A new application about 1762-34-1

There are many compounds similar to this compound(1762-34-1)Application In Synthesis of 5,5′-Dimethyl-2,2′-bipyridine. if you want to know more, you can check out my other articles. I hope it will help you,maybe you’ll find some useful information.

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Mechanism of Formic Acid Disproportionation Catalyzed by an Iridium Complex Immobilized on Bipyridine-Periodic Mesoporous Organosilica: A Case Study based on Kinetics Analysis, published in 2020, which mentions a compound: 1762-34-1, mainly applied to mesoporous organosilica supported bipyridine periodic pentamethylcyclopentadienyliridium complex preparation catalyst; formic acid disproportionation catalyzed iridium complex immobilized bipyridine kinetics, Application In Synthesis of 5,5′-Dimethyl-2,2′-bipyridine.

This work investigated the kinetics of formic acid (FA) disproportionation using an Ir complex immobilized on bipyridine-periodic mesoporous organosilica (BPy-PMO). The selectivity for methanol (MeOH) is increased using this catalyst compared to conventional homogeneous Ir complexes. This enhanced selectivity is attributed to the retention of H2 and CO2 generated by the competing FA dehydrogenation in PMO mesochannels having a high aspect ratio. However, no direct evidence for this process was previously obtained. The present work clarified the unique catalysis mechanism associated with a PMO catalyst exhibiting higher MeOH selectivity based on a hypothesis that the generation of MeOH via FA hydrogenation is promoted by the confinement of H2 in the PMO pores. The results obtained from the present kinetics study and data regarding H2 diffusion in the PMO pores strongly support this hypothesis.

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Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Brief introduction of 1762-34-1

There are many compounds similar to this compound(1762-34-1)Name: 5,5′-Dimethyl-2,2′-bipyridine. if you want to know more, you can check out my other articles. I hope it will help you,maybe you’ll find some useful information.

Name: 5,5′-Dimethyl-2,2′-bipyridine. So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic. Compound: 5,5′-Dimethyl-2,2′-bipyridine, is researched, Molecular C12H12N2, CAS is 1762-34-1, about Dynamic Helicates Self-Assembly from Homo- and Heterotopic Dynamic Covalent Ligand Strands.

The understanding and the application of reversible covalent reactions and coordination chem. together with the proper design of the mol. frameworks, allow to achieve not only well-defined output architectures but also different grades of complex behavior. In this work, the dynamic nature of the helical systems offers an addnl. level of complexity by combining self-sorting on two levels: (1) the build-up of the ligand strand constituents from their components through dynamic covalent chem.; (2) the assembly of the helicates from the ligands and the metal cations through dynamic metallo-supramol. chem. The information encoded in the ligands constituent mol. was read differently (and accurately at the same time) by metal cations that varied in the coordination algorithms. It enabled the selective formation of a specific type of helicates from a wide library of helicates formed by the possible combination of subcomponents. Ligands containing dynamic tridentate and/or bidentate binding motifs in the same strand were studied to explore the helicates self-assembly with appropriate metal cations.

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Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

New explortion of 1762-34-1

There are many compounds similar to this compound(1762-34-1)Reference of 5,5′-Dimethyl-2,2′-bipyridine. if you want to know more, you can check out my other articles. I hope it will help you,maybe you’ll find some useful information.

So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic.Mi, Zhen; Yang, Peng; Wang, Rong; Unruangsri, Junjuda; Yang, Wuli; Wang, Changchun; Guo, Jia researched the compound: 5,5′-Dimethyl-2,2′-bipyridine( cas:1762-34-1 ).Reference of 5,5′-Dimethyl-2,2′-bipyridine.They published the article 《Stable Radical Cation-Containing Covalent Organic Frameworks Exhibiting Remarkable Structure-Enhanced Photothermal Conversion》 about this compound( cas:1762-34-1 ) in Journal of the American Chemical Society. Keywords: covalent organic framework NIR photothermal therapy. We’ll tell you more about this compound (cas:1762-34-1).

