Search results for "Organische Chemie"

showing 10 items of 24 documents

Sensitive Assays by Nucleophile-Induced Rearrangement of Photoactivated Diarylethenes.

2018

Upon light-induced isomerization, diarylethenes (DAEs) equipped with reactive aldehyde moieties rearrange selectively in the presence of amines, accompanied by decoloration. In a comprehensive study, the probe structure was optimized with regard to its inherent reactivity in the nucleophile-triggered rearrangement reaction. Detailed structure−reactivity relationships could be derived, in particular with regard to the type of integrated (het)aryl moieties as well as the location of the formyl residue, and the probes’ intrinsic reactivity with primary and secondary amines was optimized. Utilizing an ancillary base, the initially formed rearrangement product can engage in a subsequent catalyti…

010402 general chemistry01 natural sciencesBiochemistryAldehydeCatalysischemistry.chemical_compoundPhotochromismColloid and Surface ChemistryNucleophile541 Physikalische ChemieReactivity (chemistry)Rearrangement reactionsensingchemistry.chemical_classification010405 organic chemistryArylGeneral ChemistryphotochromismCombinatorial chemistry0104 chemical sciences540 Chemie und zugeordnete WissenschaftenaminechemistryCatalytic cycleddc:540diaryletheneddc:541547 Organische ChemieIsomerizationddc:547Journal of the American Chemical Society
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Cycloaddition of Strained Cyclic Alkenes and Ortho-Quinones : A Distortion/Interaction Analysis

2020

The chemistry of strained unsaturated cyclic compounds has experienced remarkable growth in recent years via the development of metal–free click reactions. Among these reactions, the cycloaddition of cyclopropenes and their analogues to ortho-quinones has been established as a highly promising click reaction. The present work investigates the mechanism involved in the cycloaddition of strained dienes to ortho-quinones and structural factors that would influence this reaction. For this purpose, we use B97D density functional theory calculations throughout, and for relevant cases, we use spin component–scaled MP2 calculations and single–point domain-based local pair natural orbital coupled cl…

010405 organic chemistryChemistryOrganic ChemistryInteraction model010402 general chemistry01 natural sciencesOrganische ChemieArticleCycloaddition0104 chemical sciencesCyclic AlkenesCoupled clusterCompostos orgànicsComputational chemistryDistortionClick chemistryLife ScienceDensity functional theorySpin (physics)Química orgànicaVLAG
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Covariation and phenotypic integration in chemical communication displays: biosynthetic constraints and eco-evolutionary implications

2018

Chemical communication is ubiquitous. The identification of conserved structural elements in visual and acoustic communication is well established, but comparable information on chemical communication displays (CCDs) is lacking. We assessed the phenotypic integration of CCDs in a meta‐analysis to characterize patterns of covariation in CCDs and identified functional or biosynthetically constrained modules. Poorly integrated plant CCDs (i.e. low covariation between scent compounds) support the notion that plants often utilize one or few key compounds to repel antagonists or to attract pollinators and enemies of herbivores. Animal CCDs (mostly insect pheromones) were usually more integrated t…

0106 biological sciences0301 basic medicineEco evolutionaryanalysisPhysiologyPlant ScienceAnimal Breeding and GenomicsBiologyfloral scentsChemical communicationFloral scentsphenotypic integration010603 evolutionary biology01 natural sciencesChemical communication03 medical and health sciencesPhenotypic integrationbiosynthetic constraintsFokkerij en Genomicavegetative scentsLaboratory of Entomologycorrelation networkEcologyOrganic Chemistrychemical communicationPhenotypic integrationInsect pheromonesPE&RCLaboratorium voor Entomologiecorrelation network analysisOrganische ChemieCorrelation network analysisBiosynthetic constraints030104 developmental biologyEvolutionary biologyinternationalFloral scentIdentification (biology)EPSVegetative scentsNew Phytologist
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Symbiotic polydnavirus and venom reveal parasitoid to its hyperparasitoids

2018

Symbiotic relationships benefit organisms in utilization of new niches. In parasitoid wasps, symbiotic viruses and venom that are injected together with wasp eggs into the host caterpillar suppress immune responses of the host and enhance parasitoid survival. We found that the virus also has negative effects on offspring survival when placing these interactions in a community context. The virus and venom drive a chain of interactions that includes the herbivore and its food plant and attracts the hyperparasitoid enemies of the parasitoid. Our results shed new light on the importance of symbionts associated with their host in driving ecological interactions and highlight the intricacy of how…

0106 biological sciences0301 basic medicineWasps01 natural sciencesMultitrophic interactionParasitoidHerbivore-induced plant volatilesGene Expression Regulation PlantLaboratory of EntomologyTrophic levelPlant-mediatedLarvaMultidisciplinarybiologyPolydnavirusHerbivore-induced plant volatilePlantsBiological SciencesWaspPE&RCOrganische ChemieBiosystematiekInteraction networkinternationalLarvaSymbiosiButterfliesZoology010603 evolutionary biologyHost-Parasite Interactions03 medical and health sciencesMultitrophic interactionsSymbiosisButterflieAnimalsSymbiosisCaterpillarSalivaEcosystemHerbivoreParasitic waspVenomsHost (biology)AnimalOrganic ChemistryfungiPlantLaboratorium voor Entomologiebiology.organism_classificationVenom030104 developmental biologySettore AGR/11 - Entomologia Generale E ApplicataPolydnaviridaeHerbivoreBiosystematicsEPS
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Organiskās ķīmijas programma: Medicīnas, veterinārmedicīnas un matemātikas un dabaszinātņu fakultātēm

1942

Bez titullapas un vāka.

