Search results for "Amine gas treating"

showing 10 items of 252 documents

Core–shell-type multiarm star polyethylenimine-block-poly(ɛ-caprolactone): Synthesis and guest encapsulation potential

2006

Novel multiarm star copolymers with poly(e-caprolactone) (PCL) as the arms and hyperbranched polyethylenimine (HPEI) as the core have been successfully prepared by the tin(II) 2-ethylhexanoate catalyzed ring-opening polymerization of e-caprolactone (CL) with HPEI used directly as a macroinitiator. Not only primary but also secondary amine groups of HPEI participate in initiating the ring-opening polymerization of CL with almost 100% initiation efficiency. The average degree of polymerization of the PCL arms can be controlled by the feed ratio of the monomers to the initiating sites. Because of the polarity difference of the PCL arms and HPEI core, the obtained multiarm star polymers display…

PolyethyleniminePolymers and PlasticsOrganic ChemistryDegree of polymerizationRing-opening polymerizationchemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerAmine gas treatingCaprolactoneJournal of Polymer Science Part A: Polymer Chemistry
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Production and physicochemical characterization of a new amine derivative of gellan gum and rheological study of derived hydrogels

2020

The production of an amine derivative of gellan gum, named GG-EDA, was here obtained by functionalizing the polysaccharide backbone with pendant ethylenediamine moieties. The obtained derivative was characterized by spectroscopic, colorimetric, chromatographic and rheological analyses to study the effect of the free amino groups on the physicochemical properties of the macromolecule. A titration experiment was conducted to study the acid-base dissociation constants in aqueous media for the carboxylic and amino groups in the GG-EDA and to shed light on the possibility that the derivative shows a polyampholyte structure under physiological conditions. The rheological analysis conducted on bot…

Polymers and PlasticsEthylenediamine02 engineering and technology010402 general chemistryPolysaccharide01 natural sciencesBiomedical deviceGellan gumPolyampholyte polymerschemistry.chemical_compoundBiomedical devicesMaterials ChemistryOrganic chemistryAmine derivatized gellan gumchemistry.chemical_classificationOrganic ChemistryHydrogels021001 nanoscience & nanotechnologyGellan gum0104 chemical sciencesHydrogelchemistrySelf-healing hydrogelsAmine gas treatingTitrationPOLYMERS0210 nano-technologyDerivative (chemistry)MacromoleculeCarbohydrate Polymers
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L -lysine and EDTA polymer mimics as resins for the quantitative and reversible removal of heavy metal ion water pollutants

2012

Traditional precipitation methods for inorganic micropollutant removal from waters are increasingly being replaced by sorption methods based on both natural and synthetic materials. In this context, two novel effective heavy metal ions absorbers are presented. These resins, LYMA and LMT85, were crosslinked poly(amidoamine)s carrying amine and carboxyl groups in their repeating units. In particular, the LYMA-repeating unit contains one carboxyl and two amine groups and is a mimic of L-lysine, whereas LMT85 contains two amine and five carboxyl groups and is a mimic of EDTA. Both resins were prepared at moderate cost by simple eco-friendly procedures. The heavy metal ion set adopted as benchma…

Polymers and PlasticsMetal ions in aqueous solutionInorganic chemistryAmidoamineContext (language use)Metalchemistry.chemical_compoundmetal-polymer complexePolymer chemistryMaterials Chemistrypoly(amidoamine)Materials Chemistry2506 Metals and AlloylysinePolymers and PlasticPrecipitation (chemistry)ChemistryOrganic ChemistryEDTAselective complexationSorptionheavy metalvisual_artvisual_art.visual_art_mediumresinAmine gas treatingpollutantAbsorption (chemistry)hydrogel
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Atom transfer radical polymerization with different halides (F, Cl, Br, and I): Is the process "living" in the presence of fluorinated initiators?