The production of a radical cation-containing covalent organic framework (COF) has been accomplished by sequential in situ reactions, quaternization, and one-electron reduction of the 2,2′-bipyridine-based COFs. The acid-catalyzed COF formation enables the cis configuration of 2,2′-bipyridyl moieties in the structure, of which the stability arises from the eclipsed stacking of the two-dimensional layered structure. The postfunctionalization generates cyclic alkylated diquats as the sole products from the controlled quaternization. The reduction of diquat cations on the COF skeletons results in a large number of radical cations, which delocalize and uniaxially stack on top of one another by virtue of interlayered π-electronic couplings. The absorption of the near-IR (NIR) region exhibited by the cationic radical COF is remarkably high owing to the intercharge transfer across the π-coupling interlayers. Also, the long-range array of extended and planar frameworks in such a COF leads to the extra stability of the radical cations against external stresses. The structure-enhanced performance of the COF material is witnessed with photothermal conversion efficiencies of as high as 63.8 and 55.2% when exposed to 808 and 1064 nm lasers, resp. Further PEG modification on such a COF allows photoacoustic imaging and photothermal therapy in vivo under NIR light illumination to be manifested.

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Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Some scientific research tips on 1762-34-1

There are many compounds similar to this compound(1762-34-1)Synthetic Route of C12H12N2. if you want to know more, you can check out my other articles. I hope it will help you,maybe you’ll find some useful information.

Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 1762-34-1, is researched, Molecular C12H12N2, about Tuning of Ionic Second Coordination Sphere in Evolved Rhenium Catalyst for Efficient Visible-Light-Driven CO2 Reduction, the main research direction is carbon dioxide rhenium catalyst photoreduction quantum yield optical property; carbon dioxide reduction; ionic liquids; photocatalysis; secondary coordination sphere; visible light.Synthetic Route of C12H12N2.

Developing an efficient and easy-to-handle strategy in designing catalysts for CO2 reduction into CO by harnessing sunlight is a promising project. Here, a facile strategy was developed to design a Re catalyst modified with an ionic secondary coordination sphere for photoreduction of CO2 to CO by visible light. By adding ionic liquids or tuning a different ionic secondary coordination sphere, it was discovered that an outstanding optical property, other than CO2 absorption ability or the ability to dissociation of chloride anion, is the prerequisite for catalyst design. Accordingly, a novel Re catalyst, {Re[BpyMe(tris(2-hydroxyethyl)amine)](CO)3Cl}Br (Re-THEA), was designed, screened, and resulted in a relative high quantum yield (up to 34 %) for visible-light-induced CO2 reduction with a single-mol. system. DFT calculations, combined with exptl. outcomes, suggested the pendant ionic tris(2-hydroxyethyl)amino (THEA) group on Re-THEA can enhance visible-light absorption, stabilize reaction intermediates, and suppress the Re-Re dimer formation.

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Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Chemical Properties and Facts of 1762-34-1

There are many compounds similar to this compound(1762-34-1)Safety of 5,5′-Dimethyl-2,2′-bipyridine. if you want to know more, you can check out my other articles. I hope it will help you,maybe you’ll find some useful information.

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Dehydrogenative Synthesis of 2,2′-Bipyridyls through Regioselective Pyridine Dimerization, published in 2019, which mentions a compound: 1762-34-1, mainly applied to pyridine palladium catalyst regioselective dimerization dehydrogenative silver pivalic acid; bipyridyl preparation; 2,2′-bipyridyls; C−H arylation; dehydrogenative coupling; palladium; pyridines, Safety of 5,5′-Dimethyl-2,2′-bipyridine.

2,2′-Bipyridyls have been utilized as indispensable ligands in metal-catalyzed reactions. The most streamlined approach for the synthesis of 2,2′-bipyridyls is the dehydrogenative dimerization of unfunctionalized pyridine. Herein, we report on the palladium-catalyzed dehydrogenative synthesis of 2,2′-bipyridyl derivatives The Pd catalysis effectively works with an AgI salt as the oxidant in the presence of pivalic acid. A variety of pyridines regioselectively react at the C2-positions. This dimerization method is applicable for challenging substrates such as sterically hindered 3-substituted pyridines, where the pyridines regioselectively react at the C2-position. This reaction enables the concise synthesis of twisted 3,3′-disubstituted-2,2′-bipyridyls as an underdeveloped class of ligands.

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Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

New downstream synthetic route of 1762-34-1

There are many compounds similar to this compound(1762-34-1)Recommanded Product: 1762-34-1. if you want to know more, you can check out my other articles. I hope it will help you,maybe you’ll find some useful information.

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Synthesis, crystal structure, thermal, luminescent property and antibacterial activity of lanthanide ternary complexes with p-chlorobenzoic acid and 5,5′-dimethyl-2,2′-bipyridine, published in 2020-01-15, which mentions a compound: 1762-34-1, mainly applied to rare earth chlorobenzoic acid bipyridine ternary complex preparation structure; antibacterial crystal structure thermal property fluorescence rare earth complex, Recommanded Product: 1762-34-1.

