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Issue Info: 
  • Year: 

    2001
  • Volume: 

    12
  • Issue: 

    1
  • Pages: 

    27-31
Measures: 
  • Citations: 

    0
  • Views: 

    553
  • Downloads: 

    228
Abstract: 

Thiophosgene and 1-chloroethyl chlorothionoformate react readily with TERTIARY AMINES, and give the dialkylamine hydrochloride after hydrolysis of the initial product with water. Benzyl and allyl groups are cleaved in preference to methyl and other alkyl groups. The rection with the isoquinoline alkaloid narcotine occurs particularly easily.

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Issue Info: 
  • Year: 

    621
  • Volume: 

    10
  • Issue: 

    5
  • Pages: 

    897-905
Measures: 
  • Citations: 

    0
  • Views: 

    100
  • Downloads: 

    0
Abstract: 

A total of 11 new a,a-dioxoketene- N,S -acetals (2a–2k) and two new a,a-dioxoketene- N,N -acetals (3j and 3k) have been synthesised by treating 3-[bis(methylthiol)methylene]pentane-2,4-dione (1) with increasing mole ratios of SECONDARY ALIPHATIC AMINES at room temperature, in either toluene or ethanol. Eight non-cyclic N -methylalkyl and N -ethylalkyl AMINES and the azacyclopentane of pyrrolidine yielded exclusively mono-substituted N,S -acetals (2a–2i), while the azacyclohexanes of piperidine and morpholine yielded the mono-substituted N,S -acetals 2j and 2k and the double-substituted N,N -acetals 3j and 3k. The conversion yields for the reactions in ethanol are considerably higher than those in toluene. Furthermore, the SECONDARY ALIPHATIC AMINES with an N -methylalkyl moiety, which have one primary a-carbon and less steric crowding around the nucleophilic nitrogen, appear to be more reactive towards 1 than those with the N -ethylalkyl group, which have two primary a-carbons; further, the latter AMINES are more reactive than the AMINES with SECONDARY a-carbons.

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Author(s): 

GOWDA SH.K.N. | MAHENDRA K.N.

Issue Info: 
  • Year: 

    2007
  • Volume: 

    16
  • Issue: 

    3 (81)
  • Pages: 

    161-171
Measures: 
  • Citations: 

    0
  • Views: 

    533
  • Downloads: 

    462
Abstract: 

Maleimide modified epoxy compounds were prepared by reacting N-(4-hydroxyphenyl) maleimide (HPM) with diglycidylether of bisphenol-A. Triphenylphosphine was used as a catalyst and methylethylketone as a solvent. The resulting compound possessed both the oxirane ring and maleimide group. The curing reaction of the maleimide-epoxy compound with amine curing agents such as ethylenediamine (EDA), diethylenetriamine (DETA) and triethylenetetramine (TETA) were studied. Incorporation of maleimide groups in the epoxy resin provides cyclic imide structure and high cross-linking density to the cured resins. The cured samples were found to have good thermal stability, chemical (acid/alkali/solvent) and water absorption resistance. The morphology of cured epoxy systems were also studied by scanning electron microscopy (SEM).

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Author(s): 

KEYKHAEI M.R. | SAFARI F.

Issue Info: 
  • Year: 

    2008
  • Volume: 

    19
  • Issue: 

    2
  • Pages: 

    111-117
Measures: 
  • Citations: 

    1
  • Views: 

    469
  • Downloads: 

    183
Abstract: 

The electrochemical coating technique was used for the preparation of a polypyrrole coating on a stainless-steel wire, and applied as a fibre for solid phase microextraction (SPME). The polypyrrole fibre was employed for analyzing four volatile ALIPHATIC AMINES (ethylamine, propylamine, butylamine and pentylamine) in water by headspace SPME using gas chromatography-flame ionization detection (GC-FID). Results showed that this fibre coating is suitable for the successful extraction of the target analytes. The effects of the extraction parameters including exposure time, sampling temperature, salt concentration, and stirring rate on the extraction efficiency was optimized. Relative standard deviations (RSDs) were determined ≤4.3%. The correlation coefficient was satisfactory (r2 > 0.98) for the studied analytes. Detection limits were between 0.9 and 1.6mg.L-1. Good recoveries (99-106 %) were obtained when spiked water and wastewater samples were analyzed

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Issue Info: 
  • Year: 

    2000
  • Volume: 

    19
  • Issue: 

    1
  • Pages: 

    24-28
Measures: 
  • Citations: 

    0
  • Views: 

    317
  • Downloads: 

    0
Abstract: 

A phosgene-free synthesis of symmetrical N,N"-disubstituted ureas by the reaction of aromatic and ALIPHATIC primary AMINES and urea promoted by microwave irradiation in the presence of a suitable energy-transfer solvent such as N,N-dimethylacetamide is described.

