共查询到20条相似文献,搜索用时 31 毫秒
1.
Fangfang Dang Xinwei Wang Guoping Han Yahong Yao 《Monatshefte für Chemie / Chemical Monthly》2009,140(6):615-617
Abstract A 3D metal-organic framework, [C6H3CdN2O4]·NH4, was synthesized solvothermally and structurally characterized by single-crystal X-ray structure determination. This compound
crystallizes in the tetragonal system with the space group P42/nmc. The crystal structure presents a 3D framework and open channels, exhibiting guest-coordination sites at channel walls and
strong fluorescent emission.
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2.
Wael A. El-Sayed Ibrahim F. Nassar Adel A.-H. Abdel-Rahman 《Monatshefte für Chemie / Chemical Monthly》2009,140(4):365-370
Abstract New C-furyl glycosides bearing pyrazolines, isoxazolines, and dihydropyrimidine-2(1H)-thiones were synthesized in order to increase the number of tested compounds screened for antimicrobial activity. The antimicrobial
activity screening showed that the pyrazoline derivatives were the most active compounds.
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3.
Emanuel Makrlík Petr Vaňura Jan Budka 《Monatshefte für Chemie / Chemical Monthly》2009,140(6):583-585
Abstract The stability constant of the dibenzo-18-crown-6·H3O+ cationic complex species dissolved in nitrobenzene saturated with water has been determined from extraction experiments in
the two-phase water–nitrobenzene system and from γ-activity measurements. Various structures of protonated dibenzo-18-crown-6 are discussed.
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4.
M. Dabiri Ali A. Mohammadi Hassan Qaraat 《Monatshefte für Chemie / Chemical Monthly》2009,140(4):401-404
Abstract An efficient and direct procedure for the synthesis of novel spiro[isoindoline-1,2′-quinazoline]-3,4′(3′H)-dione derivatives is described. The process employs a condensation reaction of 2-aminobenzamides and isatins in the presence
of a catalytic amount of KAl(SO4)2.12H2O (alum) in ethanol under reflux.
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5.
Amin Rostami Sadegh Rahmati Ardeshir Khazaei 《Monatshefte für Chemie / Chemical Monthly》2009,140(6):663-667
Abstract Molecular iodine generated in situ from Fe(NO3)3·9H2O/NaI acts as a highly efficient catalyst for tetrahydropyranylation of various alcohols and phenols with 3,4-dihydro-2H-pyran in almost quantitative yields. The reaction occurs rapidly in dichloromethane at room temperature, and use of toxic
molecular iodine is avoided.
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6.
Kamal Amani Mohammad Ali Zolfigol Arash Ghorbani-Choghamarani Maryam Hajjami 《Monatshefte für Chemie / Chemical Monthly》2009,140(1):65-68
Abstract A mild, efficient, and highly selective oxidation method of sulfides to sulfoxides using Fe(NO3)3·9H2O and catalytic amounts of KBr or NaBr in the presence of wet SiO2 (50% w/w) has been developed. A variety of aliphatic and aromatic sulfides were selectively oxidized at room temperature in good to
excellent yields.
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7.
Emanuel Makrlík Ji?í Dybal Petr Vaňura 《Monatshefte für Chemie / Chemical Monthly》2009,286(1):1289-1292
Abstract From extraction experiments in the two-phase water–nitrobenzene system and γ-activity measurements, the stability constant
of protonated tetraethyl p-tert-butylcalix[4]arene tetraacetate in nitrobenzene saturated with water was determined. By using DFT calculations, the most
probable structure of the tetraethyl p-tert-butylcalix[4]arene tetraacetate·H3O+ complex species was derived.
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8.
Abstract One-pot, three-components synthesis of 2,4,6-triarylpyridines and 5-unsubstituted-3,4-dihydropyrimidin-2(1H)-ones was performed under solvent-free conditions using molecular iodine as the catalyst in moderate to good product yields.
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9.
Farough Nasiri Morteza Bidar Bahareh Atashkar 《Monatshefte für Chemie / Chemical Monthly》2009,140(4):463-466
Abstract The reaction between dibenzoylacetylene and enol systems, such as acetylaceton or cyclohexane-1,3-dione in the presence of
triphenylphosphine in THF/H2O, leads to 4-acetyl-3-benzoyl-1-phenyl-1,5-hexanedione and 2-hydroxy-3-(2-oxo-2-phenylethyl)-2-phenyl-3,5,6,7-tetrahydro-1-benzofuran-4(2H)-one. Subsequently, these compounds undergo cyclization and elemination reactions in acidic dichloromethane at room temperature
to produce known highly functionalized furan derivatives.
