Month: April 2022

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.HPLC of Formula: 2160535-56-6. The article 《Thermodynamics of the Adsorption of Isomeric Dipyridyls and Their Derivatives from Water-Organic Solutions on HYPERCARB Porous Graphitic Carbon》 in relation to this compound, is published in Russian Journal of Physical Chemistry A. Let’s take a look at the latest research on this compound (cas:1762-34-1).

High-performance liquid chromatog. is used under near-equilibrium conditions to study the adsorption of isomeric dipyridyls and their derivatives from water-acetonitrile, water-methanol, and water-isopropanol solutions onto Hypercarb graphite-like carbon material in the region of Henry’s law. It is shown that the possibility of forming strong intramol. C-H-N’-hydrogen bonds in a mol. of 2,2′-dipyridyl or its derivatives strengthens the adsorption bonding of adsorbate mols. and the surface of the graphite-like material due to stabilization of their planar conformation. Destabilizing this intramol. hydrogen bond by adding substituents in different positions of the pyridine rings enhances the specific intermol. interaction between adsorbate mols. and the solvent’s components and distorts the planar conformation of dipyridyls, weakening their retention on the Hypercarb material. Pos. adsorption from the water-organic medium on the carbon adsorbent is observed for all of the investigated dipyridyls, with the exception of 2,2′-dipyridyl-N,N’-dioxide, which is adsorbed weaker than the solvent components. Anomalous medium-property dependences are found for the thermodn. characteristics of the adsorption of dipyridyls on porous graphitic carbon, and are attributed to the predominance of adsorbate-adsorbent π-π interactions over hydrophobic ones and the resolvation of adsorbate mols. with acetonitrile in proportion to lowering the content of water in the bulk solution

Although many compounds look similar to this compound(1762-34-1)HPLC of Formula: 1762-34-1, numerous studies have shown that this compound(SMILES:CC1=CN=C(C=C1)C1=NC=C(C)C=C1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

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

The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: (R)-N-((R)-(5-(Diphenylphosphanyl)-9,9-dimethyl-9H-xanthen-4-yl)(4-methoxyphenyl)methyl)-2-methylpropane-2-sulfinamide( cas:2160535-56-6 ) is researched.HPLC of Formula: 2160535-56-6.Wang, Yidong; Zhang, Peichao; Di, Xiaoyu; Dai, Qiang; Zhang, Zhan-Ming; Zhang, Junliang published the article 《Gold-Catalyzed Asymmetric Intramolecular Cyclization of N-Allenamides for the Synthesis of Chiral Tetrahydrocarbolines》 about this compound( cas:2160535-56-6 ) in Angewandte Chemie, International Edition. Keywords: gold catalyzed asym intramol cyclization allenamide chiral hydrocarboline synthesis; chiral sulfinamide phosphine ligand gold catalyzed asym intramol cyclization; desbromoarborescidine A synthesis desbromoarborescidine C formal synthesis; deplancheine formal synthesis; desymmetrization allenamide; allenamides; cyclization; enantioselectivity; gold; tetrahydrocarboline. Let’s learn more about this compound (cas:2160535-56-6).

Highly enantioselective gold-catalyzed intramol. cyclization of N-allenamides was implemented by utilizing a designed chiral sulfinamide phosphine ligand (PC-Phos) [e.g., allenamide I → tetrahydrocarboline II (99%, 96% ee) in presence of Me2S.AuCl, AgNTf2 and ligand III in CH2Cl2 at -50°]. This represents the first example of highly enantioselective intramol. cyclization of N-allenamides. The practicality of this reaction was validated in the total synthesis of (R)-desbromoarborescidine A and formal synthesis of (R)-desbromoarborescidine C and (R)-deplancheine. Moreover, the catalyst system PC-Phos/AuNTf2 proved to be specifically efficient to promote the desymmetrization of N-allenamides in excellent yields with satisfactory ee values.

Compounds in my other articles are similar to this one((R)-N-((R)-(5-(Diphenylphosphanyl)-9,9-dimethyl-9H-xanthen-4-yl)(4-methoxyphenyl)methyl)-2-methylpropane-2-sulfinamide)HPLC of Formula: 2160535-56-6, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

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

The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 5,5′-Dimethyl-2,2′-bipyridine( cas:1762-34-1 ) is researched.Product Details of 1762-34-1.Qian, Bing-Feng; Wang, Jun-Ling; Jia, Ai-Quan; Shi, Hua-Tian; Zhang, Qian-Feng published the article 《Syntheses, reactivity, structures and photocatalytic properties of mononuclear ruthenium(II) complexes supported by 1,4,7-trimethyl-1,4,7-triazacyclononane (Me3tacn) ligands》 about this compound( cas:1762-34-1 ) in Inorganica Chimica Acta. Keywords: preparation mononuclear ruthenium trimethyltriazacyclononane bipyridine complex; crystal structure mononuclear ruthenium trimethyltriazacyclononane bipyridine complex; cyclic voltammetry mononuclear ruthenium trimethyltriazacyclononane bipyridine complex; water slitting photocatalyst mononuclear ruthenium trimethyltriazacyclononane bipyridine complex. Let’s learn more about this compound (cas:1762-34-1).

