Search results for "Butane"

showing 10 items of 184 documents

Squaric acid mediated chemoselective PEGylation of proteins: reactivity of single-step-activated α-amino poly(ethylene glycol)s.

2012

The covalent attachment of poly(ethylene glycol) (PEG) to therapeutically active proteins (PEGylation) has become an important method to deal with the pharmacological difficulties of these polypeptides, such as short body-residence times and immunogenicity. However, the derivatives of PEG used for PEGylation lack further functional groups that would allow the addition of targeting or labeling moieties. Squaric acid diethyl ester was used for the chemoselective single-step activation of poly(ethylene glycol)s into the respective ester amides. The resultant selective protein-reactive poly(ethylene glycol)s were investigated with respect to their selectivity towards amino acid residues in bovi…

Magnetic Resonance SpectroscopyLysineSquaric acidCatalysisPolyethylene GlycolsHydrolysischemistry.chemical_compoundDrug Delivery SystemsDrug StabilityPEG ratioOrganic chemistryBovine serum albuminChemoselectivityAmino AcidsbiologyProtein StabilityOrganic ChemistryProteinsSerum Albumin BovineGeneral ChemistryMolecular WeightchemistrySpectrometry Mass Matrix-Assisted Laser Desorption-Ionizationbiology.proteinPEGylationElectrophoresis Polyacrylamide GelEthylene glycolCyclobutanesChemistry (Weinheim an der Bergstrasse, Germany)
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Pillar[5]arene-Diketopyrrolopyrrole Fluorescent Copolymer: A Promising Recognition and Adsorption Material for Adiponitrile by Selective Formation of…

2017

Conjugated pillar[5]arene-diketopyrrolopyrrole copolymer (P1) is synthesized by the copolymerization of a difunctionalized pillar[5]arene and a diketopyrrolopyrrole-based monomer, which shows large extinction coefficients (1.1 × 104 m-1 cm-1 ) at 519 nm and strong emission at 587 nm. P1 exhibits very strong host-guest binding affinity towards adiponitrile but low binding affinity towards 1,4-dihalobutane and 1,4-bis(imidazol-1-yl)butane. Such an enhanced selectivity is first found in the polypseudorotaxane between pillararene and neutral guests in organic solution and is successfully used for the recognition and adsorption of adiponitrile by the formation of a P1-adiponitrile polypseudorota…

Materials scienceRotaxanesPolymers and PlasticsPolymers010405 organic chemistryOrganic ChemistryButaneConjugated systemPillararene010402 general chemistryAdiponitrile01 natural sciencesFluorescence0104 chemical scienceschemistry.chemical_compoundAdsorptionMonomerchemistryNitrilesPolymer chemistryMaterials ChemistryCopolymerAdsorptionMacromolecular Rapid Communications
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Growth of Rhodococcus sp. strain BCP1 on gaseous n-alkanes: New metabolic insights and transcriptional analysis of two soluble di-iron monooxygenase …

2015

none 7 si Rhodococcus sp. strain BCP1 was initially isolated for its ability to grow on gaseous n-alkanes, which act as inducers for the co-metabolic degradation of low-chlorinated compounds. Here, both molecular and metabolic features of BCP1 cells grown on gaseous and short-chain n-alkanes (up to n-heptane) were examined in detail. We show that propane metabolism generated terminal and sub-terminal oxidation products such as 1- and 2-propanol, whereas 1-butanol was the only terminal oxidation product detected from n-butane metabolism. Two gene clusters, prmABCD and smoABCD—coding for Soluble Di-Iron Monooxgenases (SDIMOs) involved in gaseous n-alkanes oxidation—were detected in the BCP1 g…

Microbiology (medical)Gaseous n-alkaneSoluble di-iron monooxygenaseStrain (chemistry)lcsh:QR1-502Monooxygenase gene expressionMetabolismgaseous n-alkanesMonooxygenaseBiologyLyaseRedoxMicrobiologyPrimer extensionlcsh:MicrobiologyChaperoninRhodococcus sp strain BCP1; soluble di-iron monooxygenase; propane and n-butane oxidation; gaseous n-alkanes; monooxygenase gene expressionBiochemistryRhodococcus sp. strain BCP1Rhodococcus sp strain BCP1Propane and n-butane oxidationGeneOriginal Researchpropane and butane oxidation
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(2S,3S)-2-(N,N-dibenzylamino)butane-1,3-diol refined using a multipolar atom model.

