125775-57-7

Upstream product

• 20441-00-3 4-(diphenylamino)benzonitrile 
• 7440-44-0 pyrographite 
• 36809-26-4 4-N,N-diphenylamino-1-bromobenzene 
• 4181-05-9 4-(diphenylamino)benzaldehyde 
• 1194-02-1 4-fluorobenzonitrile 
• 122-39-4 diphenylamine 

Downstream Products

• 521971-76-6 2-{4'-(6-methacryloyloxy-1-hexyloxy)biphenyl-4-yl}-5-(4-N,N-diphenylaminophenyl)-1,3,4-oxadiazole 
• 521971-81-3 2-{4'-(11-methacryloyloxy-1-undecyloxy)biphenyl-4-yl}-5-(4-N,N-diphenylaminophenyl)-1,3,4-oxadiazole 
• 1309459-83-3 4-(5-(3-bromophenyl)-1,3,4-oxadiazol-2-yl)-N,N-diphenylaniline 
• 1309459-86-6 N,N-diphenyl-4-(5-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1,3,4-oxadiazol-2-yl)aniline 
• 1309459-78-6 C₆₆H₄₄N₆O₂ 
• 1309459-79-7 C₇₄H₆₀N₆O₂ 
• 758119-08-3 2-(4-N,N'-diphenylaminophenyl)-5-(4-formalphenyl)-1,3,4-oxadiazole 
• 863315-13-3 4-(5-(4-bromophenyl)-1,3,4-oxadiazol-2-yl)-N,N-diphenylaniline 
• 863315-14-4 NC₅H₄C₆H₄C₂N₂OC₆H₄N(C₆H₅)2 

Relevant academic research and scientific papers

Nonvolatile electrical switching and write-once read-many-times memory effects in functional polyimides containing triphenylamine and 1,3,4-oxadiazole moieties

This work reports the synthesis and characterization of a series of functional aromatic polyimides (OXTA-PI)s containing triphenylamine and 1,3,4-oxadiazole moieties. All the polyimides exhibit high glass transition temperatures of 309-319 °C. A resistive

Synthesis and characterization of di-hexyl-fluorene and triphenylamine based copolymers containing 1,3,4-oxadiazole pendants

π-Conjugated polymers, poly(N-(4-(5-(4-tert-butylphenyl)-1,3,4- oxadiazol-2-yl)phenyl)-4-(9,9-dihexyl-9H-fluoren-2-yl)-N-phenyl-benzenamine (TPAOXDPF) and poly(N-(4-butylphenyl)-4-(9,9-dihexyl-9H-fluoren-2-yl)-N- phenylbenzenamine) (TPAPF), were synthesiz

D-A-π-A organic dyes for dye-sensitized solar cells: Effect of π-bridge length between two acceptors on photovoltaic properties

We report synthesis, photophysical and photovoltaic properties of organic dyes with D-A-π-A backbone having 1,3,4-oxadiazole moiety as an auxiliary acceptor, triphenylamine as donor with varying π-bridges and acceptors. The effect of increased distance be

Thermal activation delayed fluorescence material and application thereof

The invention provides a thermal activation delayed fluorescence material and an application thereof. The thermal activation delayed fluorescence material has the following structure: a compound taking tris([1, 2, 4] triazole)[4, 3-a: 4', 3'-c: 4'', 3''-e][1, 3, 5] triazine as a receptor core has the property of thermally activated delayed fluorescence, and the receptor has a rigid planar structure, so that the thermal stability of the material is effectively improved; a large torsion angle between a donor unit and an acceptor unit can inhibit intermolecular accumulation; the solubility and the film-forming property are improved; meanwhile, the larger torsion angle can reduce overlapping of molecular front line orbits, so that the lowest excited singlet state-triplet state energy level difference is reduced, triplet state excitons can return to the singlet state through reverse intersystem crossing and finally return to the ground state in a radiation transition mode to emit fluorescence, the exciton utilization rate is increased, and finally the purpose of improving the device efficiency is achieved.

PHOTOSENSITIZERS, METHOD OF MAKING THEM AND THEIR USE IN PHOTOELECTRIC CONVERSION DEVICES

Disclosed are novel photosensitizers, method of making them, and their use in photoelectric conversion devices such as the Dye Sensitized Solar Cell (DSSC). The photosensitizers have the Formula M(L1)2L2L3, M(L1)3L4 and ML4L5 where L

METAL COMPLEX, COMPOSITION COMPRISING SAME AND LIGHT-EMITTING ELEMENT USING SAME

The invention provides a metal complex having a structure represented by the following formula (1): wherein M represents a metal atom such as copper; C1 and C2 are each an sp3 carbon atom; A1-A4 each independent

Efficient deep-blue emitters comprised of an anthracene core and terminal bifunctional groups for nondoped electroluminescence

Four blue fluorescent host emitters with bifunctional charge transport groups appended to the 9- and 10-positions of the anthracene core have been designed and synthesized. By introducing peripheral bulky aryl-substitution groups to the emissive core, the

Synthesis of efficient blue and red light emitting phenanthroline derivatives containing both hole and electron transporting properties

Two phenanthroline derivatives containing a hole transporting triphenylamine and an electron transporting 1,3,4-oxadiazole unit have been prepared with high yield. UVa€"vis absorption and fluorescence measurement indicated they are high efficient light-em

Oxadiazole compounds containing 4,6-bis-trichloromethyl-S-triazin-2-yl groups, process for their preparation

Compounds of general formula I are disclosed STR1 wherein R1 denotes an unsubstituted or substituted carbocyclic or heterocyclic aryl radical, R2 and R3 are different from each other and either denote a hydrogen atom or a 4,6-bis-trichloromethyl-s-triazin-2-yl group, and n and m independently of each other, denote one of the numbers 0 and 1. The compounds are effective free-radical-forming photoinitiators and photolytically-activatable acid donors for photosensitive compositions.