Treatment of ruthenium(II) precursor [(Me3tacn)Ru(DMSO)Cl2] (Me3tacn = 1,4,7-trimethyl-1,4,7-triazacyclononane, DMSO = dimethylsulfoxide) (1) with concentrated HCl in the presence of air afforded a ruthenium(III) complex [(Me3tacn)RuCl3·H2O] (2). Reaction of 2, 2,2′-bipyridine or substituted 2,2′-bipyridine, and zinc metal powder in the presence of sodium perchlorate gave the corresponding cationic aquaruthenium(II) complex [(Me3tacn)Ru(R-bpy)(H2O)](ClO4)2 (bpy = 2,2′-bipyridine, R = H, 3; 4,4′-Me2, 4; 5,5′-Me2, 5; 4,4′-di-tBu, 6). The hydrate ligand in complexes 3 and 5 could be substituted by acetonitrile or pyridine forming complexes [(Me3tacn)Ru(5,5′-Me2-bpy)(MeCN)](ClO4)2 (7) and [(Me3tacn)Ru(R-bpy)(py)](ClO4)2 (py = pyridine, R = H (8), R = 5,5′-Me2 (9)), resp. Interaction of [(Me3tacn)Ru(bpy)(H2O)](PF6)2 with phenylacetylene in methanol afforded a ruthenium-carbene complex [(Me3tacn)(bpy)Ru:C(OMe)CH2Ph](PF6)2 (10). All complexes are well characterized by IR, UV/visible, and NMR spectroscopies. The mol. structures of 1, 1·2H2O, 4·2H2O, 7, 8, 9, and 10 were also established by single-crystal X-ray diffraction. The photocatalysis properties of complexes 3, 5, and 6 for H2 evolution by water splitting were also studied.

Compounds in my other articles are similar to this one(5,5′-Dimethyl-2,2′-bipyridine)Product Details of 1762-34-1, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

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

Electric Literature of C12H12N2. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: 5,5′-Dimethyl-2,2′-bipyridine, is researched, Molecular C12H12N2, CAS is 1762-34-1, about Near-UV-excitable, green-emitting Tb3+-based complexes. Author is Assuncao, Israel P.; Bredol, Michael; Kasprzycka, Ewa; Kynast, Ulrich H.; Lezhnina, Marina.

While numerous Eu3+ complexes are known now that can efficiently be exploited at 350-400 nm excitation range, corresponding green Tb3+ emitter complexes are hard to find. Tb3+ salts of fenamic acid and derivatives thereof are interesting candidates for applications using near-UV excitation: on addnl. co-coordination with e.g. 5,5′-dimethyl-2,2′-bipyridine, excitation maximum at 380 nm, at the same time maintaining high efficiencies, can be accomplished. Such coordination compounds hold the promise of being useful as versatile marker mols. in a variety of soft chem. environments.

Compounds in my other articles are similar to this one(5,5′-Dimethyl-2,2′-bipyridine)Electric Literature of C12H12N2, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

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

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: 5,5′-Dimethyl-2,2′-bipyridine, is researched, Molecular C12H12N2, CAS is 1762-34-1, about Theoretical and experimental study of torsional potentials, molecular structure (monomer and dimer), vibrational analysis and molecular characteristics of some dimethyl bipyridines, the main research direction is dimethyl bipyridine conformer hydrogen bond HOMO IR spectra.Quality Control of 5,5′-Dimethyl-2,2′-bipyridine.

This study deals with the determination of torsional potentials, mol. geometry in monomer and dimer form and vibrational assignments of 4,4′-dimethyl-2,2′-bipyridine (4DB); 5,5′-dimethyl-2,2′-bipyridine (5DB); and 6,6′-dimethyl-2,2′-bipyridine (6DB) using quantum chem. calculations carried out by d. functional theory (DFT) employing B3LYP functional in conjunction with 6-311++G(d,p) basis set. Existence of inter-mol. hydrogen bonds was predicted. Fourier Transform IR (FTIR) and Fourier Transform Raman (FT-Raman) spectra were recorded and vibrational anal. of the mols. was made using potential energy distribution (PED) and eigen vectors obtained in the computations. Observed and calculated frequencies agreed with an rms error 9.20, 8.21, and 8.33 cm-1 for 4DB, 5DB, and 6DB, resp. 1H and 13C NMR spectra were simulated using time-dependent DFT ; compared with the recorded exptl. spectra of the samples in Chloroform-d (CDCl3) solvent and observed that the chem. shifts agree well with their theor. counterparts. Electronic transitions were analyzed using exptl. and simulated UV-Vis spectra of the three mols. Mol. characteristics like HOMO-LUMO; thermodn. parameters; and mol. electrostatic surface potential (MESP) quantified with natural charges obtained by NBO anal. are also investigated.