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Issue Info: 
  • Year: 

    2024
  • Volume: 

    11
  • Issue: 

    3
  • Pages: 

    160-166
Measures: 
  • Citations: 

    0
  • Views: 

    9
  • Downloads: 

    0
Abstract: 

Objectives: This study aims to conduct a quantitative risk analysis and evaluate control measures for workplace exposure to ALIPHATIC AMINES, focusing on a case study in the foundry sector.Methods: The study comprised four main phases: risk analysis, determination of weight coefficients for reducing exposure probability, uncertainty analysis, and evaluation of implemented risk control measures. During the risk analysis phase, air samples were collected and analyzed to identify the presence of ALIPHATIC AMINES and assess associated risk levels. Weight coefficients for reducing exposure probability were established using the Full Consistency Method (FUCOM), where a panel of experts ranked workplace, administrative, and individual controls. Uncertainty analysis utilized the Monte Carlo (MC) method to generate triangular distributions for the weight coefficients, enabling a comprehensive evaluation of potential uncertainties.Results: Environmental monitoring in the industry revealed the presence of five ALIPHATIC AMINES, with specific units (B and C) showing exposure risks to tri-ethylamine above the adjusted TLV. Additionally, the risk of exposure to mixed ALIPHATIC AMINES was significant across all units. Deterministic weighting using the FUCOM method allocated the highest importance (0.66) to workplace controls for reducing risk probability. Uncertainty analysis using MC adjusted the weighted coefficients to 0.78 for workplace controls, 0.18 for administrative controls, and 0.13 for individual controls, with confidence levels of 85-95%. Evaluation of implemented controls in the industry indicated specific effectiveness across different control levels, with experts estimating risk reduction levels of 10.4% for individual controls, 9% for administrative controls, and 7.8% for workplace controls.Conclusion: These findings highlight the critical importance of implementing and evaluating control measures for workplace exposure to ALIPHATIC AMINES in the studied industry.

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Author(s): 

Issue Info: 
  • Year: 

    2021
  • Volume: 

    403
  • Issue: 

    -
  • Pages: 

    123657-123657
Measures: 
  • Citations: 

    1
  • Views: 

    15
  • Downloads: 

    0
Keywords: 
Abstract: 

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Author(s): 

Nazari Mohadese

Issue Info: 
  • Year: 

    2023
  • Volume: 

    5
  • Issue: 

    4
  • Pages: 

    394-415
Measures: 
  • Citations: 

    0
  • Views: 

    16
  • Downloads: 

    23
Abstract: 

SAPO-34 has emerged as a highly versatile and valuable substance with exceptional capabilities across a wide range of industries, including the production of light olefins. Its high pore volume, excellent shape selectivity, suitable acidity, and superior hydrothermal stability make it a highly sought-after material. AMINES, as structure-directing agents, play a vital role in the synthesis of SAPO-34. A diverse array of AMINES have been proposed for the synthesis of SAPO-34, each with a different templating behavior that can significantly impact the physiochemical properties of the resulting material. This review comprehensively investigates the templating behavior of AMINES based on pivotal factors such as size, shape, alkalinity, polarity, volatility, and environmental friendliness. This article provides a detailed overview of the most popular AMINES used for the SAPO-34 synthesis and exAMINES the effects of the characteristics of each of these AMINES on the properties of synthesized SAPO-34, including crystallinity, purity, acidity, and surface area. This analytical view of the issue can aid in the targeted selection of AMINES for synthesizing SAPO-34 with desired characteristics.

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Issue Info: 
  • Year: 

    2014
  • Volume: 

    20
Measures: 
  • Views: 

    205
  • Downloads: 

