Theoretical studies of new Schiff base ligand derived from 1,3‐diaminopropane and 2‐acetyl ferrocene and studying some applications of its metal complexes

A novel bidentate Schiff base ligand (L) and some d‐transition metal chelates (Cr (III), Mn (II), Fe (III), Co (II), Ni (II), Cu (II), Zn (II) and Cd (II)) were synthesized and characterized using various physicochemical and spectroscopic techniques like elemental analysis, IR, mass, UV–visible and thermal analysis. The spectroscopic data suggested that the parent Schiff base ligand coordinated to the metal ions through both imine nitrogen atoms. The molecular and electronic structure of the free ligand was optimized theoretically, and the quantum chemical parameters were calculated. The molecular structure can be used to investigate the coordination sites and the total charge density around each atom. The free ligand and its complexes were screened for their antimicrobial activities for various pathogenic bacteria and fungi. The anticancer activities of the free ligand, Cr (III), Mn (II) and Fe (III) complexes were screened against MCF‐7 cell line and found that Mn (II) complex has the lowest IC₅₀ (15.90 μg/ml). Molecular docking was used to predict the binding between the free ligand with receptor of mutant human androgen (ARccr) derived from androgen‐independent prostate cancer (1GS4), crystal structure of yeast‐specific serine/threonine protein phosphatase (ppz1) of Candida Albicans (5JPE) and crystal structure of renal tumor suppressor protein, folliculin (3 V42) and to identify the binding mode and the crucial functional groups interacting with the three proteins.     

Synthesis,spectroscopic and X‐ray single‐crystal structure study of bis(2‐methoxy‐ethanolato)‐bis(8‐quinolinato)titanium(IV)

Reaction of Ti(OCH₂CH₂OR)₄ (R?CH₃ and C₂H₅) with 8‐hydroxyquinoline in benzene at room temperature resulted in the formation of Ti(C₉H₆NO)₂(OCH₂CH₂OR)₂, characterized by IR, ¹H‐NMR, UV and mass spectroscopies. The molecular structure of Ti(C₉H₆NO)₂(OCH₂CH₂OCH₃)₂ has been determined by single‐crystal X‐ray structure analysis. The geometry at titanium is a distorted octahedron, with the nitrogen atoms of quinolinate occupying the trans position with respect to oxygens of the 2‐methoxyethoxy groups. The prepared quinolinate derivatives of titanium alkoxides are very stable towards hydrolysis and harsh conditions are required for hydrolytic cleavage. Copyright © 2005 John Wiley & Sons, Ltd.     

Crystallographic report: Dicyclohexyltin N‐[(E)‐(5‐chloro‐2‐hydroxyphenyl) methylene]‐(L)‐isoleucinate

The tin atom in the title compound is in a distorted trigonal bipyramidal geometry and forms a five‐ and six‐membered chelate rings with the tridentate ligand. Copyright © 2004 John Wiley & Sons, Ltd.     

Synthesis and X‐ray single‐crystal structure study of 5,5′‐bis(silyl)‐functionalized 3,3′‐dibromo‐2,2′‐dithiophenes

A high‐yield synthesis toward 5,5′‐bis(silyl)‐functionalized 3,3′‐dibromo‐2,2′‐dithiophenes with very efficient work‐up procedure is presented. The molecular structures of two silyl functionalized dibromo‐dithiophenes in the solid state have been determined to investigate the structural influences of different functional groups on the degree of π‐conjugation within the dithiophene moieties, as well as their packing properties. The planar alignment of the tert‐butyldimethylsilyl‐functionalized dibromo‐dithiophene shows a significantly higher degree of conjugation of the π‐system with a more favorable molecular packing than the skewed arrangement of the triisopropylsilyl‐substituted species. Copyright © 2005 John Wiley & Sons, Ltd.     

