3030-97-5Relevant articles and documents
Synthesis and structural studies of mono- and dinuclear Cu(II) complexes with an ONO donor Schiff base ligand: Self-assembly and sulfato-bridged
Vafazadeh, Rasoul,Esteghamat-Panah, Roya,Willis, Anthony C.,Hill, Anthony F.
, p. 51 - 57 (2012)
Five Cu(II) complexes, [CuL(NO3)] (1), [CuLBr][CuLCH 3OH]2Br2 (2), [CuLN3] (3), [CuL(ClO4)]2 (4) and [H2OLCu(μ-SO 4)CuLH2O] (5), where L is the s
Synthesis of O-Sulfated Human Syndecan-1-like Glyco-polypeptides by Incorporating Peptide Ligation and O-Sulfated Glycopeptide Cassette Strategies
Huang, Xuefei,Li, Tianlu,Ramadan, Sherif,Yang, Weizhun
, p. 6429 - 6433 (2020)
A successful synthesis of O-sulfated syndecan-1-like (Q23-E120) glyco-polypeptide was accomplished. The synthesis features the integration of an O-sulfated carbohydrate-bearing glycopeptide cassette with efficient protein ligation strategies, overcoming the acid lability of carbohydrate sulfates as a major hurdle in solid-phase peptide synthesis. Crucial to the synthesis is the microwave-assisted Ag(I) ligation, which afforded the ligation product in improved overall yield. This O-sulfated syndecan-1 (Q23-E120) is the longest O-sulfated glyco-polypeptide prepared to date.
Spectroscopic studies, structural characterization and electrochemical studies of two cobalt (III) complexes with tridentate hydrazone Schiff base ligands: Evaluation of antibacterial activities, DNA-binding, BSA interaction and molecular docking
Fekri, Roghayeh,Salehi, Mehdi,Asadi, Asadollah,Kubicki, Maciej
, (2018)
Co(III) complexes of tridentate Schiff base ligands derived from N-(2-hydroxybenzylideneamino)benzamide (H2L1) and 2-(2-hydroxybenzylidene)hydrazine-1-carboxamide (H2L2) were synthesized and characterized using
Synthesis, characterization, molecular structure and supramolecular architectures of some copper(II) complexes derived from salicylaldehyde semicarbazone
Salem, Nahed M.H.,Rashad, Amal R.,El Sayed, Laila,Foro, Sabine,Haase, Wolfgang,Iskander, Magdi F.
, p. 231 - 242 (2015)
A series of new copper(II) complexes, [Cu(HSalsc)Cl]·1/2H2O (1), [{Cu(HSalsc)}2(NO3)2][{Cu(HSalsc)}2(NO3)·H2O]NO3 (2), [{Cu(Salsc)}2]H2O (3), [Cu
Structure and spectral properties of dinuclear zinc complex containing semicarbazonate ligands
Jing-Lin, Wang,Jiao, Feng,Mei-Ping, Xu,Bin-Sheng, Yang
, p. 1245 - 1249 (2011)
The dinuclear Zn2+ complex [Zn(HSSC)OAc]2·2DMF (H2SSC = salicylaldehyde semicarbazone; HOAc = acetic acid; DMF = N,N-dimethylfomamide) was prepared and structurally characterized by single crystal X-ray. The basic structural unit of the complex is a dinuclear complex [Zn(HSSC)OAc]2 in which the semicarbazone ligand adopts the phenol-imine form. The deprotonated phenol group forms a one-atom bridge between the two zinc centers, and both of the zinc centers are five-coordinated. The local coordination environment of Zn2+ can be approximately considered as square pyramidal. UV spectral studies show that the H 2SSC provides strong binding of Zn2+ in a 1:1 ratio in solution. The conditional binding constant of the complex is lg KZn-L = 12.89 ± 0.76 in 0.05 M Tris-HCl buffer at pH 7.4. The H2SSC exhibits an enhanced fluorescence effect by the addition of Zn2+, and affords an excellent selectivity for Zn2+ under physiological conditions.
