Category: 1991/2/1

Hajjami, Maryam published the artcileSynthesis and Characterization of Magnetic Functionalized Ni and Cu Nano Catalysts and Their Application in Oxidation, Oxidative Coupling and Various Multi-Component Reactions, Quality Control of 91-02-1, the publication is Catalysis Letters (2021), 151(8), 2420-2435, database is CAplus.

Two magnetic nano catalysts of nickel and copper, Fe₃O₄@SiO₂@DOP-BenPyr-M(II), (M=Ni and Cu) have been synthesized. These catalysts were applied as recoverable, efficient and new heterogeneous catalysts for the high yielding and room temperature one-pot procedure of selective oxidation of sulfides to sulfoxides and oxidative coupling of thiols to disulfides. In addition, the catalytic activity of Fe₃O₄@SiO₂@DOP-BenPyr-Ni(II) was investigated as heterogeneous nanocatalyst for synthesis of 2,3-dihydroquinazolin-4(1H)-ones, 5-substituted 1H-tetrazoles and polyhydroquinolines. The synthesized catalysts were characterized by FT-IR, TGA, XRD, VSM, EDX, ICP and SEM techniques. These catalysts were recovered by an external magnet and reused several times without significant loss of catalytic efficiency.

Catalysis Letters published new progress about 91-02-1. 91-02-1 belongs to pyridine-derivatives, auxiliary class Pyridine,Benzene,Ketone, name is Phenyl(pyridin-2-yl)methanone, and the molecular formula is C12H9NO, Quality Control of 91-02-1.

Referemce:
https://en.wikipedia.org/wiki/Pyridine,
Pyridine | C5H5N – PubChem

Zhang, Jun published the artcileConstruction and regulation of imidazo[1,5-a]pyridines with AIE characteristics via iodine mediated Csp²-H or Csp-H amination, Related Products of pyridine-derivatives, the publication is Chinese Chemical Letters (2021), 32(10), 3083-3086, database is CAplus.

The widespread applications of aggregation-induced emission luminogens (AIEgens) inspire the creation of AIEgens with novel structures and functionalities. In this work, we focused on the direct and efficient synthesis of a new type of AIEgens, imidazo[1,5-a]pyridine derivatives, via iodine mediated cascade oxidative Csp²-H or Csp-H amination route from phenylacetylene or styrenes under mild conditions. The resulted compounds showed excellent AIE characteristics with tunable maximum emissions, attractive bioimaging performance, and potential anti-inflammatory activity, which exert broad application prospects in material, biol., medicine, and other relevant areas.

Chinese Chemical Letters published new progress about 91-02-1. 91-02-1 belongs to pyridine-derivatives, auxiliary class Pyridine,Benzene,Ketone, name is Phenyl(pyridin-2-yl)methanone, and the molecular formula is C10H10O6, Related Products of pyridine-derivatives.

Referemce:
https://en.wikipedia.org/wiki/Pyridine,
Pyridine | C5H5N – PubChem

Emami, Marzieh published the artcileSynthesis, Study, and Application of Pd(II) Hydrazone Complexes as the Emissive Components of Single-Layer Light-Emitting Electrochemical Cells, Product Details of C12H9NO, the publication is Inorganic Chemistry (2021), 60(2), 982-994, database is CAplus and MEDLINE.

For the first time, square planar Pd(II) complexes of hydrazone ligands have been investigated as the emissive components of light-emitting electrochem. cells (LECs). The neutral transition metal complex, [Pd(L¹)₂]·2CH₃OH (1), (HL¹ = (E)-Nâ€?(phenyl(pyridin-2-yl)methylene)isonicotinhydrazide), was prepared and structurally characterized. Complex 1 displays quasireversible redox properties and is emissive at room temperature in solution with a λ_max of 590 nm. As a result, it was subsequently employed as the emissive material of a single-layer LEC with configuration FTO/1/Ga/In, where studies reveal that it has a yellow color with CIE(x, y) = (0.33, 0.55), a luminance of 134 cd cm^-2, and a turn-on voltage of 3.5 V. Protonation of the pendant pyridine nitrogen atoms of L¹ afforded a second ionic complex [Pd(L¹H)₂](ClO₄)₂ (2) which is also emissive at room temperature with a λ_max of 611 nm, resulting in an orange LEC with CIE(x, y) = (0.43, 0.53). The presence of mobile anions and cations in the second inorganic transition metal complex resulted in more efficient charge injection and transport which significantly improved the luminance and turn-on voltage of the device to 188.6 cd cm^-2 and 3 V, resp. This study establishes Pd(II) hydrazone complexes as a new class of materials whose emissive properties can be chem. tuned and provides proof-of-concept for their use in LECs, opening up exciting new avenues for potential applications in the field of solid state lighting. The emissive properties of two Pd(II) hydrazone complexes have been exploited for the fabrication of single-layer light-emitting electrochem. cells. We demonstrate that a neutral Pd(II) complex capable of undergoing proton transfer with the solvent can support a suitable ionic medium for LECs. Furthermore, selective protonation of the hydrazone ligands and the introduction of perchlorate counterions afford a second LEC device with increased c.d., a red-shifted emission, and significantly improved brightness.

