Category: pyridine-derivatives

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. 144750-52-7, Name is Methyl 2-(2-chlorophenyl)-2-(4,5-dihydrothieno[2,3-c]pyridin-6(7H)-yl)acetate hydrochloride, SMILES is O=C(OC)C(C1=CC=CC=C1Cl)N2CCC(C=CS3)=C3C2.[H]Cl, in an article , author is Han, Yujie, once mentioned of 144750-52-7, Category: pyridine-derivatives.

Hydrothermal synthesis of polydopamine-functionalized cobalt-doped lanthanum nickelate perovskite nanorods for efficient water oxidation in alkaline solution

Perovskite oxides have attracted great attention recently for their low cost and high intrinsic activity in the electrochemical oxygen evolution reaction (OER). In this work, we synthesized highly efficient OER electrocatalysts in alkaline solution by carbonization of polydopamine (PDA)-functionalized cobalt-doped lanthanum nickelate perovskite nanorod (La5Ni3Co2) complexes. The calcination temperature and molar ratio for La, Ni, and Co were optimized. The as-prepared complex with a molar ratio of 5:3:2 (La:Ni:Co) and a calcination temperature of 500 degrees C displayed enhanced OER activity and excellent durability. In 1.0 M KOH, the overpotential of the as-prepared catalyst at a current density of 10 mA cm(-2) was 0.360 V, which is comparable to those of noble metal-based materials or perovskite-based materials. The Tafel slope is 48.1 mV dec(-1), which is smaller than those of prepared composites. The satisfactory oxygen evolution activity could be attributed to the increased Co3O4, O-2(2-)/O-, pyridine N, and quaternary N species after calcination treatment, and the improved amount of Ni3+ during the OER process, as well as the high surface area and electrochemical surface area.

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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. 695-34-1, Name is 4-Methylpyridin-2-amine, SMILES is C1=C(C=CN=C1N)C, in an article , author is Mukherjee, Shuvam, once mentioned of 695-34-1, Application In Synthesis of 4-Methylpyridin-2-amine.

Chemically sulfated arabinoxylans from Plantago ovata seed husk: Synthesis, characterization and antiviral activity

Limited options for the treatments of diseases triggered through viral infections revealed the quest for novel antiviral drugs. Polysaccharide sulfates owing to their unique mode of action are prominent antiviral drug candidates. Herein, the arabinoxylan of Plantago ovata seed husk was simultaneously extracted and chemically sulfated using sulphur trioxide-pyridine reagent in N,N-dimethylformamide solvent (SO3.Py/DMF). Thus, three arabinoxylan sulfates (IS1201-IS1203) holding variable degrees of sulfation (DS: 0.1-0.9), molar masses (18.4-31.3 kDa) and glycosyl makeup (Ara: Xyl::10-19:81-90; molar ratio) were produced and then characterized. According to the results, these polymers displayed anti-herpes simplex virus type 1 activity and their potency depends upon DS. The utmost effective compound (IS1203, IC50: 2.9 mu g mL(-1)) was a 18.4 kDa arabinoxylan possessing sulfate groups at O-3 and O-2,3 positions of xylopyranosyl (Xylp), and O-5 of arabinofuranosyl (Araf) residues. Besides, this polymer showed no cytotoxicity at concentration up to 1000 mu g mL(-1). Given that polysaccharide sulfates have antiviral activities, synthesis of new molecules possessing diverse structures will be a useful addition to the arsenal of antivirals.

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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. 766-11-0, Name is 5-Bromo-2-fluoropyridine, SMILES is FC1=NC=C(Br)C=C1, in an article , author is Li, Xinmin, once mentioned of 766-11-0, COA of Formula: https://www.ambeed.com/products/766-11-0.html.

