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Metal complexes driven from Schiff bases and semicarbazones for biomedical and allied applications: a review

https://doi.org/10.1016/j.mtchem.2019.100195
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The 175 checked references that resolve
resolves10.1016/j.cct.2003.09.003
The challenge of cyclic and acyclic schiff bases and related derivatives
resolves10.1002/prac.19311290112
Innere Komplexsalze von Oxyaldiminen und Oxyketiminen
resolves10.1002/prac.19361450304
Hochatomare Nebenvalenzringe mit meta‐ und para‐Kondensation
resolves10.1021/jm990383f
Novel 1,5-Diphenylpyrazole Nonnucleoside HIV-1 Reverse Transcriptase Inhibitors with Enhanced Activity versus the Delavirdine-Resistant P236L Mutant:  Lead Identification and SAR of 3- and 4-Substituted Derivatives
resolves10.1016/0223-5234(96)89555-9
Carbonic anhydrase activators. Part 14. Syntheses of mono and bis pyridinium salt derivatives of 2-amino-5-(2-aminoethyl)- and 2-amino-5-(3-aminopropyl)-1,3,4-thiadiazole and their interaction with isozyme II
resolves10.1016/j.saa.2013.07.056
Metal based pharmacologically active agents: Synthesis, structural characterization, molecular modeling, CT-DNA binding studies and in vitro antimicrobial screening of iron(II) bromosalicylidene amino acid chelates
resolves10.1016/j.bioorg.2016.10.009
Some new nano-sized Fe(II), Cd(II) and Zn(II) Schiff base complexes as precursor for metal oxides: Sonochemical synthesis, characterization, DNA interaction, in vitro antimicrobial and anticancer activities
resolves10.1016/j.jphotobiol.2017.04.003
DNA interaction, antimicrobial, anticancer activities and molecular docking study of some new VO(II), Cr(III), Mn(II) and Ni(II) mononuclear chelates encompassing quaridentate imine ligand
resolves10.1002/aoc.4527
Synthesis, theoretical investigations, biocidal screening, DNA binding, <i>in vitro</i> cytotoxicity and molecular docking of novel Cu (II), Pd (II) and Ag (I) complexes of chlorobenzylidene Schiff base: Promising antibiotic and anticancer agents
resolves10.1002/aoc.4699
Some new Ag(I), VO(II) and Pd(II) chelates incorporating tridentate imine ligand: Design, synthesis, structure elucidation, density functional theory calculations for DNA interaction, antimicrobial and anticancer activities and molecular docking studies
resolves10.4236/ijoc.2013.33A008
Biological Activities of Schiff Bases and Their Complexes: A Review of Recent Works
resolves10.1081/SIM-120027314
Synthesis, Characterization, and Catalytic Activity of Metal Schiff Base Complexes Derived from Pyrrole‐2‐carboxaldehyde
resolves10.1023/A:1006945006419
Synthesis, characterization, electrochemical behaviour and catalytic activity of manganese(II) complexes with linear and tripodal tetradentate ligands derived from Schiff bases
resolves10.1016/0277-5387(96)00163-5
Crystal structure and some properties of a novel potent Cu2Zn2SOD model schiff base copper(II) complex ∗[Cu(bppn)](ClO4)2∗2 · H2O
resolves10.1016/S0277-5387(96)00555-4
Synthesis, characterization and electrochemical behaviour of some copper(II) complexes with linear and tripodal tetradentate ligands derived from Schiff bases
resolves10.1246/bcsj.76.137
Schiff-Base Metal(II) Complexes as New Catalysts in the Efficient, Mild and Regioselective Conversion of 1,2-Epoxyethanes to 2-Hydroxyethyl Thiocyanates with Ammonium Thiocyanate
resolves10.1016/j.molstruc.2013.02.023
Synthesis, physicochemical studies, embryos toxicity and DNA interaction of some new Iron(II) Schiff base amino acid complexes
resolves10.1016/j.jphotobiol.2016.06.052
Sonochemical synthesis, DNA binding, antimicrobial evaluation and in vitro anticancer activity of three new nano-sized Cu(II), Co(II) and Ni(II) chelates based on tri-dentate NOO imine ligands as precursors for metal oxides