Compounds in my other articles are similar to this one(5,5′-Dimethyl-2,2′-bipyridine)Quality Control of 5,5′-Dimethyl-2,2′-bipyridine, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

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

Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Journal of Coordination Chemistry called Five new cobalt(II) complexes based on indazole derivatives: synthesis, DNA binding and molecular docking study, Author is Long, Bing-Fan; Huang, Qin; Wang, Shu-Long; Mi, Yan; Wang, Meng-Fan; Xiong, Ting; Zhang, Shu-Cong; Yin, Xian-Hong; Hu, Fei-Long, which mentions a compound: 1762-34-1, SMILESS is CC1=CN=C(C=C1)C1=NC=C(C)C=C1, Molecular C12H12N2, Category: benzodioxans.

Five cobalt(II) complexes based on 1H-indazole-3-carboxylic acid (H2L), [Co(phen)(HL)2]·H2O (1), [Co(5,5′-dimethyl-2,2′-bipy)(HL)2] (2), [Co(2,2′-bipy)2(HL)]·5H2O (3), [Co2(2,9-dimethyl-1,10-phen)2(L)2] (4) and [Co2(6,6′-dimethyl-2,2′-bipy)2(L)2]·H2O (5) (2,2′-bipy = 2,2′-bipyridine, phen = 1,10-phenanthroline), were synthesized and structurally characterized by elemental analyses, IR and UV-visible spectroscopies and single-crystal X-ray crystallog. 1-3 Possess mononuclear Co(II) structures, while 4 and 5 exhibit binuclear structure. 1D water tape which is linked by the multiple hydrogen bonds was embedded in the 3D motif of complex 3. Complexes 4 and 5 show two orthogonal planes of motif that was constituted by phen/2,2′-bipy and indazole acid, resp. The intermol. interactions including hydrogen bonding and π-π stacking interactions are stabilizing these complexes. The interactions of the synthesized complexes with calf-thymus DNA (CT-DNA) were studied by UV-visible absorption titration, ethidium bromide displacement assay and viscosity measurements. The complexes could interact with CT-DNA via a groove binding mode. Their behavior rationalization was further theor. studied by mol. docking.

Compounds in my other articles are similar to this one(5,5′-Dimethyl-2,2′-bipyridine)Category: benzodioxans, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

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

Recommanded Product: 1762-34-1. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: 5,5′-Dimethyl-2,2′-bipyridine, is researched, Molecular C12H12N2, CAS is 1762-34-1, about Unusual Photoelectrochemical Properties of Electropolymerized Films of a Triphenylamine-Containing Organic Small Molecule. Author is Yin, Hong; Yang, Tong; Wang, Ke-Zhi; Tong, Jin; Yu, Shu-Yan.

The electropolymerized films of poly(L)n on In-Sn oxide (ITO) electrode was prepared by anodic electrooxidation of a CH2Cl2 solution of a triphenylamine-carrying organic mol. L, and were characterized/studied by UV-visible absorption spectroscopy, XPS, x-ray diffraction, electrochem. impedance spectroscopy, cyclic voltammetry and photoelectrochem. measurements. Poly(L)n films show surface-controlled TPA•+1/0 associated quasi-reversible redox and exceptionally high photocurrent generation properties. At a zero external bias potential and under 100 mW/cm2 white light irradiation, a photoelectrochem. device composed of a Poly(L)1-modified ITO as working electode, a Pt disk counter electrode and SCE reference electrode in a 0.1M Na2SO4 aqueous solution exhibited a significant cathode photocurrent d. of 2.2μA/cm2, which could be switched to be anodic and outperform most previously reported mol.-based modified ITO electrodes under similar exptl. conditions. Poly(L)n films offer a number of future perspectives ranging from organic photovoltaic to photoelectrochem. catalysis and sensing.

