Comparable catalytic and biological behavior of alternative polar dioxo-molybdenum (VI) Schiff base hydrazone chelates

[1]  Hany Elsawy,et al.  Polar and nonpolar iron (II) complexes of isatin hydrazone derivatives as effective catalysts in oxidation reactions and their antimicrobial and anticancer activities , 2022, Applied Organometallic Chemistry.

[2]  O. I. Alajrawy,et al.  Dioxomolybdenum (VI) and Oxomolybdenum (IV) Complexes with N, O, and S Bidentate Ligands, Syntheses, Spectral Characterization, and DFT Studies , 2022, Journal of Molecular Structure.

[3]  N. El‐Metwaly,et al.  Novel isatin-based complexes of Mn(II) and Cu(II) ions: characterization, homogeneous catalysts for sulfides oxidation, bioactivity screening and theoretical implementations via DFT and pharmacokinetic studies , 2022, Journal of Molecular Liquids.

[4]  Sidhali U. Parsekar,et al.  Synthesis, Characterization, Crystal Structure, DNA and HSA Interactions, and Anticancer Activity of a Mononuclear Cu(II) Complex with a Schiff Base Ligand Containing a Thiadiazoline Moiety , 2022, ACS omega.

[5]  R. Behjatmanesh-Ardakani,et al.  Synthesis, spectra (FT-IR, NMR) investigations, DFT, FMO, MEP, NBO analysis and catalytic activity of MoO2(VI) complex with ONO tridentate hydrazone Schiff base ligand , 2021 .

[6]  N. El‐Metwaly,et al.  Effect of oxy-vanadium (IV) and oxy-zirconium (IV) ions in O,N-bidentate arylhydrazone complexes on their catalytic and biological potentials that supported via computerized usages , 2021, Journal of the Taiwan Institute of Chemical Engineers.

[7]  Samuel Suárez‐Pantiga,et al.  Deoxygenation reactions in organic synthesis catalyzed by dioxomolybdenum(VI) complexes. , 2021, Organic and biomolecular chemistry.

[8]  Mustafa Özyürek,et al.  Dioxomolybdenum(VI) complexes with 4-benzyloxysalicylidene-N/S-alkyl thiosemicarbazones: Synthesis, structural analysis, antioxidant activity and xanthine oxidase inhibition , 2021, Polyhedron.

[9]  R. Behjatmanesh-Ardakani,et al.  Synthesis, spectral characterization, SC-XRD, HSA, DFT and catalytic activity of a dioxidomolybdenum complex with aminosalicyl-hydrazone Schiff base ligand: An experimental and theoretical approach , 2021 .

[10]  R. Behjatmanesh-Ardakani,et al.  Binuclear Zn(II) Schiff base complexes: Synthesis, spectral characterization, theoretical studies and antimicrobial investigations , 2021, Inorganica Chimica Acta.

[11]  N. El‐Metwaly,et al.  New Cu(II) and VO(II)-O,N,O-aroylhydrazone complexes: Biological evaluation, catalytic performance, ctDNA interaction, DFT, pharmacophore, and docking simulation , 2021 .

[12]  Mahmoud A. Noamaan,et al.  Synthesis, spectral characterization, DFT calculations, pharmacological studies, CT-DNA binding and molecular docking of potential N, O-multidentate chelating ligand and its VO(II), Zn(II) and ZrO(II) chelates. , 2021, Bioorganic chemistry.

[13]  T. Mondal,et al.  Synthesis, characterization, DFT calculations, protein binding and molecular docking studies of mononuclear dioxomolybdenum(VI) complexes with ONS donor ligand , 2021 .

[14]  R. Behjatmanesh-Ardakani,et al.  Oxovanadium and dioxomolybdenum complexes: synthesis, crystal structure, spectroscopic characterization and applications as homogeneous catalysts in sulfoxidation , 2021 .

[15]  R. Behjatmanesh-Ardakani,et al.  Synthesis, crystal structure, theoretical calculation, spectroscopic and antibacterial activity studies of copper(II) complexes bearing bidentate schiff base ligands derived from 4-aminoantipyrine: Influence of substitutions on antibacterial activity , 2021, Journal of Molecular Structure.