Physicochemical studies and heterogeneous hydroxylation of benzene on FeII, FeIII-Semicarbazone/zeolite-y clathrates
Ahmed, Ayman H.,Thabet
, p. 1632 - 1641 (2015)
Complexes of Fe(II) and Fe(III) with semicarbazone (SALSC) derived from salicylaldehyde and semicarbazide hydrochloride have been trapped in zeolite-Y super cages using "ship-in-a-bottle technique." The synthesized new clathrates have been structurally ch
Manganese(ii) complex of an oxygen-nitrogen donor Schiff base ligand showing efficient catechol oxidase activity: Synthesis, spectroscopic and kinetic study
Adak, Piyali,Mondal, Antu,Chattopadhyay, Shyamal Kumar
, p. 3748 - 3754 (2020/03/17)
Tridentate O,N,O-donor Schiff base ligand (E)-1-(2-hydroxybenzylidene)semicarbazide (H2L1) and its Mn(ii) complex have been synthesized. Both the ligand and the complex have been characterized by analytical and spectroscopic techniques. X-ray crystal structure determination of the Mn(ii) complex shows that the Mn(ii) atom is in a distorted octahedral environment and there are two crystallographically different manganese atoms in the unit cell. The Mn(ii) complex shows very high catalytic activity for catechol oxidation (kcat = 3.10 × 106 h-1, kcat/KM = 3.25 × 108 h-1 M-1), which is the highest catalytic efficiency for catechol oxidation by a manganese complex reported in the literature. The probable mechanism of the catalytic reaction is explored using ESI-MS and EPR spectroscopy.
Polymer-anchored mononuclear and binuclear CuII Schiff-base complexes: Impact of heterogenization on liquid phase catalytic oxidation of a series of alkenes
Maurya, Abhishek,Kesharwani, Neha,Kachhap, Payal,Mishra, Vivek Kumar,Chaudhary, Nikita,Haldar, Chanchal
, (2019/08/12)
Liquid phase catalytic oxidation of a number of alkenes, for example, cyclohexene, cis-cyclooctene, styrene, 1-methyl cyclohexene and 1-hexene, was performed using polymer-anchored copper (II) complexes PS-[Cu (sal-sch)Cl] (5), PS-[Cu (sal-tch)Cl] (6), PS-[CH2{Cu (sal-sch)Cl}2] (7) and PS-[CH2{Cu (sal-tch)Cl}2] (8). Neat complexes [Cu (sal-sch)Cl] (1), [Cu (sal-tch)Cl] (2), [CH2{Cu (sal-sch)Cl}2] (3) and [CH2{Cu (sal-tch)Cl}2] (4) were isolated by reacting CuCl2·2H2O with [Hsal-sch] (I), [Hsal-tch] (II), [H2bissal-sch] (III) and [H2bissal-tch] (IV), respectively, in refluxing methanol. Complexes 1–4 have been covalently anchored in Merrifield resin through the amine nitrogen of the semicarbazide or thiosemicarbazide moiety. A number of analytical, spectroscopic and thermal techniques, such as CHNS analysis, Fourier transform-infrared, UV–Vis, PMR, 13C-NMR, electron paramagnetic resonance, scanning electron microscopy, energy-dispersive X-ray analysis, thermogravimetric analysis, atomic force microscopy, atomic absorption spectroscopy, and electrospray ionization-mass spectrometry, were used to analyze and establish the molecular structure of the ligands (I)–(IV) and complexes (1)–(8) in solid state as well as in solution state. Grafted complexes 5–8 were employed as active catalysts for the oxidation of a series of alkenes in the presence of hydrogen peroxide. Copper hydroperoxo species ([CuIII (sal-sch)-O-O-H]), which is believed to be the active intermediate, generated during the catalytic oxidation of alkenes, are identified. It was found that supported catalysts are very economical, green and efficient in contrast to their neat complexes as well as most of the recently reported heterogeneous catalysts.