Dyketopyrrolopyrrole polymers for use in organic semiconductor devices
US-9221943-B2 · Dec 29, 2015 · US
US9985211B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9985211-B2 |
| Application number | US-201414900482-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 3, 2014 |
| Priority date | Jun 21, 2013 |
| Publication date | May 29, 2018 |
| Grant date | May 29, 2018 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The invention relates to novel conjugated polymers containing one or more [1,2,5]Thiadiazolo[3,4-e]isoindole-5,7-dione (TID) repeating units, to methods for their preparation and educts or intermediates used therein, to polymer blends, mixtures and formulations containing them, to the use of the polymers, polymer blends, mixtures and formulations as organic semiconductors in, or for the preparation of, organic electronic (OE) devices, especially organic photovoltaic (OPV) devices and organic photodetectors (OPD), and to OE, OPV and OPD devices comprising, or being prepared from, these polymers, polymer blends, mixtures or formulations.
Opening claim text (preview).
The invention claimed is: 1. A process of preparing a polymer comprising: one or more units of formula T (TID units) wherein * each means a chemical linkage to an adjacent unit or to a terminal group in the polymer, X is S, Se, O or NR, R denotes H or straight-chain, branched or cyclic alkyl with 1 to 30 C atoms, in which one or more CH 2 groups are optionally replaced by —O—, —S—, —C(═O)—, —C(═S)—, —C(═O)—O—, —O—C(═O)—, —NR 0 —, —SiR 0 R 00 —, —CF 2 —, —CHR 0 ═CR 00 —, —CY 1 ═CY 2 — or —C≡C— in such a manner that O and/or S atoms are not linked directly to one another, and in which one or more H atoms are optionally replaced by F, Cl, Br, I or CN, or denotes aryl or heteroaryl with 5 to 15 ring atoms, which is mono- or polycyclic and unsubstituted or substituted, Y 1 and Y 2 are independently of each other H, F, Cl or CN, R 0 and R 00 are independently of each other H or optionally substituted C 1-40 carbyl or hydrocarbyl, optionally one or more distinct donor units having electron donor properties, optionally one or more distinct acceptor units having electron acceptor properties, one or more distinct spacer units which are located between each of said TID units, optional donor units and optional acceptor units, thereby preventing said TID units, optional donor units and optional acceptor units from having directly connected to each other in the polymer chain, said optional donor units, optional acceptor units and spacer units being different from the TID units, and being arylene or heteroarylene groups that are optionally substituted, wherein the polymer formed is a random copolymer formed by co-polymerising at least three different monomers comprising said TID units, spacer units, optional donor units and/or optional acceptor units, said process, comprising: coupling three or more monomers of the following formulae with each other and/or with one or more co-monomers in an aryl-aryl coupling reaction R 7 —U—R 8 MI R 7 -Sp-R 8 MII R 7 -(Sp) x -U-(Sp) y -R 8 MIII wherein U denotes a unit of formula T or T1 wherein T1 is a donor unit or an acceptor unit wherein said donor or acceptor unit is arylene or heteroarylene that is different from formula I, has 5 to 30 ring atoms, and is optionally substituted by one or more groups R S , wherein R S is on each occurrence identically or differently F, Br, Cl, —CN, —NC, —NCO, —NCS, —OCN, —SCN, —C(O)NR 0 R 00 , —C(O)X 0 , —C(O)R 0 , —C(O)OR 0 , —NH 2 , —NR 0 R 00 , —SH, —SR, —SO 3 H, —SO 2 R 0 , —OH, —NO 2 , —CF 3 , —SF 5 , optionally substituted silyl, carbyl or hydrocarbyl with 1 to 40 C atoms that is optionally substituted and optionally comprises one or more hetero atoms, and at least one of the monomers is of formula MI or MIII wherein U denotes a unit of formula T, Sp denotes a spacer unit wherein the spacer units are: x and y are independently of each other 0, 1 or 2, and R 7 and R 8 are, independently of each other, an activated C—H bond, Cl, Br, I, O-tosylate, O-triflate, O-mesylate, O-nonaflate, —SiMe 2 F, —SiMeF 2 , —O—SO 2 Z 1 , —B(OZ 2 ) 2 , —CZ 3 ═C(Z 3 ) 2 , —C≡CH, —C≡CSi(Z 1 ) 3 , —ZnX 0 or —Sn(Z 4 ) 3 , wherein X 0 is halogen, Z 1-4 are alkyl or aryl, each being optionally substituted, and two groups Z 2 may also together form a cyclic group, and * each means a chemical linkage to an adjacent unit or to a terminal group in the polymer. 2. The process according to claim 1 , wherein the donor units have the following formulae wherein R 11 , R 12 , R 13 , R 14 , R 15 , R 16 , R 17 and R 18 independently of each other denote H or have one of the meanings of R S wherein R S is on each occurrence identically or differently F, Br, Cl, —CN, —NC, —NCO, —NCS, —OCN, —SCN, —C(O)NR 0 R 00 , —C(O)X 0 , —C(O)R 0 , —C(O)OR 0 , —NH 2 , —NR 0 R 00 , —SH, —SR 0 , —SO 3 H, —SO 2 R 0 , —OH, —NO 2 , —CF 3 , —SF 5 , optionally substituted silyl, carbyl or hydrocarbyl with 1 to 40 C atoms that is optionally substituted and optionally comprises one or more hetero atoms, and * each means a chemical linkage to an adjacent unit or to a terminal group in the polymer. 3. The process according to claim 1 , wherein the acceptor units have the following formulae
containing hetero atoms · CPC title
Photovoltaic applications · CPC title
Electricity · mapped topic
Electricity · mapped topic
containing heteroatoms · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.