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Here is a brief introduction to this compound(1762-34-1)Computed Properties of C12H12N2, if you want to know about other compounds related to this compound(1762-34-1), you can read my other articles.

Computed Properties of C12H12N2. 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 The laser-induced potential jump: A method for rapid electron injection into oxidoreductase enzymes.

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

Research on new synthetic routes about 1762-34-1

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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, Inorganica Chimica Acta called Near-UV-excitable, green-emitting Tb3+-based complexes, Author is Assuncao, Israel P.; Bredol, Michael; Kasprzycka, Ewa; Kynast, Ulrich H.; Lezhnina, Marina, which mentions a compound: 1762-34-1, SMILESS is CC1=CN=C(C=C1)C1=NC=C(C)C=C1, Molecular C12H12N2, Category: benzodioxans.

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.

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

Some scientific research about 1762-34-1

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Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 1762-34-1, is researched, SMILESS is CC1=CN=C(C=C1)C1=NC=C(C)C=C1, Molecular C12H12N2Journal, Polyhedron called Synthesis and characterization of Lanthanum(III) complexes containing 4,4,4-trifluoro-1-(naphthalen-2yl)butane-1,3-dionate, Author is Mautner, Franz A.; Bierbaumer, Florian; Gyurkac, Marcell; Fischer, Roland C.; Torvisco, Ana; Massoud, Salah S.; Vicente, Ramon, the main research direction is lanthanum fluoronaphthyldiketonate bipyridine terpyridine complex preparation crystal structure; optimized mol structure lanthanum fluoronaphthyldiketonate bipyridine terpyridine complex.Quality Control of 5,5′-Dimethyl-2,2′-bipyridine.

Seven La(III) complexes with the β-diketonate anion 4,4,4-trifluoro-1-(2-naphthyl)butane-1,3-dionato(1-) (ntfa) have been synthesized, namely: [La(ntfa)3(MeOH)3] (1a), [La(ntfa)3(H2O)2(EtOH)](EtOH) (1b), [La(ntfa)3(bipy)2] (2), [La(ntfa)3(Me2bipy)] (3), [La(ntfa)3(terpy)] (4), (NEt4)[La(ntfa)4] (5) and [La(ntfa)4Na(H2O)(EtOH)(Methyl-β-naphthylketone)] (6), where bipy = bipyridine, Me2bipy = 5,5′-dimethyl-bipyridine, terpy = terpyridine, NEt4+ = tetraethylammonium ion and structurally characterized. The tris-β-diketonate compounds 1a,b, 2-4 form neutral monomeric complexes with C. N. nine for 1a, 1b and 4, eight for 3, and ten in case of 2. The tetrakis-β-diketonato complexes 5 and 6 have coordination number eight.

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

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Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 1762-34-1, is researched, SMILESS is CC1=CN=C(C=C1)C1=NC=C(C)C=C1, Molecular C12H12N2Journal, Applied Organometallic Chemistry called Synthesis, structures, thermal behaviour, luminescence and magnetic properties of lanthanide complexes constructed from 2,6-dimethylbenzoic acid and 5,5′-dimethyl-2,2′-bipyridine, Author is Li, Ying-Ying; Ren, Ning; He, Shu-Mei; Wang, Shu-Ping; Zhang, Jian-Jun, the main research direction is lanthanide methylbenzoate bipyridine complex preparation thermal decomposition luminescence magnetism; crystal structure lanthanide methylbenzoate bipyridine complex.Safety of 5,5′-Dimethyl-2,2′-bipyridine.

Six new lanthanide complexes, with the formula [La(2,6-DMBA)3(5,5′-DM-2,2′-bipy)(H2O)]2 (1) and [Ln(2,6-DMBA)3(5,5′-DM-2,2′-bipy)]2 (Ln = Tb(2), Dy(3), Ho(4), Pr(5), Nd(6)) (2,6-DMBA = 2,6-dimethylbenzoate, 5,5′-DM-2,2′-bipy = 5,5′-dimethyl-2,2′-bipyridine) have been successfully synthesized and characterized. These title complexes have three different structural types. The structure of complex 1(type I) contains coordination water mols., and the coordination number is 8. The coordination numbers of complexes 2-4 and 5-6 are 8 and 9, showing a distorted square antiprism geometry and distorted monocapped square anti-prismatic geometry, resp. However they have the same general formula and they can be all assembled into the same 1D, 2D supramol. structures via the C-H···O hydrogen bonding interactions, which is interesting in previous lanthanide complexes. The complexes were analyzed by TG-DSC/FTIR. In addition, the visible light luminescence experiments of Tb (III) complex was carried out, and the characteristic luminescence behavior of strong green color was shown. And the fluorescence lifetime and intrinsic quantum yield were calculated The magnetic properties of complexes 2-4 were also studied, and the results showed that complex 3 and complexes 2, 4 have ferromagnetic interactions and antiferromagnetic interactions, resp.

