Search results for "amide"

showing 10 items of 3119 documents

The Instability of Ni{N(SiMe3)2}2: A Fifty Year Old Transition Metal Silylamide Mystery

2015

The characterization of the unstable NiII bis(silylamide) Ni{N(SiMe3)2}2 (1), its THF complex Ni{N(SiMe3)2}2(THF) (2), and the stable bis(pyridine) derivative trans-Ni{N(SiMe3)2}2(py)2 (3), is described. Both 1 and 2 decompose at ca. 25 °C to a tetrameric NiI species, [Ni{N(SiMe3)2}]4 (4), also obtainable from LiN(SiMe3)2 and NiCl2(DME). Experimental and computational data indicate that the instability of 1 is likely due to ease of reduction of NiII to NiI and the stabilization of 4 through dispersion forces. peerReviewed

magneettiset ominaisuudetdispersiovuorovaikutussteeriset vuorovaikutuksetmagnetisminikkelidispersion effectsnikkelikompleksitsilyyliamidiligandisilylamidesteric effects
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Self-Complementary Dimers of Oxalamide-Functionalized Resorcinarene Tetrabenzoxazines

2018

Self‐complementarity is a useful concept in supramolecular chemistry, molecular biology and polymeric systems. Two resorcinarene tetrabenzoxazines decorated with four oxalamide groups were synthesized and characterized. The oxalamide groups possessed self‐complementary hydrogen bonding sites between the carbonyls and amide groups. The self‐complementary nature of the oxalamide groups resulted in self‐included dimeric assemblies. The hydrogen bonding interactions within the tetrabenzoxazines gave rise to the formation of dimers, which were confirmed by single‐crystal X‐ray diffractions analysis and supported by NMR spectroscopy and mass spectrometry. The self‐included dimers were connected b…

massaspektrometriaspectroscopyNoncovalent interactionsobligaatiotspektroskopiaSupramolecular chemistrycarbonylsdimers ; noncovalent interactions ; resorcinarenes ; supramolecular chemistry ; X-ray diffraction010402 general chemistry01 natural sciencesBiochemistryoligomerchemistry.chemical_compounddimersAmidePolymer chemistryNon-covalent interactionsresorcinarenesta116mass spectrometrychemistry.chemical_classificationbondsta114010405 organic chemistryHydrogen bondOrganic ChemistryIntermolecular forceGeneral ChemistryNuclear magnetic resonance spectroscopyPolymerResorcinareneX-ray diffraction0104 chemical sciencesoligomeeriamideschemistryvetyamidithydrogenself-complementaritySupramolecular chemistrykarbonyylitChemistry: An Asian Journal
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Morphology and mechanical properties of nanofilled polymer blends

2009

mechanical propertiepolyethylene/polyamide blends
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Monoclonal antibody TeM 106 reacts with a tonoplast intrinsic protein of 106 kDa from Brassica oleracea L

1995

A monoclonal antibody, designated TeM 106, that recognizes an intrinsic protein from the vacuole membrane (tonoplast) of cauliflower (Brassica oleracea L. var. botrytis) is described. Mice were immunized with a tonoplast fraction that had been purified from differentiating meristematic cells from the cauliflower head. Hybridomas were generated and screened by means of Enzyme Linked Immuno Sorbent Assays for differential reactivity to tonoplast over non-related proteins (bovine serum albumin). One out of 14 reactive murine clones was selected on the basis of its stability, secretory efficiency, and high affinity of the secreted antibodies. TeM 106 is an IgM which was shown by indirect immuno…

medicine.drug_classBlotting WesternFluorescent Antibody TechniqueMannoseEnzyme-Linked Immunosorbent AssayBrassicaVacuoleMonoclonal antibodyEpitopeMicechemistry.chemical_compoundAntigenAntibody SpecificityConcanavalin AmedicineAnimalsElectrophoresis Gel Two-DimensionalBovine serum albuminPlant ProteinsGel electrophoresisbiologyAntibodies MonoclonalMembrane ProteinsSerum Albumin BovineIntracellular MembranesCell BiologyMolecular biologyMolecular WeightKineticsBiochemistrychemistryVacuolesbiology.proteinElectrophoresis Polyacrylamide GelPlant LectinsAntibodyJournal of Cell Science
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Identification and characterization of a monoclonal antibody to the membrane fatty acid binding protein

1992

A monoclonal antibody to the rat liver membrane fatty acid binding protein (MFABP) was prepared by immunizing mice with purified MFABP isolated from solubilized rat liver plasma membrane proteins by oleate-agarose affinity chromatography technique. The monoclonal antibody K15/6 identified a single 40 kDa protein in rat liver plasma membranes with pI values of 8.5, 8.8 and 9.0, which is identical to the authentic MFABP, but clearly distinct from rat mitochondrial GOT. The antibody K15/6 selectively inhibited cellular influx as well as membrane binding of fatty acids, but not of cholesterol or vitamin E. The same antibody was used in immunofluorescence, ELISA and Western blot analysis to dete…

medicine.drug_classBlotting WesternImmunoblottingBiophysicsFluorescent Antibody TechniqueEnzyme-Linked Immunosorbent AssayNerve Tissue ProteinsFatty Acid-Binding ProteinsMonoclonal antibodyBiochemistryFatty acid-binding proteinCell LineMiceEndocrinologyAffinity chromatographymedicineAnimalsHumanschemistry.chemical_classificationMice Inbred BALB CbiologyMembrane transport proteinTumor Suppressor ProteinsBinding proteinCell MembraneFatty AcidsAntibodies MonoclonalFatty acidMolecular biologyNeoplasm ProteinsRatsLiverchemistryMembrane proteinBiochemistrybiology.proteinElectrophoresis Polyacrylamide GelAntibodyCarrier ProteinsFatty Acid-Binding Protein 7Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism
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Theoretical prediction of the photoinduced chemiluminescence of pesticides