resolves10.1016/S0010-8545(01)00367-8
Catalytic oxidations in carbon dioxide-based reaction media, including novel CO2-expanded phases
resolves10.1016/S0022-328X(01)00882-8
Diazadioxadecalin and salen podands and macrocycles within dynamic combinatorial virtual libraries: structure, prototropy, complexation and enantioselective catalysis
resolves10.1080/10610279508032519
Catalytic and physico-chemical properties of new schiff base complexes in zeolites
resolves10.1039/b402318h
Tetradentate Schiff base platinum(ii) complexes as new class of phosphorescent materials for high-efficiency and white-light electroluminescent devicesElectronic supplementary information (ESI) available: synthesis and spectroscopic, thermal (TGA), photophysical, electrochemical and EL characterization; CIF. See http://www.rsc.org/suppdata/cc/b4/b402318h/
resolves10.1021/ja01210a012
Stability of Chelate Compounds. II. Polarographic Reduction of Copper Chelates
resolves10.1016/S0010-8545(00)80330-6
Transition metal complexes with binucleating ligands
resolves10.1016/S0010-8545(00)80018-1
Structural aspects of metal complexes with some tetradentate schiff bases
resolves10.3390/70700511
Synthetic Studies on Optically Active Schiff-base Ligands Derived from Condensation of 2-Hydroxyacetophenone and Chiral Diamines
resolves10.1007/s10895-016-2020-z
Ni(II) and Zn(II) Complexes Containing Alkynyl Functionalized Salicylaldimine Ligand and Heterocyclic Coligand: Synthesis, Characterization and Luminescence Properties
resolves10.1016/j.molstruc.2016.08.083
Syntheses, structural characterization, luminescence and optical studies of Ni(II) and Zn(II) complexes containing salophen ligand
resolves10.1021/ed062p974
The synthetic analogs of O2-binding heme proteins
resolves10.1016/0010-8545(94)80072-3
Structural survey of technetium complexes
resolves10.1021/jp5081884
Photoswitching of Conductance through Salicylidene Methylamine
resolves10.1021/jp510476h
Structural Correlations between Luminescent Properties and Excited State Internal Proton Transfer in Some Zinc(II) <i>N,N</i>′-Bis(salicylidenes)
resolves10.1016/j.poly.2011.12.001
Induction of photoluminescence and columnar mesomorphism in hemi-disc salphen type Schiff bases via nickel(II) coordination
resolves10.1016/j.stam.2005.11.023
Manganese and cobalt 3-oxobutylideneaminato complexes: Design and application for enantioselective reactions
resolves10.1016/j.biopha.2004.04.013
Synthesis of aryl semicarbazones as potential anticonvulsant agents
resolves10.25004/IJPSDR.2011.030216
SYNTHESIS AND EVALUATION OF ANTIOXIDANT ACTIVITY OF SEMICARBAZONE DERIVATIVES
resolves10.3923/rjbsci.2011.632.634
Evaluation of Anti-Fungal Activity of Synthesized Chalcone Semicarbazone Derivatives
resolves10.1016/S0010-8545(00)80276-3
Transition metal complexes of thiosemicarbazide and thiosemicarbazones
resolves10.1016/0010-8545(85)80022-9
Transition metal complexes of semicarbazones and thiosemicarbazones
resolves10.2298/JSC0312919L
Transition metal complexes with thiosemicarbazide-based ligands, part 46: Synthesis and physico-chemical characterization of mixed ligand cobalt(III)-complexes with salicylaldehyde semi-, thiosemi- an
resolves10.1016/S0010-8545(00)00363-5
Main group metal complexes of semicarbazones and thiosemicarbazones. A structural review
resolves10.1016/0026-265X(80)90239-8
Analytical applications of biacetyl bis(4-phenyl-3-thiosemicarbazone) and bipyridylglyoxal bis(4-phenyl-3-thiosemicarbazone)
resolves10.1016/0039-9140(78)80163-5
Analytical applications of thiosemicarbazones and semicarbazones: A review
resolves10.1016/S0010-8545(02)00100-5
Biomedical uses and applications of inorganic chemistry. An overview
resolves10.1016/j.cct.2003.11.004
Contribution to the SAR field of metallated and coordination complexes
resolves10.1039/a908712e
