1446139-66-7

Basic information

• Product Name: C₃₀H₃₉BrN₂S₃
• CAS NO: 1446139-66-7
• Molecular Weight: 603.755
• Mol File: 1446139-66-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₃₀H₃₉BrN₂S₃(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₀H₃₉BrN₂S₃(1446139-66-7)
• EPA Substance Registry System: C₃₀H₃₉BrN₂S₃(1446139-66-7)

Safety Data

• Hazardous Substances Data: 1446139-66-7(Hazardous Substances Data)

Upstream product

• 1446139-63-4 4-bromo-7-[5-(2-hexyldecyl)-thiophen-2-yl]-benzo[2,1,3]thiadiazole 
• 1215857-68-3 2-(2-hexyldecyl)thiophene 
• 52997-43-0 7-(bromomethyl)pentadecane 
• 1446139-65-6 C₃₀H₄₀N₂S₃ 

Relevant articles and documents

Tuning optical and electronic properties of star-shaped conjugated molecules with enlarged π-delocalization for organic solar cell application

Three structurally related conjugated molecules (BTT-BTD-0, BTT-BTD-1 and BTT-BTD-2) in star shape have been designed and synthesized as donor materials for small molecule based bulk heterojunction (BHJ) solar cells. The structural features of these molecules include a planarized benzo[1,2-b:3,4-b′:5,6- b″]trithiophene (BTT) with a C3h symmetry as the central core and three conjugated arms incorporating electron deficient benzo[2,1,3] thiadiazole (BTD) units, with arms being linked to the core via different number of thiophene connecting units (e.g., 0, 1, 2 corresponding to BTT-BTD-0, BTT-BTD-1 and BTT-BTD-2, respectively). Comparative analyses of optical and electronic properties indicate that the molecules bearing more thiophene units between the BTT core and the BTD arms possess higher-lying HOMO levels while their LUMO levels remain almost unchanged. The improvement of BHJ device performance, with [6,6]-phenyl-C61-butyric acid methyl ester (PC 61BM) as the acceptor, is observed with increasing number of thiophene units between the BTT core and BTD arms, from BTT-BTD-0 to BTT-BTD-1 and BTT-BTD-2. The BTT-BTD-2:PC61BM based BHJ devices show the highest power conversion efficiency (PCE) of 0.74%, with an open-circuit voltage (Voc) of 0.69 V, a short-circuit current density (Jsc) of 2.93 mA cm-2, and a fill factor (FF) of 0.37 under 1 sun (100 mW cm-2) AM 1.5G simulated solar illumination. The PV performance of BTT-BTD-2 is further improved when [6,6]-phenyl-C71-butyric acid methyl ester (PC71BM) is used as the electron acceptor, yielding the best device performance with Jsc of 4.13 mA cm-2, V oc of 0.72 V, FF at 0.46 and PCE of 1.36%. The effect of the different number of thiophenes linking the BTT core and the conjugated BTD arms has been clearly demonstrated on regulating optical and electrochemical properties of the three molecules and their BHJ device performances.