The important role of 4,4′-Dibromobiphenyl

About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Chen, X; Ichige, A; Chen, JH; Fukushima, I; Kuwabara, J; Kanbara, T or concate me.. Product Details of 92-86-4

Recently I am researching about MICROWAVE-ASSISTED POLYCONDENSATION; C-H ARYLATION; PALLADIUM COMPLEXES; HIGHLY EFFICIENT; POLYMERIZATION; BOND; (HETERO)ARYLATION; HETEROARENES; SOLVENT, Saw an article supported by the JSPSMinistry of Education, Culture, Sports, Science and Technology, Japan (MEXT)Japan Society for the Promotion of Science [17H03063, 18K19103]. Product Details of 92-86-4. Published in ELSEVIER SCI LTD in OXFORD ,Authors: Chen, X; Ichige, A; Chen, JH; Fukushima, I; Kuwabara, J; Kanbara, T. The CAS is 92-86-4. Through research, I have a further understanding and discovery of 4,4′-Dibromobiphenyl

Facile polymerization reaction conditions were developed for synthesizing conjugated polymers via direct arylation and the Buchwald-Hartwig aryl amination reactions under aerobic conditions. Refluxing the reaction solvent and using XPhos Pd G2 as a precatalyst proved to be a tolerant polymerization protocol for direct arylation polycondensation, which eliminates the need for an inert gas atmosphere and can successfully proceed using commercially available, reagent-grade N,N-dimethylformamide (DMF) as the solvent. This strategy was also successfully applied to the Buchwald-Hartwig aryl amination polycondensation in toluene, which provided poly(triarylamine)s in air.

About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Chen, X; Ichige, A; Chen, JH; Fukushima, I; Kuwabara, J; Kanbara, T or concate me.. Product Details of 92-86-4

Reference:
Benzoxazole – Wikipedia,
,Benzoxazole | C7H5NO – PubChem

Can You Really Do Chemisty Experiments About 4,4′-Dibromobiphenyl

About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Li, MH; Zhang, WH; Hou, YL; Sun, RH; Li, Y or concate me.. HPLC of Formula: C12H8Br2

Authors Li, MH; Zhang, WH; Hou, YL; Sun, RH; Li, Y in HARD published article about POLYCHLORINATED-BIPHENYLS PCBS; AIR PARTITION-COEFFICIENTS; LIQUID-VAPOR PRESSURES; PREDICTION; TRANSPORT in [Li, Minghao; Zhang, Wenhui; Hou, Yilin; Sun, Ruihao; Li, Yu] North China Elect Power Univ, Moe Key Lab Resources & Environm Syst Optimizat, Beijing, Peoples R China in 2020, Cited 34. HPLC of Formula: C12H8Br2. The Name is 4,4′-Dibromobiphenyl. Through research, I have a further understanding and discovery of 92-86-4

The long-range migration ability of persistent organic pollutants was characterized by both K-OA and P-L. It is difficult for a traditional model of 3D-QSAR to capture the relationship between the double activities of pollutants and their structures. To this end, a log-normalized method was employed to treat a given data set (K-OA and P-L values) to obtain a comprehensive activity (Z) that represents the long-range migration ability of polyhalogenated biphenyls. Then, the relationship between the comprehensive activity of polyhalogenated biphenyls and their structures could be constructed; the proposed model was named the three-dimensional quantitative structure-double-activities relationship (3D-QSA(2)R) model. Two new PCB-52 molecules with a reduced ability for long-range migration were designed after analyses of the contour maps, with Z values increasing significantly by 30.44-41.30%, and the environmental persistence, bioconcentration and biotoxicity decreased by 3.37-8.99%, 26.86-26.73% and -1.17-3.50%, respectively, compared with those of PCB-52. logK(OA) and logP(L) values of the novel modified PCB-52 were predicted as 3.20-4.57% and 74.57-79.19%, respectively, by the EPI database software, and these values showed a consistent increasing trend with the Z values predicted by 3D-QSA(2)R, indicating that the established 3D-QSA(2)R could be used to deal with the relationship between the multi-activities of organic pollutants and their structures.

About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Li, MH; Zhang, WH; Hou, YL; Sun, RH; Li, Y or concate me.. HPLC of Formula: C12H8Br2

Reference:
Benzoxazole – Wikipedia,
,Benzoxazole | C7H5NO – PubChem

Properties and Exciting Facts About 92-86-4

HPLC of Formula: C12H8Br2. About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Chumkaeo, P; Poonsawat, T; Meechai, T; Somsook, E or concate me.