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

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Here is a brief introduction to this compound(1762-34-1)Formula: C12H12N2, if you want to know about other compounds related to this compound(1762-34-1), you can read my other articles.

Shao, Qing; Zhang, Shaodong; Hu, Zhen; Zhou, Yongfeng published the article 《Multimode Self-Oscillating Vesicle Transformers》. Keywords: multimode self oscillating vesicle transformer rhythmic oscillatory; ruthenium complex bipyridine copolymer polythioether; copolymers; materials chemistry; ruthenium; self-assembly; vesicles.They researched the compound: 5,5′-Dimethyl-2,2′-bipyridine( cas:1762-34-1 ).Formula: C12H12N2. Aromatic heterocyclic compounds can be divided into two categories: single heterocyclic and fused heterocyclic. In addition, there is a lot of other information about this compound (cas:1762-34-1) here.

Engineering synthetic materials that mimic the complex rhythmic oscillatory behavior of living cells is a fundamental challenge in science and technol. Up to now, the reported synthetic model system still cannot compete with nature in oscillatory modes and amplitudes. Presented here is a novel alternating copolymer vesicle that exhibits drastic and multimode shape oscillations in real time, which are controlled by polymer concentrations and driven by the Belousov-Zhabotinsky oscillatory reaction, including swelling/deswelling, twisting/detwisting, stretching/shrinking, fusion/fission, and multiple division. Some of them, especially the fission oscillation, have not been observed before. In addition, the oscillation magnitude with regard to diameter is much larger than that of previously reported self-oscillating vesicles. Such a self-oscillating vesicle transformer would extend the complexity and capacity of membrane deformations in synthetic systems, approaching those of natural cells.

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

Introduction of a new synthetic route about 1762-34-1

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Quality Control of 5,5′-Dimethyl-2,2′-bipyridine. Aromatic compounds can be divided into two categories: single heterocycles and fused heterocycles. Compound: 5,5′-Dimethyl-2,2′-bipyridine, is researched, Molecular C12H12N2, CAS is 1762-34-1, about Synthesis, structural characterization and in vitro cytotoxic evaluation of mixed Cu(II)/Co(II) levofloxacin-bipyridyl complexes. Author is Bashir, Masrat; Yousuf, Imtiyaz.

This work features synthesis, structural characterization and biol. evaluation of two Cu(II)/Co(II)-based complexes (1 and 2) synthesized from levofloxacin (lvXn) and bipyridyl ligands. The structural elucidation of complexes 1 and 2 was carried out by anal., spectral (UV-vis, FTIR, EPR) and single crystal x-ray crystallog. techniques. The crystallog. details of complex 1 revealed a triclinic crystal system with P-1 space group and lattice parameters a = 10.32(7) Å, b = 11.75(8) Å, c = 14.85(9) Å, and α = 87.40°, β = 77.55°, γ = 66.26°. The DFT studies were performed to study the electronic structure and localization of HOMO and LUMO electron densities on the complexes. authors have also performed comparative in vitro DNA/BSA binding studies of complexes 1 and 2 by multispectroscopic methods to evaluate the cytotoxic potential of synthesized complexes which revealed better binding potential of copper analog. Furthermore, the cytotoxic assessment of copper analog was examined on a panel of five human cancer cell lines employing SRB assay which revealed remarkably good and selective cytotoxic activity towards A498 (kidney), HeLa (cervical) and HepG2 (hepatoma) cancer cell lines.

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

A small discovery about 1762-34-1

Here is a brief introduction to this compound(1762-34-1)Safety of 5,5′-Dimethyl-2,2′-bipyridine, if you want to know about other compounds related to this compound(1762-34-1), you can read my other articles.