Inorganic Chemistry published new progress about 91-02-1. 91-02-1 belongs to pyridine-derivatives, auxiliary class Pyridine,Benzene,Ketone, name is Phenyl(pyridin-2-yl)methanone, and the molecular formula is C12H9NO, Product Details of C12H9NO.

Referemce:
https://en.wikipedia.org/wiki/Pyridine,
Pyridine | C5H5N – PubChem

Jayakumar, K. published the artcileSpectral, thermal and DFT studies of novel nickel(II) complexes of 2-benzoylpyridine-N⁴-methyl-3- thiosemicarbazone: Crystal structure of a square planar azido-nickel(II) complex, COA of Formula: C12H9NO, the publication is Journal of Molecular Structure (2022), 132257, database is CAplus.

Novel six Ni(II) complexes of an NNS donor 2-benzoylpyridine-N⁴-methyl-3- thiosemicarbazone(HL) were synthesized and characterized. Various physicochem. techniques are applied for the study of the coordination behavior of the thiosemicarbazone to the nickel center. In all the complexes, thiosemicarbazone is coordinated in the thiolate form. A four coordinated Ni(II) complex [NiLN₃] is crystallized and its mol. and crystal structures are determined by single-crystal x-ray crystallog. Single-crystal XRD reveals that the complex got crystallized in the monoclinic space group P2₁/n and nickel(II) has a square planar environment. Intramol. hydrogen bonding interactions make the complex more rigid and in the crystal lattice, the intermol. hydrogen bonding interactions generate a supramol. 1 D chain. The chem. reactivity behavior of the HL and six Ni(II) complexes was evaluated with the CAM-B3LYP quantum chem. calculations The validity of electronic structure principles like Maximum Hardness, Min. Polarizability, and Min. Electrophilicity Principle in the study is discussed.

Journal of Molecular Structure published new progress about 91-02-1. 91-02-1 belongs to pyridine-derivatives, auxiliary class Pyridine,Benzene,Ketone, name is Phenyl(pyridin-2-yl)methanone, and the molecular formula is C12H9NO, COA of Formula: C12H9NO.

Referemce:
https://en.wikipedia.org/wiki/Pyridine,
Pyridine | C5H5N – PubChem

Joshi, Abhisek published the artcileRu-Catalyzed Selective C-H Functionalization of Pyridotriazoles with Acrylates, Quality Control of 91-02-1, the publication is SynOpen (2021), 5(4), 294-300, database is CAplus.

Ruthenium-catalyzed efficient and selective C-H alkenylation of pyridotriazoles with acrylates is described. The combination of metals (Ru and Fe) plays a crucial role in achieving quant. yields of the desired products. The reaction is proposed to involve the formation of a ruthenium cyclometalated intermediate.

SynOpen published new progress about 91-02-1. 91-02-1 belongs to pyridine-derivatives, auxiliary class Pyridine,Benzene,Ketone, name is Phenyl(pyridin-2-yl)methanone, and the molecular formula is C12H9NO, Quality Control of 91-02-1.

Referemce:
https://en.wikipedia.org/wiki/Pyridine,
Pyridine | C5H5N – PubChem

Arora, Bhavya published the artcileFabrication of a recyclable magnetic halloysite-based cobalt nanocatalyst for the efficient degradation of bisphenol A and malachite green, Quality Control of 91-02-1, the publication is Materials Advances (2022), 3(15), 6373-6384, database is CAplus.