Base-Controlled One-Pot Chemoselective Suzuki-Miyaura Reactions for the Synthesis of Unsymmetrical Terphenyls

We report a chemoselective Suzuki-Miyaura reaction protocol of using bromophenyl fluorosulfonate as building block for the preparation of unsymmetrical terphenyls. The chemoselective cross-coupling of bromophenyl fluorosulfonate and arylboronic acids can be achieved by controlling base species without using any ligands. Under this methodology, various of m- and p-unsymmetrical terphenyls were obtained in moderate to good yields.

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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

Chemistry, like all the natural sciences, Product Details of 144750-52-7, begins with the direct observation of nature— in this case, of matter.144750-52-7, Name is Methyl 2-(2-chlorophenyl)-2-(4,5-dihydrothieno[2,3-c]pyridin-6(7H)-yl)acetate hydrochloride, SMILES is O=C(OC)C(C1=CC=CC=C1Cl)N2CCC(C=CS3)=C3C2.[H]Cl, belongs to pyridine-derivatives compound. In a document, author is Shen, Fang-Fang, introduce the new discover.

Purely organic light-harvesting phosphorescence energy transfer by beta-cyclodextrin pseudorotaxane for mitochondria targeted imaging

A new type of purely organic light-harvesting phosphorescence energy transfer (PET) supramolecular assembly is constructed from 4-(4-bromophenyl)-pyridine modified beta-cyclodextrin (CD-PY) as a donor, cucurbit[8]uril (CB[8]) as a mediator, rhodamine B (RhB) as an acceptor, and adamantane modified hyaluronic acid (HA-ADA) as a cancer cell targeting agent. Interestingly, the complexation of free CD-PY, which has no RTP emission in aqueous solution, with CB[8] results in the formation of CD-PY@CB[8] pseudorotaxane with an RTP emission at 510 nm. Then the addition of RhB leads to an efficient light-harvesting PET process with highly efficient energy transfer and an ultrahigh antenna effect (36.42) between CD-PY@CB[8] pseudorotaxane and RhB. Importantly, CD-PY@CB[8]@RhB assembles with HA-ADA into nanoparticles with further enhanced delayed emission at 590 nm. The nanoparticles could be successfully used for mitochondria targeted imaging in A549 cancer cells. This aqueous-state PET based on a supramolecular assembly strategy has potential application in delayed fluorescence cell imaging.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 144750-52-7. Product Details of 144750-52-7.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, such as the rate of change in the concentration of reactants or products with time. 72830-09-2, Name is 2-Chloromethyl-3,4-dimethoxypyridinium chloride, formurla is C8H11Cl2NO2. In a document, author is Aganda, Kim Christopher C., introducing its new discovery. Product Details of 72830-09-2.

Visible-light-mediated direct C3-arylation of 2H-indazoles enabled by an electron-donor-acceptor complex

A mild visible-light-mediated, photocatalyst-free arylation of 2H-indazoles was developed. The formation of an electron donor-acceptor complex by 2H-indazoles and aryl diazonium salts in the presence of pyridine allows the direct arylation of 2H-indazoles under visible-light irradiation. This process provides an efficient route for the synthesis of C3-arylated-2H-indazoles, which are important scaffolds of various bioactive compounds.

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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. 5223-06-3, Name is 2-(5-Ethylpyridin-2-yl)ethanol, SMILES is CCC1=CN=C(CCO)C=C1, in an article , author is Kalkman, Eric D., once mentioned of 5223-06-3, Formula: https://www.ambeed.com/products/5223-06-3.html.

