1120-82-7Relevant articles and documents
X-ray crystal structures and MMA polymerization of cadmium(II) complexes with bidentate pyrazole ligands: The formation of monomers or dimers as a function of a methyl substituent on the pyrazole and aniline rings
Kim, Dongil,Kim, Sunghoon,Woo, Hyun Yul,Lee, Ha-Jin,Lee, Hyosun
, p. 445 - 453 (2014)
The reaction of CdBr2·4H2O with ancillary ligands, N,N-bis(1H-pyrazolyl-1-methyl)aniline (L1), N,N-bis(1H-pyrazolyl-1-methyl)-p-methylaniline (L2), N,N-bis(1H-pyrazolyl-1-methyl)-3,5-dimethylaniline (L3), N,N-bis(3,5-dimethyl-1H-pyrazolyl-1-methyl)aniline (L4) and N,N-bis(1H-pyrazolyl-1-methyl)-2,6-dimethylaniline (L5) in ethanol yields novel Cd(II) bromide complexes, [L1CdBr2] 2, [L2CdBr2]2, [L 3CdBr2]2, [L4CdBr2] and [L5CdBr2]. The X-ray crystal structures of [L 1CdBr2]2, [L2CdBr2] 2 and [L3CdBr2]2 reveal a bromo-bridged dimeric species with crystallographic inversion symmetry. Conversely, [L4CdBr2] and [L5CdBr2] exist as monomeric complexes, presumably due to the steric hindrance between the methyl substituents of the two pyrazole groups in the ligand and cadmium centre for [L4CdBr2], and crowding around the cadmium metal by methyl substituents on the aniline residue in the ligand for [L 5CdBr2]. The geometry at each Cd(II) centre for [L 1CdBr2]2, [L2CdBr2] 2 and [L3CdBr2]2 is best described as a distorted trigonal bipyramid. A distorted trigonal bipyramid is achieved in [L4CdBr2] by coordinative interaction of the nitrogen atom of the aniline unit and the cadmium atom with a σ plane of symmetry, based on the bond length of Cd-Naniline (2.759(7) A). [L 5CdBr2] exists with a distorted tetrahedral geometry involving non-coordination of the nitrogen atom of aniline and the Cd centre, resulting in the formation of an eight-membered chelate ring. The catalytic activity of monomeric, five-coordinated [L4CdBr2] in the polymerization of methyl methacrylate (MMA) in the presence of modified methylaluminoxane (MMAO) at 60°C resulted in a higher molecular weight and a narrower polydispersity index (PDI) than those obtained with dimeric [L nCdBr2]2 (Ln=L1, L 2, L3) or monomeric tetrahedral [L5CdBr 2]. Copyright
New binuclear copper(ii) coordination polymer based on mixed pyrazolic and oxalate ligands: Structural characterization and mechanical properties
López Marzo, Adaris M.,Guerrero, Miguel,Calvet, Teresa,Font-Bardia, Mercè,Pellicer, Eva,Baró, Maria Dolors,Pons, Josefina,Sort, Jordi
, p. 32369 - 32375 (2015)
A new inorganic-organic coordination polymer based on a copper(ii) binuclear complex coordinated with pyrazole (L1), 1-(hydroxymethyl)pyrazole) (L2) and oxalate (Ox) ligands has been unexpectedly obtained. The crystal structure of this coordination polymer has been unequivocally determined from single crystal X-ray diffraction. One copper(ii) center (Cu1) is four-coordinated with two nitrogens (N2, L1 and N3, L2), one oxygen (O1, L1) and one chlorine atom, while the other copper(ii) nucleus (Cu2) is five-coordinated with one nitrogen (N1, L1), three oxygens (O1, L2; O2 and O3, Ox) and one chlorine atom, giving slightly distorted square-planar and square-pyramidal geometries, respectively. To the best of our knowledge, such coordination environments have never been previously observed to coexist in the same structure. The terminal chlorine (Cl1) forms the connecting bridge between the planar binuclear [Cu2Cl(Ox)0.5(L1)(L2)]n units ending in an attractive structural framework. An extended layered structure staggered along the b-axis is observed in the supramolecular view. Nanoindentation experiments were carried out and relevant mechanical parameters such as hardness, Young's modulus, indentation energies and elastic recovery were determined. Additionally, a comparative analysis between the supramolecular structure and the mechanical properties is reported. This journal is
Design, synthesis and evaluation of second generation MurF inhibitors based on a cyanothiophene scaffold
Hrast, Martina,Anderluh, Marko,Knez, Damijan,Randall, Christopher P.,Barreteau, Hélène,O'Neill, Alex J.,Blanot, Didier,Gobec, Stanislav
, p. 83 - 96 (2014)
MurF ligase is a crucial enzyme that catalyses the ultimate intracellular step of bacterial peptidoglycan biosynthesis, and thus represents an attractive target for antibacterial drug discovery. We designed, synthesized and evaluated a new series of cyanothiophene-based inhibitors of MurF enzymes from Streptococcus pneumoniae and Escherichia coli. The target compounds had increased polarity compared to the first generation of inhibitors, with demonstrated enzyme inhibitory potencies in the low micromolar range. Furthermore, the best inhibitors displayed promising antibacterial activities against selected Gram-positive and Gram-negative strains. These results represent an important step towards the development of new antibacterial agents targeting peptidoglycan biosynthesis.