Gold complexes with thiosemicarbazones: reactions of bi- and tridentate thiosemicarbazones with dichloro[2-(dimethylaminomethyl)phenyl-C 1,N ]gold(III), [Au(damp-C 1,N )Cl2]
resolves10.1021/jm0512241
Novel Antitrypanosomal Agents Based on Palladium Nitrofurylthiosemicarbazone Complexes:  DNA and Redox Metabolism as Potential Therapeutic Targets
resolves10.1021/jm049529n
Copper(II) and Cobalt(III) Pyridoxal Thiosemicarbazone Complexes with Nitroprusside as Counterion:  Syntheses, Electronic Properties, and Antileukemic Activity
resolves10.1016/j.ejmech.2005.03.014
Antiproliferative activities of iron and platinum conjugates of salicylaldehyde semi-/thiosemicarbazones against C6 glioma cells
resolves10.1016/S0162-0134(02)00419-1
Synthesis, structure, spectroscopic and in vitro antitumour studies of a novel gallium(III) complex with 2-acetylpyridine 4N-dimethylthiosemicarbazone
resolves10.1016/S0079-6468(08)70259-5
7 The Chemistry and Biological Activity of α -(N)-Heterocyclic Carboxaldehyde Thiosemicarbazones
resolves10.1007/s10593-008-0162-x
Directed synthesis of semicarbazones, thiosemicarbazones, and guanylhydrazones of 1-vinylpyrrole-2-carbaldehydes
resolves10.1016/j.jinorgbio.2005.04.012
Nickel (II) complexes of naphthaquinone thiosemicarbazone and semicarbazone: Synthesis, structure, spectroscopy, and biological activity
resolves10.1016/j.poly.2016.10.039
Synthesis of novel Zn(II) and Cd(II) complexes of semicarbazones and their utility as precursors for respective metal selenide quantum dots
resolves10.1016/S0162-0134(01)00220-3
Synthesis, structure and biological activity of nickel(II) complexes of 5-methyl 2-furfural thiosemicarbazone
resolves10.1590/S0103-50532001000300002
The chemistry of isatins: a review from 1975 to 1999
resolves10.1016/S0277-5387(02)01035-5
Synthesis and structures of acetylferrocene thiosemicarbazones and their dimethylthallium(III) complexes, which have four- or five-membered chelate rings
resolves10.1007/s10876-015-0883-9
Synthesis, Crystal Structure and Properties of Three Metal Complexes Based on a Flexible Schiff Base Ligand
resolves10.1016/j.ejmech.2011.07.038
Biological evaluation of a novel water soluble sulphur bridged binuclear copper(II) thiosemicarbazone complex
resolves10.1007/BF01062223
Antifungal and antitumor activity of heterocyclic thiosemicarbazones and their metal complexes: current status
resolves10.1016/0006-2952(94)90105-8
Inhibitors of ribonucleotide reductase
resolves10.1021/ic000915e
Chemical Control on the Coordination Mode of Benzaldehyde Semicarbazone Ligands. Synthesis, Structure, and Redox Properties of Ruthenium Complexes
resolves10.1021/cr0406458
Advances in Homogeneous and Heterogeneous Catalytic Asymmetric Epoxidation
resolves10.1007/s11434-013-5786-2
Synthesis, structure, optoelectronic properties of novel zinc Schiff-base complexes
resolves10.14429/dsj.56.1905
Transition Metal Carbohydrazide Nitrates: Burn-rate Modifiers for Propellants
resolves10.1002/ejic.201100465
New Energetic Complexes of Copper(II) and the Acetone Carbohydrazide Schiff Base as Potential Flame Colorants for Pyrotechnic Mixtures
resolves10.1016/j.jlumin.2011.06.030
Electroluminescence of colloidal ZnSe quantum dots
resolves10.1016/j.ica.2004.11.026
Cd(II) and Cu(II) complexes of polydentate Schiff base ligands: synthesis, characterization, properties and biological activity
resolves10.1007/s11243-008-9135-2
Syntheses, characterization, antimicrobial and genotoxic activities of new Schiff bases and their complexes
resolves10.1080/00958970903093694
Synthesis, characterization, and biological activity of a Schiff-base Zn(II) complex
resolves10.1016/S0014-827X(99)00075-0
Synthesis and antimicrobial activity of Schiff and Mannich bases of isatin and its derivatives with pyrimidine
resolves10.1016/j.saa.2005.03.031