Worsening water quality has drawn considerable attention from the scientific fraternity owing to its serious impact on human health and environmental ecosystem. In this regard, magnetic halloysite-based organic-inorganic hybrid materials with a hollow nanotubular structure and surface tunable chem. have emerged as an excellent platform for the efficient removal of recalcitrant water contaminants. The fabrication of nanocatalyst involves a simple yet versatile covalent immobilization strategy, wherein a chelating ligand, 2-benzoylpyridine (2-BPy) was grafted onto silane-functionalized magnetic halloysite nanotubes with subsequent anchoring of cobalt ions. Various physico-chem. techniques such as FT-IR spectroscopy, P-XRD, VSM, FE-SEM, TEM and XPS provided valuable insights into the crystallinity, magnetic attributes and morphol. of the designed nanocomposites. The exptl. results indicated that a Co(II)@2-BPy@APTES@MHNTs/H₂O₂ catalytic system not only exhibits immense catalytic potential in accelerating the degradation process but also shows impressive features such as shorter reaction time and ambient reaction conditions. With the assistance of coumarin fluorescent probe technique and radical scavenging studies, the mechanistic pathway has been proposed, and it has been found that in situ generated highly reactive hydroxyl radicals play a crucial role in achieving outstanding degradation efficiency. The kinetic characteristics of the degradation profile demonstrate that pseudo-first-order kinetics is followed with an apparent rate constant of 0.1179 min^-1 for BPA and 0.1242 min^-1for MG. Fascinatingly, the splendid magnetic properties of the designed Co(II)@2-BPy@APTES@MHNTs furnished their facile recovery and reusability for nine subsequent runs. Remarkably, the new findings demonstrated here will deepen our understanding of the fabrication and utilization of heterogeneous catalysts for wastewater treatment via a greener approach.

Materials Advances published new progress about 91-02-1. 91-02-1 belongs to pyridine-derivatives, auxiliary class Pyridine,Benzene,Ketone, name is Phenyl(pyridin-2-yl)methanone, and the molecular formula is C12H9NO, Quality Control of 91-02-1.

Referemce:
https://en.wikipedia.org/wiki/Pyridine,
Pyridine | C5H5N – PubChem

Munshi, Sadeka J. published the artcileMetal(II) chloride complexes containing a tridentate N-donor Schiff base ligand: syntheses, structures and antimicrobial activity, Synthetic Route of 91-02-1, the publication is Journal of Coordination Chemistry (2021), 74(12), 2004-2016, database is CAplus.

One new tridentate N-coordinate ligand, N’-phenyl-N”-(phenyl(pyridin-2-yl)methylene)ethane-1,2-diamine (L), were synthesized and characterized. The tridentate N₃-coordinate ligand L were used in the synthesis of a series of three mononuclear complexes [M(L)Cl₂] [M = Cu(II), Co(II), and Zn(II)] and one polynuclear Cd(II) complex [Cd(L)Cl₂]_n and these complexes were characterized by spectroscopic techniques. The structure of all the complexes has been solved by single-crystal X-ray diffraction studies and the data reveal that all mononuclear complexes have distorted square pyramidal geometry and the polynuclear Cd(II) complex has distorted octahedral geometry. The antimicrobial activity of all complexes was investigated against Gram-pos. (Bacillus subtilis, Staphylococcus aureus) and Gram-neg. (Escherichia coli, Proteus vulgaris) bacteria by disk diffusion method. The compounds demonstrated significant antimicrobial activity while [Cu(L)Cl₂] exhibited the best antibacterial activity among all the synthesized complexes.

Journal of Coordination Chemistry published new progress about 91-02-1. 91-02-1 belongs to pyridine-derivatives, auxiliary class Pyridine,Benzene,Ketone, name is Phenyl(pyridin-2-yl)methanone, and the molecular formula is C12H9NO, Synthetic Route of 91-02-1.

Referemce:
https://en.wikipedia.org/wiki/Pyridine,
Pyridine | C5H5N – PubChem

Sarkar, Nabin published the artcileAluminum-catalyzed selective hydroboration of carbonyls and dehydrocoupling of alcohols, phenols, amines, thiol, selenol, silanols with HBpin, Name: Phenyl(pyridin-2-yl)methanone, the publication is Polyhedron (2022), 115902, database is CAplus.

