25407-11-8

Upstream product

• 609-73-4 o-nitroiodobenzene 
• 74-86-2 acetylene 
• 99558-11-9 copper(I) 2-nitrophenylacetylide 
• 860756-31-6 α-chloro-2,2'-dinitro-stilbene 
• 577-19-5 2-nitrophenyl bromide 
• 16433-96-8 2-ethynyl-1-nitrobenzene 
• 75867-47-9 trimethyl((2-nitrophenyl)ethynyl)silane 
• 141-52-6 sodium ethanolate 
• 3284-77-3 1-(dichloromethyl)-2-nitrobenzene 
• 124-41-4 sodium methylate 

Downstream Products

• 133253-56-2 2,2'-dinitrobenzil 
• 681462-57-7 2.2'-dinitro-tolan dibromide 
• 116668-54-3 (Z)-2,2'-diaminostilbene 
• 131298-21-0 2-[(2-aminophenyl)ethynyl]phenylamine 
• 157869-16-4 1-(2'-aminophenyl)-2-(2'-nitrophenyl)ethyne 
• 873411-82-6 α,α,3',5'-tetrachloro-2'-nitro-2-nitroso-deoxybenzoin 
• 42467-40-3 2,2'-dinitrostilbene 
• 42467-39-0 2,2'-dinitrostilbene 
• 131298-23-2 17,17,18,18-Tetradehydro-1,10-bis(p-tolylsulfonyl)-1,10-diaza<2>(1,3)benzeno<2>(1,2)benzeno<2>(1,2)benzenophan 
• 131298-24-3 17,17,18,18-Tetradehydro-8-methyl-1,10-bis(p-tolylsulfonyl)-1,10-diaza<2>(1,3)benzeno<2>(1,2)benzeno<2>(1,2)benzenophan 
• 131298-26-5 8-Brom-17,17,18,18-tetradehydro-1,10-bis(p-tolylsulfonyl)-1,10-diaza<2>(1,3)benzeno<2>(1,2)benzeno<2>(1,2)benzenophan 
• 131298-27-6 8-Cyan-17,17,18,18-tetradehydro-1,10-bis(p-tolylsulfonyl)-1,10-diaza<2>(1,3)benzeno<2>(1,2)benzeno<2>(1,2)benzenophan 
• 131298-25-4 17,17,18,18-Tetradehydro-8-methoxy-1,10-bis(p-tolylsulfonyl)-1,10-diaza<2>(1,3)benzeno<2>(1,2)benzeno<2>(1,2)benzenophan 
• 131298-28-7 17,17,18,18-Tetradehydro-8-nitro-1,10-bis(p-tolylsulfonyl)-1,10-diaza<2>(1,3)benzeno<2>(1,2)benzeno<2>(1,2)benzenophan 

Relevant academic research and scientific papers

Sodium methylthiolate as an efficient deprotecting agent for dicobalt hexacarbonyl complexes of acetylenes

Various dicobalt hexacarbonyl acetylene complexes were efficiently converted to the unprotected acetylene by the reaction of two molar equivalents of sodium methylthiolate. Yields and reaction times depend upon the choice of solvent. DMF proved to be the

Double anchor indolo[3,2-: B] indole-derived metal-free dyes with extra electron donors as efficient sensitizers for dye-sensitized solar cells

Two new di-acceptors metal-free organic dyes based on indolo[3,2-b]indole donor backbone with extra electron donors were designed, synthesized, and applied for dye-sensitized solar cells (DSSCs). In this study, the effect of the additional donors was inve

Dipyrrole derivative and preparation method thereof as well as organic light-emitting device

The invention provides a dipyrrole derivative and a preparation method thereof as well as an organic light-emitting device and belongs to the technical field of organic optoelectronic materials. According to the dipyrrole derivative disclosed by the inven

HETEROCYCLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

A heterocyclic compound and an organic light-emitting device including the heterocyclic compound, the heterocyclic compound being represented by Formula 1:

Dicyanovinyl-substituted indolo[3,2-b] indole derivatives: Low-band-gap π-conjugated molecules for a single-component ambipolar organic field-effect transistor

A series of low-band-gap π-conjugated molecules comprising N,N′-dihexylindolo[3,2-b]indole as an electron donor (D) and dicyanovinyl as an electron acceptor (A) with A-π-D-π-A architecture have been designed and synthesized to fabricate a single-component

Solution processed bulk heterojunction solar cells based on A-D-A small molecules with a dihydroindoloindole (DINI) central donor and different acceptor end groups

Four acceptor-donor-acceptor (A-D-A) small molecules with dihydroindoloindole (DINI) as the central donor unit and different acceptor end groups such as dicyanovinylene (DCV), indenedione (IND), cyanoacrylate (CA) and rhodanine (Rho) linked through bithiophene as the π-linker, DINI-DCV, DINI-IND, DINI-CA and DINI-Rho, were designed and synthesized for the application as donor materials along with PC71BM as an acceptor for solution processed organic bulk heterojunction solar cells. The effect of acceptor end groups on the photovoltaic performance was investigated. The organic solar cells (OSCs) based on as cast DINI-IND showed the highest power conversion efficiency of 3.04%, as cast DINI-CA showed the lowest PCE of 1.63% and the other two exhibit a PCE in between them. These results showed that acceptor end groups affect the overall performance of the cells. The PCE of OSCs has been further improved up to 7.04% and 6.16% employing two-step annealing (TSA) treated DIN-IND:PC71BM (1:2) and DIN-CN:PC71BM (1:2), respectively. The enhancement in the PCE of OSCs with TSA treated active layers is attributed to the better nanophase morphology, the increase in the crystalline nature and light harvesting efficiency and more balanced charge transport and charge collection probability.

ELECTROACTIVE MATERIALS

There is disclosed a compound having Formula (I), Formula (II), Formula (III), Formula (VIII), Formula (IX), or Formula (X) The variables are described in detail in the application.

Compound and organic light-emitting device comprising the same

Provided are a compound of Formula 1 and an organic light-emitting device including the compound of Formula 1: The compounds of Formula 1 are particularly useful as fluorescent dopants in the emission layer of the organic light-emitting device.

Synthesis and characterization of new dihydroindolo[3,2-b]indole and 5,6-Bis(octyloxy)-4,7-di(thiophen-2-yl)benzo[c][1,2,5]thiadiazole-based polymer for bulk heterojunction polymer solar cells

We have designed and developed a new ladder type tetrafused π-conjugated building block such as dihydroindolo[3,2-b]indole (DINI) and investigated its role as an electron rich unit. The photovoltaic properties of a new semiconducting π-conjugated polymer,

Synthesis and Characterization of Indolo[3,2-b]indole Based Copolymers for Bulk Heterojunction Polymer Solar Cell

A series of donor-acceptor low band gap polymers (DINIBT-C8, DINIBT-C10 and DINIBT-EH) containing 5,10-dihydroindolo[3,2-b]indole (DINI) as an electron donating unit and benzothiadiazole (BT) as an electron accepting unit with various kinds of alkyl chain