IP Library Granted Patent US 8,598,575
Granted Patent B2
US 8,598,575 · App. 13/775,211 · Granted Dec 3, 2013

Semiconducting compounds and related compositions and devices

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Quick Facts
Patent No.
US 8,598,575
App. No.
13/775,211
Granted
Dec 3, 2013
Kind
B2
Abstract

Disclosed are new semiconductor materials prepared from thienocoronene-based compounds and related heteroaromatic analogs. Such compounds can exhibit high carrier mobility and/or good current modulation characteristics. In addition, the compounds of the present teachings can possess certain processing advantages such as solution-processability and/or good stability at ambient conditions.

Claims (49)

1. A compound having formula I:

wherein:

W 1 and W 2 independently are —(CR c R d ) m — or —(SiR e R f )—;

X and X′ are selected from the group consisting of S, O, NR a and CR b , provided that one of X and X′ is selected from the group consisting of S, O, and NR a , and the other X and X′ is CR b ;

Y and Y′ are selected from the group consisting of S, O, NR a′ and CR b′ , provided that one of Y and Y′ is selected from the group consisting of S, O, and NR a′ , and the other Y and Y′ is CR b′ ;

Z 1 and Z 2 independently are selected from the group consisting of O, S, —C≡C—, and a covalent bond;

R a and R a ′ independently are selected from the group consisting of H, a C 1-20 alkyl group, a C 2-20 alkenyl group, and a C 1-20 haloalkyl group;

R b and R b ′ independently are selected from the group consisting of H, a C 1-20 alkyl group, a C 2-20 alkenyl group, and a C 1-20 haloalkyl group;

R c and R d independently are selected from the group consisting of H, a C 1-20 alkyl group, and a C 1-20 haloalkyl group;

R e and R f independently are selected from the group consisting of H, a C 1-20 alkyl group, and a C 1-20 haloalkyl group;

R 1 , R 1 ′, R 2 , and R 2 ′ independently are selected from the group consisting of a linear C 1-40 alkyl group, a linear C 2-40 alkenyl group, and a linear C 1-40 haloalkyl group; and

m, at each occurrence, independently is 0, 1, 2, 3, or 4.

2. The compound of claim 1 , wherein the compound has the formula IIa or IIIa:

wherein R 1 , R 1 ′, R 2 , R 2 ′, Z 1 , Z 2 , and m are as defined in claim 1 .

3. The compound of claim 1 , wherein the compound has the formula IVa or Va:

wherein R 1 , R 1 ′, R 2 , R 2 ′, Z 1 , Z 2 , and m are as defined in claim 1 .

4. The compound of claim 2 , wherein Z 1 and Z 2 independently are O or a covalent bond.

5. The compound of claim 2 , wherein each m independently is 0, 1, or 2.

6. The compound of claim 2 , wherein R 1 and R 2 independently are selected from the group consisting of a linear C 3-40 alkyl group, a linear C 4-40 alkenyl group, and a linear C 3-40 haloalkyl group; and R 1 ′ and R 2 ′ independently are selected from the group consisting of CH 3 , CF 3 , C 2 H 5 , C 2 F 5 , CH 2 CF 3 , CF 2 CH 3 , CH 2 CH 2 CH 3 , CF 2 CF 2 CF 3 , CH 2 CH 2 CF 3 , CH 2 CH 2 CH 2 CH 3 , CF 2 CF 2 CF 2 CF 3 , and CH 2 CH 2 CH 2 CF 3 .

7. The compound of claim 1 , wherein the compound has the formula IIb or IIIb:

wherein R 1 and R 2 independently are selected from the group consisting of a linear C 3-40 alkyl group, a linear C 4-40 alkenyl group, and a linear C 3-40 haloalkyl group; R 1 ′ and R 2 ′ independently are selected from the group consisting of CH 3 , CF 3 , C 2 H 5 , C 2 F 5 , CH 2 CF 3 , CF 2 CH 3 , CH 2 CH 2 CH 3 , CF 2 CF 2 CF 3 , CH 2 CH 2 CF 3 , CH 2 CH 2 CH 2 CH 3 , CF 2 CF 2 CF 2 CF 3 , and CH 2 CH 2 CH 2 CF 3 ; and m 1 and m 2 independently are 0, 1, or 2.

8. The compound of claim 1 , wherein the compound has the formula IVb or Vb:

wherein R 1 and R 2 independently are selected from the group consisting of a linear C 3-40 alkyl group, a linear C 4-40 alkenyl group, and a linear C 3-40 haloalkyl group; R 1 ′ and R 2 ′ independently are selected from the group consisting of CH 3 , CF 3 , C 2 H 5 , C 2 F 5 , CH 2 CF 3 , CF 2 CH 3 , CH 2 CH 2 CH 3 , CF 2 CF 2 CF 3 , CH 2 CH 2 CF 3 , CH 2 CH 2 CH 2 CH 3 , CF 2 CF 2 CF 2 CF 3 , and CH 2 CH 2 CH 2 CF 3 ; and m 1 and m 2 independently are 0, 1, or 2.

9. The compound of claim 1 , wherein the compound has the formula IIc, IIIc, IVc, or Vc:

wherein R 1 and R 2 independently are selected from the group consisting of a linear C 3-40 alkyl group, a linear C 4-40 alkenyl group, and a linear C 3-40 haloalkyl group; R 1 ′ and R 2 ′ independently are selected from the group consisting of CH 3 , CF 3 , C 2 H 5 , C 2 F 5 , CH 2 CF 3 , CF 2 CH 3 , CH 2 CH 2 CH 3 , CF 2 CF 2 CF 3 , CH 2 CH 2 CF 3 , CH 2 CH 2 CH 2 CH 3 , CF 2 CF 2 CF 2 CF 3 , and CH 2 CH 2 CH 2 CF 3 ; and m 1 and m 2 independently are 0, 1, or 2.

10. A compound having formula VI:

wherein:

X and X′ are selected from the group consisting of S, O, NR a and CR b , provided that one of X and X′ is selected from the group consisting of S, O, and NR a , and the other X and X′ is CR b ;

Y and Y′ are selected from the group consisting of S, O, NR a′ and CR b′ , provided that one of Y and Y′ is selected from the group consisting of S, O, and NR a′ , and the other Y and Y′ is CR b′ ;

Z 3 and Z 4 independently are selected from the group consisting of O, S, and —C≡C—;

R a and R a ′ independently are selected from the group consisting of H, a C 1-20 alkyl group, a C 2-20 alkenyl group, and a C 1-20 haloalkyl group;

R b and R b ′ independently are selected from the group consisting of H, a C 1-20 alkyl group, a C 2-20 alkenyl group, and a C 1-20 haloalkyl group; and

R 3 and R 4 independently are selected from the group consisting of a linear or branched C 1-40 alkyl group, a linear or branched C 2-40 alkenyl group, a linear or branched C 2-40 alkynyl group, a linear or branched C 1-40 haloalkyl group, and a Si(C 1-40 alkyl) 3 group.

11. The compound of claim 10 , wherein the compound has the formula VII or VIII:

wherein R 3 and R 4 are as defined in claim 10 .

12. A compound having formula IX, X, XI, or XII:

wherein:

Z 5 and Z 6 independently are selected from the group consisting of O, S, —C≡C—, and a covalent bond;

Z 7 and Z 8 independently are selected from the group consisting of O, S, —C≡C—, and a covalent bond;

R 5 and R 6 independently are selected from the group consisting of a linear or branched C 1-40 alkyl group, a linear or branched C 2-40 alkenyl group, a linear or branched C 2-40 alkynyl group, a linear or branched C 1-40 haloalkyl group, and a Si(C 1-40 alkyl) 3 group; and

R 7 and R 8 independently are selected from the group consisting of a linear or branched C 1-40 alkyl group, a linear or branched C 2-40 alkenyl group, a linear or branched C 2-40 alkynyl group, a linear or branched C 1-40 haloalkyl group, and a Si(C 1-40 alkyl) 3 group.

13. A thin film semiconductor comprising a compound of claim 1 .

14. A composite comprising a substrate and the thin film semiconductor of claim 13 deposited on the substrate.

15. An electronic device, an optical device, or an optoelectronic device comprising the thin film semiconductor of claim 13 .

16. An electronic device, an optical device, or an optoelectronic device comprising the composite of claim 14 .

17. A field effect transistor device comprising a source electrode, a drain electrode, a gate electrode, and the thin film semiconductor of claim 13 in contact with a dielectric material.

18. The field effect transistor device of claim 17 , wherein the field effect transistor has a structure selected from top-gate bottom-contact structure, bottom-gate top-contact structure, top-gate top-contact structure, and bottom-gate bottom-contact structure.

19. The field effect transistor device of claim 18 , wherein the dielectric material comprises an organic dielectric material.

20. The field effect transistor device of claim 18 , wherein the dielectric material comprises an inorganic dielectric material or a hybrid organic/inorganic dielectric material.

Assignments (6)
ASSET PURCHASE AGREEMENT Recorded Dec 13, 2025
From: FLEXTERRA, INC.; FLEXTERRA TAIWAN CORPORATION LIMITED
To: USINVEST, LLC
Reel/Frame 073948/0751 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 5, 2025
From: FLEXTERRA, INC.
To: USINVEST LLC
Reel/Frame 073464/0376 →
SECURITY INTEREST Recorded Oct 17, 2024
From: FLEXTERRA, INC.
To: SAES GETTERS INTERNATIONAL LUXEMBOURG S.A., IN ITS CAPACITY AS COLLATERAL AGENT
Reel/Frame 069191/0563 →
SECURITY INTEREST Recorded Nov 23, 2021
From: FLEXTERRA, INC.
To: SAES GETTERS INTERNATIONAL LUXEMBOURG S.A., IN ITS CAPACITY AS COLLATERAL AGENT
Reel/Frame 058226/0591 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 7, 2017
From: POLYERA CORPORATION
To: FLEXTERRA, INC.
Reel/Frame 041197/0650 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 23, 2013
From: FACCHETTI, ANTONIO; CHEN, ZHIHUA; USTA, HAKAN; NEWMAN, CHRISTOPHER; YAN, HE
To: POLYERA CORPORATION
Reel/Frame 031464/0346 →