2008

The crystal structure of the title compound, C18H23NO2, was determined using the experimental library multipolar atom model. The refinement showed a significant improvement of crystallographic statistical indices when compared with a conventional spherical neutral atom refinement.

Models MolecularBenzylaminesEnergetic neutral atomMolecular Structure010405 organic chemistryChemistryStatistical indexDiolButaneGeneral MedicineCrystal structure010402 general chemistryCrystallography X-Ray01 natural sciencesGeneral Biochemistry Genetics and Molecular Biology3. Good health0104 chemical sciencesCrystallographychemistry.chemical_compound[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM]Chemical SciencesButylene GlycolsComputingMilieux_MISCELLANEOUSAtom modelActa crystallographica. Section C, Crystal structure communications
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Experimental and Theoretical Studies on Magnetic Exchange in Silole-Bridged Diradicals.

2006

International audience; Five bis(tert-butylnitroxide) diradicals connected by a silole [2,5-R2-3,4-diphenylsilole; R = Me3CN(®O.bul.)Z; Z = p-C6H4 (7a), p-C6H4C6H4-p (7b), 1,4-naphthalenediyl (7c), m-C6H4 (7d)] or a thiophene [2,5-R2-thiophene; R = p-Me3CN(®O.bul.)C6H4 (12)] ring as a coupler were studied. Compd. 12 crystallizes in the orthorhombic space group Pna21 with a 20.752(5), b 5.826(5), and c 34.309(5) .ANG.. X-ray crystal structure detn., electronic spectroscopy, variable-temp. EPR spectroscopy, SQUID measurements and DFT computations (UB3LYP/6-31+G*) were used to study the mol. conformations and electronic spin coupling in this series of mols. Whereas compds. 7b, 7c, and 7d are q…

Models MolecularFree RadicalsSiloleCrystal structure010402 general chemistryRing (chemistry)01 natural sciencesDFTCatalysislaw.inventionchemistry.chemical_compoundNitroxide diradicalMagnetic interactionslawComputational chemistryThiopheneAntiferromagnetismOrganosilicon CompoundsSinglet stateTriplet stateElectron paramagnetic resonance010405 organic chemistryChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic ChemistryElectron Spin Resonance SpectroscopyGeneral Chemistry0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryCrystallographyModels ChemicalButanesDiamagnetismEPR spectroscopy
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Experimental and Theoretical Study on the Cycloreversion of a Nucleobase-Derived Azetidine by Photoinduced Electron Transfer.

2018

[EN] Azetidines are interesting compounds in medicine and chemistry as bioactive scaffolds and synthetic intermediates. However, photochemical processes involved in the generation and fate of azetidine-derived radical ions have scarcely been reported. In this context, the photoreduction of this four-membered heterocycle might be relevant in connection with the DNA (6-4) photoproduct obtained from photolyase. Herein, a stable azabipyrimidinic azetidine (AZT(m)), obtained from cycloaddition between thymine and 6-azauracil units, is considered to be an interesting model of the proposed azetidine-like intermediate. Hence, its photoreduction and photo-oxidation are thoroughly investigated throug…

