Synthesis, Physicochemical Characterization, Biological Evaluation, In Silico and Molecular Docking Studies of Pd(II) Complexes with P, S-Donor Ligands.

One homoleptic () and three heteroleptic (-) palladium(II) complexes were synthesized and characterized by various physicochemical techniques, i.e., elemental analysis, FTIR, Raman spectroscopy, H, C, and P NMR.

Fabrication and prospective applications of graphene oxide-modified nanocomposites for wastewater remediation.

Water bodies have become polluted with heavy metals and hazardous contaminants as a result of fast development. Many strategies have been devised by researchers in order to remove hazardous contaminants from the aquatic environment. Utilizing graphene oxide-based composite materials as efficient adsorbents for waste water treatment, desalination, separation, and purification is gaining attraction nowadays.

Copper sulfide nanostructures: synthesis and biological applications.

Over the past few years, considerable attention has been paid to biomedical applications of copper sulfide nanostructures owing to their enhanced physiochemical and pharmacokinetics characteristics in comparison to gold, silver, and carbon nanomaterials. The small-sized Cu S nanoparticles have the advantage to absorb efficiently in the near-infrared region (NIR) above 700 nm and the absorption can be tuned by altering their stoichiometries. Moreover, their easy removal through the kidneys overpowers the issue of toxicity caused by many inorganic substances.

Two new monofunctional platinum(II) dithiocarbamate complexes: -type axial protection, equatorial-axial conformational isomerism, and anticancer and DNA binding studies.

The syntheses of two platinum(ii) dithiocarbamate complexes (1 and 2) that show quinoplatin- and phenanthriplatin-type axial protection of the Pt-plane are described. The Pt-plane of complex 2 is axially more protected than that of complex 1. Furthermore, both complexes adopt two different stereochemical conformations in the solid state (based on single-crystal X-ray structures) owing to the structurally flexible piperazine backbone; i.

Micro-Raman high-pressure investigation on the malaria pigment hematin anhydride (β-hematin).

The effect of pressure on the Raman and fluorescence spectra of hematin anhydride (β-hematin) is reported. In a diamond-anvil cell, DAC, with applied pressures up to 41 kbar, the Raman spectrum undergoes a series of intensity enhancements and increases in energy for many of the Raman-active bands up to a pressure of ~27 kbar. At higher pressures, there is either a leveling out or a decrease in the energies of these vibrational modes.

Correction: Synthesis of γ-alumina (AlO) nanoparticles and their potential for use as an adsorbent in the removal of methylene blue dye from industrial wastewater.

[This corrects the article DOI: 10.1039/C8NA00014J.].

Synthesis of γ-alumina (AlO) nanoparticles and their potential for use as an adsorbent in the removal of methylene blue dye from industrial wastewater.

Non-toxic nanomaterials have gained significant importance recently in the treatment of industrial wastewater that sometimes contains organic dyes such as methylene blue. We report here an easy approach for the synthesis of γ-alumina (AlO) nanoparticles a method that incorporates the use of formamide and the non-ionic surfactant Tween-80. Together, formamide and Tween-80 serve as an effective precipitating agent and a convenient synthetic template, respectively, in directing the growth of the alumina nanoparticles.

An Overview of the Potential Therapeutic Applications of CO-Releasing Molecules.

Carbon monoxide (CO) has long been known as the "silent killer" owing to its ability to form carboxyhemoglobin-the main cause of CO poisoning in humans. Its role as an endogenous neurotransmitter, however, was suggested in the early 1990s. Since then, the biological activity of CO has been widely examined via both the direct administration of CO and in the form of so-called "carbon monoxide releasing molecules (CORMs).

Synthesis, spectroscopic investigation, and DFT study of N,N'-disubstituted ferrocene-based thiourea complexes as potent anticancer agents.

In the present work, the synthesis, characterization (FT-IR, multinuclear (H and C) NMR, AAS, Raman, and elemental analyses), DNA binding (cyclic voltammetry, UV-Vis spectroscopy), and in vitro biological screening of nine new ferrocene-incorporated thioureas (A1-A9) are reported. Furthermore, the single-crystal X-ray structure of compound A8 was also determined. The ferrocene-based N,N'-disubstituted thioureas were derived by allowing the ferrocenyl anilines to react with freshly prepared isothiocyanates under a N atmosphere in dry acetone.

Facile synthesis of fluoro, methoxy, and methyl substituted ferrocene-based urea complexes as potential therapeutic agents.

In the present work, the synthesis, characterization (FT-IR, multinuclear (H and C) NMR, AAS, Raman, and elemental analysis), DNA binding (cyclic voltammetry, UV-Vis spectroscopy and viscometry), and in vitro biological assessment of nine new ferrocene-based ureas are reported. The desulphurization of ferrocenyl thioureas to the corresponding oxo analogues using aqueous sodium hydroxide and mercuric chloride led to the ferrocenyl ureas (F1-F9) in high yields. The DNA binding studies performed by cyclic voltammetry and UV-Vis spectroscopy produced results that are in close agreement with one another for the binding constants (K) and an electrostatic mode of interaction was observed.

Cellulose derivatives modified by sodium tellurate and a chromium(III) tellurate complex.

A novel cellulose (Cell) derivative, sodium-tellurato (Cell-TeO(OH)4(ONa)/Cell-Cl), has been synthesized from the reaction of 6-chloro-6-deoxycellulose (Cell-Cl) with telluric acid in the presence of sodium hydroxide. The subsequent reaction of this polymeric material with chromium(III) in aqueous solution yields the [Cr(Cell-TeO3(OH)3/Cell-Cl)(Cell-TeO2(OH)4/Cell-Cl)(H2O)3] complex. The molecular structures and morphology of the new polymer and the Cr(III) complex have been examined using elemental analysis, solid-state (13)C NMR, UV-vis, XRD and FTIR spectroscopy, and SEM-EDX, TGA and magnetic measurements.

Ferrocene-Based Bioactive Bimetallic Thiourea Complexes: Synthesis and Spectroscopic Studies.

Bioactive 1,1'-(4,4'-di-ferrocenyl)di-phenyl thiourea and various metal complexes of this ligand have been successfully synthesized and characterized by using physicoanalytical techniques such as FT-IR and multinuclear ((1)H and (13)C) NMR spectroscopy along with melting point and elemental analyses. The interaction of the synthesized compounds with DNA has been investigated by using cyclic voltammetric and viscometric measurements. The intercalation of the complexes into the double helix structure of DNA is presumably occurring.

Infrared and Raman spectroscopic characterization of some organic substituted hybrid silicas.

Nine hybrid silicas bearing the organic substituent groups methyl, octyl, octadecyl, vinyl, phenyl, mercaptopropyl, isocyanatopropyl, chloropropyl and glycidoxypropyl were synthesized by an acid-catalyzed, hydrolytic sol-gel process. The resulting solid materials were characterized by their absorbance and attenuated total reflection (ATR) IR and Raman spectra. The latter technique proved to be particularly useful in the identification of the organic moieties in the hybrid silicas.

Pressure-tuning micro-Raman spectra of artists' pigments: α- and β-copper phthalocyanine polymorphs.

The two polymorphs of copper phthalocyanine, α- and β-CuPc, have been examined by micro-Raman spectroscopy at pressures approaching 5.0 GPa. The metastable α-polymorph does not exhibit any structural changes, while the more thermodynamically stable β-polymorph does exhibit a reversible phase transition at 2.

Determination of the network structure of sensor materials prepared by three different sol-gel routes using Fourier transform infrared spectroscopy (FT-IR).

Solid acid-base sensor materials were prepared by encapsulating three pH indicators (alizarin red, brilliant yellow, and acridine) within a silica matrix using a sol-gel approach through three different routes: (1) non-hydrolytic, (2) acid-catalyzed, and (3) base-catalyzed. Raman and Fourier transform infrared spectroscopies were used to evaluate the silica-indicator interactions. Because vibrational bands assigned to functional groups present in the indicator molecules were not detected, the main silica stretching mode νSi-O between approximately 1300 and 1000 cm(-1) was used to detect the presence of our indicators within the silica matrix.

Pressure-tuning infrared and Raman microscopy study of the DNA bases: adenine, guanine, cytosine, and thymine.

Diamond-anvil cell, pressure-tuning infrared (IR), and Raman microspectroscopic measurements have been undertaken to examine the effects of high pressures up to about 45 kbar on the vibrational spectra of the four DNA bases, adenine, cytosine, guanine, and thymine. Small structural changes were evident for all the four bases, viz., for adenine and cytosine at 28-31 kbar; for guanine at 16-19 kbar; and for thymine at 25-26 kbar.

High-pressure resonance Raman spectroscopic study of ultramarine blue pigment.

The resonance Raman spectrum of ultramarine has been studied as a function of pressure up to 5 GPa. The overtone progressions of the ν(1) fundamental and the combination bands of S(3)(-) and the ν(1) band of S(2)(-) were measured and the pressure dependences were determined. The symmetric stretching mode of S(3)(-) is nearly harmonic.

Azobenzene photoisomerization under high external pressures: testing the strength of a light-activated molecular muscle.

The photoinduced isomerization and thermal back relaxation of an azobenzene-functionalized polymer poly(disperse red 1 acrylate) were investigated at increasing external pressures up to 1.5 GPa inside a diamond-anvil spectroscopic cell. The thermal cis-trans isomerization was monitored by laser pump-probe spectroscopy, which demonstrated an increase in the half-life of the isomerization process with increasing pressure.

Raman, FTIR, photoacoustic-infrared, and inelastic neutron scattering spectra of ternary metal hydride salts A2MH5, (A = Ca, Sr, Eu; M = Ir, Rh) and their deuterides.

The vibrational spectra of the ternary metal hydride (deuteride) salts, A(2)MH(5) and A(2)MD(5), where A = calcium, strontium and europium and M = iridium(I) and rhodium(I), have been assigned using Raman, Fourier transform infrared, photoacoustic infrared, and inelastic neutron scattering spectroscopies and density functional theory (DFT) calculations. The wavenumbers of the infrared-active stretching vibrations depend upon the ionization energies of the central metal atom and the cation. The phase transition in calcium pentahydridoiridate(I) was studied as a function of temperature and pressure.

Synthesis, characterization and anticancer studies of mixed ligand dithiocarbamate palladium(II) complexes.

Six mixed ligand dithiocarbamate Pd(II) complexes (1-6) of general formula [(DT)Pd(PR(3))Cl], where DT = dimethyldithiocarbamate (1, 5), diethyldithiocarbamate (2, 3), dicyclohexyldithiocarbamate (4), bis(2-methoxyethyl)dithiocarbamate (6); PR(3) = benzyldiphenylphosphine (1), diphenyl-2-methoxyphenylphosphine (2), diphenyl-p-tolylphosphine (3), diphenyl-m-tolylphosphine (4), tricyclohexylphosphine (5), diphenyl-2-pyridylphosphine (6) have been synthesized and characterised using Elemental analysis, FT-IR, Raman and multinuclear magnetic resonance (NMR) spectroscopy. Compounds 1 and 2 were also characterized by single crystal X-ray diffraction technique (XRD). The XRD study reveals that the Pd(II) moiety has a pseudo square-planar geometry, in which two positions are occupied by the dithiocarbamate ligand in a bidentate fashion, while at the remaining two positions organophosphine and chloride are present.

Preparation, characterization and pH-metric measurements of 4-hydroxysalicylidenechitosan Schiff-base complexes of Fe(III), Co(II), Ni(II), Cu(II), Zn(II), Ru(III), Rh(III), Pd(II) and Au(III).

