US2016133858A1PendingUtilityA1

Semiconducting Compounds and Devices Incorporating Same

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Assignee: MARKS TOBIN JPriority: Mar 24, 2011Filed: Jan 18, 2016Published: May 12, 2016
Est. expiryMar 24, 2031(~4.7 yrs left)· nominal 20-yr term from priority
H10K 30/50H10K 85/6576H01L 51/0074H01L 51/0558C07D 495/04H01L 51/0068H01L 51/0072C07D 519/00Y02E10/549B82Y 10/00H10K 85/655H10K 10/484H10K 85/6572H10K 10/466H10K 85/113H10K 10/464H10K 30/30H10K 85/215
56
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Claims

Abstract

Disclosed are molecular and polymeric compounds having desirable properties as semiconducting materials. Such compounds can exhibit desirable electronic properties and possess processing advantages including solution-processability and/or good stability. Organic transistor and photovoltaic devices incorporating the present compounds as the active layer exhibit good device performance.

Claims

exact text as granted — not AI-modified
We claim: 
     
         1 . An electronic, optical or optoelectronic device comprising a molecular semiconductor component, the molecular semiconductor component comprising a compound having formula (II): 
       
         
           
           
               
               
           
         
       
       wherein:
 R 1  and R 2  independently are a C 1-20  alkyl group or a C 1-20  haloalkyl group; 
 Ar 1 , Ar 2 , Ar 3 , and Ar 4  independently are an optionally substituted C 6-14  aryl group or an optionally substituted 5-14 membered heteroaryl group; 
 π, at each occurrence, independently is an optionally substituted polycyclic aryl or heteroaryl group; 
 m 1 , m 2 , m 3  and m 4  independently are 1, 2, 3 or 4; and 
 p is 0 or 1. 
 
     
     
         2 . The device of  claim 1 , wherein Ar 1 , Ar 2 , Ar 3 , and Ar 4  independently are an optionally substituted thienyl group or an optionally substituted bicyclic heteroaryl group comprising a thienyl group fused with a 5-membered heteroaryl group. 
     
     
         3 . The device of  claim 1 , wherein the compound has the formula: 
       
         
           
           
               
               
           
         
       
       wherein:
 R 3 , R 4 , R 5 , and R 6 , at each occurrence, independently are selected from H and R 7 , wherein R 7 , at each occurrence, independently is selected from a halogen, CN, a C 1-20  alkyl group, a C 1-20  haloalkyl group, a C 1-20  alkoxy group, and a C 1-20  alkylthio group; and 
 R 1 , R 2 , π, and p are as defined in  claim 1 . 
 
     
     
         4 . The device of  claim 3 , wherein p is 1. 
     
     
         5 . The device of  claim 4 , wherein π is an optionally substituted heteroaryl group represented by a formula selected from: 
       
         
           
           
               
               
           
         
       
       wherein Het, at each occurrence, is a monocyclic moiety including at least one heteroatom in its ring and optionally substituted with 1-2 R 10  groups, wherein R 8 , R 9 , and R 10  independently can be H or R 7 , wherein R 7 , at each occurrence, independently is selected from a halogen, CN, a C 1-20  alkyl group, a C 1-20  haloalkyl group, a C 1-20  alkoxy group, and a C 1-20  alkylthio group. 
     
     
         6 . The device of  claim 1 , wherein the compound is: 
       
         
           
           
               
               
           
         
       
       wherein R 1 , R 2  and R 10  independently are a C 1-20  alkyl group. 
     
     
         7 . A compound having formula (II): 
       
         
           
           
               
               
           
         
       
       wherein:
 R 1  and R 2  independently are a C 1-20  alkyl group or a C 1-20  haloalkyl group; 
 Ar 1 , Ar 2 , Ar 3 , and Ar 4  independently are an optionally substituted C 6-14  aryl group or an optionally substituted 5-14 membered heteroaryl group; 
 π, at each occurrence, independently is an optionally substituted polycyclic aryl or heteroaryl group; 
 m 1 , m 2 , m 3  and m 4  independently are 1, 2, 3 or 4; and 
 p is 0 or 1.

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