    84
Abstract: 

A KINETIC SPECTROPHOTOMETRIC METHOD BASED ON THE REACTION OF 1, 2- NAPHTHOQUINONE-4-SULPHONATE (NQS) WITH AMINES COUPLED WITH MULTIVARIATE CURVE RESOLUTION-ALTERNATING LEAST SQUARES (MCR-ALS) HAS BEEN PROPOSED FOR SIMULTANEOUS DETERMINATION OF ETHYLAMINE, PROPYLAMINE AND BUTYLAMINE. THE MCR-ALS METHODOLOGY ADEQUATELY EXPLOITS THE SECONDORDER ADVANTAGE [1] WHICH ENABLES QUANTITATION OF ANALYTE IN THE PRESENCE OF UNKNOWN AND UNCALIBRATED INTERFERENCES. ETHYLAMINE, PROPYLAMINE AND BUTYLAMINE REACT WITH NQS AT PH 9.5 TO PRODUCE SPECTROPHOTOMETRICALLY DETECTABLE DERIVATIVES. THE DERIVATIVES SHOW SPECTRA WITH CONSIDERABLE OVERLAPPING. THESE AMINES ARE DIFFICULT TO BE DETERMINED ON THE BASIS OF THEIR RESPECTIVE ABSORPTION SPECTRA OF THEIR DERIVATIVES WITH NQS. THEREFORE, DETERMINATION OF THESE THREE ALIPHATIC AMINES HAS BEEN CARRIED OUT DUE TO THE DIFFERENCE BETWEEN THEIR REACTION RATES. QUANTITATIVE DETERMINATION OF AN ANALYTE IN THE MIXTURE IS PERFORMED USING A SYNTHETIC SOLUTION AS STANDARD CONTAINING ONLY THE ANALYTE OF INTEREST. INITIAL ESTIMATES OF CONCENTRATION PROFILES OF DIFFERENT ANALYTE WERE BUILT USING EVOLVING FACTOR ANALYSIS (EFA) APPROACH. MCRALS ALGORITHM WAS APPLIED TO THE EXPERIMENTAL DATA UNDER THE NON-NEGATIVITY, UNIMODALITY AND CLOSURE CONSTRAINTS. THE QUANTITATIVE DETERMINATION OF THESE COMPOUNDS IN DIFFERENT SYNTHETIC MIXTURES AND SOME REAL SAMPLES SUCH AS RIVER WATER, WELL WATER, TAP WATER AND SOIL HAS BEEN PERFORMED AND SATISFACTORY RESULTS HAVE BEEN OBTAINED. USING THE PROPOSED METHOD, ACCURATE QUANTITATION IS POSSIBLE EVEN IN THE PRESENCE OF RANK DEFICIENCY. GOOD RECOVERIES WERE OBTAINED IN THE RANGE OF 88.41-114.96% FOR ALL THE COMPOUNDS.

Yearly Impact:   مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Issue Info: 
  • Year: 

    2014
  • Volume: 

    22
Measures: 
  • Views: 

    165
  • Downloads: 

    113
Abstract: 

ORGANIC AZIDES ARE USEFUL INTERMEDIATES FOR THE SYNTHESISOF NITROGEN-CONTAINING COMPOUNDS.THEY ARE A WELL-STUDIED CLASS OF COMPOUNDS THAT ARE EASILY PREPARED AND TRANSFORMED INTO A VARIETY OF FUNCTIONAL GROUPS (AMINES, TRIAZENES, AZA-YLIDES AND ISOCYANATES), REACTIVE INTERMEDIATES (NITRENES, NITRENIUM IONS) AND NITROGEN-CONTAINING HETEROCYCLES (AZIRINES, AZIRIDINES, TRIAZOLES, TRIAZOLINES AND AZOLES).AZIDES HAVE SEVERAL DEFENSE AND INDUSTRIAL APPLICATIONS, INCLUDING USE AS PROPELLANTS, EXPLOSIVES, POLYMER CROSS LINKERS, RUBBER VULCANIZATION AGENTS, REACTIVE DYES AND BLOWING AGENTS, AND ARE ALSO FOUND IN BIOLOGICALLY AND PHARMACEUTICALLY ACTIVE COMPOUNDS [1].ORGANICAZIDES ARE USED AS EQUIVALENTS OF PRIMARY AMINESAND ARE EMPLOYED IN THE STAUDINGER REACTION. RECENTLY, A 1, 3-DIPOLE REACTION OF ORGANIC AZIDES ANDTERMINAL ALKYNES WASWIDELY USED AS CLICK REACTION.VARIOUS SYNTHETIC METHODS FOR PREPARATION OF ORGANIC AZIDES HAVE BEEN DEVELOPED. AMONG THEM, THE NUCLEOPHILIC SUBSTITUTION OF ORGANIC COMPOUNDS HAVING A LEAVING GROUP WITH AN AZIDE ION IS A COMMON METHOD [2]. ONE OF THE METHODS FOR SYNTHESIS OF AZIDES IS THE USE OF VINYL ALCOHOL IN PRESENCE OF TMSN3/BF3.OET2 AND SODIUM AZIDE [3] AND USE OF CARBOXYLIC ACIDS USING PH2PCL2/I2 AND SODUMAZIDE [4]. IN THIS WORK, INITIALLY, WE HAVE CONVERTED PRIMARY AMINES TO DIAZONIUM SALTS USING NANO2 AND P2O5/SAWDUST. THEN DIAZONIUM SALTS WERE REACTED WITH SODIUM AZIDE FOR PREPARATION OF ARYL OR ALKYL AZIDES AT ROOM TEMPERATURE.

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