Compounds in my other articles are similar to this one(5,5′-Dimethyl-2,2′-bipyridine)Recommanded Product: 1762-34-1, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

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

SDS of cas: 1762-34-1. 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 Heteroleptic NiII complexes: Synthesis, structural characterization, computational studies and amoebicidal activity evaluation. Author is Hernandez-Ayala, Luis Felipe; Toledano-Magana, Yanis; Ortiz-Frade, Luis; Flores-Alamo, Marcos; Galindo-Murillo, Rodrigo; Reina, Miguel; Garcia-Ramos, Juan Carlos; Ruiz-Azuara, Lena.

In this work, we present the synthesis, characterization, electrochem. studies, DFT calculations, and in vitro amoebicidal effect of seven new heteroleptic NiII coordination compounds The crystal structures of [H2(pdto)](NO3)2 and [Ni(pdto)(NO3)]PF6 are presented, pdto = 2,2′-[1,2-ethanediylbis-(sulfanediyl-2,1-ethanediyl)]dipyridine. The rest of the compounds have general formulas: [Ni(pdto)(N-N)](PF6) where N-N = 2,2′-bipyridine (bpy), 4,4′-dimethyl-2,2′-bipyridine (44dmbpy), 5,5′-dimethyl-2,2′-bipyridine (55dmbpy), 1,10-phenanthroline (phen), 4,7-dimethyl-1,10-phenanthroline (47dmphen) and 5,6-dimethyl-1,10-phenanthroline (56dmphen). The size of N-N ligand and its substituents modulate the compound electronic features and influence their antiproliferative efficiency against Entamoeba histolytica, 56dmphen derivative, shows the biggest molar volume and presents a powerful amoebicidal activity (IC50 = 1.2μM), being seven times more effective than the first-line drug for human amoebiasis metronidazole. Also, increases the reactive oxygen species concentration within the trophozoites. This could be the trigger of the E. histolytica growth inhibition. The antiparasitic effect is described using NiII electron d., molar volume, estimated by DFT, as well as the exptl. redox potential and diffusion coefficients In general, amoebicidal efficiency is directly proportional to the increment of the molar volume and decreases when the redox potential becomes more pos.

Compounds in my other articles are similar to this one(5,5′-Dimethyl-2,2′-bipyridine)SDS of cas: 1762-34-1, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

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

Safety of 5,5′-Dimethyl-2,2′-bipyridine. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: 5,5′-Dimethyl-2,2′-bipyridine, is researched, Molecular C12H12N2, CAS is 1762-34-1, about Four rare earth complexes with chlorinated carboxylic acids and bipyridine ligands: crystal structures, thermal analysis and luminescence properties. Author is Zhou, Meng-xue; Ren, Ning; Zhang, Jian-jun.

Four new complexes were successfully synthesized by solvothermal method or conventional solution method, namely [Ln2(5,5′-DM-2,2′-bipy)2 (3,4-DClBA)6 (H2O)(C2H5OH)](Ln=Sm(1), Eu(2)) and [Ln(5,5′-DM-2,2′-bipy)(3,5-DClBA)3]2 (Ln=Sm(3), Eu(4); 3,4-HDClBA=3,4-dichlorobenzoic acid, 3,5-HDClBA=3,5-dichlorobenzoic acid, 5,5′-DM-2,2′-bipy=5,5′-dimethyl-2,2′-bipyridine). Complexes 1 and 2 are isostructure and each metal center is eight-coordinated forming a distorted square antiprismatic. Complexes 1 and 2 are connected to form 2D supermol. structure by C-HCl hydrogen bonding and π-π interactions. The geometry of complex 3 is a nine coordinated distorted monocapped square antiprismatic, and the two-dimensional supramol. structure is formed by different π-π stacking interactions between mols. Thermogravimetric-IR combined technol. revealed the thermal stability and thermal decomposition mechanism of complexes 1∼4. The fluorescence and lifetime of complexes 2 and 4 were studied. The results showed that both complexes could emit the characteristic fluorescence of Eu3+ ions.

Compounds in my other articles are similar to this one(5,5′-Dimethyl-2,2′-bipyridine)Safety of 5,5′-Dimethyl-2,2′-bipyridine, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

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

Name: 5,5′-Dimethyl-2,2′-bipyridine. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: 5,5′-Dimethyl-2,2′-bipyridine, is researched, Molecular C12H12N2, CAS is 1762-34-1, about Tuning of Ionic Second Coordination Sphere in Evolved Rhenium Catalyst for Efficient Visible-Light-Driven CO2 Reduction. Author is Chen, Kai-Hong; Wang, Ning; Yang, Zhi-Wen; Xia, Shu-Mei; He, Liang-Nian.

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.

Compounds in my other articles are similar to this one(5,5′-Dimethyl-2,2′-bipyridine)Name: 5,5′-Dimethyl-2,2′-bipyridine, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

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