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An article Formation of Metal-Based 21-and 22-Membered Macrocycles from Dinuclear Organotin Tectons and Ditopic Organic Ligands Carrying Carboxylate or Dithiocarbamate Groups WOS:000473116400007 published article about RAY STRUCTURAL-CHARACTERIZATION; SOLID-STATE STRUCTURES; BIDENTATE LEWIS-ACIDS; BRIDGED DOUBLE LADDER; CRYSTAL-STRUCTURES; COORDINATION POLYMERS; TRANSESTERIFICATION REACTIONS; MOLECULAR TECTONICS; TETRATIN COMPOUNDS; HYDROGEN-BONDS in [Rojas-Leon, Iran; Vasquez-Rios, Maria G.; Gomez-Jaimes, Gelen; Hopfl, Herbert] Univ Autonoma Estado Morelos, Inst Invest Ciencias Basicas & Aplicadas, Ctr Invest Quim, Ave Univ 1001, Cuernavaca 62209, Morelos, Mexico; [Rojas-Leon, Iran; Alnasr, Hazem; Jurkschat, Klaus] Tech Univ Dortmund, Fak Chem & Chem Biol, D-44221 Dortmund, Germany; [Hernandez-Ahuactzi, Iran F.] Univ Guadalajara, Ctr Univ Tonala, Ave Nuevo Perifer 555, Tonala 45425, Jalisco, Mexico; [Santillan, Rosa] IPN, Dept Quim, Ctr Invest & Estudios Avanzados, Ave Inst Politecn Nacl 2508, Mexico City 07360, DF, Mexico in 2019, Cited 183. Recommanded Product: 92-86-4. The Name is 4,4′-Dibromobiphenyl. Through research, I have a further understanding and discovery of 92-86-4

Four dinuclear organotin halides of composition XnPh(3-n)SnCH2Si(Me)(2)-C12H8-Si(Me)(2)CH2-SnPh(3-n)Xn (X = Cl, I; n = 1, 2) were prepared and combined in 1:1 stoichiometric reactions with potassium 2,5-pyridinedicarboxylate, 3,5-pyridinedicarboxylate, and piperazine bis-dithiocarbamate, respectively. The reactions yielded a total of five [1 + 1] aggregates with either 21- or 22-membered macrocyclic structures that were fully characterized by elemental analysis, mass spectrometry, IR and NMR (H-1, C-13, Si-29, and Sn-119) spectroscopy, and, in three cases, additionally by single-crystal X-ray diffraction analysis. In solution, the macrocycles exhibit conformational and configurational equilibria being fast on the NMR time scale, which, for one of the macrocycles, were closer examined by variable temperature NMR spectroscopy and DFT calculations.

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Product Details of 92-86-4. Authors Lovell, TC; Colwell, CE; Zakharov, LN; Jasti, R in ROYAL SOC CHEMISTRY published article about in [Lovell, Terri C.; Colwell, Curtis E.; Jasti, Ramesh] Univ Oregon, Inst Mat Sci, Dept Chem & Biochem, Eugene, OR 97403 USA; [Zakharov, Lev N.] Univ Oregon, CAMCOR Ctr Adv Mat Characterizat Oregon, Eugene, OR 97403 USA in 2019, Cited 38. The Name is 4,4′-Dibromobiphenyl. Through research, I have a further understanding and discovery of 92-86-4

[n]Cycloparaphenylenes, or carbon nanohoops, are unique conjugated macrocycles with radially oriented pi-systems similar to those in carbon nanotubes. The centrosymmetric nature and conformational rigidity of these molecules lead to unusual size-dependent photophysical characteristics. To investigate these effects further and expand the family of possible structures, a new class of related carbon nanohoops with broken symmetry is disclosed. In these structures, referred to as meta[n]cycloparaphenylenes, a single carbon-carbon bond is shifted by one position in order to break the centrosymmetric nature of the parent [n]cycloparaphenylenes. Advantageously, the symmetry breaking leads to bright emission in the smaller nanohoops, which are typically non-fluorescent due to optical selection rules. Moreover, this simple structural manipulation retains one of the most unique features of the nanohoop structures-size dependent emissive properties with relatively large extinction coefficients and quantum yields. Inspired by earlier theoretical work by Tretiak and co-workers, this joint synthetic, photophysical, and theoretical study provides further design principles to manipulate the optical properties of this growing class of molecules with radially oriented pi-systems.