Synthesis, characterization and biological activity of some transition metals with Schiff base derived from 2-thiophene carboxaldehyde and aminobenzoic acid
resolves10.1023/A:1006917704209
Synthesis, characterization and antibacterial properties of Schiff bases and Schiff base metal complexes derived from 2,3-diamino- pyridine
resolves10.1016/0277-5387(95)00310-X
The synthesis, characterization and bioactivities of some copper(II) complexes of the 2-acetylpyridine schiff bases of s-methyl- and s-benzyldithiocarbazate, and the x-ray crystal structure of the nitrato(s-benzyl-β-n-(2-acetylpyridyl) methylenedithiocarbazato)copper(II) complex
resolves10.1080/00945719909351739
Synthesis, Characterization and Antifungal Activity of Some Transition Metal Complexes of the Schiff Base Derived from 4-Acetylbi-Phenyl and S-Benzyldithiocarbazate
resolves10.1080/14756360290005598
Antibacterial Schiff Bases of Oxalyl-hydrazine/diamide Incorporating Pyrrolyl and Salicylyl Moieties and of Their Zinc(II) Complexes
resolves10.1007/BF02704255
Synthesis, characterisation and electrochemical behaviour of Cu(II), Co(II), Ni(II) and Zn(II) complexes derived from acetylacetone andp-anisidine and their antimicrobial activity
resolves10.1016/j.bmcl.2005.12.035
Schiff base conjugates of p-aminosalicylic acid as antimycobacterial agents
resolves10.4489/MYCO.2008.36.2.093
Antibacterial and Antifungal Studies on Some Schiff Base Complexes of Zinc(II)
resolves10.1631/jzus.2007.B0446
Synthesis of Schiff bases of naphtha[1,2-d]thiazol-2-amine and metal complexes of 2-(2′-hydroxy)benzylideneaminonaphthothiazole as potential antimicrobial agents
resolves10.1016/j.poly.2013.04.016
Novel binuclear Cu(II) complexes combining a semicarbazone Schiff base with distinct bridging ligands: Structure and antimicrobial activity
resolves10.3109/14756366.2011.582686
Synthesis, characterization and biological properties of thienyl derived triazole Schiff bases and their oxovanadium(IV) complexes
resolves10.2174/092986706776873023
Current Advances in Antifungal Targets and Drug Development
resolves10.1111/jcmm.12508
Antibacterial, antifungal and <i>in vitro</i> antileukaemia activity of metal complexes with thiosemicarbazones
resolves10.1016/j.saa.2005.04.005
Spectroscopic and biological studies on newly synthesized nickel(II) complexes of semicarbazones and thiosemicarbazones
resolves10.1360/03wb0174
Characteristic spectral studies and in vitro antifungal activity of some Schiff bases and their organotin (?) complexes
resolves10.3390/molecules14010174
Coordination Modes of a Schiff Base Pentadentate Derivative of 4-Aminoantipyrine with Cobalt(II), Nickel(II) and Copper(II) Metal Ions: Synthesis, Spectroscopic and Antimicrobial Studies
resolves10.4489/MYCO.2006.34.4.214
Antifungal Activities of Biorelevant Complexes of Copper(II) with Biosensitive Macrocyclic Ligands
resolves10.1016/j.saa.2012.08.042
Retraction notice to: Experimental FT-IR, FT-Raman spectra and quantum chemical studies of optimized molecular structures, conformers and vibrational characteristics of Nicotinic acid and Thio-nicotinic acid [Spectrochim. Acta Part A: Mol. Biomol. Spectrosc. 96 (2012) 163–178]
resolves10.1081/SIM-120021656
Synthesis, Spectral and Antifungal Activity of Ru(II) Mixed‐Ligand Complexes
resolves10.1016/0020-1693(96)05098-0
The preparation, characterization, crystal structure and biological activities of some copper(II) complexes of the 2-benzoylpyridine Schiff bases of S-methyl- and S-benzyldithiocarbazate
resolves10.1007/BF00167006
Synthesis, physico-chemical and biological studies on oxovanadium(IV) derivatives of mercaptotriazoles
resolves10.1002/cbdv.201200126
Synthesis and Evaluation of Gambogic Acid Derivatives as Antitumor Agents. Part III
resolves10.15252/embj.201694732
Discrete cytosolic macromolecular BRAF complexes exhibit distinct activities and composition
resolves10.1038/222385a0