2016

Atom transfer radical polymerization (ATRP) is often used for grafting from fluorinated polymers. Nevertheless, the possibility to initiate an ATRP from a C-F functionality and the activity of the catalysts in the presence of fluoride anions are essentially unexplored. Therefore, we investigated the thermodynamics and kinetics of C-F bond activation by ATRP catalysts and compared it with other halide systems. The ATRP equilibrium constant was estimated to be small for the reaction between [CuITPMA]+ and benzyl fluoride (TPMA = tris(2-pyridylmethyl)- amine). However, [CuITPMA] + could react with the more active initiator diethyl fluoromalonate (DEFM). With DEFM as initiator and CuIBr/TPMA as…

Polymers and PlasticsPOLY(VINYLIDENE FLUORIDE) ATRP HALOGEN EXCHANGE FLUORIDE INITIATORSHalide02 engineering and technologyATRP010402 general chemistry01 natural sciencesCatalysisStyreneInorganic Chemistrychemistry.chemical_compoundBenzyl fluoridePolymer chemistryFLUORIDE INITIATORSMaterials ChemistryMethyl acrylateEquilibrium constantMaterials Chemistry2506 Metals and AlloyPolymers and PlasticChemistryAtom-transfer radical-polymerizationOrganic ChemistryHALOGEN EXCHANGESettore ING-IND/27 - Chimica Industriale E Tecnologica021001 nanoscience & nanotechnology0104 chemical sciencesAmine gas treating0210 nano-technologyPOLY(VINYLIDENE FLUORIDE)
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Ultra-small gold nanoclusters assembled on plasma polymer-modified zeolites: a multifunctional nanohybrid with anti-haemorrhagic and anti-inflammator…

2021

Refereed/Peer-reviewed Hemostatic agents are pivotal for managing clinical and traumatic bleeding during emergency and domestic circumstances. Herein, a novel functional hybrid nanocomposite material consisting of plasma polymer-modified zeolite 13X and ultra-small gold nanoclusters (AuNCs) was fabricated as an efficient hemostatic agent. The surface of zeolite 13X was functionalised with amine groups which served as binding sites for carboxylate terminated AuNCs. Protein corona studies revealed the enhanced adsorption of two proteins, namely, coagulation factors and plasminogen as a result of AuNCs immobilization on the zeolite surface. The immune response studies showed that the hybrid na…

PolymersAnti-Inflammatory AgentsProtein CoronaHemorrhagezeolites02 engineering and technology010402 general chemistry01 natural sciencesNanoclustersAdsorptionprotein coronaHumansGeneral Materials ScienceZeoliteHemostatic AgentNanocompositebiologyChemistry021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical scienceshemostatic agentsbiology.proteinZeolitesAmine gas treatingVitronectinGold0210 nano-technology
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Zn-Enhanced Asp-Rich Antimicrobial Peptides N-Terminal Coordination by Zn(II) and Cu(II), Which Distinguishes Cu(II) Binding to Different Peptides

2021

The antimicrobial activity of surfactant-associated anionic peptides (SAAPs), which are isolated from the ovine pulmonary surfactant and are selective against the ovine pathogen Mannheimia haemolytica, is strongly enhanced in the presence of Zn(II) ions. Both calorimetry and ITC measurements show that the unique Asp-only peptide SAAP3 (DDDDDDD) and its analogs SAAP2 (GDDDDDD) and SAAP6 (GADDDDD) have a similar micromolar affinity for Zn(II), which binds to the N-terminal amine and Asp carboxylates in a net entropically-driven process. All three peptides also bind Cu(II) with a net entropically-driven process but with higher affinity than they bind Zn(II) and coordination that involves the N…

Pore Forming Cytotoxic Proteins0301 basic medicineStereochemistryQH301-705.5Metal ions in aqueous solutionAntimicrobial peptidesPeptide010402 general chemistry01 natural sciencesArticleCatalysisInorganic Chemistry03 medical and health scienceschemistry.chemical_compoundthermodynamicsDeprotonationZn(II) and Cu(II) bioinorganic chemistryPulmonary surfactantAmidePhysical and Theoretical ChemistryBiology (General)Mannheimia haemolyticaMolecular BiologyQD1-999Spectroscopychemistry.chemical_classificationOrganic ChemistryElectron Spin Resonance SpectroscopyGeneral Medicine0104 chemical sciencesComputer Science ApplicationsZincChemistry030104 developmental biologyMembranechemistryAmine gas treatingmetal-antimicrobial peptide interactionsPeptidesCopperInternational Journal of Molecular Sciences
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Efficient Synthesis of Multifunctional Chelating Agents Based on Tetraazacycloalkanes