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: 5,5′-Dimethyl-2,2′-bipyridine, is researched, Molecular C12H12N2, CAS is 1762-34-1, about Construction of lanthanide complexes based on 2,6-dimethylbenzoic acid and 5,5′-dimethyl-2,2′-bipyridine: Supramolecular structures, thermodynamic properties and luminescence.Safety of 5,5′-Dimethyl-2,2′-bipyridine.

By using conventional solution method, two novel binuclear lanthanide complexes, [Eu(2,6-DMBA)3(5,5′-DM-2,2′-bipy)]2(1), and [Sm(2,6-DMBA)3(5,5′-DM-2,2′-bipy)]2(2) (2,6-DMBA = 2,6-dimethylbenzoate, 5,5′-DM-2,2′-bipy = 5,5′-dimethy-2,2′-bipyridine), have been synthesized at room temperature The two complexes are characterized by element anal., single-crystal X-ray diffraction analyses and powder X-ray diffraction. The single-crystal analyses results indicate they are isomorphous in the monoclinic space group of P2(1)c. The binuclear complexes 1 and 2 are linked to form 1D, 2D supramol. structures through the same C-H···O hydrogen bonding interactions. The thermal decomposition process of these complexes is investigated by TG-DSC/FTIR technol. and the FTIR spectra of the escaped gas also are measured. In addition within a temperature range from 295.15 K to 410.15 K, heat capacities of the title complexes are measured by a DSC instrument, which indicates that no phase transition occurs in this range, and the heat capacity values of the complexes gradually increases with rising temperature Not only that, the thermodn. functions values (HT-H298.15K) and (ST-S298.15K) of the complexes 1 and 2 are calculated according to the fitted polynomial equations and the thermodn. equation. The luminescent behavior of complex 1 is investigated in the solid state. The complex 1 with Eu3+ ion shows strong red luminescence behavior, and the luminescence lifetime and fluorescent quantum yield are calculated to be 1.442 ms and 18.96%.

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

Discovery of 1762-34-1

Here is a brief introduction to this compound(1762-34-1)Formula: C12H12N2, if you want to know about other compounds related to this compound(1762-34-1), you can read my other articles.

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, Organometallics called Group 6 Metal Complexes as Electrocatalysts of CO2 Reduction: Strong Substituent Control of the Reduction Path of [Mo(η3-allyl)(CO)2(x,x’-dimethyl-2,2′-bipyridine)(NCS)] (x = 4-6), Author is Taylor, James O.; Veenstra, Florentine L. P.; Chippindale, Ann M.; Calhorda, Maria Jose; Hartl, Frantisek, which mentions a compound: 1762-34-1, SMILESS is CC1=CN=C(C=C1)C1=NC=C(C)C=C1, Molecular C12H12N2, Formula: C12H12N2.

[Mo(η3-allyl)(CO)2(x,x’-dmbipy)(NCS)] (dmbipy = dimethyl-2,2′-bipyridine; x = 4-6) were synthesized and their electrochem. reduction studied using combined cyclic voltammetry (CV) and variable-temperature spectroelectrochem. (IR/UV-visible SEC) in THF and butyronitrile (PrCN), at Au and Pt electrodes. The exptl. results, strongly supported by d. functional theory (DFT) calculations, indicate that the general cathodic path of these Group 6 organometallic complexes is closely related to that of the intensively studied class of Mn tricarbonyl α-diimine complexes, which, themselves, have recently been identified as important smart materials for catalytic CO2 reduction The di-Me substitution on the 2,2′-bipyridine ligand backbone has presented new insights into this emerging class of catalysts. For the 1st time, the 2e- reduced 5-coordinate anions [Mo(η3-allyl)(CO)2(x,x’-dmbipy)]- were directly observed with IR spectroelectrochem. (IR SEC). The role of steric and electronic effects in determining the reduction-induced reactivity was also studied. For the 6,6′-dmbipy, the primary 1e- reduced radical anions exert unusual stability, radically changing the follow-up cathodic path. The 5-coordinate anion [Mo(η3-allyl)(CO)2(6,6′-dmbipy)]- remains stable at low temperature in strongly coordinating butyronitrile and does not undergo dimerization at elevated temperature, in sharp contrast to reactive [Mo(η3-allyl)(CO)2(4,4′-dmbipy)]- that tends to dimerize in a reaction with the parent complex. The complex with the 5,5′-dmbipy ligand combines both types of reactivity. Under aprotic conditions, the different properties of [Mo(η3-allyl)(CO)2(x,x’-dmbipy)]- are also reflected in their reactivity toward CO2. Preliminary CV and IR SEC results reveal differences in the strength of CO2 coordination at the free axial position. Catalytic waves attributed to the generation of the 5-coordinate anions were observed using CV, but only a modest catalytic performance toward the production of formate was demonstrated by IR SEC. For 6,6′-dmbipy, a stronger catalytic effect was observed for the Au cathode, compared to Pt.