An article Synergistic Activities in the Ullmann Coupling of Chloroarenes at Ambient Temperature by Pd-Supported Calcined Ferrocenated La2O3 WOS:000454321800050 published article about PALLADIUM CATALYST; ARYL CHLORIDES; ALLOY NANOCLUSTERS; BOND ACTIVATION; SUZUKI-MIYAURA; NANOPARTICLES; CARBON; HALIDES; NANOCATALYSTS; EFFICIENT in [Somsook, Ekasith] Mahidol Univ, Fac Sci, NANOCAST Lab, Ctr Catalysis Sci & Technol,Dept Chem, 272 Rama 6 Rd, Bangkok 10400, Thailand; [Somsook, Ekasith] Mahidol Univ, Fac Sci, Ctr Excellence Innovat Chem, 272 Rama 6 Rd, Bangkok 10400, Thailand in 2019, Cited 42. HPLC of Formula: C12H8Br2. The Name is 4,4′-Dibromobiphenyl. Through research, I have a further understanding and discovery of 92-86-4

Novel palladium-doped nanoparticles have been explored to serve as the first metal oxide-derived heterogeneous catalyst for Ullmann reaction of chloroarenes under mild condition (34 degrees C). This heterogeneous catalyst exhibited high catalytic activity towards the Ullmann homocoupling of chloroarenes into a series of useful symmetrically biaryl products with good to excellent yields in the presence of ethanol and NaOH, thereby leading to green and economical Ullmann reaction. The produced nanoparticles were successfully characterized by various techniques including PXRD, XPS, HRTEM, SEM-EDS, BET, TGA techniques, elemental mapping analysis and ICP-OES. Interestingly, based on characterization and experimental data, a reasonable mechanism has been proposed. Also, the formation of aryl methyl ketone as a by-product has been further confirmed by isotopic labelling experiments that the acetyl moiety is derived from ethanol. Moreover, the catalyst was stable and could be easily reused up to 5 times under atmospheric air without suffering significant loss in catalytic activity.

HPLC of Formula: C12H8Br2. About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Chumkaeo, P; Poonsawat, T; Meechai, T; Somsook, E or concate me.

Reference:
Benzoxazole – Wikipedia,
,Benzoxazole | C7H5NO – PubChem

Extracurricular laboratory: Synthetic route of C12H8Br2

About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Guo, W; Zou, JH; Guo, BB; Xiong, JH; Liu, C; Xie, ZH; Wu, L or concate me.. Category: benzoxazole

Category: benzoxazole. Guo, W; Zou, JH; Guo, BB; Xiong, JH; Liu, C; Xie, ZH; Wu, L in [Guo, Wei; Zou, Junhua; Guo, Binbin; Xiong, Jinhua; Liu, Cheng; Wu, Ling] Fuzhou Univ, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350116, Peoples R China; [Xiong, Jinhua] Longyan Univ, Coll Chem & Mat Sci, Longyan 364000, Peoples R China; [Xie, Zenghong] Fuzhou Univ, Inst Food Safety & Environm Monitoring, Fuzhou 350108, Peoples R China published Pd nanoclusters/TiO2(B) nanosheets with surface defects toward rapid photocatalytic dehalogenation of polyhalogenated biphenyls under visible light in 2020, Cited 60. The Name is 4,4′-Dibromobiphenyl. Through research, I have a further understanding and discovery of 92-86-4.

Constructing effective photocatalysts with visible light response to achieve rapid dehalogenation of polyhalogenated compounds remains a challenge nowadays. Herein, Pd nanoclusters-decorated TiO2 nanosheets with surface defects (Pd/TNS) are designed for polyhalogenated biphenyls dehalogenation under visible light. Pd/TNS is able to rapidly remove bromine atoms of 4-bromobiphenyl in 30 min. Experimental results reveal that oxygen vacancies and Ti3+ are in-situ generated in TNS during Pd photodeposition, which extend the absorption band edge of Pd/TNS to visible light region. Besides, the unique two-dimensional nanosheets structure of TNS contributes to a high surface area for high dispersion of Pd nanoclusters. Importantly, the Pd nanoclusters serve to activate carbon-halogen bond in polyhalogenated biphenyls and hydrogen-oxygen in H2O. The high dehalogenation efficiency could be assigned to a strong chemical interaction and synergistic effect between the Pd nanoclusters and TiO2(B) nanosheets. Finally, a collaborative mechanism is proposed for photocatalytic dehalogenation of polyhalogenated biphenyls on Pd/TNS.