Platinum Compounds: a New Class of Potent Antitumour Agents
resolves10.1038/nrc2167
The resurgence of platinum-based cancer chemotherapy
resolves10.1128/AAC.31.11.1798
N-methylisatin-beta-4',4'-diethylthiosemicarbazone, an inhibitor of Moloney leukemia virus protein production: characterization and in vitro translation of viral mRNA
resolves10.1016/0042-6822(79)90096-5
Inhibition of vaccinia virus late protein synthesis by isatin-β-thiosemicarbazone: Characterization and in vitro translation of viral mRNA
resolves10.1021/jm960603e
Design, Synthesis, and Evaluation of Nonpeptidic Inhibitors of Human Rhinovirus 3C Protease
resolves10.1016/j.bmcl.2005.04.027
Synthesis and evaluation of isatin derivatives as effective SARS coronavirus 3CL protease inhibitors
resolves10.1016/j.antiviral.2006.03.004
Antiviral drug resistance
resolves10.1007/s00706-013-1034-3
Synthesis, characterization, and antiviral activity of novel fluorinated isatin derivatives
resolves10.1016/j.ejmech.2011.09.031
Novel platinum(II) and palladium(II) complexes of thiosemicarbazones derived from 5-substitutedthiophene-2-carboxaldehydes and their antiviral and cytotoxic activities
resolves10.1097/00001813-200003000-00009
Structure-activity studies on gossypol in tumor cell lines
resolves10.2298/JSC0807727C
Ni(II), Pd(II) and Pt(II) complexes with ligand containing thiosemicarbazone and semicarbazone moiety: Synthesis, characterization and biological investigation
resolves10.1021/jm00164a023
Design, synthesis, testing, and quantitative structure-activity relationship analysis of substituted salicylaldehyde Schiff bases of 1-amino-3-hydroxyguanidine tosylate as new antiviral agents against coronavirus
resolves10.1590/1414-431x20176390
Two novel Co(II) complexes with two different Schiff bases: inhibiting growth of human skin cancer cells
resolves10.1016/j.poly.2011.02.037
Searching for gallium bioactive compounds: Gallium(III) complexes of tridentate salicylaldehyde semicarbazone derivatives
resolves10.1021/ic2020308
Effect of N(4)-Phenyl Substitution in 2-Oxo-1,2-dihydroquinoline-3-carbaldehyde Semicarbazones on the Structure, DNA/Protein Interaction, and Antioxidative and Cytotoxic Activity of Cu(II) Complexes
resolves10.1016/j.jinorgbio.2008.11.009
Biological effects of a complex of vanadium(V) with salicylaldehyde semicarbazone in osteoblasts in culture: Mechanism of action
resolves10.1016/j.jinorgbio.2010.11.001
Vanadium polypyridyl compounds as potential antiparasitic and antitumoral agents: New achievements
resolves10.1021/jm000979z
Synthesis, Cytotoxicity, and Antitumor Activity of Copper(II) and Iron(II) Complexes of <sup>4</sup><i>N</i>-Azabicyclo[3.2.2]nonane Thiosemicarbazones Derived from Acyl Diazines
resolves10.1002/ejic.201100898
Synthesis, Characterisation, and Preliminary In Vitro Studies of Vanadium(IV) Complexes with a Schiff Base and Thiosemicarbazones as Mixed Ligands
resolves10.1016/j.ejmech.2010.04.009
Mn(II), Co(II) and Zn(II) complexes with heterocyclic substituted thiosemicarbazones: Synthesis, characterization, X-ray crystal structures and antitumor comparison
resolves10.1002/cjoc.20010191122
Synthesis, characterization of diorganotin (IV) schiff base complexes and their <i>in vitro</i> antitumor activity
resolves10.1002/adma.19950070703
The Colloid Chemical Approach to Nanostructured Materials**
resolves10.1126/science.281.5385.2013
Semiconductor Nanocrystals as Fluorescent Biological Labels
resolves10.1016/j.pquantelec.2013.04.001
On the physics of semiconductor quantum dots for applications in lasers and quantum optics
resolves10.3233/CBM-2008-4603
Quantum dot bioconjugates for in vitro diagnostics &amp; in vivo imaging
resolves10.1103/PhysRevLett.92.186601
High Efficiency Carrier Multiplication in PbSe Nanocrystals: Implications for Solar Energy Conversion
resolves10.1038/nbt764