Unusual Electronic Effects of Ancillary Ligands on the Perfluoroalkylation of Aryl Iodides and Bromides Mediated by Copper(I) Pentafluoroethyl Complexes of Substituted Bipyridines

Several perfluoroalkylcopper compounds have been reported previously that serve as reagents or catalysts for the perfluoroalkylation of aryl halides. However, the relationships between the reactivity of such complexes and the electronic properties of the ancillary ligands are unknown, and such relationships are not well-known in general for copper complexes that mediate or catalyze cross coupling. We report the synthesis and characterization of a series of pentafluoroethylcopper(I) complexes ligated by bipyridine ligands possessing varied electronic properties. In contrast to the limited existing data on the reactivity of L2Cu(I)-X complexes bearing amine and pyridine-type ligands in Ullmann-type aminations with aryl halides, the reactions of aryl halides with pentafluoroethylcopper(I) complexes bearing systematically varied bipyridine ligands were faster for complexes bearing less electron-donating bipyridines than for complexes bearing more electron-donating bipyridines. Analysis of the rates of reaction and the relative populations of the neutral complexes [(R(2)bpy)CuC2F5] and ionic complexes [(R(2)bpy)(2)Cu][Cu(C2F5)(2)] formed by these reagents in solution suggests that this effect of electronics on the reaction rate results from an unusual trend of faster oxidative addition of aryl halides to [(R(2)bpy)CuC2F5] complexes containing less electron-donating R(2)bpy ligands than to those containing more electron-donating R(2)bpy ligands.

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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, such as the rate of change in the concentration of reactants or products with time. 31251-41-9, Name is 8-Chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-one, formurla is C14H10ClNO. In a document, author is Guo, Beibei, introducing its new discovery. SDS of cas: 31251-41-9.

Hydration of nitriles using a metal-ligand cooperative ruthenium pincer catalyst

Nitrile hydration provides access to amides that are important structural elements in organic chemistry. Here we report catalytic nitrile hydration using ruthenium catalysts based on a pincer scaffold with a dearomatized pyridine backbone. These complexes catalyze the nucleophilic addition of H2O to a wide variety of aliphatic and (hetero)aromatic nitriles in (BuOH)-Bu-t as solvent. Reactions occur under mild conditions (room temperature) in the absence of additives. A mechanism for nitrile hydration is proposed that is initiated by metal-ligand cooperative binding of the nitrile.

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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

117977-21-6, Name is 2-[[[4-(3-Methoxypropoxy)-3-methylpyridine-2-yl ]methyl]thio]-1H-benzimidazole, molecular formula is C18H21N3O2S, belongs to pyridine-derivatives compound, is a common compound. In a patnet, author is Lapointe, Sebastien, once mentioned the new application about 117977-21-6, SDS of cas: 117977-21-6.

Nickel(II) Complexes with Electron-Rich, Sterically Hindered PNP Pincer Ligands Enable Uncommon Modes of Ligand Dearomatization

We report the reactivity and characterization of hydride, methyl, and bromo Ni-II complexes with a new class of electron-rich and sterically hindered PNP pincer ligands, Me4PNPR (R = Pr-i, Bu-t), in which a classical metal-ligand cooperative mode of reactivity via CH2 arm deprotonation is blocked by methylation. This enables new, uncommon modes of PNP ligand dearomatization that involve reactivity in the para position of the pyridine ring. In particular, the reduction of [(Me4PNPiPr) (NiMe)-Me-II]B(Ar-F)(4) with KC8 leads to the formation of a new C-C bond via dimerization of two complexes through the para position. This reactivity stands in sharp contrast to the previously reported bromo or chloro complexes, where stable Ni-I halogen moieties are formed. Computational analysis showed a greater propensity for ligand-centered radical formation for the presumed intermediate one-electron-reduced species. UV-induced homolysis of the Ni-II-Me bond in [(Me4PNPiPr) (NiMe)-Me-II]B(Ar-F)(4) leads to the formation of a Me radical detected by radical traps and Ni(I )intermediates that can be trapped in the presence of halide ions to give previously characterized, stable Ni-I halogen complexes. In addition, treatment of the bromo complexes [(Me4PNPR)(NiBr)-Br-II]BPh4 with a powerful hydride source, LiBEt3H, leads to the reduction of the pyridine ring and the formation of Ni-II complexes with an anionic amide donor reduced pincer ligand, although aromatic Ni-II hydride complexes could also be obtained with a weaker hydride source. We have observed that steric bulk at the phosphine donors controls the reactivity of the resulting Ni(II)H( )complexes. While t-Bu-substituted [(Me4PNPtBu) (NiH)-H-II]Y(Y=BPh4, B(Ar-F)(4)) does not react with O-2, the less sterically hindered Pr-i-substituted [(Me4PNPiPr)(NiH)-H-II]Y reacts instantaneously to give an unstable superoxide adduct that can be observed by EPR.