About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Guo, W; Zou, JH; Guo, BB; Xiong, JH; Liu, C; Xie, ZH; Wu, L or concate me.. Category: benzoxazole

Reference:
Benzoxazole – Wikipedia,
,Benzoxazole | C7H5NO – PubChem

An overview of features, applications of compound:92-86-4

About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Tian, YC; Wang, JB; Cheng, XY; Liu, K; Wu, TZ; Qiu, XQ; Kuang, ZJ; Li, ZY; Bian, JL or concate me.. Recommanded Product: 4,4′-Dibromobiphenyl

An article Microwave-assisted unprotected Sonogashira reaction in water for the synthesis of polysubstituted aromatic acetylene compounds WOS:000518034000029 published article about ORGANIC-SYNTHESIS; CATALYST; POLYMER; CO2; NANOPARTICLES; ADSORPTION; FRAMEWORKS; EFFICIENT in [Tian, Yucheng; Wang, Jubo; Cheng, Xinying; Liu, Kang; Wu, Tizhi; Qiu, Xiaqiu; Kuang, Zijian; Li, Zhiyu; Bian, Jinlei] China Pharmaceut Univ, Sch Pharm, Dept Med Chem, Jiangsu Key Lab Drug Design & Optimizat, Nanjing 210009, Peoples R China in 2020, Cited 37. Recommanded Product: 4,4′-Dibromobiphenyl. The Name is 4,4′-Dibromobiphenyl. Through research, I have a further understanding and discovery of 92-86-4

A microwave-assisted, efficient and rapid Sonogashira reaction was developed for the synthesis of polysubstituted aromatic alkynes. The reaction was made environmentally friendly and easy to perform by replacing the traditional amine solvents with water. The optimized reaction conditions yielded the products with high yields, while reducing the dependence on anaerobic reaction conditions with no inert gas protection. The reaction also achieved the product on the milligram level, overcoming the problem of TMSA volatilization in small-scale reactions. The environmentally friendly reaction solvent, mild reaction conditions, high reaction yields and short reaction time made the reaction highly promising for various applications, especially for synthesizing porous aromatic frameworks.

About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Tian, YC; Wang, JB; Cheng, XY; Liu, K; Wu, TZ; Qiu, XQ; Kuang, ZJ; Li, ZY; Bian, JL or concate me.. Recommanded Product: 4,4′-Dibromobiphenyl

Reference:
Benzoxazole – Wikipedia,
,Benzoxazole | C7H5NO – PubChem

A new application about92-86-4

Recommanded Product: 4,4′-Dibromobiphenyl. About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Shieh, MH; Liu, YH; Wang, CC; Jian, H; Lin, CN; Chen, YM; Huang, CY or concate me.

Recommanded Product: 4,4′-Dibromobiphenyl. Recently I am researching about TRINUCLEAR COPPER(I) ACETYLIDES; N-HETEROCYCLIC CARBENES; CARBONYL-COMPLEXES; CLUSTERS; ELECTROCHEMISTRY; NANOPARTICLES; CHEMISTRY; TE; CONSTRUCTION; SPECTROSCOPY, Saw an article supported by the Ministry of Science and Technology of TaiwanMinistry of Science and Technology, Taiwan [107-2113-M-003-006]. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Shieh, MH; Liu, YH; Wang, CC; Jian, H; Lin, CN; Chen, YM; Huang, CY. The CAS is 92-86-4. Through research, I have a further understanding and discovery of 4,4′-Dibromobiphenyl