New N,N,N',N'-tetradentate pyrazoly agents: Synthesis and evaluation of their antifungal and antibacterial activities
Abrigach, Farid,Bouchal, Btissam,Riant, Olivier,Macé, Yohan,Takfaoui, Abdelilah,Radi, Smaail,Oussaid, Abdelouahad,Bellaoui, Mohammed,Touzani, Rachid
, p. 83 - 89 (2016)
A new library of N,N,N',N'-tetradentate pyrazoly compounds containing a pyrazole moiety was synthesized by the condensation of (3,5-dimethyl-1H-pyrazol-1-yl)methanol 2a or (1H-pyrazol-1-yl)methanol 2b with a series of primary diamines in refluxed acetonitrile for 6h. The antifungal activity against the budding yeast Saccharomyces cerevisiae, as well as the antibacterial activity against Escherichia coli of these new tetradentate ligands were studied. We found that these tetradentate ligands act specifically as antifungal agents and lack antibacterial activity. Their biological activities depend on the nature of the structure of the compounds.
New arylselanylpyrazole-copper catalysts: Highly efficient catalytic system for C–Se and C–S coupling reactions
Coelho, Felipe Lange,Dresch, Lucielle Codeim,Stieler, Rafael,Campo, Leandra Franciscato,Schneider, Paulo Henrique
, p. 19 - 26 (2019/01/04)
We describe herein the use of arylselanylpyrazole–copper complexes as versatile catalysts for C–Se and C–S coupling reactions. The performance of these complexes for C–Se reactions was investigated in chalcogenoacetylene synthesis. The reactions were carried out under mild and aerobic conditions and afforded selanylalkynes bearing a variety of electron-withdrawing and electron-donating groups. The performance of these catalysts for C–S coupling was investigated through the reaction of aryl halides with thiols and products were obtained in moderate to excellent yields. A plausible mechanism for selenoacetylene synthesis is also suggested, and the 77Se NMR results show that these arylselanylpyrazole ligands act as hemilabile ligands. High-resolution mass spectrometry was used to investigate the intermediates and also to corroborate the proposed catalytic cycle.
ZINC COMPLEX INCLUDING N,N-BISPYRAZOLYL BASED LIGAND, CATALYST FOR POLYMERIZATION OF MONOMER HAVING A RING-TYPE ESTER GROUP, AND METHOD OF FORMING POLYMER USING THE CATALYST
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Paragraph 0078; 0079, (2017/07/13)
The present invention relates to a zinc complex containing an N,N-bispyrazolyl based ligand, a catalyst for polymerizing a monomer having a cyclic ester group, and a method of forming a polymer by using the same, wherein the zinc complex is represented by chemical formula 1, and in the chemical formula 1, Ar represents a cycloalkyl group, an alkoxy group, or a halogen group; L represents -(CH_2)_y- (while y is an integer of 1 to 5) or an arylene group; R_1 to R_4 represent independently hydrogen or an alkyl group; and X represents a halogen group.COPYRIGHT KIPO 2017