[16]  F. Ullah,et al.  Mononucleating nicotinohydazone complexes with VO2+, Cu2+, and Ni2+ ions. Characteristic, catalytic, and biological assessments , 2021, Journal of Molecular Liquids.

[17]  H. A. Rudbari,et al.  Synthesis, characterization, crystal structures, Hirshfeld surface analysis, DFT computational studies and catalytic activity of novel oxovanadium and dioxomolybdenum complexes with ONO tridentate Schiff base ligand , 2021, Polyhedron.

[18]  N. El‐Metwaly,et al.  Tailoring, structural inspection of novel oxy and non-oxy metal-imine chelates for DNA interaction, pharmaceutical and molecular docking studies , 2021 .

[19]  A. Quintard Copper Catalyzed Decarboxylative Functionalization of Ketoacids , 2021, The chemical record.

[20]  Lise‐Marie Chamoreau,et al.  Can the Stereogenic 1,1’‐Bi‐2‐naphtol Molecule Be Coordinated to W(VI) or Mo(VI) Peroxo Moieties? , 2021 .

[21]  V. Mirkhani,et al.  Synthesis, characterization, crystal structures, DFT, TD-DFT, molecular docking and DNA binding studies of novel copper(II) and zinc(II) complexes bearing halogenated bidentate N,O-donor Schiff base ligands , 2021, Polyhedron.

[22]  V. Mirkhani,et al.  Novel copper(II) and zinc(II) complexes of halogenated bidentate N,O-donor Schiff base ligands: Synthesis, characterization, crystal structures, DNA binding, molecular docking, DFT and TD-DFT computational studies , 2021 .

[23]  N. El‐Metwaly,et al.  Targeting ctDNA binding and elaborated in-vitro assessments concerning novel Schiff base complexes: Synthesis, characterization, DFT and detailed in-silico confirmation , 2020 .

[24]  M. Gandelman,et al.  Decarboxylative Halogenation of Organic Compounds , 2020, Chemical reviews.

[25]  S. Shaaban,et al.  Bis‐dioxomolybdenum (VI) oxalyldihydrazone complexes: Synthesis, characterization, DFT studies, catalytic epoxidation potential, molecular modeling and biological evaluations , 2020 .

[26]  F. Ullah,et al.  Biological and catalytic potential of sustainable low and high valent metal-Schiff base sulfonate salicylidene pincer complexes , 2019, RSC advances.

[27]  A. Pombeiro,et al.  Cu(ii) complexes of N-rich aroylhydrazone: magnetism and catalytic activity towards microwave-assisted oxidation of xylenes. , 2019, Dalton transactions.

[28]  Subhasis Ghosh,et al.  Oxovanadium(V) and Dioxomolybdenum(VI) Complexes of Amide-Imine Conjugates: Structures, Catalytic and Antitumor Activities. , 2019, ACS applied bio materials.

[29]  Luyao Xu,et al.  An acetohydroxamate-coordinated oxidovanadium(V) complex derived from pyridinohydrazone ligand with urease inhibitory activity , 2019, Inorganic Chemistry Communications.

[30]  Sabyasachi Ta,et al.  Exploring Anticancer and (Bio)catalytic Activities of New Oxovanadium(V), Dioxomolybdenum(VI), and Copper(II) Complexes of Amide–Imine Conjugates , 2019, ACS Applied Bio Materials.

[31]  Ryan R. Langeslay,et al.  Catalytic Applications of Vanadium: A Mechanistic Perspective. , 2018, Chemical reviews.

[32]  G. Mohamed,et al.  Transition metal complexes of nano bidentate organometallic Schiff base: Preparation, structure characterization, biological activity, DFT and molecular docking studies , 2018, Applied Organometallic Chemistry.

[33]  E. El-Samanody,et al.  Molecular modeling, spectral investigation and thermal studies of the new asymmetric Schiff base ligand; (E)‐N'‐(1‐(4‐((E)‐2‐hydroxybenzylideneamino)phenyl)ethylidene)morpholine‐4‐carbothiohydrazide and its metal complexes: Evaluation of their antibacterial and anti‐molluscicidal activity , 2018 .