The zwitterionic structure of 2‐hydroxy‐4‐[(2‐hydroxybenzylidene)amino]benzoic acid

The title compound, C₁₄H₁₁NO₄, exists in the solid phase in the zwitterionic form, 2‐{[(4‐carboxy‐3‐hydroxyphenyl)iminiumyl]methyl}phenolate, with the H atom from the phenol group on the 2‐hydroxybenzylidene ring transferred to the imine N atom, resulting in a strong intramolecular N—H...O hydrogen bond between the iminium H atom and the phenolate O atom, forming a six‐membered hydrogen‐bonded ring. In addition, there is an intramolecular O—H...O hydrogen bond between the carboxylic acid group and the adjacent hydroxy group of the other ring, and an intermolecular C—H...O contact involving the phenol group and the C—H group adjacent to the imine bond, connecting the molecules into a two‐dimensional network in the (10) plane. π–π stacking interactions result in a three‐dimensional network. This study is important because it provides crystallographic evidence, supported by IR data, for the iminium zwitterionic form of Schiff bases.<!?tpb=12pt>     

Synthesis and Characterization of Organotin Compounds of a New Schiff Base Ligand with α‐Oxoglutaric Acid Isonicotinyl Hydrazone

Organotin compounds are a recurring motif in organometallic chemistry. The syntheses and characterization of new diorganotin compounds with α‐oxoglutaric acid isonicotinyl hydrazone are described, prepared compounds were characterized by elemental analysis, UV/Vis, ¹H, and ¹³C NMR spectroscopy, and X‐ray diffraction. They both have a distorted pentagonal bipyramidal arrangement, with a heptacoordinated central tin atom. Compound 1 presents a centrosymmetric dinuclear framework. Interestingly, intermolecular O–H ··· N and O–H ··· O hydrogen bonds contribute to the two‐dimensional network. Compound 2 is a simple mononuclear compound, which exhibits a rare one‐dimensional chain constructed by intermolecular O–H ··· Cl and N–H ··· O hydrogen bonds.     

X‐ray characterization and magnetic properties of dioxygen‐bridged CuII and MnIII Schiff base complexes

The coordination chemistry of multinuclear metal compounds is important because of their relevance to the multi‐metal active sites of various metalloproteins and metalloenzymes. Multinuclear Cu^II and Mn^III compounds are of interest due to their various properties in the fields of coordination chemistry, inorganic biochemistry, catalysis, and optical and magnetic materials. Oxygen‐bridged binuclear Mn^III complexes generally exhibit antiferromagnetic interactions and a few examples of ferromagnetic interactions have also been reported. Binuclear Cu^II complexes are important due to the fact that they provide examples of the simplest case of magnetic interaction involving only two unpaired electrons. Two novel dioxygen‐bridged copper(II) and manganese(III) Schiff base complexes, namely bis(μ‐4‐bromo‐2‐{[(3‐oxidopropyl)imino]methyl}phenolato)dicopper(II), [Cu₂(C₁₀H₁₀BrNO₂)₂], (1), and bis(diaqua{4,4′‐dichloro‐2,2′‐[(1,1‐dimethylethane‐1,2‐diyl)bis(nitrilomethanylylidene)]diphenolato}manganese(III)) bis{μ‐4,4′‐dichloro‐2,2′‐[(1,1‐dimethylethane‐1,2‐diyl)bis(nitrilomethanylylidene)]diphenolato}bis[aquamanganese(III)] tetrakis(perchlorate) ethanol disolvate, [Mn(C₁₈H₁₆Cl₂N₂O₂)(H₂O)₂]₂[Mn₂(C₁₈H₁₆Cl₂N₂O₂)₂(H₂O)₂](ClO₄)₄·2C₂H₅OH, (2), have been synthesized and single‐crystal X‐ray diffraction has been used to analyze their crystal structures. The structure analyses of (1) and (2) show that each Cu^II atom is four‐coordinated, with long weak Cu…O interactions of 2.8631 (13) Å linking the dinuclear halves of the centrosymmetric tetranucelar molecules, while each Mn^III atom is six‐coordinated. The shortest intra‐ and intermolecular nonbonding Mn…Mn separations are 3.3277 (16) and 5.1763 (19) Å for (2), while the Cu…Cu separations are 3.0237 (3) and 3.4846 (3) Å for (1). The magnetic susceptibilities of (1) and (2) in the solid state were measured in the temperature range 2–300 K and reveal the presence of antiferromagnetic spin‐exchange interactions between the transition metal ions.     

