I):

##STR00001## F.sup.1 has formula (IIa) and F.sup.2 has formula (IIb):

##STR00002## in which g and d, which are identical or different, represent an integer equal to 1, 2 or 3; R.sup.1 to R.sup.12 represent a hydrogen atom or an alkyl radical of 1 to 22 carbon atoms; x and y are integers such that the sum x+y is 0 to 2; R.sup.13 is an oxygen or sulphur atom or a divalent CH.sub.2 radical; n1, n2, m, p1 and p2 are an integer or equal to 0 and such that the molecular weight Mn of the polymer of formula (I) is between 400 and 100 000 g/mol, a process for the preparation of the polymer by ring-opening metathesis polymerization, and use as adhesive in mixture with an amino compound having at least two amine groups.

An exemplary embodiment of the present disclosure provides a method of designing a polymer. The method can include: providing a set of polymer data; generating a set of polymer structures; providing one or more target properties for the polymer, predicting properties of each polymer structure of the set of polymer structures, and design considerations for the set of polymer structures; and selecting one or more polymer structures from the set of polymer structures, based at least in part, on the predicted properties of the polymer structures. The polymer data can include a set of monomer structures.

The present disclosure is directed to methods of making a polymer, including exposing a reaction mixture including a strained cyclic unsaturated monomer and an organic initiator to a stimulus to provide an activated organic initiator, whereby the activated organic initiator is effective to polymerize the strained cyclic unsaturated monomer via a 4-membered carbocyclic intermediate to provide a polymer having constitutional units derived from the strained cyclic unsaturated monomer.

An organic semiconducting donor-acceptor (D-A) small molecule, as well as a semiconductor device that can incorporate the D-A small molecule, are disclosed. The D-A small molecule can have electron deficient substituents and R group substituents that can be C.sub.1-C.sub.20 linear alkyl chains, C.sub.2-C.sub.24 branched alkyl chains, hydrogen atoms, etc. The D-A small molecule can be can be synthesized in a reaction between a dithienofuran (DTF) core monomer and an electron deficient monomer. Additionally, the D-A small molecule can be part of an organic semiconducting copolymer. A semiconductor device that can incorporate the D-A small molecule in a photoactive layer is also disclosed herein. Additionally, 3,4-dibrominated furan compound that can, in some embodiments, be a precursor for the D-A small molecule is disclosed. The 3,4-dibrominated furan compound can be synthesized in a reaction involving a furan-2,5-dicarboxylic dimethyl ester (FDME), which can have a bio-renewable precursor.

The present disclosure is directed to methods of making a polymer, including exposing a reaction mixture including a strained cyclic unsaturated monomer and an organic initiator to a stimulus to provide an activated organic initiator, whereby the activated organic initiator is effective to polymerize the strained cyclic unsaturated monomer via a 4-membered carbocyclic intermediate to provide a polymer having constitutional units derived from the strained cyclic unsaturated monomer.

Disclosed are methods for preparing and collecting a polyaromatic compound. Also disclosed are products comprising a polyaromatic compound.