A popular N,N’-chelated NacNac analog, i.e., conjugated bis-guanidinate (CBG) stabilized aluminum dihydride LAlH₂ [1; L = ArNC(ArNH):NC:(NHAr)NAr, where Ar = 2,6-Et₂-C₆H₃], demonstrates excellent catalytic hydroboration of a wide array of carbonyls with pinacolborane (HBpin) under neat conditions with good tolerance of reducible functional groups such as alkyl, alkene, halide, nitrile, nitro, ester, amide, and heteroaryl. In addition, we investigated complex 1 catalyzed cross-dehydrocoupling (CDC) of alcs., phenols, amines, thiol, selenol, and silanols with HBpin under mild reaction conditions. Furthermore, several control experiments have been performed to understand the mechanisms in hydroboration and CDC reactions. All corresponding catalytic intermediates have been identified and characterized by ¹H and ¹³C{¹H} NMR spectroscopic methods. In contrast to several reports on metal-catalyzed hydroboration of carbonyls, this is the second report for the mol. aluminum catalyzed CDC of organic substrates with HBpin.

Polyhedron published new progress about 91-02-1. 91-02-1 belongs to pyridine-derivatives, auxiliary class Pyridine,Benzene,Ketone, name is Phenyl(pyridin-2-yl)methanone, and the molecular formula is C12H9NO, Name: Phenyl(pyridin-2-yl)methanone.

Referemce:
https://en.wikipedia.org/wiki/Pyridine,
Pyridine | C5H5N – PubChem

Kos, Martin published the artcileEnantioenriched Ruthenium-Tris-Bipyridine Complexes Bearing One Helical Bipyridine Ligand: Access to Fused Multihelicenic Systems and Chiroptical Redox Switches, Application of Phenyl(pyridin-2-yl)methanone, the publication is Inorganic Chemistry (2021), 60(16), 11838-11851, database is CAplus and MEDLINE.

The synthesis and photophys. and chiroptical properties of novel aza[n]helicenes (6a–d, 10a,b, n = 4-7) substituted with one or two 2-pyridyl groups are described. The preparation was performed via an adapted Mallory reaction using aromatic imines as precursors. The obtained novel class of helical 2,2′-bipyridine ligands was then coordinated to Ru(bipy)₂²⁺ units, thus affording the first diastereomerically and enantiomerically pure [RuL(bipy)₂]²⁺ (11a,c, L = 6a,c) or [Ru₂L'(bipy)₄]⁴⁺ (12, L’ = 10b) complexes. The topol. and stereochem. of these novel metal-based helical architectures were studied in detail, notably using X-ray crystallog. Interestingly, the coordination to ruthenium(II) enabled the preparation of fused multihelical systems incorporating aza- and ruthena-helicenes within the same scaffold. The photophys., chiroptical, and redox properties of these complexes were examined in detail, and efficient redox-triggered chiroptical switching activity was evidenced.

Inorganic Chemistry published new progress about 91-02-1. 91-02-1 belongs to pyridine-derivatives, auxiliary class Pyridine,Benzene,Ketone, name is Phenyl(pyridin-2-yl)methanone, and the molecular formula is C12H9NO, Application of Phenyl(pyridin-2-yl)methanone.

Referemce:
https://en.wikipedia.org/wiki/Pyridine,
Pyridine | C5H5N – PubChem

Xu, Pengcheng published the artcilePalladium-catalyzed dearomative cyclocarbonylation of allyl alcohol for the synthesis of quinolizinones, Computed Properties of 91-02-1, the publication is Organic & Biomolecular Chemistry (2021), 19(6), 1274-1277, database is CAplus and MEDLINE.

An approach for the synthesis of quinolizinone I (R = H, 6-Me, 7-F, etc.; R¹ = H, Me, Ph; R² = H, Me, pentyl; R³ = H, Me; X = N, CH) with potential bioactivity has been developed via palladium-catalytic dearomative cyclocarbonylation of allyl alc. R⁴C(R¹)=C(R²)CH(R³)OH (R⁴ = pyridin-2-yl, 5-fluoropyridin-2-yl, pyrazin-2-yl, etc.). Diverse quinolizinone compounds I could be attained with good efficiencies. A feasible reaction pathway could be a successive procedure of allylation, dearomatization, CO insertion and the Heck reaction.

Organic & Biomolecular Chemistry published new progress about 91-02-1. 91-02-1 belongs to pyridine-derivatives, auxiliary class Pyridine,Benzene,Ketone, name is Phenyl(pyridin-2-yl)methanone, and the molecular formula is C10H10O2, Computed Properties of 91-02-1.

Referemce:
https://en.wikipedia.org/wiki/Pyridine,
Pyridine | C5H5N – PubChem