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1.
In this report, we described the synthesis and characterization of a variety of diaminotriarylmethane derivatives with dimethylamino
functional groups. These compounds were synthesized by the tandem regio-selective electrophilic aromatic substitution reaction
of N,N-dimethylaniline with aryl aldehydes to form the corresponding diaminotriarylmethane compounds. In our strategy, Bi(NO3)3 was used as a catalyst under solvent free conditions to afford the desired products in good to excellent yields.
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2.
A one-pot multi-component reaction is developed for the efficient synthesis of 4,5-dibenzylidene octahydroacridines in high
yields. The reaction is performed by the tandem reaction of three molar equivalent aromatic aldehydes with two molar equivalent
4-alkylcyclohexanone in the system of NH4OAc/HOAc under microwave irradiation.
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3.
Sandip A. Sadaphal Kiran F. Shelke Swapnil S. Sonar Murlidhar S. Shingare 《Central European Journal of Chemistry》2008,6(4):622-626
1-benzyl-3-methyl imidazolium hydrogen sulphate [bnmim][HSO4] was found to be an effective catalyst for the condensation reaction of indoles and derivatives with benzaldehydes in microwave
irradiation with lower reaction time and higher yields to give bis(indolyl) methanes.
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4.
Phase equilibria established in the PbO - BiVO4 system over the whole component concentration range up to 1000°C have been investigated. A phase diagram has been constructed
using DTA and XRD.
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5.
Petr Bělina Petra Šulcová Miroslav Trojan Pavel Mazurek 《Central European Journal of Chemistry》2007,5(3):706-714
New binary lanthanum-aluminum triphosphates were synthesized by thermal-condensation method from H3PO4, La2O3 and Al(OH)3. These pigments could be potentially used as special inorganic pigments; their corrosion-inhibition properties were widely
studied. Synthesis conditions were determined on the basis of DTA and TG measurements. The products were also characterized
by X-ray diffraction analysis. Physical properties — density by pycnometric method, particle size distribution, oil number
and critical pigment volume concentration (CPVC), pH and specific conductivity of their aqueous extracts were also determined.
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6.
Jinzhang Gao Haifeng Fan Wu Yang Xiangli Sun Chongyang Li Xuefeng Mao Jie Wang Rong Wang Zhengping Jia 《Central European Journal of Chemistry》2008,6(4):617-621
A rapid, simple and reliable capillary electrophoresis method for the separation and quantitation of inorganic cations with
indirect UV detection at 214 nm was developed. The electrolyte was: 12 mM imidazole as background absorbance provider; 5 mM
malic acid and 1.0 mM 18-crown-6 ether as complexing agents; and 20% D2O (v/v) to improve ion mobility. The pH was 4.25. The applied voltage was 22 kV at 22°C. Nine ions were completely separated
and determined with correlation coefficients of 0.9979-0.9992. The relative standard deviations (RSD) were less than 0.5%
for migration time and less than 5.2% for peak area (n=8). The detection limits (S/N=3) were from 0.08 mg L−1 (for Na+) to 0.51 mg L−1 (for Cu2+). To assess the reliability atomic absorption (AA) was also used to determine the same samples. Satisfactory results were
obtained for real samples of jasmine tea drink and coconut milk.
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7.
Nadezhda Rangelova Lachezar Radev Sanchi Nenkova Isabel M. Miranda Salvado Maria H. Vas Fernandes Michael Herzog 《Central European Journal of Chemistry》2011,9(1):112-118
Methylcellulose (MC) / SiO2 organic / inorganic hybrid materials have been prepared from MC and methyltriethoxysilane or ethyltrimethoxysilane, and characterized
by XRD, FTIR and AFM. XRD showed peak shifts. FTIR shows intermolecular hydrogen bonding between MC and SiO2. AFM depicts surface roughness which depends on the silica precursor and MC content.
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8.
Raluca Turdean Elena Bogdan Anamaria Terec Anca Petran Laurian Vlase Ioan Turcu Ion Grosu 《Central European Journal of Chemistry》2009,7(1):111-117
The synthesis of new 3,7-dibromophenothiazine derivatives bearing bromoalkyl, mercaptoalkyl and alkylthioacetate groups on
the N atom at position 10 is reported. The Suzuki coupling reaction of one of these derivatives via the bromine atoms at positions
3 and 7 with bromothiophene derivatives is also discussed.
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9.
D. A. Svechkarev G. V. Karpushina L. L. Lukatskaya A. O. Doroshenko 《Central European Journal of Chemistry》2008,6(3):443-449
Three 2-(benzimidazol-2-yl)-3-hydroxychromone derivatives were synthesized. Their spectroscopic and fluorescent properties,
due to excited state intramolecular proton transfer (ESIPT) from OH to carbonyl, were studied. Theoretical possibility of
an alternative intramolecular H-bonding and experimental evidence for such behavior are discussed.
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10.
Jorge Luis Sague Doimeadios 《Central European Journal of Chemistry》2008,6(4):505-508
Herein, the first example of a co-crystal system formed by an imidazolium nitrate, a carbene precursor, and copper (II) nitrate,
{[Cu(NO3)2(H2O)2]L1(NO3)2} (1) (L1 = 1,1′-dibenzyl-3,3′-butyl-diimidazolium-2,2′-diylidene) is reported. These two building blocks are connected in the solid
state through hydrogen bonds to generate a three-dimensional supramolecular network.
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11.