A novel family of N-heterocyclic carbene (NHC)-incorporated Se-Fe-Cu compounds, bis-1,3-dimethylimidazol-2-ylidene (bis-Me-2-imy)-containing compound [(mu(4)-Se)Fe-3(CO)(9){Cu(Me-2-imy)}(2)] (2), bis-N-methyl- or bis-N-isopropyl-substituted benzimidazol-2-ylidene (bis-Me-2-bimy or bis-Pr-i(2)-bimy)-incorporated compounds [(mu(4)-Se)Fe-3(CO)(9){Cu(Me-2-bimy)}(2)] (3) or [(mu(4)-Se)Fe-3(CO)(9){Cu(Pr-i(2)-bimy)}(2)] (4), and a bis-1,3-dimethyl-4,5-dichloroimidazol-2-ylidene (bis-Me-2-Cl-2-imy)-containing compound [(mu(3)-Se)Fe-3(CO)(9){Cu(Me-2-Cl-2-imy)}(2)] (5), were synthesized in moderate yields in facile one-pot reactions of the ternary pre-designed compound [(mu(3)-Se)Fe-3(CO)(9){Cu(MeCN)}(2)] (1) with the corresponding imidazolium salts and (KOBu)-Bu-t in THF in an ice-water bath. Single-crystal X-ray analyses revealed that the Me-2-imy compound 2 or the Me-2-bimy compound 3 each exhibited a trigonal bipyramidal SeFe3(CO)(9)Cu geometry with an Fe2Cu plane further capped by a Cu(Me-2-imy) or Cu(Me-2-bimy) fragment, respectively, with one long Cu-Cu covalent bond. In addition, compound 4 also comprised a trigonal bipyramidal SeFe3(CO)(9)Cu core structure, but the second Cu(Pr-i(2)-bimy) group bridged the equatorial Fe-Fe edge with two unbonded Cu atoms, due to the presence of a sterically bulky Pr-i(2)-bimy fragment. On the other hand, the strong electron-withdrawing chloro-containing NHC compound 5 showed a comparatively open tetrahedral SeFe3(CO)(9) metal core, where two Fe-Fe edges each were further bridged by a Cu(Me-2-Cl-2-imy) fragment. Due to the nonclassical C-H center dot center dot center dot O(carbonyl) hydrogen bonds between the CO groups of the SeFe3(CO)(9)Cu-2 core and CH moieties of the neighboring NHC ligands, both compounds 2 and 3 comprised a one-dimensional network, while compounds 4 and 5 each were made up of a two-dimensional framework in the solid state, which efficiently enhanced the stability of these Se-Fe-Cu NHC compounds. Importantly, all of these synthesized Se-Fe-Cu NHC compounds 2-5 had pronounced catalytic activities for the homocoupling of arylboronic acids with high catalytic yields. Finally, these Se-containing Fe-Cu NHC compounds further represented excellent models for studying chalcogen effects in comparison to their Te analogs, as demonstrated by their catalytic performances and electrochemical behaviors, and by DFT calculations.

Recommanded Product: 4,4′-Dibromobiphenyl. About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Shieh, MH; Liu, YH; Wang, CC; Jian, H; Lin, CN; Chen, YM; Huang, CY or concate me.

Reference:
Benzoxazole – Wikipedia,
,Benzoxazole | C7H5NO – PubChem

An update on the compound challenge: 92-86-4

Category: benzoxazole. About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Escalona, C; Estrany, F; Ahumada, JC; Borras, N; Soto, JP; Aleman, C or concate me.

Category: benzoxazole. In 2020 POLYM BULL published article about CONDUCTING POLYMERS; SELECTIVE DETECTION; CARBAZOLE; 3,4-ETHYLENEDIOXYTHIOPHENE; POLY(3,4-ETHYLENEDIOXYTHIOPHENE); ELECTROPOLYMERIZATION; SEMICONDUCTORS; MULTILAYERS; THIOPHENE; FILMS in [Escalona, Cindy; Ahumada, Juan C.; Soto, Juan P.] Pontificia Univ Catolica Valparaiso, Fac Ciencias, Lab Polimeros, Inst Quim, Ave Brasil 2950, Valparaiso, Chile; [Escalona, Cindy; Estrany, Francesc; Borras, Nuria; Aleman, Carlos] Univ Politecn Cataluna, EEBE, Dept Engn Quim, C Eduard Maristany 10-14, Barcelona 08019, Spain; [Estrany, Francesc; Aleman, Carlos] Univ Politecn Cataluna, Barcelona Res Ctr Multiscale Sci & Engn, C Eduard Maristany 10-14, Barcelona 08019, Spain in 2020, Cited 47. The Name is 4,4′-Dibromobiphenyl. Through research, I have a further understanding and discovery of 92-86-4.