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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 5431-44-7, Name is 2,6-Pyridinedicarboxaldehyde, molecular formula is C7H5NO2. In an article, author is Boyd, Derek R.,once mentioned of 5431-44-7, Quality Control of 2,6-Pyridinedicarboxaldehyde.

Toluene Dioxygenase-Catalyzed cis-Dihydroxylation of Quinolines: A Molecular Docking Study and Chemoenzymatic Synthesis of Quinoline Arene Oxides

Molecular docking studies of quinoline and 2-chloroquinoline substrates at the active site of toluene dioxygenase (TDO), were conducted using Autodock Vina, to identify novel edge-to-face interactions and to rationalize the observed stereoselective cis-dihydroxylation of carbocyclic rings and formation of isolable cis-dihydrodiol metabolites. These in silico docking results of quinoline and pyridine substrates, with TDO, also provided support for the postulated cis-dihydroxylation of electron-deficient pyridyl rings, to give transient cis-dihydrodiol intermediates and the derived hydroxyquinolines. 2-Chloroquinoline cis-dihydrodiol metabolites were used as precursors in the chemoenzymatic synthesis of enantiopure arene oxide and arene dioxide derivatives of quinoline, in the context of its possible mammalian metabolism and carcinogenicity.

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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

Synthetic Route of 211915-84-3, The transformation of simple hydrocarbons into more complex and valuable products via catalytic C–H bond functionalisation has revolutionised modern synthetic chemistry. 211915-84-3, Name is Ethyl 3-(2-(((4-cyanophenyl)amino)methyl)-1-methyl-N-(pyridin-2-yl)-1H-benzo[d]imidazole-5-carboxamido)propanoate, SMILES is O=C(OCC)CCN(C1=NC=CC=C1)C(C2=CC=C3N(C)C(CNC4=CC=C(C#N)C=C4)=NC3=C2)=O, belongs to pyridine-derivatives compound. In a article, author is Xie, Fangxi, introduce new discover of the category.

Mechanism for Zincophilic Sites on Zinc-Metal Anode Hosts in Aqueous Batteries

The zinc-metal anode (ZMA) is a critical component of rechargeable Zn-based batteries. Zinc-dendrite formation on ZMA during cycling causes an internal short-circuit, thereby limiting long-term practical operation of batteries. A strategy of introducing zincophilic sites shows promise in suppressing dendrite growth. However, the mechanism is not understood. Here, a detailed study of the mechanism of zincophilic sites based on multiple in situ/ex situ techniques is reported. Using a carbon-host as a model system with nitrogen sites as zincophilic sites and both ex situ near-edge X-ray absorption fine structure (NEXAFS) and in situ Raman spectra, it is shown that zinc ions are bonded with pyridine sites to form Zn-N bonds. The Zn-N bonds induce spacious nucleation of zinc on carbon-hosts and suppress zinc-dendrite formation. The host with zincophilic sites exhibits a homogenous Zn deposition, together with boosted electrochemical performance. This finding underscores the impact of nitrogen zincophilic sites in suppressing zinc-dendrite formation. It is shown that bonding between zinc ions and zincophilic sites is the mechanism for zincophilic nucleation in the ZMA host. These findings are expected to be of immediate benefit to researchers in battery technologies and materials science.

Synthetic Route of 211915-84-3, The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 211915-84-3 is helpful to your research.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem