IP Library Granted Patent US 9,708,346
Granted Patent B2
US 9,708,346 · App. 15/298,160 · Granted Jul 18, 2017

Semiconducting compounds and related devices

Inventors: Antonio Facchetti (Chicago, IL); Zhihua Chen (Skokie, IL); Jennifer E. Brown (Chicago, IL)
Assignee: Flexterra, Inc.
C07D513/04C08G61/126H01L51/0036H01L51/0043C08G2261/124C08G2261/1412C08G2261/18C08G2261/228C08G2261/3223C08G2261/3243C08G2261/3244C08G2261/3246C08G2261/91C08G2261/92H01L51/0541H01L51/0545H01L51/0558H01L51/4253
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,708,346
App. No.
15/298,160
Granted
Jul 18, 2017
Kind
B2
Abstract

The present teachings relate to new semiconducting compounds including one or more moieties represented by formula (I): wherein X is a chalcogen; and one or more linear conjugated moieties and/or one or more cyclic conjugated moieties other than the moieties represented by formula (I). The present compounds can be used to prepare thin film semiconductor components which can be incorporated into various electronic, optical, and optoelectronic devices.

Claims (78)

1. A compound comprising one or more moieties represented by formula (I):

wherein X is a chalcogen; and one or more linear conjugated moieties and/or one or more cyclic conjugated moieties other than the moieties represented by formula (I).

2. The compound of claim 1 , wherein the compound comprises one or more moieties represented by formula (II):

wherein R 1 , at each occurrence, independently is selected from the group consisting of H, halogen, —CN, NO 2 , R 2 , -L-R 3 , OH, OR 2 , OR 3 , NH 2 , NHR 2 , N(R 2 ) 2 , NHR 3 , NR 2 R 3 , N(R 3 ) 2 , SH, SR 2 , SR 3 , S(O) 2 OH, —S(O) 2 OR 2 , —S(O) 2 OR 3 , C(O)H, C(O)R 2 , C(O)R 3 , C(O)OH, C(O)OR 2 , C(O)OR 3 , C(O)NH 2 , C(O)NHR 2 , C(O)N(R 2 ) 2 , C(O)NHR 3 , C(O)NR 2 R 3 , C(O)N(R 3 ) 2 , SiH 3 , SiH(R 2 ) 2 , SiH 2 (R 2 ), and Si(R 2 ) 3 , wherein L is selected from the group consisting of a divalent C 1-40 alkyl group, a divalent C 2-40 alkenyl group, a divalent C 1-40 haloalkyl group, and a covalent bond; R 2 is selected from the group consisting of a C 1-40 alkyl group, a C 2-40 alkenyl group, a C 2-40 alkynyl group, and a C 1-40 haloalkyl group; and R 3 is selected from the group consisting of a C 3-10 cycloalkyl group, a C 6-14 aryl group, a C 6-14 haloaryl group, a 3-12 membered cycloheteroalkyl group, and a 5-14 membered heteroaryl group, each of which optionally is substituted with 1-5 substituents selected from the group consisting of a halogen, —CN, NO 2 , R 2 , OR 2 , and SR 2 .

3. The compound of claim 1 , wherein X is selected from the group consisting of O, S, and Se.

4. The compound of claim 3 , wherein the compound comprises one or more moieties represented by formula (III) or (IV):

5. The compound of claim 1 , wherein the compound is a polymer having a first repeating unit M 1 selected from the group consisting of:

wherein:

pi-2 is an optionally substituted conjugated polycyclic moiety;

Ar, at each occurrence, is independently an optionally substituted 5- or 6-membered aryl or heteroaryl group;

Z is a conjugated noncyclic linker;

m and m′ independently are 0, 1, 2, 3, 4, 5 or 6, provided that at least one of m and m′ is not 0;

p and p′ independently are 0 and 1, provided that at least one of p and p′ is 1; and

the polymer has a degree of polymerization (n) ranging from 3 to 1,000.

6. The compound of claim 5 , wherein the compound is a polymer having a first repeating unit M 1 selected from the group consisting of:

7. The compound of claim 2 , wherein the compound is a polymer having a first repeating unit M 1 selected from the group consisting of:

wherein:

pi-2 is an optionally substituted conjugated polycyclic moiety;

Ar, at each occurrence, is independently an optionally substituted 5- or 6-membered aryl or heteroaryl group;

Z is a conjugated noncyclic linker;

m and m′ independently are 0, 1, 2, 3, 4, 5 or 6, provided that at least one of m and m′ is not 0;

p and p′ independently are 0 and 1, provided that at least one of p and p′ is 1; and

the polymer has a degree of polymerization (n) ranging from 3 to 1,000.

8. The compound of claim 7 , wherein the compound is a polymer having a first repeating unit M 1 selected from the group consisting of:

9. The compound of claim 8 , wherein R 1 , at each occurrence, independently is selected from the group consisting of H, F, Cl, —CN, —NO 2 , R 2 , OR 2 , and SR 2 , wherein R 2 is selected from the group consisting of a linear or branched C 1-40 alkyl group, a linear or branched C 2-40 alkenyl group, and a linear or branched C 1-40 haloalkyl group.

10. The compound of claim 9 , wherein R′, at each occurrence, independently is selected from the group consisting of H, F, Cl, —CN, a C 3-20 alkyl group, a C 3-20 alkoxy group, and a C 3-20 haloalkyl group.

11. The compound of claim 8 further comprising one or more additional repeating units M 2 that are different from the first repeating unit M 1 , said additional repeating units M 2 being selected from the group consisting of:

wherein:

pi-2 is an optionally substituted conjugated polycyclic moiety;

Ar, at each occurrence, is independently an optionally substituted 5- or 6-membered aryl or heteroaryl group;

Z is a conjugated noncyclic linker;

m and m′ independently are 0, 1, 2, 3, 4, 5 or 6, provided that at least one of m and m′ is not 0;

m″ is 1, 2, 3, 4, 5 or 6; and

p and p′ independently are 0 and 1, provided that at least one of p and p′ is 1.

12. The compound of claim 11 represented by formula (V) or (VI):

wherein n is an integer ranging from 3 to 1,000.

13. The compound of claim 12 , wherein pi-2 in the first repeating unit M 1 and any additional repeating unit M 2 is an optionally substituted C 8-26 aryl group or 8-26 membered heteroaryl group.

14. The compound of claim 13 , wherein pi-2 is selected from the group consisting of:

wherein:

R a is selected from the group consisting of H, F, Cl, —CN, R, —OR, —SR, —C(O)R, —OC(O)R, and —C(O)OR;

R b is selected from the group consisting of H, R, and -L′-R f ;

R c is H or R;

R d is selected from the group consisting of H, F, Cl, —CN, R, —OR, —SR, —C(O)R, —OC(O)R, —C(O)OR, and -L′-R f ;

R e is selected from the group consisting of H, F, Cl, —CN, R, —OR, —SR, —C(O)R, —OC(O)R, —C(O)OR, and R f ;

R f is a C 6-20 aryl group or a 5-20-membered heteroaryl group, each optionally substituted with 1-8 groups independently selected from the group consisting of F, Cl, —CN, R, —OR, and —SR;

L′ is selected from the group consisting of —O—, —S—, —C(O)—, —OC(O)—, —C(O)O—, and a covalent bond; and

R is selected from the group consisting of a C 1-40 alkyl group, a C 1-40 haloalkyl group, a C 2-40 alkenyl group, and a C 2-40 alkynyl group.

15. The compound of claim 8 , wherein Ar in (Ar) m , (Ar) m′ , and (Ar) m″ in the first repeating unit M 1 and any additional repeating unit M 2 is represented by:

wherein each W independently is selected from the group consisting of N, CH, and CR 4 , wherein R 4 is selected from the group consisting of F, Cl, —CN, R 2 , OR 2 , SR 2 , C(O)R 2 , OC(O)R 2 , and C(O)OR 2 , and wherein R 2 is selected from the group consisting of a C 1-40 alkyl group, a C 2-40 alkenyl group, a C 2-40 alkynyl group, and a C 1-40 haloalkyl group.