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10.
Mohammad Rahimizadeh Mehdi Pordel Mehdi Bakavoli Zahra Bakhtiarpoor Ala Orafaie 《Monatshefte für Chemie / Chemical Monthly》2009,140(6):633-638
Abstract New imidazo[4,5-a]acridone derivatives were synthesized from the rearrangement of 3H-imidazo[4′,5′:3,4]benzo[c]isoxazoles. New imidazo[4,5-a]acridines were obtained from the reaction of imidazo[4,5-a]acridones in boiling POCl3. All of these compounds exhibited antimicrobial activities comparable to streptomycin as reference drug.
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11.
Arash Ghorbani-Choghamarani Maryam Hajjami Hamid Goudarziafshar Mohsen Nikoorazm Shadpour Mallakpour Fatemeh Sadeghizadeh Gouhar Azadi 《Monatshefte für Chemie / Chemical Monthly》2009,140(6):607-610
Abstract A simple and efficient catalytic oxidation of urazoles and a bis-urazole to the corresponding triazolinediones by treatment
with Al(NO3)3.9H2O in the presence of a catalytic amount of silica sulfuric acid is described. A good range of urazole derivatives was selectively
oxidized in CH2Cl2 at room temperature in good to excellent yields.
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12.
Maher F. El-Zohry Thanaa A. Mohamed Essam M. Hussein 《Monatshefte für Chemie / Chemical Monthly》2009,140(3):265-272
Abstract 2-Methylbenzimidazole 1 reacted with 3-dicyanomethylidine-1-ethyl-2-oxoindoline 2 in ethyl acetate to afford 1-amino-2-cyano-3,4-dihydro-1′-ethylspiro{benzimidazo[1,2-a]pyridine-3,3′-indolin}-2′-one 6, which was used as a key intermediate in the synthesis of fused spiropolyheterocyclic derivatives of benzimidazopyridopyrimidine
and/or benzimidazonaphthyridine nucleus incorporating an indoline moiety.
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13.
Ruta Lazauskaite Maryte Daskeviciene Vytautas Getautis Juozas V. Grazulevicius 《Monatshefte für Chemie / Chemical Monthly》2009,140(5):565-571
Abstract Photoinitiated cationic polymerizations of various epoxy monomers bearing a carbazole moiety, 9-[3-(allyloxy)-2-(oxiran-2-ylmethoxy)propyl]-9H-carbazole, 9-[3-methoxy-2-(oxiran-2-ylmethoxy)propyl]-9H-carbazole, 9-[2-(oxiran-2-ylmethoxy)ethyl]-9H-carbazole, as well as a composition of 3,6-dibromo-9-(oxiran-2-ylmethyl)-9H-carbazole with 3,4-epoxycyclohexylmethyl 3,4-epoxycyclohexane carboxylate were investigated in bulk using triphenyl carbenium
salts having anions such as BF4
−, SnCl5
−, and SbCl6
−. Dark polymerizations of the carbazolyl monomers in the presence of the initiators are studied. These photoinduced polymerization
reactions give oligomers of degree of polymerization 4-22. The effect of the anion of the photoinitiator and polymerization
time on the polymerization reaction is discussed.
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14.
Marco Rupprich Clemens Decristoforo Barbara Matuszczak 《Monatshefte für Chemie / Chemical Monthly》2009,140(4):405-407
Abstract In contrast to the results presented in a previous report, the direct conversion of alcohols to alkyl fluorides with triphenylphosphine
and potassium fluoride in CCl4/DMF under mild conditions failed.
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15.
Abstract UV–visible spectral observations indicate that the J-aggregation of protonated meso-tetra(4-sulfonatophenyl)porphyrin ([H2TSPP]2+) under acidic conditions is completely inhibited by the π–π counteraction between 1-butyl-pyridinium tetrafluoroborate ([bpy]BF4) and [H2TSPP]2+. The studies also suggest that the intermolecular π–π force is of relative importance for the J-aggregates of [H2TSPP]2+ and the intermolecular electrostatic force for the H-aggregates.
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16.
