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52066-64-5

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52066-64-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52066-64-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,6 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 52066-64:
(7*5)+(6*2)+(5*0)+(4*6)+(3*6)+(2*6)+(1*4)=105
105 % 10 = 5
So 52066-64-5 is a valid CAS Registry Number.

52066-64-5Downstream Products

52066-64-5Relevant academic research and scientific papers

Donor-acceptor materials exhibiting deep blue emission and thermally activated delayed fluorescence with tris(triazolo)triazine

Hojo, Ryoga,Hudson, Zachary M.,Mayder, Don M.

, p. 14342 - 14350 (2021/11/01)

Five luminescent donor-acceptor compounds based on the tris(triazolo)triazine (TTT) acceptor were prepared. Out of the series of emitters,TTT-3HMATexhibits deep blue emission with CIE(x,y) (0.16, 0.05) and a photoluminescence quantum yield (PLQY) of 0.9

Polymer Dots with Enhanced Photostability, Quantum Yield, and Two-Photon Cross-Section using Structurally Constrained Deep-Blue Fluorophores

Algar, W. Russ,Burke, Sarah A.,Darwish, Ghinwa H.,Gupta, Rupsa,Hudson, Zachary M.,Kamal, Saeid,Lix, Kelsi,Mayder, Don M.,Nguyen, Giang D.,Tom, Gary,Tonge, Christopher M.,Tran, Michael V.

, p. 16976 - 16992 (2021/10/25)

Semiconducting polymer dots (Pdots) have emerged as versatile probes for bioanalysis and imaging at the single-particle level. Despite their utility in multiplexed analysis, deep blue Pdots remain rare due to their need for high-energy excitation and sens

Bis(hexamethylazatriangulene)sulfone: A high-stability deep blue-violet fluorophore with 100% quantum yield and CIE: Y < 0.07

Tonge, Christopher M.,Zeng, Jiajie,Zhao, Zujin,Tang, Ben Zhong,Hudson, Zachary M.

supporting information, p. 5150 - 5155 (2020/04/27)

Efficient deep blue-violet fluorophores are highly sought after as emitters for OLEDs and as labels for fluorescent imaging. Despite significant progress in the development of deep blue luminescent materials, highly efficient emitters in the deep-blue/violet region of the visible spectrum with good photostability remain rare. Here we describe the preparation of two violet-blue emitters based on hexamethylazatriangulene (HMAT) donors and weakly accepting sulfone and sulfoxide acceptors, with CIE coordinates in solution as low as (0.16, 0.02) and quantum yields of unity. By restricting freedom of motion in the HMAT donor, stability of the sp2 C-N bonds is increased significantly, increasing photostability over controls with nonplanar donors while also narrowing the emission bandwidth to 39.5 nm FWHM. These materials were then evaluated in proof-of-concept experiments for both two-photon excited fluorescence and as emitters in OLEDs to demonstrate their potential applications in optoelectronics.

Planar triphenylamine derivative having crosslinkable group and synthesis method of same

-

, (2020/04/17)

The invention relates to a planar triphenylamine derivative having a crosslinkable group and a synthesis method of same, wherein the compound is synthesized through reactions such as Ullmann couplingreaction, Grignard reaction, ring-closing reaction, halogenation reaction and Suzuki reaction. The structure of the planar triphenylamine derivative is represented as the following structure, whereinF, G, H and I in the planar triphenylamine derivative have more than one of styryl or trifluorovinyl crosslinking groups, so that after crosslinking, an anti-solvent network thin film can be formed, and interlayer miscibility of a device is effectively prevented. The oxidization potentials of the F, G, H, I and J, tested by the cyclic voltammetry method, are 0.3 eV, 0.29 eV, 0.27 eV, 0.32 eV and 0.33 eV, respectively, which are lower than the oxidization potential (0.36 eV) of planar triphenylamine, which is beneficial to carrier transport. The planar triphenylamine derivative has important application prospect in the field of organic photovoltaic devices and organic electroluminescence devices.

Heterocyclic compound and organic light emitting device including the same

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, (2020/07/15)

Provided are a heterocyclic compound and an organic light-emitting device including the same. The heterocyclic compound may be represented by Formula 1: in the Formula 1, A1, X2, Y1, Y2, m1, m2, R10,R20, R30, b10, b20 and b30 are same as described in the description.

Novel compounds for organic electronic material and organic electronic device using the same

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, (2016/10/08)

The present invention refers to novel organic for electronic material containing the same compound and relates to organic electronic devices, particularly for electronic material organic the present invention according to formula 1 or formula 2 compound i

Bridged-triarylamine starburst oligomers as hole transporting materials for electroluminescent devices

Fang, Zhen,Chellappan, Vijila,Webster, Richard D.,Ke, Lin,Zhang, Tianfu,Liu, Bin,Lai, Yee-Hing

experimental part, p. 15397 - 15404 (2012/09/25)

Two bridged-triphenylamine starburst molecules were designed and synthesized. Their electrochemical properties were studied in detail using cyclic voltammetry (CV) and square wave voltammetry (SWV) methods. The bridged molecular structure stabilizes the o

Bridged triphenylamine-based dendrimers: Tuning enhanced two-photon absorption performance with locked molecular planarity

Fang, Zhen,Teo, Tang-Lin,Cai, Liping,Lal, Yee-Hing,Samoc, Anna,Samoc, Marek

supporting information; experimental part, p. 1 - 4 (2009/08/07)

Triphenylamine derivatives bridged by methylene units afford a near planar molecular platform in a series of one dimer and two oligomers exhibiting increased structural rigidity compared to that of their parent triphenylamines. This series of dendrimers s

12-Organyldibenzazocine-5,7-diones

Hellwinkel, Dieter,Ittemann, Peter

, p. 3165 - 3197 (2007/10/02)

The title compounds 10, 23 are formed in low yields on treatment of 2,2'-organylimino-bisbenzoic acid esters 8 with methyllithium, but in high yields in the intramolecular ester condensation with sodium hydride of triarylamines 12, containing o-acetyl-, a

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