:NATURAL SCIENCES::Chemistry::Organic chemistry [Research Subject Categories]Ķīmija - studiju programmasLatvijas Universitātes studiju programmasOrganische Chemie - StudienprogrammeOrganiskā ķīmija - studiju programmasLatvijas Universitātes vēsture
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Kinetics of the Strain-Promoted Oxidation-Controlled Cycloalkyne-1,2-quinone Cycloaddition: Experimental and Theoretical Studies

2018

Stimulated by its success in both bioconjugation and surface modification, we studied the strain-promoted oxidation-controlled cycloalkyne–1,2-quinone cycloaddition (SPOCQ) in three ways. First, the second-order rate constants and activation parameters (ΔH⧧) were determined of various cyclooctynes reacting with 4-tert-butyl-1,2-quinone in a SPOCQ reaction, yielding values for ΔH⧧ of 4.5, 7.3, and 12.1 kcal/mol, for bicyclo[6.1.0]non-4-yne (BCN), cyclooctyne (OCT), and dibenzoazacyclooctyne (DIBAC), respectively. Second, their reaction paths were investigated in detail by a range of quantum mechanical calculations. Single-configuration theoretical methods, like various DFT and a range of MP2…

Bicyclic molecule010405 organic chemistryChemistryOrganic ChemistryKineticsSolvationCycloalkyne010402 general chemistryOrganische Chemie01 natural sciencesArticleCycloaddition0104 chemical sciencesQuinonechemistry.chemical_compoundReaction rate constantComputational chemistryLife ScienceSurface modificationQuímica orgànicaVLAGThe Journal of Organic Chemistry
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Supramolecular polymerization of sulfated dendritic peptide amphiphiles into multivalent L-selectin binders

2021

The synthesis of a sulfate-modified dendritic peptide amphiphile and its self-assembly into one-dimensional rod-like architectures in aqueous medium is reported. The influence of the ionic strength on the supramolecular polymerization was probed via circular dichroism spectroscopy and cryogenic transmission electron microscopy. Physiological salt concentrations efficiently screen the charges of the dendritic building block equipped with eight sulfate groups and trigger the formation of rigid supramolecular polymers. Since multivalent sulfated supramolecular structures mimic naturally occurring L-selectin ligands, the corresponding affinity was evaluated using a competitive SPR binding assay…

Circular dichroismSupramolecular chemistryPeptidemacromolecular substancesFull Research Paperlcsh:QD241-441lcsh:Organic chemistryAmphiphilePeptide amphiphilelcsh:Sciencel-selectin binderssupramolecular polymerschemistry.chemical_classificationOrganic Chemistrytechnology industry and agriculture547multivalencyCombinatorial chemistryself-assembly in waterSupramolecular polymersChemistry500 Naturwissenschaften und Mathematik::540 Chemie::547 Organische ChemiechemistryPolymerizationIonic strengthlcsh:QBeilstein Journal of Organic Chemistry
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On the Stability and Formation of Pillar[n]arenes: a DFT Study

2021

The increased use of both pillar[5]arenes and pillar[6]arenes, stimulated by increasingly efficient syntheses of both, has brought forward the question as to what drives the intermediates in this Friedel-Crafts ring formation to form a pillar[5]arene, a pillar[6]arene, or any other sized macrocycle. This study sets out to answer this question by studying both the thermodynamics and kinetics involved in the absence and presence of templating solvents using high-end wB97XD/6-311G(2p,2d) DFT calculations.

CrystallographyChemistryKineticsOrganic ChemistryPillarLife ScienceRing (chemistry)Organische ChemieQuímica orgànicaVLAG
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Bis(imidazolium) salts derived from amino acids as receptors and transport agents for chloride anions

2015

The binding properties of bis(imidazolium) hosts 1a–c derived from amino acids towards different anions have been studied by 1H NMR titration experiments in 95 : 05 CD3CN : H2O at 303 K, ESI-MS and theoretical calculations. Among this family, the salt 1c showed a strong and high selectivity for chloride anions. Transmembrane chloride transport activity has also been studied for the three bis(imidazolium) based transporters in POPC liposome models, and compound 1a was identified as an active chloride/nitrate exchanger.

General Chemical EngineeringChemistry OrganicSalt (chemistry)Medicinal chemistryChlorideCompostos orgànics Síntesichemistry.chemical_compoundmedicineLife ScienceOrganic chemistryPOPCVLAGchemistry.chemical_classificationLiposomeamino acidsOrganic Chemistrychloride anionsQuímica orgánicaGeneral ChemistryOrganische ChemieTransmembrane proteinAmino acidchemistryProton NMRbis(imidazolium)TitrationAminoàcidsmedicine.drug
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Rapid Surface Functionalization of Hydrogen-Terminated Silicon by Alkyl Silanols

2017

Surface functionalization of inorganic semiconductor substrates, particularly silicon, has focused attention toward many technologically important applications, involving photovoltaic energy, biosensing and catalysis. For such modification processes, oxide-free (H-terminated) silicon surfaces are highly required, and different chemical approaches have been described in the past decades. However, their reactivity is often poor, requiring long reaction times (2-18 h) or the use of UV light (10-30 min). Here, we report a simple and rapid surface functionalization for H-terminated Si(111) surfaces using alkyl silanols. This catalyst-free surface reaction is fast (15 min at room temperature) and…

HydrogenSiliconSilici Compostoschemistry.chemical_element02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesBiochemistryCatalysisArticleQuímica de superfíciesCatalysisColloid and Surface ChemistryMonolayerLife ScienceOrganic chemistryReactivity (chemistry)AlkylVLAGchemistry.chemical_classificationOrganic ChemistryGeneral ChemistryPolymer021001 nanoscience & nanotechnologyOrganische Chemie0104 chemical scienceschemistrySurface modification0210 nano-technologyJournal of the American Chemical Society
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