2018

An efficient route has been developed for the synthesis of multifunctional tetraazacycloalkanes (in particular 1,4,7,10-tetraazacyclotridecane) incorporating an aminomethyl pendant arm on the carbon skeleton. Starting from the appropriate C-functionalized bisaminal-protected intermediate, the target macrocycles were easily obtained by means of a step-by-step introduction of the desired functional groups onto the free primary amine group, followed by deprotection of the bisaminal intermediates. This straightforward and versatile synthetic approach paves the way for the design of a new family of multifunctional chelators.

Primary (chemistry)010405 organic chemistryLigandChemistryOrganic ChemistryCarbon skeletonRegioselectivity010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesAmine gas treatingChelationPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Generation of 6,7-Dihydro-5H-1,3,4-thiadiazolo[3,2-a]pyridines — Unexpected Products in the Reaction of 5-Ethylthio-1,3,4-thiadiazole-2-amine and 3-(…

1998

PropiophenonesChemistryOrganic ChemistryAmine gas treatingPhysical and Theoretical ChemistryMedicinal chemistryEuropean Journal of Organic Chemistry
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Synthesis of C3/C1-Substituted Tetrahydroisoquinolines

2015

A broad biological screening of the natural alkaloid N-methylisosalsoline (2) extracted from Hammada scoparia leaves against a panel of human and parasitic proteases revealed an interesting activity profile of 2 towards human 20S proteasome. This outcome suggests that the 1,2,3,4-tetrahydroisoquinoline skeleton may be exploited as a template for the development of novel anticancer agents. In this article, we report the synthesis and chemical characterization of a new series of isosalsoline-type alkaloids (10-11) with variations at N2 and C3 positions with respect to the natural Compound 2, obtained by a synthetic strategy that involves the Bischler-Napieralski cyclization. The substrate for…

Proteases<i>N</i>-methylisosalsolineStereochemistryPharmaceutical SciencenitroalkeneNitroalkene20s proteasomeArticleAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryTetrahydroisoquinolinesN-methylisosalsolineDrug DiscoveryAnimalsHumansParasitesPhysical and Theoretical ChemistryBischler-Napieralski condensationCell ProliferationBischler-Napieralski condensation; N-methylisosalsoline; nitroalkene; proteasome; tetrahydroisoquinolineChemistryTetrahydroisoquinolineAlkaloidOrganic ChemistrySubstrate (chemistry)Hammada scopariaproteasomeChemistry (miscellaneous)Molecular MedicineCattleAmine gas treatingtetrahydroisoquinolinePeptide Hydrolases
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Mechanism of aminocarbene formation by nucleophilic attack on isocyanide ligands in platinum(II)2-pyrazyl and 4-pyridyl complexes

1997

Abstract The reactions of 2-pyrazyl and 4-pyridyl isocyanide complexes [Pt(CNC 6 H 11 )(C 4 H 3 N 2 - C 2 )(dppe)ClO 4 and [Pt(CNC 6 H 11 )(C 5 H 4 N- C 4 ) (dppe)]ClO 4 ( 1 ) with amines involving the formation of aminocarbene derivatives have been studied kinetically in 1,2-dichloroethane by UV—VIS techniques. The kinetics obey the simple second-order rate law rate = k 2 [ 1 ][amine]. Low activation enthalpies and highly negative activation entropies for the k 2 term are observed. A mechanism is proposed involving direct nucleophilic attack of the amine on the isocyanide carbon with concomitant proton transfer from the amine to the isocyanide nitrogen assisted by the heterocyclic nitrogen…

ProtonChemistryLigandIsocyanideOrganic ChemistryKineticschemistry.chemical_elementPhotochemistryBiochemistryMedicinal chemistryNitrogenInorganic Chemistrychemistry.chemical_compoundNucleophileMaterials ChemistryAmine gas treatingPhysical and Theoretical ChemistryPlatinum
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