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Safety of 4,4′-Dibromobiphenyl. In 2019 J AM CHEM SOC published article about CONJUGATED POLYELECTROLYTES; SYNTHETIC POLYELECTROLYTES; METATHESIS; ANNULATION; ACID; EFFICIENCY; POLYMERS; CATIONS in [Liu, Xiaolin; Han, Ting; Qiu, Zijie; Li, Yuanyuan; Li, Qiyao; Hu, Yubing; Liu, Zhiyang; Lam, Jacky W. Y.; Tang, Ben Zhong] Hong Kong Univ Sci & Technol, Chinese Natl Engn Res Ctr Tissue Restorat & Recon, Dept Chem & Biol Engn,Kowloon, Inst Mol Funct Mat,Inst Adv Study,Dept Chem,Hong, Clear Water Bay, Hong Kong, Peoples R China; [Li, Mengge; Cao, Bing; Hu, Xianglong] South China Normal Univ, Coll Biophoton, Minist Educ, Key Lab Laser Life Sci, Guangzhou 510631, Guangdong, Peoples R China; [Li, Mengge; Cao, Bing; Hu, Xianglong] South China Normal Univ, Coll Biophoton, Inst Laser Life Sci, Guangzhou 510631, Guangdong, Peoples R China; [Liu, Xiaolin; Han, Ting; Qiu, Zijie; Li, Yuanyuan; Li, Qiyao; Hu, Yubing; Liu, Zhiyang; Lam, Jacky W. Y.; Tang, Ben Zhong] HKUST Shenzhen Res Inst, 9 Yuexing 1st Rd,South Area,Hitech Pk, Shenzhen 518057, Peoples R China; [Tang, Ben Zhong] South China Univ Technol, State Key Lab Luminescent Mat & Devices, SCUT HKUST Joint Res Inst, Ctr Aggregat Induced Emiss, Guangzhou 510640, Guangdong, Peoples R China in 2019, Cited 63. The Name is 4,4′-Dibromobiphenyl. Through research, I have a further understanding and discovery of 92-86-4.

Polyelectrolytes play an important role in both natural biological systems and human society, and their synthesis, functional exploration, and profound application are thus essential for biomimicry and creating new materials. In this study, we developed an efficient synthetic methodology for in situ generation of azonia-containing polyelectrolytes in a one-pot manner by using readily accessible nonionic reactant in the presence of commercially available cheap ionic species. The resulting polyelectrolytes are emissive in the solid state and can readily form luminescent photopatterns with different colors. The azonia-containing polyelectrolytes possess extraordinary potency of reactive oxygen species (ROS) generation, enabling them to impressively kill methicillin-resistant Staphylococcus aureus (MRSA), a drug resistant superbug, both in vitro and in vivo.

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Recommanded Product: 92-86-4. Recently I am researching about COVALENT TRIAZINE FRAMEWORKS; POROUS POLYMERS; PHOTOCATALYTIC ACTIVITY; CARBON-DIOXIDE; SURFACE-AREA; REDUCTION; CAPTURE; CONSTRUCTION; CONVERSION; PLATFORMS, Saw an article supported by the Singapore National Research FoundationNational Research Foundation, Singapore [R279-000-444-281, R279-000-483-281]; National University of SingaporeNational University of Singapore [R279-000482-133]; Singapore MOE AcRF-Tier1Ministry of Education, Singapore [2018-T1-001-072, RG 9/18]; MOE AcRF-Tier2 [MOE2016-T2-2-056]. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Dai, CH; Zhong, LX; Gong, XZ; Zeng, L; Xue, C; Li, SZ; Liu, B. The CAS is 92-86-4. Through research, I have a further understanding and discovery of 4,4′-Dibromobiphenyl