Immunofluorescent labeling of cancer marker Her2 and other cellular targets with semiconductor quantum dots
resolves10.4236/anp.2016.51001
Biotoxicity of CdS/CdSe Core-Shell Nano-Structures
resolves10.1016/0040-4020(72)80068-1
Bildung und fragmentierung von cycloalkeno-1,2,3-selenadiazolen
resolves10.1039/a807666i
Dinuclear diselenolenes derived from cycloalkeno-1,2,3-selenadiazoles and tetrakis(triphenylphosphine)palladium
resolves10.1039/dt9930000703
Synthesis and characterisation of cyclopentadienylcobalt and pentamethylcyclopentadienylcobalt diselenolenes
resolves10.1016/S0022-328X(98)00367-2
Decamethylpentasilacycloheptyne·Mo2(CO)4(η5-C5H5)2 and cycloheptyne·Mo2(CO)4(η5-C5H5)2
resolves10.1016/S0167-577X(02)01021-2
Synthesis of cadmium selenide by use of selenadiazol in ethylene glycol—a greener source of selenium
resolves10.1039/C4RA00676C
Core–shell ZnSe–CdSe quantum dots: a facile approach via decomposition of cyclohexeno-1,2,3-selenadiazole
resolves10.1007/s10593-015-1666-9
An efficient solventless synthesis of cycloalkeno-1,2,3-selenadiazoles, their antimicrobial studies, and comparison with parent semicarbazones
resolves10.1039/C7NJ00793K
Microwave synthesis of bis(cycloalkeno)-1,4-diselenins: a novel source of Se for CdSe QDs
resolves10.1039/C7NJ02994B
1,2,3-Selenadiazole-driven single family MSNCs of CdSe
resolves10.1021/nn800632j
Synthesis, Characterization, and Bioconjugation of Fluorescent Gold Nanoclusters toward Biological Labeling Applications
resolves10.1021/nl101225f
On the Ligand’s Role in the Fluorescence of Gold Nanoclusters
resolves10.1021/ar200331z
Quantum Sized Gold Nanoclusters with Atomic Precision
resolves10.1021/ar300213z
Atomically Precise Gold Nanoclusters as New Model Catalysts
resolves10.1002/ange.200702032
Gold Nanoparticles and Gold(III) Complexes as General and Selective Hydrosilylation Catalysts
resolves10.1021/ic001073m
Syntheses and Characterization of Gold(III) Tetradentate Schiff Base Complexes. X-ray Crystal Structures of [Au(sal<sub>2</sub>pn)]Cl·2.5H<sub>2</sub>O and [Au(sal<sub>2</sub>en)]PF<sub>6</sub>
resolves10.1021/ac202162u
Use of Fluorescent DNA-Templated Gold/Silver Nanoclusters for the Detection of Sulfide Ions
resolves10.1021/ac101427y
Ultrasensitive Sensing of Hg<sup>2+</sup> and CH<sub>3</sub>Hg<sup>+</sup> Based on the Fluorescence Quenching of Lysozyme Type VI-Stabilized Gold Nanoclusters
resolves10.1002/anie.201100299
Insulin‐Directed Synthesis of Fluorescent Gold Nanoclusters: Preservation of Insulin Bioactivity and Versatility in Cell Imaging
resolves10.1016/j.bioorg.2014.07.004
Synthesis of copper/nickel nanoparticles using newly synthesized Schiff-base metals complexes and their cytotoxicity/catalytic activities
resolves10.1007/s11243-010-9410-x
Hydrothermal and sonochemical synthesis of a nano-sized nickel(II) Schiff base complex as a precursor for nano-sized nickel(II) oxide; spectroscopic, catalytic and antibacterial properties
resolves10.1088/0957-4484/18/5/055602
Quasi-homogeneous catalytic hydrogenation over monodisperse nickel and cobalt nanoparticles
resolves10.1016/j.jcrysgro.2007.12.052
Morphology controllable synthesis of nickel nanopowders by chemical reduction process
resolves10.1016/j.matlet.2009.01.062
Ag-catalyzed synthesis of ultrafine nickel nanoparticles: A facile way to size control
resolves10.1143/JJAP.32.L511
Blue Electroluminescence in Thin Films of Azomethin-Zinc Complexes
resolves10.1021/ic062035r
Structural, Spectral, Electric-Field-Induced Second Harmonic, and Theoretical Study of Ni(II), Cu(II), Zn(II), and VO(II) Complexes with [N<sub>2</sub>O<sub>2</sub>] Unsymmetrical Schiff Bases of <i>S</i>-Methylisothiosemicarbazide Derivatives
resolves10.1143/JJAP.35.L1339
White-Light-Emitting Material for Organic Electroluminescent Devices
resolves10.1021/ic7020758
