Search results for " organic"

showing 10 items of 5145 documents

Defying Stereotypes with Nanodiamonds: Stable Primary Diamondoid Phosphines

2016

International audience; Direct unequal C-H bond difunctionalization of phosphorylated diamantane was achieved in high yield from the corresponding phosphonates. Reduction of the functionalized phosphonates provides access to novel primary and secondary alkyl/aryl diamantane phosphines. The prepared primary diamantyl phosphines are quite air stable compared to their adamantyl and especially alkyl or aryl analogues. This finding is corroborated by comparing the singly occupied molecular orbital energy levels of the corresponding phosphine radical cations obtained by density functional theory computations.

room-temperaturemolecular tripoddeactivated aryl chlorideshomogeneous catalysts010402 general chemistryDiamondoidselective preparationchemistry01 natural sciencesMedicinal chemistryChemical reaction[ CHIM ] Chemical Scienceschemistry.chemical_compoundOrganic chemistry[CHIM]Chemical SciencesarylationAlkylNanodiamonds ; Diamondoid Phosphines ; diamantane ; adamantane ; adamantylphosphinechemistry.chemical_classification010405 organic chemistryChemistryligandsArylOrganic Chemistrypalladiumphosphorylated adamantanes3. Good health0104 chemical sciencesChemical bondDensity functional theoryDiamantanePhosphine
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Carbon stocks in a 50‑year‑oldEucalyptus camaldulensisstand in Sicily, Italy

2015

Eucalyptus stands in semi-arid areas may contribute to enhance carbon (C) stocks in both biomass and soil. However, the limited information available is mainly focused on short-rotation plantations. In this study, the above- and below-ground C pools in five 50-year-old Eucalyptus camaldulensis Dehnh. stands planted on Miocenic evaporitic deposits in Sicily, Italy, with a xeric and thermic pedoclimate, were measured. Above-ground biomass was determined by partitioning and weighing branches, stem and leaves. Below-ground C pools included the determination of litter, root biomass, and soil organic and inorganic C. In terms of the above-ground biomass, the E. camaldulensis stand accumulated on …

rootsbelow-ground biomassSettore AGR/05 - Assestamento Forestale E Selvicolturasemi-arid Mediterranean climateSettore AGR/13 - Chimica AgrariaBiomassDeserts and xeric shrublandssoillitterbelow-ground biomaabove-ground biomassTotal organic carbonevaporitic depositsSoil organic matterabove-ground biomass; below-ground biomass; evaporitic deposits; litter; roots; semi-arid Mediterranean climate; soil; ForestryForestrySoil classificationForestryrootEucalyptusevaporitic depositEucalyptus camaldulensisAgronomySettore AGR/14 - PedologiaLitterEnvironmental scienceabove-ground biomaSouthern Forests: a Journal of Forest Science
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NMR-based quantification of rosmarinic and carnosic acids, GC-MS profile and bioactivity relevant to neurodegenerative disorders of Rosmarinus offici…

2013

Abstract A comparative study of phytochemicals content and biological properties of eight Rosmarinus officinalis (rosemary) populations (RO1–RO8) collected in different areas of Tunisia was carried out. Two of the main rosemary constituents, rosmarinic and carnosic acids, were quantified by an NMR technique. Carnosic acid content was higher than that of rosmarinic acid. The non-polar constituents were examined by GC and GC–MS. Total phenols and flavonoids content were also determined in order to discuss the possible correlation between these phytochemicals and bioactivity. Antioxidant activity was investigated through different in vitro assays. Sample RO3 from a sub-humid area showed the hi…

rosmarinic acidAntioxidantDPPHmedicine.medical_treatmentMedicine (miscellaneous)Rosmarinuschemistry.chemical_compoundAntioxidant activitymedicineAnticholinesterese activityTX341-641Settore BIO/15 - Biologia FarmaceuticaPhenolscarnosic acidNutrition and DieteticsABTSChromatographybiologyChemistryNutrition. Foods and food supplyRosmarinic acidCarnosic acidSettore CHIM/06 - Chimica OrganicaRosmarinic and carnosic acidsbiology.organism_classificationNMRBiochemistryRosmarinic and carnosic acidOfficinalisRosmarinus officinalisneurodegenerative disorderPhytochemicals contentFood Science
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SMART NANOSPONGE-BASED SYSTEMS FOR ADVANCED APPLICATIONS

2023

rosmarinic acidpolymerrelaxometrysmart materialSettore CHIM/06 - Chimica Organicaquercetinphotocatalysifolic acidcontrolled release dyecyclodextrinheuristic analysiadsorptionpH-tunabilitycalixarenenanomaterialnanospongeFFC-NMR
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3,4,5-Trimethoxy-4'-methylbiphenyl