Four novel lanthanide coordination complexes, [La(p-ClBA)3(5,5′-DM-2,2′-bipy)H2O]n (1), [Ln(p-ClBA)3(5,5′-DM-2,2′-bipy)H2O]2 (Ln = Sm 2, Eu 3, Gd 4) were obtained from the reaction between p-chlorobenzoic acid (p-ClHBA), 5,5′-dimethyl-2,2′-bipyridine (5,5′-DM-2,2′-bipy) and lanthanide nitrate under solvothermal conditions. Single crystal X-ray diffraction anal. showed that complex 1 is a 1D chain structure, crystallized in the monoclinic system, space group P2(1)/n, and formed a 2D sheet through the C-H···O hydrogen bond interactions. While complexes 2-4 were binuclear unit and crystallizes isomorphically in the triclinic system, space group Pi̅. The binuclear unit were assembled into 1D supramol. structures through the O-H···O hydrogen bond interactions along the a-axis and formed a 2D supramol. structures through the π-π stacking interactions along the b-axis. The thermal anal. of four complexes were studied by TG-DSC/FTIR. The solid state photoluminescent properties of complex 3 were investigated at room temperature Moreover, the antibacterial activities of complexes 1-4 on Candida albicans were studied.

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Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Extended knowledge of 1762-34-1

There are many compounds similar to this compound(1762-34-1)Recommanded Product: 5,5′-Dimethyl-2,2′-bipyridine. if you want to know more, you can check out my other articles. I hope it will help you,maybe you’ll find some useful information.

The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: 5,5′-Dimethyl-2,2′-bipyridine(SMILESS: CC1=CN=C(C=C1)C1=NC=C(C)C=C1,cas:1762-34-1) is researched.Recommanded Product: 5,5′-Dimethyl-2,2′-bipyridine. The article 《The laser-induced potential jump: A method for rapid electron injection into oxidoreductase enzymes》 in relation to this compound, is published in Journal of Physical Chemistry B. Let’s take a look at the latest research on this compound (cas:1762-34-1).

Oxidoreductase enzymes often perform technol. useful chem. transformations using abundant metal cofactors with high efficiency under ambient conditions. The understanding of the catalytic mechanism of these enzymes is, however, highly dependent on the availability of well-characterized and optimized time-resolved anal. techniques. We have developed an approach for rapidly injecting electrons into a catalytic system using a photoactivated nanomaterial in combination with a range of redox mediators to produce a potential jump in solution, which then initiates turnover via electron transfer (ET) to the catalyst. The ET events at the nanomaterial-mediator-catalyst interfaces are, however, highly sensitive to the exptl. conditions such as photon flux, relative concentrations of system components, and pH. Here, we present a systematic optimization of these exptl. parameters for a specific catalytic system, namely, [FeFe] hydrogenase from Chlamydomonas reinhardtii (CrHydA1). The developed strategies can, however, be applied in the study of a wide variety of oxidoreductase enzymes. Our potential jump system consists of CdSe/CdS core-shell nanorods as a photosensitizer and a series of substituted bipyridinium salts as mediators with redox potentials in the range from -550 to -670 mV (vs. SHE). With these components, we screened the effect of pH, mediator concentration, protein concentration, photosensitizer concentration, and photon flux on steady-state photoreduction and hydrogen production as well as ET and potential jump efficiency. By manipulating these exptl. conditions, we show the potential of simple modifications to improve the tunability of the potential jump for application to study oxidoreductases.

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Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Now Is The Time For You To Know The Truth About 1762-34-1

There are many compounds similar to this compound(1762-34-1)Recommanded Product: 5,5′-Dimethyl-2,2′-bipyridine. if you want to know more, you can check out my other articles. I hope it will help you,maybe you’ll find some useful information.

Recommanded Product: 5,5′-Dimethyl-2,2′-bipyridine. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: 5,5′-Dimethyl-2,2′-bipyridine, is researched, Molecular C12H12N2, CAS is 1762-34-1, about Dual Catalytic Platform for Enabling sp3 α C-H Arylation and Alkylation of Benzamides. Author is Rand, Alexander W.; Yin, Hongfei; Xu, Liang; Giacoboni, Jessica; Martin-Montero, Raul; Romano, Ciro; Montgomery, John; Martin, Ruben.

A dual catalytic sp3 α C-H arylation and alkylation of benzamides with organic halides is described. This protocol exhibits an exquisite site selectivity, chemoselectivity, and enantioselectivity pattern, offering a complementary reactivity mode to existing sp3 arylation or alkylations via transition metal catalysis or photoredox events.