Models MolecularPhotochemistryRadicalAzetidinePyrimidine dimer010402 general chemistryPhotochemistry01 natural sciencesCatalysisPhotoinduced electron transferNucleobaseCyclobutaneElectron transferElectron Transportchemistry.chemical_compoundElectron transferQUIMICA ORGANICAUracilCycloadditionAza CompoundsCycloaddition Reaction010405 organic chemistryOrganic ChemistryGeneral ChemistryRadicalsPhotochemical Processes0104 chemical sciencesThymineDensity functional calculationsPyrimidineschemistryPyrimidine DimersAzetidinesOxidation-ReductionThymineChemistry (Weinheim an der Bergstrasse, Germany)
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Theoretical insight into the intrinsic ultrafast formation of cyclobutane pyrimidine dimers in UV-irradiated DNA: thymine versus cytosine.

2008

The higher formation yields measured in the ultrafast photoinduced formation of cyclobutane thymine dimers (T T) with respect to those of cytosine (C C) are explained, on the basis of ab initio CASPT2 results, by the existence in thymine of more reactive orientations and a less efficient photoreversibility, whereas in cytosine the funnel toward the photolesion becomes competitive with that mediating the internal conversion of the excited-cytosine monomer.

Models MolecularTime FactorsUltraviolet RaysAb initioPyrimidine dimerDNAInternal conversion (chemistry)PhotochemistrySurfaces Coatings and FilmsThymineCyclobutanechemistry.chemical_compoundCytosineMonomerchemistryPyrimidine DimersMaterials ChemistryNucleic Acid ConformationPhysical and Theoretical ChemistryCytosineDNAThymineDNA DamageThe journal of physical chemistry. B
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Direct oxidation of isobutane to methacrolein over V-MCM-41 catalysts

2004

High vanadium content mesoporous vanado-silicates with MCM-41-like structure, obtained by the atrane route, catalyse the direct oxidation of isobutane to methacrolein with 30% selectivity, and a total dehydrogenation (olefin plus methacrolein) selectivity up to 74%.

Olefin fiberInorganic chemistryVanadiumchemistry.chemical_elementMethacroleinGeneral ChemistryCatalysischemistry.chemical_compoundchemistryAtraneMCM-41IsobutaneOrganic chemistryDehydrogenationSelectivityCatalysis Today
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Copper(I) Bromide: An Alternative Emitter for Blue-Colored Flame Pyrotechnics.

2015

Copper(I) bromide was evaluated as an alternative emitter for blue flame pyrotechnic compositions. CuBr and CuCl emission spectra were recorded from a butane torch flame and compared. Cu(BrO3 )2 was synthesized and used in pyrotechnic compositions as an oxidizer and the source for the generation of CuBr species. Pyrotechnic compositions, which contained copper and potassium bromates as oxidizers, were optimized for the generation of blue flames. The experimental data, including emission spectra of the flames, chromaticity coordinates, burning rates, luminous intensities, and sensitivity tests, were analyzed and compared.

Organic ChemistryAnalytical chemistryPyrotechnicschemistry.chemical_elementCopper(I) bromideNanotechnologyButaneGeneral ChemistryCopperCatalysischemistry.chemical_compoundBlue coloredchemistryBromideEmission spectrumChromaticityChemistry (Weinheim an der Bergstrasse, Germany)
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Polymer-supported molybdenyl thioglycolate as oxygen atom transfer reagent

2000

Abstract Oxo-transfer reactions of a variety of substrates in DMF or methanol using polymer-supported molybdenyl thioglycolate (PSMT) have been investigated. The clean oxidation of Me 2 PhP, n -butanethiol or benzoin to yield Me 2 PhPO, disulfide or benzil, respectively, occurs in high yield. In the presence of air or pyridine N-oxide, a catalytic cycle is accomplished which goes on until the completion of the substrate.

Process Chemistry and TechnologySubstrate (chemistry)PhotochemistryCatalysisCatalysischemistry.chemical_compoundchemistryBenzoinReagentYield (chemistry)PyridineBenzilPhysical and Theoretical ChemistryButanethiolJournal of Molecular Catalysis A: Chemical
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