The reaction mechanism between AlX and HX (X = Br, Cl, and F) have been characterized in detail using DFT as well as the ab initio method. The reaction yielding AlX3 and molecular hydrogen was calculated to be highly exothermic. The present calculations also show that the possible routes
to the trihalides species start more favorable with the primary insertion product AlX2H than with the biadduct AlX(HX)2 one.
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12.
Francis E. Appoh Marcy J. Manning Teri J. Gullon Margaret A. Hansen Emily C. Bevans Krista D. M. Hogan Courtney S. Turner Christopher M. Vogels Andreas Decken Stephen A. Westcott 《Central European Journal of Chemistry》2008,6(3):359-364
The Ugi reaction with formylphenylboronic acid derivatives as the carbonyl component proceeds to give the corresponding boron-containing
dipeptide derivatives (Ugi products) in good yields.
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13.
Tevhide Özkaya Abdulhadi Baykal Muhammet Sadaka Toprak 《Central European Journal of Chemistry》2008,6(3):465-469
Water-soluble Mn3O4 nanocrystals have been prepared through thermal decomposition in a high temperature boiling solvent, 2-pyrrolidone. The final
product was characterized with XRD, SEM, TEM, FTIR and Zeta Potential measurements. Average crystallite size was calculated
as ∼15 nm using XRD peak broadening. TEM analysis revealed spherical nanoparticles with an average diameter of 14±0.4 nm.
FTIR analysis indicated that 2-pyrrolidone coordinates with the Mn3O4 nanocrystals only via O from the carbonyl group, thus confining their growth and protecting their surfaces from interaction
with neighboring particles.
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14.
Noora Kuuloja Tuula Kylmälä Youjun Xu Robert Franzén 《Central European Journal of Chemistry》2008,6(3):390-392
Xenbucin 1, an analgesic drug, was synthesized in 4 steps using two different routes. The biaryl fragment could successfully be produced
via a Pd/C catalysed Suzuki coupling in water using sodium tetraphenylborate as a phenylation reagent. Overall yields of the
routes were 36% and 59%, respectively.
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15.
Dominique R. Duguay Matthew T. Zamora Johanna M. Blacquiere Francis E. Appoh Christopher M. Vogels Susan L. Wheaton Felix J. Baerlocher Andreas Decken Stephen A. Westcott 《Central European Journal of Chemistry》2008,6(4):562-568
The addition of formylphenylboronic acid derivatives to thiourea and ethyl acetoacetate proceeds in the presence of an additional
Lewis acid catalyst to give the corresponding 3,4-dihydropyrimidin-2(1H)-(thio)ones (Biginelli products) in moderate yield.
Compounds were tested for antifungal activity against pure cultures of Aspergillus niger, Aspergillus flavus, Candida albicans and Saccharomyces cerevisiae but, unfortunately, none showed any appreciable activity.
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16.
Afaf R. Genady Mohamed E. El-Zaria Detlef Gabel 《Central European Journal of Chemistry》2008,6(2):154-160
Derivatives of purine, adenine, guanine, and 2,6-diaminopurine linked to the azanonaborane (B8N cluster) have been prepared, for possible use as powerful agents for boron neutron capture therapy (BNCT). The synthesis
was carried out via a ligand exchange reaction. The exo-NH2R group of the azanonaborane of the type [(RH2N)B8H11NHR] can be exchanged by one hetero-nitrogen atom of the pyrimidine ring, and except for guanine, also by an N atom of the
imidazole ring. The identity of the products was confirmed by NMR, elemental analysis, IR, and mass spectrometry. No reaction
was found to occur with caffeine and theophylline under the same reaction conditions.
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17.
The relative enthalpies of melts in the system KF - K2NbF7 were measured by drop-calorimetry at the temperatures 1058, 1140 and 1208 K as a function of composition. Heat capacities
of melted mixtures and enthalpies of mixing were determined using the experimental data. The molar heat capacity of melts
diverges slightly from additivity. The molar enthalpy of mixing of melts shows small negative deviation from ideality which
decreases with decreasing temperature. The thermal effect at mixing was assigned predominantly to association reactions producing
more complex fluoroniobate anions.
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18.
Fluorescence spectroscopy and circular dichroism (CD) spectroscopy were used to investigate the interaction of coumarin-3-carboxylic
acid with human serum albumin (HSA) and bovine serum albumin (BSA) under physiological conditions in a buffer solution of
pH 7.4.
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19.
Ghasem Rezanejade Bardajee Farnaz Jafarpour Hamid Samareh Afsari 《Central European Journal of Chemistry》2010,8(2):370-374
In this report, a rapid, efficient and environmental friendly synthesis of 3-carboxycoumarins under ultrasound irradiation
in water media is described. The Knoevenagel condensation of Meldrum’s acid with substituted benzaldehydes in the presence
of zirconium oxide chloride (ZrOCl2·8H2O) and ultrasonic irradiation in water gave the corresponding 3-carboxycoumarins in good to excellent yields.
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20.
Alexander O. Terent’ev Igor B. Krylov Vera A. Vil’ Zhanna Yu. Pastukhova Sergey A. Fastov Gennady I. Nikishin 《Central European Journal of Chemistry》2012,10(2):360-367
It was found that oximes undergo deoximation in the presence of the H2O2aq-HBraq system to form ketones and bromo ketones. This reaction provided the basis for the synthesis of dibromo ketones in yields
varying from 40% to 94%. This method is environmentally friendly, sustainable, and easy to perform. The results of this investigation
extend the potential of the use of oximes for the protection of carbonyl group, thus offering the ability to perform not only
conventional deoximation but also the subsequent bromination of ketones. The reaction is easily scaled up and dibromo ketones
can be prepared in gram amounts.
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