2007

Although it is relatively easy to find chemiluminescent (CL) molecules working on the field of direct liquid phase (especially employing strong oxidants), the molecules found as chemiluminescent are normally very weak CL compounds for developing suitable analytical CL-procedures. Therefore, it is mandatory to develop new strategies to enhance in a simple way the native chemiluminescence of such a compounds, and even to increase the number of compounds to be determined by direct chemiluminescence. Photoinduced chemiluminescence (Ph-CL) results in a simple and easily on-line accessible strategy to solve these disadvantages. In the present paper, molecular connectivity, a topological method wh…

medicine.drug_classCarboxamideSulfuric acidOximeAnalytical Chemistrylaw.inventionchemistry.chemical_compoundPotassium permanganatechemistryComputational chemistrylawmedicineOrganic chemistryMoleculePhotodegradationThiocarbamatesChemiluminescenceTalanta
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Rationally designed haptens for highly sensitive monoclonal antibody-based immunoanalysis of fenhexamid.

2018

Immunochemical methods have been consolidated during the last few years as complementary analytical strategies for chemical contaminant and residue determination. However, generation of suitable immunoreagents for small organic molecules demands adequate hapten design. In this study, fenhexamid was considered as a model compound and novel haptens were designed and synthesized in order to evaluate the influence of the linker tethering site on antibody binding properties and immunoassay parameters. Haptens were conceived with the spacer arm at different positions, while the more antigenic aromatic moiety was kept free. The synthesis of these functionalized compounds was accomplished by total …

medicine.drug_classEnzyme-Linked Immunosorbent AssayTandem mass spectrometryQuechersMonoclonal antibody01 natural sciencesBiochemistryAnalytical ChemistryLimit of DetectionElectrochemistrymedicineEnvironmental ChemistrySpectroscopyDetection limitResidue (complex analysis)Chromatographymedicine.diagnostic_test010405 organic chemistryChemistry010401 analytical chemistryAntibodies MonoclonalRepeatabilityAmides0104 chemical sciencesFungicides IndustrialImmunoassayHaptenHaptensThe Analyst
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Reaction of 4-acylaminomethylpyridine N-oxides with phenylbutazone in the presence of acetic anhydride

1987

medicine.drug_classInfraredOrganic ChemistryCarboxamideBiological activityNuclear magnetic resonance spectroscopyAmine oxidechemistry.chemical_compoundAcetic anhydridechemistrymedicinePhenylbutazoneOrganic chemistrymedicine.drugJournal of Heterocyclic Chemistry
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Non-covalent interactions of N-phenyl-1,5-dimethyl-1H-imidazole-4-carboxamide 3-oxide derivatives—a case of intramolecular N-oxide hydrogen bonds

2017

The crystal structures of new N-phenyl-1,5-dimethyl-1H-imidazole-4-carboxamide 3-oxide derivatives are reported. The results of X-ray diffraction showed the existence of intramolecular hydrogen bonding between carboxamide nitrogen donors and N-oxide oxygen acceptors. The use of Quantum Theory of Atoms in Molecules allowed its classification as a strong interaction, with energy about 10 kcal/mol, and of intermediate character between closed shell and shared bonds. Comparison of experimental data and quantum theoretical calculations indicated that a substituent attached to the phenyl ring in the para position influences the strength and geometry of the title hydrogen bonding. Stronger π-elect…

medicine.drug_classLow-barrier hydrogen bondintramolecular hydrogen bondSubstituentCarboxamideN-oxide group010402 general chemistry01 natural scienceschemistry.chemical_compoundComputational chemistrymedicineNon-covalent interactionsHirshfeld surface analysisPhysical and Theoretical Chemistrychemistry.chemical_classification010405 organic chemistryHydrogen bondIntermolecular forceAtoms in moleculesCondensed Matter Physicshydrogen bonding0104 chemical sciencesCrystallographychemistryQTAIMIntramolecular forcesubstituent effectStructural Chemistry
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Stimuli-responsive bile acid-based metallogels forming in aqueous media

2015

Abstract The synthesis and gelation properties of a picolinic acid conjugated bile acid derivative in the presence of metal salts along with the stimuli-responsiveness of the systems are reported. The gels are formed in the presence of Cu 2+ ions in the solvent systems composed of 30–50% of organic solvent (MeOH, acetonitrile, or acetone) in water. The gels respond to various stimuli: they can be formed upon sonication or shaking, and their gel–sol transformation can be triggered by a variety of chemical species. NMR, MS, and SEM techniques are exploited in order to gain a deeper insight on the self-assembled systems.

medicine.drug_classSonicationClinical BiochemistryConjugated systemPicolinic acidBiochemistrystimuli-responsiveBile Acids and Saltschemistry.chemical_compoundpicolinic acidEndocrinologyAcetonemedicineOrganic chemistrybile acidPicolinic AcidsAcetonitrileMolecular Biologyta116PharmacologyMolecular StructureBile acidOrganic Chemistryself-assemblyAmideschemistrySelf-assemblymetallogelGelsCopperDerivative (chemistry)Steroids
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