2,2′‐[(Disulfanediyl)bis{5‐[(1E)‐(2‐hydroxybenzylidene)amino]‐1,3‐thiazole‐4,2‐diyl}]diphenol: synthesis,crystal structure and calculation of molecular hyperpolarizability

The title Schiff base compound {systematic name: 2‐[5‐[(E )‐(2‐hydroxybenzylidene)amino]‐4‐(2‐{5‐[(E )‐(2‐hydroxybenzylidene)amino]‐2‐(2‐hydroxyphenyl)‐1,3‐thiazol‐4‐yl}disulfanyl)‐1,3‐thiazol‐2‐yl]phenol}, C₃₂H₂₂N₄O₄S₄, incorporating a disulfanediyl (dithio) linkage, was obtained from the condensation reaction between two equivalents of salicylaldehyde and one equivalent of dithiooxamide in dimethylformamide, and was characterized by elemental analysis, IR spectroscopic analysis and single‐crystal X‐ray diffraction. A one‐dimensional chain is formed along the b axis via double intermolecular C—H…S hydrogen bonds. The HOMO (highest occupied molecular orbital) and LUMO (lowest unoccupied molecular orbital) energies and some related molecular parameters were calculated at the B3LYP/6‐311G(d,p) level of theory. The molecular hyperpolarizability was also calculated.     

Online wide‐angle X‐ray diffraction/small‐angle X‐ray scattering measurements for the CO2‐laser‐heated drawing of poly(ethylene terephthalate) fiber

Fiber‐structure‐development in the poly(ethylene terephthalate) fiber drawing process was investigated with online measurements of wide‐angle and small‐angle X‐ray scattering with both a high‐luminance X‐ray source and a CO₂‐laser‐heated drawing system. The intensity profile of the transmitted X‐ray confirmed the location of the neck‐drawing point. The diffraction images had a time resolution of several milliseconds, and this still left much room for improvement. Crystal diffraction appeared in the wide‐angle X‐ray images almost instantaneously about 20 ms after necking, whereas a four‐point small‐angle X‐ray scattering pattern appeared immediately after necking. With the elapse of time after necking, the four‐point scattering pattern changed into a meridional two‐point shape. © 2005 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 43: 1090–1099, 2005     

A mixed‐ligand quinazoline‐based Ni(II) Schiff base complex: Synthesis,characterization, crystal structure,antimicrobial investigation and catalytic activity for the synthesis of 2H–indazolo[2,1‐b]phthalazine‐triones

A tridentate Schiff base ligand, (E)‐3‐((2‐hydroxy‐3‐methoxybenzylidene)amino)‐2‐methylquinazolin‐4(3H)‐one [HL], and its mixed‐ligand Ni(II) complex [Ni(L)(imi)], were synthesized and fully characterized using elemental analysis, FT‐IR, UV–Vis and ¹HNMR spectroscopy techniques. The structure of the synthesized ligand and complex was determined with single crystal X‐ray diffraction method. In the complex, a square planner geometry was observed around the Ni(II) central atom coordinated with the donor atoms of the Schiff base ligand and one nitrogen of imidazole group. In addition, the catalytic activity of the complex on the three‐component condensation of hydrazine hydrate with phthalic anhydride and dimedone to obtain 2H–indazolo[2,1‐b]phthalazine‐triones was investigated. Furthermore, in‐vitro antimicrobial studies were performed that indicated the great antibacterial activities of the Ni(II) complex against Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa and Bacillus cereus bacteria.     

Synthesis,Spectral, X‐Ray Diffraction,DFT, and Nematicidal Activity of Mixed Ligand Complexes of Ethyl 2‐(2‐Hydroxybenzylidine)‐Hydrazine Carboxylate and 1,10‐Phenanthroline with Some Transition Metals

In this work, mixed ligand complexes derived from ethyl 2‐(2‐hydroxybenzylidine)‐hydrazine carboxylate (HL) and 1,10‐phenanthroline (Phen) as ligands were synthesized and their structures elucidated by elemental analysis, infrared (IR), electronic,¹H NMR, and mass spectra, X‐ray diffraction (XRD), magnetic susceptibility measurements, and TG/DTG analyses. The analytical and spectral data support the formation of the complexes with the central ion in each complex six‐coordinated and a slightly distorted octahedral geometry. The IR spectra showed that HL and Phen ligands act as neutral bidentates. The XRD patterns of the complexes showed their crystalline nature. The calculated bond length and the force constant F (U═O) in the uranyl complex are 1.738 Å and 685.90 Nm⁻¹, respectively. The molar conductance values of the synthetic complexes in DMF were found to be in the range 5.00–274.06 S cm²/mol at room temperature. The thermodynamic parameters were evaluated by using the Coats–Redfern (CR) and Horowitz–Metzeger (HM) methods. Theoretical molecular structures were investigated by the density functional theory/B3LYP method using the Gaussian 98 W basis set. The nematicidal activity of the ligands and its metal complexes was also studied.     

Synthesis,structure and property of diorganotin N‐[(3‐methoxy‐2‐oxyphenyl)methylene]tyrosinates

Five new diorganotin N‐[(3‐methoxy‐2‐oxyphenyl)methylene] tyrosinates, R₂Sn[2‐O‐3‐MeOC₆H₃CH=NCH (CH₂C₆H₄OH‐4)COO] (R = Me, 1 ; Et, 2 ; Bu, 3 ; Cy, 4 ; Ph, 5 ), have been synthesized and characterized by elemental analysis, IR, NMR (¹H, ¹³C and ¹¹⁹Sn) spectra, and the X‐ray single crystal diffraction. In non‐coordinated solvent, complexes 1 – 5 have penta‐coordinated tin atom. In the solid state, 1 – 3 are centrosymmetric dimmers in which each tin atom is seven‐coordinated in a distorted pentagonal bipyramid, and 4 displays discrete molecular structure with distorted trigonal bipyramidal geometry, and the tin atom of 5 is hexa‐coordinated and possess the distorted octahedral geometry with a coordinational methanol molecule. The intermolecular O‐H???O hydrogen bonds in 1 – 4 link molecules into the different one‐dimensional supramolecular chain with R₂² (30) or R₂² (20) macrocycles, and the molecules of 5 are joined into a two‐dimensional supramolecular network containing R₄⁴ (24) and R₄⁴ (28) two macrocycles. Bioassay results against human tumour cell HeLa indicated that 3 ‐ 5 belonged to the efficient cytostatic agents and the activity decreased in the order 4 > 3 > 5 > 2 > 1. The fluorescence determinations show the complexes may be explored for potential luminescent materials.     

Synthesis and conjugation of a triiodohydroxylamine for the preparation of highly X‐ray opaque poly(ε‐caprolactone) materials

To address a need for highly X‐ray opaque biodegradable materials, a series of poly(ε‐caprolactone) derivatives were prepared using oxime post‐polymerization modification to conjugate two different iodinated hydroxylamines. These materials were synthesized with up to 32 wt. % iodine content and demonstrated improved X‐ray contrast relative to both the ketone precursors and previously reported monoiodinated materials. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 787–793     

Synthesis and Spectroscopic Characterization of the Benzaldehyde Schiff Base of S‐Allyldithiocarbazate and its Copper(II) Complex and the X‐ray Crystal Structure of Bis[S‐allyl‐β‐N‐benzylidene)dithiocarbazato]Copper(II)