Maram R. Al-Dweik Jalal A. Zahra Monther A. Khanfar Mustafa M. El-Abadelah Klaus-Peter Zeller Wolfgang Voelter 《Monatshefte für Chemie / Chemical Monthly》2009,140(2):221-228
Abstract A series of ethyl 2-(substituted)-9-cyclopropyl-4-fluoro-6-oxo-1H-imidazo[4,5-h]quinoline-7-carboxylates has been prepared from ethyl 7,8-diamino-1,4-dihydroquinoline-3-carboxylate via thermally induced
reactions with model alkanoic acids or via microwave-assisted cyclocondensation with some arene carboxaldehydes. Acid-catalysed
hydrolysis of the resulting ester derivatives furnished the corresponding imidazoquinoline-7-carboxylic acids. The structures
of these new acid and ester derivatives are based on microanalytical and spectral (IR, MS, and NMR) data.
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17.
Mohammad B. Teimouri Reihaneh Bazhrang 《Monatshefte für Chemie / Chemical Monthly》2009,140(5):513-517
Abstract Protonation of the highly reactive 1:1 intermediate produced in the reaction between alkyl or aryl isocyanides and electron-deficient
acetylenic esters with 3-hydroxy-1H-phenalene-1-one leads to a vinylisonitrilium cation, which undergoes an addition reaction with the conjugate base of the
3-hydroxy-1H-phenalene-1-one to produce biologically interesting dialkyl 10-(alkyl or arylamino)-7-oxo-7H,8H-naphtho[1,8-gh]chromene-8,9-dicarboxylates in moderate to fairly good yields at room temperature.
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18.
K. M. Ibrahim I. M. Gabr G. M. Abu El-Reash R. R. Zaky 《Monatshefte für Chemie / Chemical Monthly》2009,140(6):625-632
Abstract Acetone [N-(3-hydroxy-2-naphthoyl)] hydrazone (H2AHNH) has been prepared and its structure confirmed by elemental analysis and 1H NMR spectroscopy. It has been used to produce diverse complexes with Co(II), Ni(II), Cu(II), Zn(II), Cd(II), and U(VI)O2 ions. The complexes obtained have been investigated by thermal analysis, spectral studies (1H NMR, IR, UV–visible, ESR), and magnetic measurements. IR spectra suggest that H2AHNH acts as a bidentate ligand. The electronic spectra of the complexes and their magnetic moments provide information about
geometries. The ESR spectra give evidence for the proposed structure and the bonding for some Cu(II) complexes. Thermal decomposition
of the Ni(II) and Cu(II) complexes afforded metal oxides as final products. Kinetic data were obtained for each stage of thermal
degradation of some of the complexes using the Coats–Redfern method. The formation of complexes in solution was studied pH-metrically
and the order of their stability constants (log K) was found to be U(VI)O2 > Cu(II) > Zn(II) > Ni(II) > Cd(II) > Co(II). Antimicrobial and eukaryotic DNA studies were carried out.
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19.
Suban K. Sahoo B. K. Kanungo Minati Baral 《Monatshefte für Chemie / Chemical Monthly》2009,140(2):139-145
Abstract The complexation of a tripodal amine-catechol ligand tris((2,3-dihydroxybenzylamino)ethyl)amine (TRENCAT, L) with group-13
metal ions, viz., Al(III), Ga(III), and In(III), were investigated by means of potentiometric titrations and spectrophotometric
measurements in an aqueous medium of 0.1 M KCl at 25 ± 1 °C. The ligand shows the potential to form various monomeric complexes
of the types MLH3, MLH2, MLH, and ML. At low pH, the ligand is coordinated through three more acidic ortho-catecholic O-atoms to give MLH3 species. With the rise in pH, the species MLH3 releases three protons in steps from the meta-catecholic O-atoms to form MLH2, MLH, and ML. The order of stability Ga(III) > Al(III) > In(III) for the species MLH3 and MLH2 is changed into Al(III) > Ga(III) > In(III) for the species MLH and ML. The coordination modes, binding ability, selectivity,
and the change in stability order were explained with the help of experimental evidence, molecular modeling calculations,
and available literature.
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20.
Abolghasem Davoodnia Mehdi Bakavoli Mehdi Soleimany Niloofar Tavakoli-Hoseini 《Monatshefte für Chemie / Chemical Monthly》2009,47(3):355-358
Abstract A new route to the synthesis of 2-arylthieno[2,3-d]pyrimidin-4(3H)-ones has been developed through heterocyclization of 2-amino-4,5-dimethylthiophene-3-carboxamide
with aromatic aldehydes in boiling glacial acetic acid followed by air oxidation. The unoxidized intermediates, 2-aryl-2,3-dihydrothieno[2,3-d]pyrimidin-4(1H)-ones, are isolated when the reactions are carried out either at room temperature or under a nitrogen atmosphere.
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