[34]  M. S. Adam Catalytic activity of nickel(II), copper(II) and oxovanadium(II)‐dihydroindolone complexes towards homogeneous oxidation reactions , 2018 .

[35]  J. White,et al.  Preparation, crystal structure, spectroscopic studies, DFT calculations, antibacterial activities and molecular docking of a tridentate Schiff base ligand and its cis-MoO2 complex , 2018 .

[36]  S. Gharaghani,et al.  Studies on DNA binding properties of new Schiff base ligands using spectroscopic, electrochemical and computational methods: Influence of substitutions on DNA-binding , 2018 .

[37]  K. Figarella,et al.  Antileishmanial and Antitrypanosomal Activity of Synthesized Hydrazones, Pyrazoles, Pyrazolo[1,5-a]-Pyrimidines and Pyrazolo[3,4-b]- Pyridine , 2017, Current Bioactive Compounds.

[38]  M. Tahir,et al.  Distorted square-antiprism geometry of new zirconium (IV) Schiff base complexes: Synthesis, spectral characterization, crystal structure and investigation of biological properties , 2017 .

[39]  M. Youssef,et al.  Synthesis and characterization of binary and ternary oxovanadium complexes of N,N′‐(2‐pyridyl)thiourea and curcumin: Catalytic oxidation potential, antibacterial, antimicrobial, antioxidant and DNA interaction studies , 2017 .

[40]  E. Yousif,et al.  Metal complexes of Schiff base: Preparation, characterization and antibacterial activity , 2017 .

[41]  Zhentao Wang,et al.  Silver-Catalyzed Decarboxylative Bromination of Aliphatic Carboxylic Acids. , 2017, Organic letters.

[42]  Gayathri Virupaiah,et al.  Oxidative bromination and oxidation of organic substrates catalyzed by bis[2,2'‐hydroxyphenylbenzimidazole]Fe(III) complex entrapped in zeolite‐Y cavity , 2017 .

[43]  Shivaraj,et al.  DNA interaction, antimicrobial studies of newly synthesized copper (II) complexes with 2-amino-6-(trifluoromethoxy)benzothiazole Schiff base ligands. , 2016, Journal of photochemistry and photobiology. B, Biology.

[44]  A. Crochet,et al.  A study of DNA/BSA interaction and catalytic potential of oxidovanadium(v) complexes with ONO donor ligands. , 2016, Dalton transactions.

[45]  M. S. Adam Catalytic potentials of homodioxo-bimetallic dihydrazone complexes of uranium and molybdenum in a homogeneous oxidation of alkenes , 2015, Monatshefte für Chemie - Chemical Monthly.

[46]  R. Kia,et al.  Synthesis, spectral characterization and crystal structure studies of a new hydrazone Schiff base and its dioxomolybdenum(VI) complex , 2015 .

[47]  Jun Wang,et al.  Recyclable 1,2-bis[3,5-bis(trifluoromethyl)phenyl]diselane-catalyzed oxidation of cyclohexene with H2O2: a practical access to trans-1,2-cyclohexanediol. , 2014 .

[48]  M. Maurya,et al.  Synthesis, characterization and catalytic activity of dioxidomolybdenum(VI) complexes of tribasic pentadentate ligands , 2014 .

[49]  E. Milner-White,et al.  On the antiquity of metalloenzymes and their substrates in bioenergetics. , 2013, Biochimica et biophysica acta.

[50]  Wen-jie Zheng,et al.  Microwave-assisted synthesis of arene ruthenium(II) complexes that induce S-phase arrest in cancer cells by DNA damage-mediated p53 phosphorylation. , 2013, European journal of medicinal chemistry.

[51]  F. Arjmand,et al.  Synthesis, characterization, biological studies (DNA binding, cleavage, antibacterial and topoisomerase I) and molecular docking of copper(II) benzimidazole complexes. , 2012, Journal of photochemistry and photobiology. B, Biology.

[52]  Jason M. Lynam,et al.  Synthesis and Reactivity of Molybdenum Complexes Containing Functionalized Alkynyl Ligands: A Photochemically Activated CO-Releasing Molecule (PhotoCO-RM) , 2011 .