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Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Chemical Properties and Facts of 1762-34-1

There are many compounds similar to this compound(1762-34-1)Reference of 5,5′-Dimethyl-2,2′-bipyridine. if you want to know more, you can check out my other articles. I hope it will help you,maybe you’ll find some useful information.

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called A new mononuclear nickel complex with 5,5′-dimethyl-2,2′-bipyridine: Synthesis, structural investigation and catalytic properties, published in 2020-11-05, which mentions a compound: 1762-34-1, mainly applied to preparation crystal structure mononuclear nickel dimethylbipyridine selenate complex; Thermal decomposition mononuclear nickel dimethylbipyridine selenate complex; Heck Sonogashira coupling reaction nickel dimethylbipyridine selenate complex catalyst, Reference of 5,5′-Dimethyl-2,2′-bipyridine.

The new [Ni(dmbpy)(H2O)4]SeO4 (1) complex (dmbpy = 5,5′-dimethyl-2,2′-bipyridine or C12H12N2), based on mononuclear nickel(II) and bi-at. bridging ligands was successfully synthesized by hydrothermal method. The crystals were characterized by x-ray single-crystal diffraction, crystallizing in the monoclinic system, space group P21/c. Their crystal structure consists of metallic cations octahedrally coordinated by four water mols. and two nitrogen atoms coming from the organic mol. [NiN2O4], and a selenate anion (SeO4)2-. Their crystal packing is ensured by a three-dimensional network of O-H. O hydrogen bonds between the cation and anion moieties, and π… π interactions between the pyridine rings of the organic moieties of the same layer. The thermal anal. discloses dehydration between 148° and 210°, leading to an anhydrous compound [Ni(dmbpy)]SeO4. The study of vibrational absorption and Raman scattering spectra allows bringing addnl. information to those obtained by x-ray diffraction. The optical band gap was calculated from the UV-visible absorbance spectra using classical Tauc relation which is 3.58 eV. The catalytic evaluation of [Ni(dmbpy)(H2O)4]SeO4 on Heck and Sonogashira coupling reactions, activated by ultrasonic irradiation, results in encouraging yields for a very short times with a remarkable selectivity of the form (E) with respect to (Z) during the arylation of styrene, making this complex a promising catalyst for both types of reactions. The coupling products of the Heck and Sonogashira coupling reaction ((Z)-/(E)- Stilbene and Diphenylacetylene, resp.) were examined by 13C NMR and 1H NMR. These spectroscopic measurements provide extremely valuable information on the structure of the mols. obtained.

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Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Can You Really Do Chemisty Experiments About 1762-34-1

There are many compounds similar to this compound(1762-34-1)Electric Literature of C12H12N2. if you want to know more, you can check out my other articles. I hope it will help you,maybe you’ll find some useful information.

Electric Literature of C12H12N2. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: 5,5′-Dimethyl-2,2′-bipyridine, is researched, Molecular C12H12N2, CAS is 1762-34-1, about Dual Cobalt and Photoredox Catalysis Enabled Redox-Neutral Annulation of 2-Propynolphenols. Author is Zhu, Yao; He, Yong-Qin; Tian, Wan-Fa; Wang, Mei; Zhou, Zhao-Zhao; Song, Xian-Rong; Ding, Hai-Xin; Xiao, Qiang.

A hydroxyl-assisted, organophotoredox/cobalt dual catalyzed annulation of 2-propynolphenols I [R1 = H, R2 = H, F, Cl, Br, MeO2C, Me; R1 = Cl, R2 = H; R1 = R2 = F; R3 = R4 = Me, Ph, 4-FC6H4, 3-F3CC6H4, etc.; R3 = Ph, R4 = Me, 4-ClC6H4, 2-FC6H4, 4-F3CC6H4, 2-thienyl, etc.; R3 = 4-FC6H4, R4 = 4-MeOC6H4; R3R4 = (CH2)5] to form 2-(hydroxymethyl)benzo[b]furans II has been developed by employing 1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene (4CzIPN) as photosensitizer and CoCl2(PPh3)2/5,5′-dimethyl-2,2′-bipyridine as cobalt catalytic precursor. Various substrates and functional groups were tolerated. The practical applications of this reaction were further demonstrated by enlarged gram-scale and various derivations for complex heterocycles. Primary mechanistic studies suggested the involvement of cobalt-hydride mediated hydrogen atom transfer (HAT) process.

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Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem