Facile iterative synthesis, spectral characterization, electron microscopic study and thermogravimetric analysis of phosphorus dendron with bisphenol A at the focal point

A facile iterative synthesis of a phosphorus dendron with bisphenol A at the focal point by following the divergent procedure is described. The phosphorus dendron peripherally functionalized with phenolic OH group has been accomplished in a very versatile simple fashion, using the Schiff condensation and nucleophilic substitution reactions using P(S)Cl₃, P(O)Cl₃, 3-hydroxybenzaldehyde and 3-aminopheno. The structures of intermediate dendrons were confirmed by IR, NMR (¹H, ¹³C and ³¹P), LC-Mass and C, H, N analysis. The structure of the final dendron (5) was confirmed by IR, NMR (¹H, ¹³C and ³¹P), MALDI-TOF-MS, and C, H, N analysis. The thermal stability of the resulting functionalized dendron has been checked by TGA/DTA analysis. The surface topography observed by scanning electronic microscopic study (SEM) gives the reminiscent of the dendritic structure.     

Synthesis of Adenines with a Phosphorus-Containing Group in the 9-Position

Adenine derivatives with a phosphorus-containing substituent on N⁹ have been synthesized, and their structure has been confirmed by ¹H, ¹³C, and ³¹P NMR and IR spectroscopy, X-ray diffraction, MALDI mass spectrometry, and elemental analysis.     

Synthesis and hydrolytic cleavage of tetrazolo[1,5-c]quinazolines

A series of tetrazolo[1,5-c]quinazolines were synthesized by [4 + 1]-cyclocondensation of 4-hydrazinoquinazolines with sodium nitrite with good yields. Peculiarities of this reaction were discussed, namely, the influence of halogen on the reaction yield. Hydrolytic cleavage of tetrazolo[1,5-c]quinozoline cycle was studied in order to obtain 2-(1H-tetrazolo-5-yl)anilines. The structures of the compounds were elucidated by ¹H NMR, ¹³C NMR, infrared, mass spectrometry, and elemental analysis.     

Synthesis and Characterization of Novel N-, S-, O-Substituted P-Chloranil Derivatives

A series of novel N-, S-, and O-substituted p-chloranil derivatives were synthesized from the reactions of p-chloranil (1) and related nucleophiles in sodium carbonate (Na₂CO₃) solution of acetonitrile or in chloroform with Et₃N. The structures of novel compounds were characterized by using microanalysis, Fourier transform–infrared, ¹H NMR, ¹³C NMR, and mass spectrometry.     

Synthesis and characterization of a new platinum(II) complex with L-mimosine

Synthesis and characterization of a new Pt(II)–mimosine complex are described. Elemental, mass spectrometry and thermal analyses for the complex are consistent with the formula [PtCl₂(C₈H₁₀N₂O₄)]·1.5H₂O. ¹³C NMR, ¹⁵N NMR and infrared spectroscopy indicate coordination of the ligand to Pt(II) through the N and O atoms in a square-planar geometry. The final residue after thermal treatment was identified as metallic Pt. The complex is soluble in dimethylsulfoxide.     

Diastereoselective Synthesis of New Dialkylphosphorylhydrazones

A series of 22 dialkylphosphorylydrazones (dialkyl ester, N′-[(1E)-(R₁ phenyl)methylene]-phosphorohydrazidic acid), 20 of them new, along with three new N,N′-bis (diisobutylphosphorylthioamide)diamines (bis-[diisobutyl ester), N-thioxomethylene]-, diamine)phosphora-midic acid, were prepared and characterized by IR, ¹H NMR, ¹³C NMR, ³¹P NMR, and mass spectrometry. The analysis of ¹H NMR, ¹³C NMR, ³¹P NMR, and NOE spectra confirmed the observation of the single diastereoisomer E in the synthesis of dialkylphosphorylydrazones. The results of a molecular modeling study performed in order to investigate the mechanism of the synthesis of dialkylphosphorylydrazones are in agreement with the experimental results, i.e., the favored formation of diastereoisomer E over Z.     

Preparation and characterization of aluminum phthalocyanine acetate, propionate, and benzoate

Aluminum phthalocyanine acetate, propionate and benzoate were prepared by the reaction of hydroxy aluminum phthalocyanine and the corresponding acetic, propionic, and benzoic anhydrides. The reaction products were characterized by ¹H and ¹³C NMR spectroscopy and mass spectrometry. The thermal behavior of the products was determined by thermal analysis of particular samples.     

Design,Synthesis, and Characterization of Some New bis‐thiazoles

The essential idea of the work in this article is mainly dependent on the use of bis‐hydrazonoyl halides for heterocyclic synthesis. The present work describes preparation and characterization of new bis‐thiazoles from reaction of bis‐hydrazonoyl chlorides with thiosemicarbazones. The synthetic Schemes for the final compounds are proposed and discussed. Structures of the final products were elucidated by elemental analyses and Fourier transform infrared, mass spectrometry, ¹H, and ¹³C‐NMR spectra.     

Synthesis of New Dibenzo-tetraaza and Dibenzo-dioxadiaza[14]annulene Derivatives Using 3-Bromo-substituted Vinamidinium Salt

Novel bromo-substituted derivatives of dibenzo-tetraaza and dibenzo-dioxadiaza[14]annulenes B–G were synthesized by a twofold condensation reaction of a symmetrical bromo-substituted vinamidinum salt A with ortho-diamino- and ortho-amino-hydroxyarenes such as 1,2-diaminobenzene, 1,2-diamino-4,5-dimethylbenzene, 2,3-diaminonaphthalene, 1,2-diamino-4-methylbenzene, 2-amino-1-hydroxybnzene, and 2-amino-1-hydroxy-5-methyl-benzene in acetonitrile/acetic acid as reaction medium. The ultraviolet/visible spectral behavior of these [14]annulenes was examined in dimethyl sulfoxide (DMSO). Elemental analysis, infrared, ¹H NMR, ¹³C NMR, and mass spectra confirm the molecular structure of the newly synthesized compounds.     

A facile one‐pot synthesis of [(COD)Pt(CH3)2]

A novel one‐pot synthesis of dimethyl(1,5‐cyclooctadiene)platinum(II), i.e. [(COD)Pt(CH₃)₂] (complex 1), was developed in 92% yield using platinum acetylacetonate, 1,5‐cyclooctadiene and trimethylaluminium. Complex 1 was fully characterized by ¹H and ¹³C NMR, mass spectrometry, cell dimensions and elemental analysis. Copyright © 2005 John Wiley & Sons, Ltd.     

Thermal properties and combustion behaviors of a novel UV-curable flame retarded coating containing silicon and phosphorus

A silicon-based acrylate (SHEA) was synthesized via the reaction between 2-hydroxylethyl acrylate and dimethyldichlorosilane, and characterized by Fourier transform infrared (FTIR), ¹H NMR spectroscopy and ²⁹Si NMR spectroscopy. The SHEA was blended with phosphorus-containing tri(acryloyloxyethyl) phosphate (TAEP) at different ratios to obtain a series of UV-curable flame retarded resins. The final unsaturation conversion of the SHEA films was determined by FTIR. Their combustion behaviors were examined by microscale combustion calorimetry (MCC). The thermal degradations of TAEP/SHEA composites were characterized using thermogravimetric analysis/infrared spectrometry (TG–IR). The MCC results present that the addition of TAEP into SHEA was able to decrease the HRR, HRC, T_max and THC. Among the TAEP/SHEA resins, Si1 (TAEP:SHEA is 1:1) owns the highest initial decomposition temperature and leaves the most char residue at 800 °C. The change of chemical structure during the thermal degradation process was monitored by real-time FTIR analysis to study the condensed-phase flame retarded mechanism.     

Phosphoramides: Synthesis,Spectroscopy, and X‐ray Crystallography

A series of new phosphoramides with general formula RP(O)X₂, where R = amino/p‐methylphenoxy and X = amine, were synthesized and characterized by ¹H, ¹³C, ³¹P nuclear magnetic resonance (NMR), and infrared (IR) spectroscopy and elemental analysis. The ³¹P{¹H} NMR spectra show that among compounds 7–9 containing 2‐, 3‐, and 4‐aminopyridinyl moieties, respectively, the shielding order of the P atom decreases as 7 > 9 > 8 . Also, the structure of compound 7 was determined by X‐ray crystallography. In this structure, repeated noncentrosymmetric dimers are formed by two strong intermolecular N(1)‐H(1N)…N(2) and N(3)‐H(3N)…O(1) hydrogen bonds. Taking into account weak intermolecular C(17)‐H(17C)…N(4), C(17)‐H(17E)…N(4), C(2)‐H(2A)…O(2), and also weak aromatic C—H…C interactions, a three‐dimensional polymeric chain is created in the crystalline network. The density functional theory calculations at B3LYP, B3PW91, and M06 levels using the 6–31+G** basis set were in good agreement with the X‐ray crystallography data.     

Synthesis, characterization, and polymerization of vinylmelamines

Abstract  

Vinyl functionalized melamine derivatives for cross-linking based on polymerization were synthesized as potential substitutes for harmful formaldehyde in melamine resins. Methylmelamines undergo direct vinylation with acetylene to the corresponding vinylmelamines in more than 95% conversion. Their chemical structures were fully characterized by mass spectrometry, Fourier transform infrared (FTIR) spectroscopy, elementary analysis, ¹H, ¹³C, and 2D correlation nuclear magnetic resonance (NMR) experiments. Linear and cross-linked polymers were prepared by free radical polymerization neat and in solution and characterized by size exclusion chromatography (SEC) and matrix-assisted laser desorption ionization time-of-flight (MALDI-ToF) mass spectrometry.     

Preparation, thermal properties, morphology, and microstructure of phosphorus-containing epoxy/SiO2 and polyimide/SiO2 nanocomposites

A phosphorus-containing tri-ethoxysilane (dopo-icteos) reacting from the nucleophilic addition reaction of 9,10-dihydro-9-oxa-10-phosphaphenanthrene 10-oxide (dopo) and 3-(trieoxysilyl) isocyanate (icteos) was synthesized. The structure of dopo-icteos was confirmed by ¹H, ¹³C, ³¹P NMR and IR spectra. A triethylamine catalyzed mechanism for the dopo-icteos synthesis was proposed and verified by NMR spectra. The phosphorus-containing epoxy/SiO₂ and polyimide/SiO₂ nanocomposites were prepared from the in-situ curing of diglycidyl ether of bisphenol A (DGEBA)/4,4-diaminodiphenylmethane(DDM)/dopo-icteos, and imidization of poly(amic acid) of pyromellitic dianhydride (PMDA)/4,4′-oxydianiline (ODA)/dopo-icteos, respectively. The microstructure and morphology were investigated by ²⁹Si NMR, scanning electron microscope (SEM), EDS (Si and P mapping) analysis and atomic force microscope (AFM). The thermal properties, flame retardancy and dielectric properties of the organic-inorganic hybrids were investigated by differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), limiting oxygen index (LOI), thermal gravimetric analysis (TGA) and dielectric analyzer (DEA).     

Synthesis and characterization of alt‐copoly(carbosiloxane)s containing oligodiphenylsiloxane segments

Novel α,ω‐divinyloligodiphenylsiloxanes (1,9‐divinyldecaphenylpentasiloxane, 1,7‐divinyloctaphenyltetrasiloxane, 1,5‐divinylhexaphenyltrisiloxane, and 1,3‐divinyltetraphenyldisiloxane) were prepared and copolymerized by Pt‐catalyzed hydrosilylation with α,ω‐dihydridopentasiloxanes. The molecular weights of the copolymers were measured with gel permeation chromatography, and their thermal properties were characterized with differential scanning calorimetry and thermogravimetric analysis. The polymers had high thermal stability in air and nitrogen. The oligomer and polymer structures were determined with ¹H, ¹³C, ¹⁹F, and ²⁹Si NMR and IR spectrometry. The molecular weights of the oligomers were measured with high‐resolution mass spectrometry. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 2155–2163, 2005     

Design, synthesis, and bioactivity of cyanonitrovinyl neonicotinoids as potential insecticides

Abstract  

A series of cyanonitrovinyl neonicotinoids were designed and synthesized via five steps in about 35% overall yields. All compounds were structurally characterized by ¹H nuclear magnetic resonance (NMR), ¹³C NMR, infrared (IR), and high-resolution mass spectrometry (HRMS), and single-crystal X-ray diffraction analysis of 2-[1-[(6-chloropyridin-3-yl)methyl]-2-imidazolidinylidene]-2-nitroacetonitrile revealed that the double bond is (E)-configured. The preliminary agriculture bioassay indicated that one compound exhibited moderate insecticidal activity against pea aphid.     