S‐allyl‐β‐N‐(benzylidene)dithiocarbazate (sabdtc, 1 ), prepared from hydrazine hydrate, carbon disulfide, allyl bromide and benzaldehyde, reacts with copper(II) nitrate in ethanol solution to form the complex Cu(sabdtc)₂ ( 2 ). 1 function as a single negatively charged bidentate chelating ligand and coordinates via the azomethine nitrogen atom and thioenolate sulfur atom to the metal ion. 1 and 2 were characterized by elemental analyses, ¹H NMR, ¹³C NMR, UV/Vis, IR, and mass spectra. Spectroscopic evidences suggest a four‐coordinate distorted square planar structure for 2 . The molecular and crystal structure of 2 was determined by single crystal X‐ray analysis. Crystallographic data for 2 at 291(2) K: space group C2/c, a = 20.340(3), b = 15.503(3), c = 7.659(1) Å, β = 95.96(2)°, Z = 4, R₁ = 0.044 and wR2 = 0.0689.     

Synthesis and crystal structure of the dinuclear copper(II) Schiff base complex μ‐hydroxido‐μ‐chlorido‐bis{[bis(trans‐2‐nitrocinnamaldehyde)ethylenediamine]chloridocopper(II)} dichloromethane sesquisolvate

Transition metal complexes of Schiff base ligands have been shown to have particular application in catalysis and magnetism. The chemistry of copper complexes is of interest owing to their importance in biological and industrial processes. The reaction of copper(I) chloride with the bidentate Schiff base N,N′‐bis(trans‐2‐nitrocinnamaldehyde)ethylenediamine {Nca₂en, systematic name: (1E,1′E,2E,2′E)‐N,N′‐(ethane‐1,2‐diyl)bis[3‐(2‐nitrophenyl)prop‐2‐en‐1‐imine]} in a 1:1 molar ratio in dichloromethane without exclusion of air or moisture resulted in the formation of the title complex μ‐chlorido‐μ‐hydroxido‐bis(chlorido{(1E,1′E,2E,2′E)‐N,N′‐(ethane‐1,2‐diyl)bis[3‐(2‐nitrophenyl)prop‐2‐en‐1‐imine]‐κ²N,N′}copper(II)) dichloromethane sesquisolvate, [Cu₂Cl₃(OH)(C₂₀H₁₈N₄O₄)₂]·1.5CH₂Cl₂. The dinuclear complex has a folded four‐membered ring in an unsymmetrical Cu₂OCl₃ core in which the approximate trigonal bipyramidal coordination displays different angular distortions in the equatorial planes of the two Cu^II atoms; the chloride bridge is asymmetric, but the hydroxide bridge is symmetric. The chelate rings of the two Nca₂en ligands have different conformations, leading to a more marked bowing of one of the ligands compared with the other. This is the first reported dinuclear complex, and the first five‐coordinate complex, of the Nca₂en Schiff base ligand. Molecules of the dimer are associated in pairs by ring‐stacking interactions supported by C—H…Cl interactions with solvent molecules; a further ring‐stacking interaction exists between the two Schiff base ligands of each molecule.     

Synthesis and properties of novel Schiff base oligomers based on oligo‐4‐hydroxybenzaldehyde

Condensation of oligo‐4‐hydroxybenzaldehyde with aniline, 2‐chloroaniline, 2‐aminophenol, 2‐aminotoluene, 4‐aminotoluene, and 4‐nitroaniline gave the corresponding Schiff base oligomers (OFAP, OKAP, OHAP, OOAP, OTAP, and ONAP, respectively). The products were characterized by ¹H NMR, Fourier transform infrared, ultraviolet–visible, and elemental analyses. The number‐average molecular weight, mass‐average molecular weight, and polydispersity index (PDI) values of the Schiff base oligomers were determined. Thermogravimetric analysis was used to compare the thermal stability of the oligomers, which showed the Schiff base oligomers to be resistant to thermooxidative decomposition. Weight loss of 5% and 50% occurred at temperatures of 122 and 475 °C; for OFAP, at 118 and 453 °C; for OKAP, at 182 and 491 °C; for OHAP, at 150 and 452 °C; for OOAP, at 132 and 401 °C; for OTAP, and at 193 and 414 °C for ONAP. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 1120–1125, 2004     