[53]  M. Zupan,et al.  Oxidative halogenation with "green" oxidants: oxygen and hydrogen peroxide. , 2009, Angewandte Chemie.

[54]  M. Kanai,et al.  Nucleophile generation via decarboxylation: asymmetric construction of contiguous trisubstituted and quaternary stereocenters through a Cu(I)-catalyzed decarboxylative Mannich-type reaction. , 2009, Journal of the American Chemical Society.

[55]  E. Taş,et al.  Synthesis, structural characterization, electrochemistry and spectroelectrochemistry of dinuclear copper(II) metal complexes stabilized by a tetradentate NOOO salicylaldimine ligands , 2009 .

[56]  N. Galić,et al.  Spectrometric study of tautomeric and protonation equilibria of o-vanillin Schiff base derivatives and their complexes with Cu(II). , 2008, Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.

[57]  E. Taş,et al.  The sterically hindered salicylaldimine ligands with their copper(II) metal complexes: Synthesis, spectroscopy, electrochemical and thin-layer spectroelectrochemical features , 2008 .

[58]  E. Taş,et al.  Synthesis, spectroscopic and structural studies of new Schiff bases prepared from 3,5-Bu2t-salicylaldehyde and heterocyclic amines: X-ray structure of N-(3,5-di-tert-butylsalicylidene)-1-ethylcarboxylato-4-aminopiperidine. , 2007, Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.

[59]  L. Nahar,et al.  Microtitre plate-based antibacterial assay incorporating resazurin as an indicator of cell growth, and its application in the in vitro antibacterial screening of phytochemicals , 2007, Methods.

[60]  Weisheng Liu,et al.  The crystal structures of copper(II), manganese(II), and nickel(II) complexes of a (Z)-2-hydroxy-N'-(2-oxoindolin-3-ylidene) benzohydrazide--potential antitumor agents. , 2007, Bioorganic & medicinal chemistry letters.

[61]  M. Shair,et al.  Stereoelectronic effects dictate mechanistic dichotomy between Cu(II)-catalyzed and enzyme-catalyzed reactions of malonic acid half thioesters. , 2007, Journal of the American Chemical Society.

[62]  Chun-xiang Kuang,et al.  Stereoselective synthesis of (E)-β-arylvinyl bromides by microwave-induced reaction of anti-3-aryl-2,3-dibromopropanoic acids using an AgOAc–AcOH system , 2005 .

[63]  M. Kantam,et al.  Molybdate-exchanged Mg-Al-LDH catalyst: an eco-compatible route for the synthesis of β-bromostyrenes in aqueous medium , 2004 .

[64]  M. Nethaji,et al.  Hydrolytic Cleavage of DNA by Ternary Amino Acid Schiff Base Copper(II) Complexes Having Planar Heterocyclic Ligands , 2004 .

[65]  M. Bhattacharjee,et al.  A green Hunsdiecker reaction: synthesis of β-bromostyrenes from the reaction of α,β-unsaturated aromatic carboxylic acids with KBr and H2O2 catalysed by Na2MoO4·2H2O in aqueous medium , 2001 .

[66]  Chun-xiang Kuang,et al.  Convenient and stereoselective synthesis of (Z)-1-bromo-1-alkenes by microwave-induced reaction , 2001 .

[67]  S. Mukhopadhyay,et al.  Oxidative Bromination in a Liquid−Liquid Two-Phase System to Synthesize Organic Intermediates: 2-Bromophenol, 2,6-Dibromophenol, and 2-Bromo-4-methylphenol , 1999 .

[68]  R. Bray The inorganic biochemistry of molybdoenzymes , 1988, Quarterly Reviews of Biophysics.

[69]  W. Orme-Johnson Molecular basis of biological nitrogen fixation. , 1985, Annual review of biophysics and biophysical chemistry.

[70]  J. Topich Ligand control of the redox properties of dioxomolybdenum(VI) coordination complexes , 1981 .

[71]  C. Price,et al.  The Stereochemistry and Mechanism of the Bromodecarboxylation of Unsaturated Carboxylate Ions1 , 1957 .