Synthesis and Characterization of Luminescent Zinc(II) and Cadmium(II) Complexes with N,S-Chelating Schiff Base Ligands
resolves10.1016/S1381-1169(00)00432-5
Asymmetric cyclopropanation catalyzed by copper–Schiff’s base complexes
resolves10.1016/j.poly.2015.11.050
Copper(I) complexes of 2-methoxy-(5-trifluoromethyl-phenyl)-pyridine-2yl-methylene-amine: Impact of phosphine ancillary ligands on luminescence and catalytic properties of the copper(I) complexes
resolves10.1016/j.ica.2016.10.024
Synthesis, characterization, luminescence and catalytic properties of copper(I) complexes with N-(2-pyridylmethylene)-1,5-dimethyl-2-pyrazole-3-(2H)-one and triphenylphosphine as ligands
resolves10.1016/j.ica.2005.02.006
Synthesis, crystal structure and photo-induced DNA cleavage activity of ternary copper(II) complexes of NSO-donor Schiff bases and NN-donor heterocyclic ligands
resolves10.1016/j.saa.2010.12.045
Synthesis, experimental and theoretical characterization of N,N′-dipyridoxyl (1,4-butanediamine) Schiff-base ligand and its Cu(II) complex
resolves10.1016/0304-5102(88)85009-0
Catalysis of cobalt-Schiff base complexes in oxygenation of alkenes: on the mechanism of ketonization
resolves10.1007/BF00136366
Catalytic activities of Schiff base aquocomplexes of copper(II) towards hydrolysis of amino acid esters
resolves10.1016/S1381-1169(98)00071-5
Polymer-supported palladium–nickel bimetallic catalyst for the regioselective hydroesterification of styrene
resolves10.1080/00958970801989902
Synthesis and characterization of Schiff base metal complexes: their antimicrobial, genotoxicity and electrochemical properties
resolves10.1016/j.poly.2006.11.005
Synthesis, characterization, and spectroscopic studies of tetradentate Schiff base chromium(III) complexes
resolves10.1016/S0022-328X(98)01058-4
Catalytic asymmetric reactions via π-allylpalladium complexes coordinated with chiral monophosphine ligands
resolves10.1016/S0022-328X(98)01059-6
Enantioselective palladium-catalyzed allylic substitutions with asymmetric chiral ligands
resolves10.1002/(SICI)1099-0682(199801)1998:1<43::AID-EJIC43>3.0.CO;2-S
Enantioselective Palladium-Catalysed Allylation of 1,5-Dimethylbarbituric Acid
resolves10.1016/S0926-860X(03)00414-9
Electrocatalytic effects of thionyl chloride reduction by polymeric Schiff base transition metal(II) complexes
resolves10.1021/ic061286x
Spacially Confined M<sub>2</sub>Centers (M = Fe, Co, Ni, Zn) on a Sterically Bulky Binucleating Support:  Synthesis, Structures and Ethylene Oligomerization Studies
resolves10.1016/S1381-1169(98)00283-0
Enantioselective catalysis
resolves10.1021/jo981252+
A Convenient and Highly Regioselective One-Pot Synthesis of Quinolines by Addition of a Vilsmeier-Type Reagent to <i>N</i>-Arylimines
resolves10.1016/S0040-4039(96)02414-8
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resolves10.1016/S0040-4039(97)00192-5
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resolves10.1016/j.talanta.2004.12.043
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resolves10.1007/s12161-008-9028-1
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resolves10.1002/jccs.200800049
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resolves10.1530/jrf.0.0690001
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resolves10.1021/ja00320a018
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resolves10.1248/cpb.53.22
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The 79 references without a DOI — listed, not checked
no DOI — not checked10.1016/j.mtchem.2019.100195_bib1
no DOI — not checked10.1016/j.mtchem.2019.100195_bib2
no DOI — not checked10.1016/j.mtchem.2019.100195_bib3
no DOI — not checked10.1016/j.mtchem.2019.100195_bib6
no DOI — not checked10.1016/j.mtchem.2019.100195_bib8
no DOI — not checked10.1016/j.mtchem.2019.100195_bib10c