Organic pi-conjugated polymers (CPs) have been intensively explored for a variety of critical photocatalytic applications in the past few years. Nevertheless, CPs for efficient CO2 photoreduction have been rarely reported, which is mainly due to the lack of suitable polymers with sufficient solar light harvesting ability, appropriate energy level alignment and good activity and selectivity in multi-electron-transfer photoreduction of CO2 reaction. We report here the rational design and synthesis of two novel triphenylamine (TPA) based conjugated microporous polymers (CMPs), which can efficiently catalyze the reduction of CO2 to CO using water vapor as an electron donor under ambient conditions without adding any co-catalyst. Nearly 100% selectivity and a high CO production rate of 37.15 mu mol h(-1) g(-1) are obtained for OXD-TPA, which is significantly better than that for BP-TPA (0.9 mu mol h(-1) g(-1)) as a result of co-monomer change from biphenyl to 2,5-diphenyl-1,3,4-oxadiazole. This difference could be mainly ascribed to the synergistic effect of a decreased optical band gap, improved interface charge transfer and increased CO2 uptake for OXD-TPA. This contribution is expected to spur further interest in the rational design of porous conjugated polymers for CO2 photoreduction.

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Bohlen, ML; Jeon, HP; Kim, YJ; Sung, B in [Bohlen, Marie-Leonie; Jeon, Hyun Pyo; Kim, Young Jun; Sung, Baeckkyoung] KIST Europe Forschungsgesell MbH, Saarbrucken, Germany published In Silico Modeling Method for Computational Aquatic Toxicology of Endocrine Disruptors: A Software-Based Approach Using QSAR Toolbox in 2019, Cited 39. Product Details of 92-86-4. The Name is 4,4′-Dibromobiphenyl. Through research, I have a further understanding and discovery of 92-86-4.

Computational analyses of toxicological processes enables high-throughput screening of chemical substances and prediction of their endpoints in biological systems. In particular, quantitative structure-activity relationship (QSAR) models have been increasingly applied to assess the environmental effects of a plethora of toxic materials. In recent years, some more highlighted types of toxicants are endocrine disruptors (EDs, which are chemicals that can interfere with any hormone-related metabolism). Because EDs may significantly affect animal development and reproduction, rapidly predicting the adverse effects of EDs using in silico techniques is required. This study presents an in silico method to generate prediction data on the effects of representative EDs in aquatic vertebrates, particularly fish species. The protocol describes an example utilizing the automated workflow of the QSAR Toolbox software developed by the Organization for Economic Co-operation and Development (OECD) to enable acute ecotoxicity predictions of EDs. As a result, the following are determined: (1) calculation of the numerical correlations between the concentration for 50% of lethality (LC50) and octanol-water partition coefficient (K-ow), (2) output performances in which the LC50 values determined in experiments are compared to those generated by computations, and (3) the dependence of estrogen receptor binding affinity on the relationship between K-ow and LC50.

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An article Sonogashira-Hagihara and Buchwald-Hartwig cross-coupling reactions with sydnone and sydnone imine derived catalysts WOS:000607148200009 published article about N-HETEROCYCLIC CARBENES; EFFICIENT SYNTHESIS; C-C; PALLADIUM; COMPLEXES; ARYL; AMINATION; ACID in [Lucke, Ana-Luiza; Pruschinski, Lucas; Freese, Tyll; Schmidt, Andreas] Tech Univ Clausthal, Inst Organ Chem, Leibnizstr 6, D-38678 Clausthal Zellerfeld, Germany in 2020, Cited 50. Product Details of 92-86-4. The Name is 4,4′-Dibromobiphenyl. Through research, I have a further understanding and discovery of 92-86-4

Seven different palladium complexes of sydnones and sydnone imines and a co-catalyst system consisting of lithium sydnone-4-carboxylate and Pd(PPh3)(4) catalyzed Sonogashira-Hagihara reactions between (hetero)aromatic bromides and 2-methylbut-3-yn-2-ol (52 examples, up to 100% yield). The co-catalyst system and a sydnone Pd complex were also tested in Buchwald-Hartwig reactions (9 examples, up to 100% yield). [GRAPHICS]