16. The compound of claim 15 , wherein (Ar) m , (Ar) m′ , and (Ar) m″ if present in either the first repeating unit M 1 or any additional repeating unit M 2 independently are selected from the group consisting of:

17. The compound of claim 1 , wherein the compound is a small molecule represented by formula (VII) or (VIII):

wherein:

R 1 , at each occurrence, independently is selected from the group consisting of H, halogen, —CN, NO 2 , R 2 , -L-R 3 , OH, OR 2 , OR 3 , NH 2 , NHR 2 , N(R 2 ) 2 , NHR 3 , NR 2 R 3 , N(R 3 ) 2 , SH, SR 2 , SR 3 , S(O) 2 OH, —S(O) 2 OR 2 , —S(O) 2 OR 3 , C(O)H, C(O)R 2 , C(O)R 3 , C(O)OH, C(O)OR 2 , C(O)OR 3 , C(O)NH 2 , C(O)NHR 2 , C(O)N(R 2 ) 2 , C(O)NHR 3 , C(O)NR 2 R 3 , C(O)N(R 3 ) 2 , SiH 3 , SiH(R 2 ) 2 , SiH 2 (R 2 ), and Si(R 2 ) 3 , wherein L is selected from the group consisting of a divalent C 1-40 alkyl group, a divalent C 2-40 alkenyl group, a divalent C 1-40 haloalkyl group, and a covalent bond; R 2 is selected from the group consisting of a C 1-40 alkyl group, a C 2-40 alkenyl group, a C 2-40 alkynyl group, and a C 1-40 haloalkyl group; and R 3 is selected from the group consisting of a C 3-10 cycloalkyl group, a C 6-14 aryl group, a C 6-14 haloaryl group, a 3-12 membered cycloheteroalkyl group, and a 5-14 membered heteroaryl group, each of which optionally is substituted with 1-5 substituents selected from the group consisting of a halogen, —CN, NO 2 , R 2 , OR 2 , and SR 2 ;

R 5 and R 6 independently are selected from the group consisting of H, R 2 , OR 2 , SR 2 , C(O)R 2 , OC(O)R 2 , and C(O)OR 2 ;

Q 1 and Q 2 independently are selected from the group consisting of:

wherein:

pi-2 is an optionally substituted conjugated polycyclic moiety;

Ar, at each occurrence, is independently an optionally substituted 5- or 6-membered aryl or heteroaryl group;

Z is a conjugated noncyclic linker;

m and m′ independently are 0, 1, 2, 3, 4, 5 or 6, provided that at least one of m and m′ is not 0;

m″ is 1, 2, 3, 4, 5 or 6; and

p and p′ independently are 0 and 1, provided that at least one of p and p′ is 1.

18. The compound of claim 1 , wherein the compound is a small molecule represented by formula (IX) or (X):

wherein:

Ar, at each occurrence, is independently an optionally substituted 5- or 6-membered aryl or heteroaryl group;

m and m′ independently are 0, 1, 2, 3, 4, 5 or 6, provided that at least one of m and m′ is not 0;

R 5 and R 6 independently are selected from the group consisting of H, R 2 , OR 2 , SR 2 , C(O)R 2 , OC(O)R 2 , and C(O)OR 2 ;

Q is absent or selected from the group consisting of:

and a covalent bond,

wherein:

pi-2 is an optionally substituted conjugated polycyclic moiety;

Ar, at each occurrence, is independently an optionally substituted 5- or 6-membered aryl or heteroaryl group;

Z is a conjugated noncyclic linker;

m and m′ independently are 0, 1, 2, 3, 4, 5 or 6, provided that at least one of m and m′ is not 0;

m″ is 1, 2, 3, 4, 5 or 6; and

p and p′ independently are 0 and 1, provided that at least one of p and p′ is 1.

19. The compound of claim 18 , wherein the compound is a small molecule represented by formula (XI), (XII), (XIII), (XIV), (XV), or (XVI):

20. The compound of 19 , wherein X is S.

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 Nov 13, 2016
From: FACCHETTI, ANTONIO; CHEN, ZHIHUA; BROWN, JENNIFER E.
To: POLYERA CORPORATION
Reel/Frame 040608/0499 →
Continuity (2)
Provisional Application 62243141 · Oct 19, 2015
Related Publication 20170110666A1 · Apr 20, 2017