The preparation of copolymers bearing N-methylcarbazole and 2,7-linked 3,4-ethylenedioxythiophene units has been carried out using the N-methyl-2,7-di(2-(3,4-ethylenedioxythienyl))carbazole monomer, which has been chemically synthesized through the Stille coupling reaction of 2,7-dibromo-N-methylcarbazole and tributyl-stannylated 3,4-ethylenedioxythiophene. Then, the monomer was electropolymerized by chronoamperometry in acetonitrile with 0.1 M LiClO4 under a constant potential of 0.70 V and using steel AISI 316 electrodes. The electrochemical activity and stability, charge-discharge capacity, charge transfer resistance and surface properties (i.e. morphology, topography and wettability) of the resulting polymer have been characterized and compared with those reported for poly(3,4-ethylenedioxythiophene). Finally, the polymer has been obtained by potentiodynamic sweep, applying around 100 cyclic voltammetry steps to an acetonitrile solution of the N-methyl-2,7-di(2-(3,4-ethylenedioxythienyl))carbazole monomer with 0.1 M LiClO4. Results show that although this technique has been mostly used to electropolymerize diheteroaromatic-subtituted carbazoles, the resulting material presents serious disadvantages with respect to that produced by chronoamperometry under a constant potential.

Category: benzoxazole. About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Escalona, C; Estrany, F; Ahumada, JC; Borras, N; Soto, JP; Aleman, C or concate me.

Reference:
Benzoxazole – Wikipedia,
,Benzoxazole | C7H5NO – PubChem

Simple exploration of C12H8Br2

About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Isci, R; Gunturkun, D; Yalin, AS; Ozturk, T or concate me.. Category: benzoxazole

Category: benzoxazole. Isci, R; Gunturkun, D; Yalin, AS; Ozturk, T in [Isci, Recep; Gunturkun, Dilara; Yalin, Ahsen Sare; Ozturk, Turan] Istanbul Tech Univ, Dept Chem, Maslak, Turkey; [Ozturk, Turan] TUBITAK UME, Chem Grp Labs, Gebze, Turkey published Copolymers of 4-thieno[3,2-b]thiophen-3-ylbenzonitrile with anthracene and biphenyl; synthesis, characterization, electronic, optical, and thermal properties in 2021, Cited 35. The Name is 4,4′-Dibromobiphenyl. Through research, I have a further understanding and discovery of 92-86-4.

Two novel copolymers of 4-thieno[3,2-b]thiophen-3-ylbenzonitrile (TT-CN), possessing electron withdrawing cyano moiety, with anthracene (P1) and biphenyl (P2) were prepared via Suzuki coupling. Optic, electronic, and thermal properties of the copolymers were investigated through UV-Vis spectroscopy, cyclic voltammetry, gel permeation chromatography, and thermal gravimetric analysis. The polymers with anthracene and biphenyl had electronic band gaps of 2.01 and 1.90 eV, respectively. Both polymers demonstrated excellent large Stokes shifts of 101 (anthracene) and 105 nm (biphenyl) as well as very good thermal properties. As they had good optical, electronic, and thermal properties, they are promising candidates for electronic applications.

About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Isci, R; Gunturkun, D; Yalin, AS; Ozturk, T or concate me.. Category: benzoxazole

Reference:
Benzoxazole – Wikipedia,
,Benzoxazole | C7H5NO – PubChem

Some scientific research about 92-86-4

Product Details of 92-86-4. About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Guo, W; Zou, JH; Guo, BB; Xiong, JH; Liu, C; Xie, ZH; Wu, L or concate me.

Product Details of 92-86-4. In 2020 APPL CATAL B-ENVIRON published article about POLYBROMINATED DIPHENYL ETHERS; BROMINATED FLAME RETARDANTS; DECABROMODIPHENYL ETHER; TITANIUM-DIOXIDE; DEBROMINATION; PBDES; TIO2; NANOPARTICLES; DEGRADATION; OXIDATION in [Guo, Wei; Zou, Junhua; Guo, Binbin; Xiong, Jinhua; Liu, Cheng; Wu, Ling] Fuzhou Univ, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350116, Peoples R China; [Xiong, Jinhua] Longyan Univ, Coll Chem & Mat Sci, Longyan 364000, Peoples R China; [Xie, Zenghong] Fuzhou Univ, Inst Food Safety & Environm Monitoring, Fuzhou 350108, Peoples R China in 2020, Cited 60. The Name is 4,4′-Dibromobiphenyl. Through research, I have a further understanding and discovery of 92-86-4.