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

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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 Molecular engineering towards tunable morphology of metal-organic complex microcrystals for efficient and multicolor electrochemiluminescence, the main research direction is mol engineering towards tunable morphol metal organic complex microcrystals; multicolor electrochemiluminescence.Recommanded Product: 1762-34-1.

Electrochemiluminescence (ECL) of crystalline materials has recently attracted increasing attention due to their unique characteristics and applications, such as crystallization-induced emission, active waveguiding, and biosensing. Tris(2,2′-bipyridine)ruthenium(II), [Ru(bpy)3]2+, a classical metal-organic complex for ECL studies, has been fully investigated in solution as well as its derivatives However, the dependence of ECL properties on the mol. structure and crystal morphol. of these complexes has not been illustrated, partially due to the difficulty in the controlled crystal growth. Here, we adopt a facile mol. engineering strategy to obtain microcrystals of [Ru(bpy)3]2+ derivatives with well-defined morphol. (rods, wires, or polyhedrons) and varied phosphorescence emission colors (yellow, orange, and red) by simply changing the position and number of Me substituents on the bipyridine ligands. The packing modes of mols. influenced by Me groups play a vital role in crystal growth based on attachment energy anal. The obtained microcrystals could act as ECL luminophores when modified on glassy carbon electrode surfaces. Those with one-dimensional (1D) morphol. generally show superior ECL efficiency and stability to three-dimensional (3D) shaped microcrystals. ECL biosensors made of stable 1D microcrystals show reliable and sensitive responses to hydroxyproline, demonstrating their capacity in recyclable detections. This work demonstrates the great potential of mol. engineering in controlling the morphol., emission colors, and ECL properties of mol. crystals, paving the way for the development of high-performance ECL biosensing and optoelectronic devices.

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

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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.Kondori, Tahere; Akbarzadeh-T, Niloufar; Ghaznavi, Habib; Karimi, Zeinab; Shahraki, Jafar; Sheervalilou, Roghayeh; Shahraki, Omolbanin researched the compound: 5,5′-Dimethyl-2,2′-bipyridine( cas:1762-34-1 ).Related Products of 1762-34-1.They published the article 《A binuclear iron(III) complex of 5,5′-dimethyl-2,2′-bipyridine as cytotoxic agent》 about this compound( cas:1762-34-1 ) in BioMetals. Keywords: binuclear iron complex dimethyl bipyridine cytotoxic agent; 5,5′-dimethyl-2,2′-bipyridine; Binuclear iron(III) complex; Cytotoxicity; Fish salmon DNA. We’ll tell you more about this compound (cas:1762-34-1).

The binuclear iron(III) complex (1), namely, {[Fe(5,5′-dmbpy)2(OH2)]2(O)}(NO3)4 with a distorted octahedral coordination, formed by four nitrogen and two oxygen atoms, was previously reported by our team. In this study the DNA-binding and cytotoxicity evaluation for target complex were studied. The results indicated strong cytotoxicity activity against A549 cells comparable to cisplatin values. The binding interaction between complex 1 and FS-DNA was investigated by UV-Vis, fluorescence spectroscopy, and gel electrophoresis at physiol. pH (7.2). The DNA binding investigation has shown groove binding interactions with complex 1, therefore the hydrogen binding plays an important role in the interaction of DNA with complex 1. The calculated thermodn. parameters (ΔH°, ΔS° and ΔG°) show that hydrogen bonding and Vander-Waals forces have an important function in Fe(III) complex-DNA interaction. Moreover, DNA cleavage was studied using agarose gel electrophoresis. Viscosity measurements illustrated that relative viscosity of DNA was unchanged with the adding concentrations of Fe(III) complex. Mol. docking simulation results confirmed the spectroscopic and viscosity titration outcomes.

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