The Structure of 2‐[(1S)‐(+)‐10‐camphorsulfonamino]‐6‐aminopyridine in the Solid State and in Solution; Unprecedented Cocrystallization of Four Stereoisomers

The solid and solution structures of a new optically active aminopyridine compound, 2‐[(1S)‐(+)‐10‐camphorsulfonamino]‐6‐aminopyridine [(S)‐csaap], 1 , are reported. Crystal data: space group P2₁, a = 8.9729 (5), b = 10.9447 (6), c = 36.693 (2) Å, β = 96.435 (1)°, V = 3580.8 (3) ų, Z = 8, R₁ = 0.0673 and wR₂ = 0.1600 with I > 2σ(I). This chiral compound shows an unprecedented cocrystallization of four stereoisomers, which are characterized by X‐ray crystallography and NMR spectroscopy.     

New Rh(III) complexes of 5‐methyl‐5‐(pyridyl)‐2,4‐imidazolidenedione: Synthesis,X‐ray structure,electrochemical study and catalytic behaviour for hydrogenation of ketones

We describe the reaction of anion [RhCl₆]³⁻ with a series of hydantoin ligands (HL1, HL2 and HL3 = 5‐methyl‐5‐(2‐, 3‐ and 4‐pyridyl)‐2,4‐imidazolidenedione, respectively). Based on spectroscopic, cyclic voltammetric, elemental and MS analyses, the complexes have the general formula K[RhCl₂(L1)₂] ( 1 ), cis ‐ and trans ‐K[RhCl₄(HL2)₂] ( 2a and 2b ) and cis ‐ and trans ‐K[RhCl₄(HL3)₂] ( 3a and 3b ). Complexes 2a , 2b , 3a and 3b were characterized successfully using infrared, ¹H NMR and ¹³C NMR spectral analyses. Dissolution of complex 1 in dimethylsulfoxide (DMSO) led to elimination of one KL1 ligand and coordination of two DMSO molecules as ligands and transformation of this complex to cis ‐ and trans ‐[RhCl₂L1(DMSO)₂] ( 1a and 1b ). Recrystallization led to separation and isolation of crystals of 1a from the initial mixture. X‐ray analysis results showed that this complex was crystallized as solvated complex cis ‐[RhCl₂L1(DMSO)₂]DMSO. The catalytic activity of these complexes was then evaluated for the hydrogenation of various ketones.     

Spectral Characterization and Antimicrobial Activity of Some Schiff Bases Derived from 4‐Methyl‐2‐aminophenol

A series of N‐(5‐methyl‐2‐hydroxyphenyl)‐(2/3/4/5‐substituted)‐benzaldimines ( I – XIII ) were synthesized using appropriate synthetic route. Their structures were characterized by FT‐IR, UV‐Visible, ESI‐MS, ¹H‐ and ¹³C‐NMR spectroscopic techniques and analytical methods. The crystal structure of N‐(5‐methyl‐2‐hydroxyphenyl)‐3,4‐dimethoxybenzaldimine ( XIII ) was determined by X‐ray diffraction at room temperature. Relationship between the melting points and the structures of the compounds were examined. Antibacterial activities of the compounds were evaluated against Staphylococcus aureus, Staphylococcus epidermidis, Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa and Proteus mirabilis. Antifungal activities were reported for Candida albicans. Some of the Schiff bases showed considerable antimicrobial activity against S. aureus and C. albicans.     

乙酰丙酮缩联苯胺席夫碱的合成及晶体结构

一个多世纪以来,己有大量有关席夫碱方面的文献报道.许多Schiff碱金属配合物因具有良好的抗肿瘤、抗病毒、杀菌抑霉等多种生物活性而得到了广泛应用[1-3];其特殊的催化行为以及在酶模拟方面的功效引起了化学家的普遍重视[4,5].席夫碱中,β一二酮类化合物是一类良好的金属螯合剂,因为它能够为金属提供两个键合点,形成稳定的六元螯合环,其与稀土离子形成的配合物具有稳定的化学性质和优异的发光性能,因而具有广泛的应用前景[6].