1-Silantranyl nitrate

A method of synthesis of 1-silatranyl nitrate O₂NOSi(OCH₂CH₂)₃N based on the reaction of 1-hydrosilatrane with mercury nitrate in the acetonitrile medium was developed. The structure of the synthesized 1-silatranyl nitrate, mp 227°C, was confirmed by elemental analysis, ¹H, ¹³C, and ²⁹Si NMR spectoscopy, infrared spectroscopy, and mass spectrometry. Silatranyl nitrate previously described in the literature as yellowish viscous oil apparently contains impurities preventing its crystallization.     

Synthesis,cytotoxicity and anti‐metastatic properties of new pyridyl–thiazole arene ruthenium(II) complexes

A series of novel ruthenium(II)–cymene complexes ( 1 – 8 ) containing substituted pyridyl–thiazole ligands, [Ru(η⁶‐p‐cymene)(L)Cl]Cl (L = N,N‐chelating derivatives), have been synthesized and characterized using elemental analysis, infrared, ¹H NMR and ¹³C NMR spectroscopies and mass spectrometry. All these complexes not only display marked cytotoxicity in vitro against three different human cancer cell lines (HeLa, A549 and MDA‐MB‐231), but also exhibit promising anti‐metastatic activity at sub‐cytotoxic concentrations. Cell cycle analysis shows that the ruthenium(II) complex‐induced growth inhibition was mainly caused by S‐phase cell cycle arrest. Further protein level analysis suggests that compound 5 may exert antitumor activity via a p53‐independent mechanism.     

Phosphorus Schiff base ligand and its complexes: Experimental and theoretical investigations

A phosphorus-containing Schiff base was prepared from bis{3-[2-(4-amino-1,5-dimethyl-2-phenylpyrazol-3-ylideneamino)ethyl]indol-1-ylmethyl}phosphinic acid and paraformaldehyde as a novel antibacterial compound. The reaction of the Schiff base ligand with VO(IV), Ni(II), Co(II), Cu(II), Zn(II), Cd(II), Hg(II), Pd(II) and Pt(IV) led to binuclear species of metal complexes, depending on the ratio of metal ion and ligand. The ligand and its complexes were investigated using elemental analysis, Fourier transform infrared, ¹H NMR, ¹³C NMR, UV–visible and mass spectra, thermogravimetric analysis, conductivity measurements and thermal analysis. The results showed that the Schiff base behaves as a tetradentate ligand; moreover, on the basis of conductance results, of all the prepared complexes are non-electrolytes, excepting the Pt(IV) complex. The metal complexes were found to be formed with a metal-to-ligand ratio of 2:1, except for the Pt(IV) complex with a ratio of 1:1. The activation thermodynamic parameters (ΔE*, ΔH*, ΔS*, ΔG* and K) and the activation energy of thermal decomposition were determined from thermogravimetric analysis using the Coats–Redfern method. The biological activities of the metal complexes were screened against the growth of bacteria and fungi in vitro to assess the antimicrobial potential and study the toxicity of the compounds. The prepared compounds have noteworthy antimicrobial properties.     

Efficient Protocol for the Synthesis of Novel Spiro[acenaphthylene-1,2′-pyrrolidin]-2-one Compounds

An efficient catalyst-free synthesis of 3′-benzoyl-4′,5′-diphenyl-2H-spiro[acenaphthylene-1,2′-pyrrolidin]-2-one derivatives via one-pot 1,3-dipolar cycloaddition of acenaphthenequinone, arylmethyl amines, and chalcones with high regioselectivity is described. The structure of the cycloadducts were characterized by infrared, high-resolution mass spectrometry (electrospray ionization), ¹H NMR, and ¹³C NMR spectra, and the structure of 4a was confirmed using x-ray single-crystal structure analysis.