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COA of Formula: C12H8Br2. Recently I am researching about N-HETEROCYCLIC CARBENES; EFFICIENT SYNTHESIS; C-C; PALLADIUM; COMPLEXES; ARYL; AMINATION; ACID, Saw an article supported by the Deutsche Forschungsgemeinschaft (DFG)German Research Foundation (DFG). Published in ARKAT USA INC in GAINESVILLE ,Authors: Lucke, AL; Pruschinski, L; Freese, T; Schmidt, A. The CAS is 92-86-4. Through research, I have a further understanding and discovery of 4,4′-Dibromobiphenyl

Seven different palladium complexes of sydnones and sydnone imines and a co-catalyst system consisting of lithium sydnone-4-carboxylate and Pd(PPh3)(4) catalyzed Sonogashira-Hagihara reactions between (hetero)aromatic bromides and 2-methylbut-3-yn-2-ol (52 examples, up to 100% yield). The co-catalyst system and a sydnone Pd complex were also tested in Buchwald-Hartwig reactions (9 examples, up to 100% yield). [GRAPHICS]

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In 2020 GREEN CHEM 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. The Name is 4,4′-Dibromobiphenyl. Through research, I have a further understanding and discovery of 92-86-4. Product Details 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.

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SDS of cas: 92-86-4. I found the field of Polymer Science very interesting. Saw the article Polytriphenylamine and Poly(styrene-co-hydroxystyrene) Blends as High-Performance Anticorrosion Coating for Iron published in 2021, Reprint Addresses Huang, PT (corresponding author), Fu Jen Catholic Univ, Dept Chem, New Taipei 24205, Taiwan.. The CAS is 92-86-4. Through research, I have a further understanding and discovery of 4,4′-Dibromobiphenyl.

An electroactive polytriphenylamine (PTPA-C6) is blended with poly(styrene-co-hydroxystyrene) (PS-co-PHS) as coating layers to enhance protection efficiency of PTPA-C6 on iron substrate in 3.5% sodium chloride (NaCl) solution. Experimental results show that incorporation of hydroxyl group to the polystyrene not only increases the miscibility of PTPA-C6 with PS through the hydrogen bond formation, but also enhances the bonding strength between the polymer coating layer and iron substrate. These improvements lead to superior enhancement in anticorrosion performance of PTPA-C6, even after thermal treatment. Protection efficiency (PE) of PTPA-C6 increases from 81.52% of the PTPA-C6 itself to over 94.40% under different conditions (PEmax = 99.19%).

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An article Light-Promoted C-N Coupling of Aryl Halides with Nitroarenes WOS:000608259900001 published article about NICKEL-CATALYZED AMINATION; PRECATALYST; PHOTOREDOX; AMIDATION; ARYLATION; CHLORIDES; AMINES; ESTERS; ALPHA in [Li, Gang; Yang, Liu; Liu, Jian-Jun; Zhang, Wei; Cao, Rui; Wang, Chao; Zhang, Zunting; Xue, Dong] Shaanxi Normal Univ, Minist Educ, Key Lab Appl Surface & Colloid Chem, Xian 710062, Peoples R China; [Li, Gang; Yang, Liu; Liu, Jian-Jun; Zhang, Wei; Cao, Rui; Wang, Chao; Zhang, Zunting; Xue, Dong] Shaanxi Normal Univ, Sch Chem & Chem Engn, Xian 710062, Peoples R China; [Xiao, Jianliang] Univ Liverpool, Dept Chem, Liverpool L69 7ZD, Merseyside, England in 2021, Cited 56. Product Details of 92-86-4. The Name is 4,4′-Dibromobiphenyl. Through research, I have a further understanding and discovery of 92-86-4

A photochemical C-N coupling of aryl halides with nitroarenes is demonstrated for the first time. Catalyzed by a Ni-II complex in the absence of any external photosensitizer, readily available nitroarenes undergo coupling with a variety of aryl halides, providing a step-economic extension to the widely used Buchwald-Hartwig C-N coupling reaction. The method tolerates coupling partners with steric-congestion and functional groups sensitive to bases and nucleophiles. Mechanistic studies suggest that the reaction proceeds via the addition of an aryl radical, generated from a Ni-I/Ni-III cycle, to a nitrosoarene intermediate.

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