no DOI — not checked10.1016/j.mtchem.2019.100195_bib14b
no DOI — not checked10.1016/j.mtchem.2019.100195_bib16d
no DOI — not checked10.1016/j.mtchem.2019.100195_bib33c
no DOI — not checked10.1016/j.mtchem.2019.100195_bib33d
no DOI — not checked10.1016/j.mtchem.2019.100195_bib33e
no DOI — not checked10.1016/j.mtchem.2019.100195_bib33f
no DOI — not checked10.1016/j.mtchem.2019.100195_bib34b
no DOI — not checked10.1016/j.mtchem.2019.100195_bib34c
no DOI — not checked10.1016/j.mtchem.2019.100195_bib36
no DOI — not checked10.1016/j.mtchem.2019.100195_bib41
no DOI — not checked10.1016/j.mtchem.2019.100195_bib43
no DOI — not checked10.1016/j.mtchem.2019.100195_bib46
no DOI — not checked10.1016/j.mtchem.2019.100195_bib48d
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no DOI — not checked10.1016/j.mtchem.2019.100195_bib54
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no DOI — not checked10.1016/j.mtchem.2019.100195_bib66
no DOI — not checked10.1016/j.mtchem.2019.100195_bib68
no DOI — not checked10.1016/j.mtchem.2019.100195_bib69b
no DOI — not checked10.1016/j.mtchem.2019.100195_bib69c
no DOI — not checked10.1016/j.mtchem.2019.100195_bib70
no DOI — not checked10.1016/j.mtchem.2019.100195_bib71
no DOI — not checked10.1016/j.mtchem.2019.100195_bib72
no DOI — not checked10.1016/j.mtchem.2019.100195_bib73
no DOI — not checked10.1016/j.mtchem.2019.100195_bib74
no DOI — not checked10.1016/j.mtchem.2019.100195_bib76
no DOI — not checked10.1016/j.mtchem.2019.100195_bib77
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no DOI — not checked10.1016/j.mtchem.2019.100195_bib80
no DOI — not checked10.1016/j.mtchem.2019.100195_bib82
no DOI — not checked10.1016/j.mtchem.2019.100195_bib83
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no DOI — not checked10.1016/j.mtchem.2019.100195_bib97
no DOI — not checked10.1016/j.mtchem.2019.100195_bib101
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no DOI — not checked10.1016/j.mtchem.2019.100195_bib106a
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no DOI — not checked10.1016/j.mtchem.2019.100195_bib113
no DOI — not checked10.1016/j.mtchem.2019.100195_bib120
no DOI — not checked10.1016/j.mtchem.2019.100195_bib122
no DOI — not checked10.1016/j.mtchem.2019.100195_bib124
no DOI — not checked10.1016/j.mtchem.2019.100195_bib127
no DOI — not checked10.1016/j.mtchem.2019.100195_bib128
no DOI — not checked10.1016/j.mtchem.2019.100195_bib131
no DOI — not checked10.1016/j.mtchem.2019.100195_bib136
no DOI — not checked10.1016/j.mtchem.2019.100195_bib138
no DOI — not checked10.1016/j.mtchem.2019.100195_bib161
no DOI — not checked10.1016/j.mtchem.2019.100195_bib162
no DOI — not checked10.1016/j.mtchem.2019.100195_bib163
no DOI — not checked10.1016/j.mtchem.2019.100195_bib164
no DOI — not checked10.1016/j.mtchem.2019.100195_bib165
no DOI — not checked10.1016/j.mtchem.2019.100195_bib166
no DOI — not checked10.1016/j.mtchem.2019.100195_bib167
no DOI — not checked10.1016/j.mtchem.2019.100195_bib177
no DOI — not checkedChem. Abstr., 111 (1989) 22902.
no DOI — not checked10.1016/j.mtchem.2019.100195_bib182
no DOI — not checked10.1016/j.mtchem.2019.100195_bib187
no DOI — not checkedOxygen detecting agent, Jpn. Kokai 6035, 260(to a Gosei Chemical Industry Co.Ltd) 23 Feb.1985, Appl.83/142, 557, 05 Aug 1983 5PP
no DOI — not checked10.1016/j.mtchem.2019.100195_bib193
no DOI — not checkedGer Offen3, 409,082(to Bayer AG) 19 Sep.1985
no DOI — not checked10.1016/j.mtchem.2019.100195_bib195
no DOI — not checked10.1016/j.mtchem.2019.100195_bib197
no DOI — not checked10.1016/j.mtchem.2019.100195_bib198
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no DOI — not checked10.1016/j.mtchem.2019.100195_bib202
no DOI — not checked10.1016/j.mtchem.2019.100195_bib204
no DOI — not checked10.1016/j.mtchem.2019.100195_bib205
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