Constructing effective photocatalysts with visible light response to achieve rapid dehalogenation of polyhalogenated compounds remains a challenge nowadays. Herein, Pd nanoclusters-decorated TiO2 nanosheets with surface defects (Pd/TNS) are designed for polyhalogenated biphenyls dehalogenation under visible light. Pd/TNS is able to rapidly remove bromine atoms of 4-bromobiphenyl in 30 min. Experimental results reveal that oxygen vacancies and Ti3+ are in-situ generated in TNS during Pd photodeposition, which extend the absorption band edge of Pd/TNS to visible light region. Besides, the unique two-dimensional nanosheets structure of TNS contributes to a high surface area for high dispersion of Pd nanoclusters. Importantly, the Pd nanoclusters serve to activate carbon-halogen bond in polyhalogenated biphenyls and hydrogen-oxygen in H2O. The high dehalogenation efficiency could be assigned to a strong chemical interaction and synergistic effect between the Pd nanoclusters and TiO2(B) nanosheets. Finally, a collaborative mechanism is proposed for photocatalytic dehalogenation of polyhalogenated biphenyls on Pd/TNS.

Product Details of 92-86-4. About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Guo, W; Zou, JH; Guo, BB; Xiong, JH; Liu, C; Xie, ZH; Wu, L or concate me.

Reference:
Benzoxazole – Wikipedia,
,Benzoxazole | C7H5NO – PubChem

What kind of challenge would you like to see in a future of compound:92-86-4

About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Guo, W; Zou, JH; Guo, BB; Xiong, JH; Liu, C; Xie, ZH; Wu, L or concate me.. Computed Properties of C12H8Br2

An article Pd nanoclusters/TiO2(B) nanosheets with surface defects toward rapid photocatalytic dehalogenation of polyhalogenated biphenyls under visible light WOS:000552015900077 published article about POLYBROMINATED DIPHENYL ETHERS; BROMINATED FLAME RETARDANTS; DECABROMODIPHENYL ETHER; TITANIUM-DIOXIDE; DEBROMINATION; PBDES; TIO2; NANOPARTICLES; DEGRADATION; OXIDATION in [Guo, Wei; Zou, Junhua; Guo, Binbin; Xiong, Jinhua; Liu, Cheng; Wu, Ling] Fuzhou Univ, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350116, Peoples R China; [Xiong, Jinhua] Longyan Univ, Coll Chem & Mat Sci, Longyan 364000, Peoples R China; [Xie, Zenghong] Fuzhou Univ, Inst Food Safety & Environm Monitoring, Fuzhou 350108, Peoples R China in 2020, Cited 60. The Name is 4,4′-Dibromobiphenyl. Through research, I have a further understanding and discovery of 92-86-4. Computed Properties of C12H8Br2

Constructing effective photocatalysts with visible light response to achieve rapid dehalogenation of polyhalogenated compounds remains a challenge nowadays. Herein, Pd nanoclusters-decorated TiO2 nanosheets with surface defects (Pd/TNS) are designed for polyhalogenated biphenyls dehalogenation under visible light. Pd/TNS is able to rapidly remove bromine atoms of 4-bromobiphenyl in 30 min. Experimental results reveal that oxygen vacancies and Ti3+ are in-situ generated in TNS during Pd photodeposition, which extend the absorption band edge of Pd/TNS to visible light region. Besides, the unique two-dimensional nanosheets structure of TNS contributes to a high surface area for high dispersion of Pd nanoclusters. Importantly, the Pd nanoclusters serve to activate carbon-halogen bond in polyhalogenated biphenyls and hydrogen-oxygen in H2O. The high dehalogenation efficiency could be assigned to a strong chemical interaction and synergistic effect between the Pd nanoclusters and TiO2(B) nanosheets. Finally, a collaborative mechanism is proposed for photocatalytic dehalogenation of polyhalogenated biphenyls on Pd/TNS.

About 4,4′-Dibromobiphenyl, If you have any questions, you can contact Guo, W; Zou, JH; Guo, BB; Xiong, JH; Liu, C; Xie, ZH; Wu, L or concate me.. Computed Properties of C12H8Br2

Reference:
Benzoxazole – Wikipedia,
,Benzoxazole | C7H5NO – PubChem