The 4-hydroxysalicylidenechitosan Schiff-base (2CS-Hdhba) was prepared by the condensation of 2,4-dihydroxybenzaldehyde with chitosan, and its metal complexes, [M(2CS-dhba)Cl(2)(H(2)O)(2)] (M(III)=Fe, Ru, Rh), [M'(2CS-dhba)(AcO)(H(2)O)(2)] (M'(II)=Co, Ni, Cu, Zn), [Pd(2CS-dhba)Cl(H(2)O)] and [Au(2CS-dhba)Cl(2)], are reported. These complexes were characterized by elemental analysis, by spectral data (FTIR, solid-phase (13)C NMR, UV-vis and ESR spectroscopy), by morphological observations (SEM and XRD), and by magnetic and thermal measurements. The Schiff base (2CS-Hdhba) behaves as a bidentate chelate with a single negative charge.

Application of photoacoustic infrared spectroscopy in the forensic analysis of artists' inorganic pigments.

Fourier-transform photoacoustic infrared (PAIR) spectroscopy has been used in the analysis of 12 inorganic pigments commonly in use by artists today, viz., cobalt blue, ultramarine blue, Prussian blue, azurite, malachite, chromium oxide, viridian, cadmium yellow, chrome yellow, iron oxide, yellow ochre and Mars orange. The authenticity of these 12 commercial pigments was first established by recording their Raman spectra.

Antineoplastic Activity of New Transition Metal Complexes of 6-Methylpyridine-2-carbaldehyde-N(4)-ethylthiosemicarbazone: X-Ray Crystal Structures of [VO(2)(mpETSC)] and [Pt(mpETSC)Cl].

New complexes of dioxovanadium(V), zinc(II), ruthenium(II), palladium(II), and platinum(II) with 6-methylpyridine-2-carbaldehyde-N(4)-ethylthiosemicarbazone (HmpETSC) have been synthesized. The composition of these complexes is discussed on the basis of elemental analyses, IR, Raman, NMR ((1)H, (13)C, and (31)P), and electronic spectral data. The X-ray crystal structures of [VO(2)(mpETSC)] and [Pt(mpETSC)Cl] are also reported.

Synthesis, spectroscopic characterization, X-ray structure and evaluation of binding parameters of new triorganotin(IV) dithiocarboxylates with DNA.

Three new triorganotin(IV) dithiocarboxylates (1-3) with general formula R(3)SnL, where R=C(4)H(9) (1), C(6)H(11) (2), C(6)H(5) (3) and L=4-(4-nitrophenyl)piperazine-1-carbodithioate, have been synthesized and characterized by elemental analysis, Raman, FT-IR, multinuclear NMR ((1)H, (13)C and (119)Sn) and mass spectrometry. The crystal structure of complex 3 confirmed distorted trigonal-bipyramidal geometry around Sn atom. The interaction of compounds 1-3 with DNA was investigated by cyclic voltammetry (CV) and UV-vis spectroscopy.

Synthesis, characterization, and biological studies of organotin(IV) derivatives with o- or p-hydroxybenzoic acids.

Organotin(IV) complexes with o- or p-hydroxybenzoic acids (o-H(2)BZA or p-H(2)BZA) of formulae [R(2)Sn(HL)(2)] (where H(2)L = o-H(2)BZA and R = Me- (1), n-Bu- (2)); [R(3)Sn(HL)] (where H(2)L = o-H(2)BZA and R = n-Bu- (3), Ph- (4) or H(2)L = p-H(2)BZA and R = n-Bu- (5), Ph- (6)) were synthesized by reacting a methanolic solution of di- and triorganotin(IV) compounds with an aqueous solution of the ligand (o-H(2)BZA or p-H(2)BZA) containing equimolar amounts of potassium hydroxide. The complexes were characterized by elemental analysis, FT-IR, Far-IR, TGA-DTA, FT-Raman, Mössbauer spectroscopy, (1)H, (119)Sn-NMR, UV/Vis spectroscopy, and Mass spectroscopy. The X-ray crystal structures of complexes 1 and 2 have also been determined.