IP Library Granted Patent US 7,838,624
Granted Patent B2
US 7,838,624 · App. 12/153,180 · Granted Nov 23, 2010

Mixed halogen polymerization

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Quick Facts
Patent No.
US 7,838,624
App. No.
12/153,180
Granted
Nov 23, 2010
Kind
B2
Abstract

Synthesis of regioregular thiophene-based polymers (PTs) and their functionalized counterparts via metal assisted cross-coupling polymerizations utilizing mixed halogen substituted aryl halide monomer precursors. The described method provides a means to control structural homogeneity and regioregularity and the electronic/spectroscopic properties of functionalized PTs, and leads to improved performance of organic semiconductor devices such as OPVs and/or OFETs. Asymmetrical monomers can be used.

Claims (28)

1. A method of making poly(3-arylsubstituted) thiophene, comprising:

providing at least one monomer represented by:

wherein X is I and X′ is Br, or X is I and X′ is Cl, or X is Br and X′ is Cl; and

polymerizing the monomer; and

wherein the aryl group is a substituted phenyl group comprising a branched alkyl substituent.

2. The method of claim 1 , wherein X is I, and X′ is Br.

3. The method of claim 1 , wherein the aryl group is 4-octylphenyl group or 4-(2-ethylhexyl)phenyl group.

4. The method of claim 1 , wherein the polymerizing step comprises (i) reacting the monomer with an organomagnesium reagent to form an intermediate, and (ii) reacting the intermediate with at least one metal complex.

5. The method of claim 1 , wherein the polymerizing step comprises (i) reacting the monomer with an organomagnesium reagent comprising an organomagnesium component and a metal activation agent to form an intermediate, and (ii) reacting the intermediate with at least one metal complex.

6. The method of claim 1 , wherein the polymerizing step comprises dissolving the monomer in at least one solvent to form a mixture, adding at least one organomagnesium reagent to the mixture, adding an initiator to the mixture, recovering a poly(3-arylsubstituted thiophene).

7. The method of claim 1 , wherein the polymerizing step is carried out under substantially living conditions.

8. The method of claim 1 , wherein the polymerizing is carried out to produce a homopolymer.

9. The method of claim 1 , wherein X is I and X′ is Br, and wherein the aryl group is an optionally substituted phenyl group, and wherein the polymerizing step comprises (i) reacting the monomer with an organomagnesium reagent to form an intermediate, and (ii) reacting the intermediate with at least one metal complex.

10. A method comprising:

providing an unsaturated ring compound comprising at least two halogen ring substituents, wherein a first halogen ring substituent is iodo and a second halogen ring substituent is bromo,

providing an organomagnesium reagent comprising an organomagnesium component and a metal activation agent,

combining the unsaturated ring compound with the reagent to form a second compound by metal-halogen exchange, wherein the metal activation agent activates the metal halogen exchange,

exposing the second compound to at least one transition metal initiator to produce an oligomerization or polymerization reaction;

wherein the unsaturated ring compound is a thiophene compound substituted at the 3-position with a substituted phenyl group comprising a branched alkyl substitutent.

11. The method of claim 10 , wherein the thiophene compound is substituted at the 2-position with bromo and substituted at the 5-position with iodo group.

12. The method of claim 10 , wherein the metal activation agent comprises lithium, magnesium, potassium, or zinc.

13. The method of claim 10 , wherein the metal activation agent comprises lithium.

14. A method comprising:

providing at least one asymmetrical organic dihalogen polymerization monomer adapted for metal-assisted cross coupling polymerization, wherein the monomer comprises at least one thiophene ring which is substituted with an aryl group, and wherein the monomer comprises an X halogen group and an X′ halogen group, wherein X and X′ are different and independently Cl, Br, or I,

polymerizing the monomer;

wherein the thiophene ring is substituted at the 3-position with a substituted phenyl group comprising a branched alkyl substitutent.

15. The method of claim 14 , wherein the polymerizing step comprises (i) reacting the monomer with an organomagnesium reagent comprising an organomagnesium component and a metal activation agent to form an intermediate, and (ii) reacting the intermediate with at least one metal complex.

16. The method of claim 14 , wherein the polymerizing step is carried out under substantially living conditions.

Assignments (9)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 31, 2014
From: PLEXTRONICS, INC.
To: SOLVAY USA INC.
Reel/Frame 032568/0780 →
RELEASE OF SECURITY INTEREST Recorded Mar 31, 2014
From: SOLVAY AMERICA, INC.
To: PLEXTRONICS, INC.
Reel/Frame 032568/0619 →
RELEASE OF SECURITY INTEREST Recorded Mar 31, 2014
From: SOLVAY AMERICA, INC.
To: PLEXTRONICS, INC.
Reel/Frame 032568/0641 →
RELEASE OF SECURITY INTEREST Recorded Mar 31, 2014
From: SOLVAY AMERICA, INC.
To: PLEXTRONICS, INC.
Reel/Frame 032568/0742 →
SECURITY AGREEMENT Recorded Jan 30, 2014
From: PLEXTRONICS, INC.
To: SOLVAY AMERICA, INC.
Reel/Frame 032141/0680 →
SECURITY AGREETMENT Recorded Sep 23, 2013
From: PLEXTRONICS, INC.
To: SOLVAY AMERICA, INC.
Reel/Frame 031347/0336 →
SECURITY AGREEMENT Recorded May 24, 2013
From: PLEXTRONICS, INC.
To: SOLVAY AMERICA, INC.
Reel/Frame 030486/0137 →
SECURITY AGREEMENT Recorded Aug 30, 2011
From: PLEXTRONICS, INC.
To: SOLVAY NORTH AMERICA INVESTMENTS, LLC
Reel/Frame 026826/0084 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 27, 2008
From: LAIRD, DARIN; SHEINA, ELENA
To: PLEXTRONICS, INC.
Reel/Frame 021494/0422 →