2013

In the title compound, C16H18O3, the dihedral angle between the benzene rings is 33.4 (2)°. In the crystal, mol­ecules are packed in a zigzag arrangement along the b-axis and are inter­connected via weak C—H⋯O hydrogen bonds, and C—H⋯π inter­actions involving the meth­oxy groups and the benzene rings of neighbouring molecules.

röntgendiffraktiocrystal structure010405 organic chemistryHydrogen bonddendrimeeri prekursoriGeneral ChemistrykiderakenneDihedral angle010402 general chemistryCondensed Matter Physics01 natural sciencesOrganic Papers3. Good health0104 chemical sciencesX-ray diffractionCrystalchemistry.chemical_compoundCrystallographychemistryZigzagdendrimer precursorMoleculeGeneral Materials ScienceBenzeneta116Acta Crystallographica Section E-Structure Reports Online
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3,5-Dimethoxy-4'-methylbiphenyl

2013

The title compound, C15H16O2, crystallizes with three independent mol­ecules in the asymmetric unit. The intra­molecular torsion angle between the aromatic rings of each mol­ecule are −36.4 (3), 41.3 (3) and −37.8 (3)°. In the crystal, the complicated packing of the mol­ecules forms wave-like layers along the b and c axes. The mol­ecules are connected via extensive meth­oxy–phenyl C—H…π inter­actions. A weak C—H…O hydrogen-bonding network also exists between meth­oxy O atoms and aromatic or meth­oxy H atoms.

röntgendiffraktiocrystal structuredendrimeeri prekursori010405 organic chemistryChemistryX-ray DiffractionAromaticitykiderakenneGeneral ChemistryDihedral angle010402 general chemistryCondensed Matter PhysicsBioinformaticsOrganic Papers01 natural sciences0104 chemical sciences3. Good healthCrystalCrystallographydendrimer precursorGeneral Materials Scienceta116
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3,4-Dimethoxy-4'-methylbiphenyl

2013

In the title compound, C15H16O2, the dihedral angle between the planes of the aromatic rings is 30.5 (2). In the crystal, molecules are linked via C—HO hydrogen bonds and C— H interactions, forming a two-dimensional network lying parallel to (100). peerReviewed

röntgendiffraktiocrystal structuredendrimeeri prekursori010405 organic chemistryHydrogen bondChemistryAromaticitykiderakenneGeneral ChemistryDihedral angle010402 general chemistryCondensed Matter Physics01 natural sciencesOrganic PapersX-ray diffraction0104 chemical sciences3. Good healthCrystalCrystallographydendrimer precursorGeneral Materials Scienceta116Acta Crystallographica Section E-Structure Reports Online
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Methyl 3',5'-dimethoxybiphenyl-4-carboxylate

2013

In the title compound, C16H16O4, the dihedral angle between the benzene rings is 28.9 (2)°. In the crystal, mol­ecules are packed in layers parallel to the b axis in which they are connected via weak inter­molecular C-H...O contacts. Face-to-face π-π inter­actions also exist between the benzene rings of adjacent mol­ecules, with centroid-centroid and plane-to-plane shift distances of 3.8597 (14) and 1.843 (2) Å, respectively.

röntgendiffraktiocrystal structuredendrimeeri prekursorikiderakenneDihedral angle010402 general chemistryBioinformatics01 natural sciencesOrganic PapersCrystalchemistry.chemical_compoundGeneral Materials ScienceBenzeneta116Biphenyl010405 organic chemistryHydrogen bondGeneral ChemistryMeth-Condensed Matter PhysicsX-ray diffraction0104 chemical sciences3. Good healthCrystallographychemistrydendrimer precursorLayer (electronics)
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Polyphenols and Pharmacological Screening of a Monarda fistulosa L. dry Extract Based on a Hydrodistilled Residue By-Product

2021

This study aimed to determine the composition and content of polyphenols in the dry extract obtained from the hydrodistilled residue by-product of the wild bergamot (Monarda fistulosa L., Lamiaceae Martinov family) herb (MFDE) and to evaluate its safety and pharmacological properties. The total phenolic content (TPC) in the MFDE was 120.64 mg GAE/g. The high-performance liquid chromatography (HPLC) analysis showed the presence of a plethora of phenolic compounds, including hydroxycinnamic acids and flavone derivatives in the MFDE, with rosmarinic acid and luteolin-7-O-glucoside being the main components. With an IC50 value of 0.285 mg/mL, it was found to be a strong DPPH radical scavenger. …

safetyDPPHRM1-950phenolic compoundsMonarda fistulosa01 natural sciencesHigh-performance liquid chromatographywild bergamot03 medical and health scienceschemistry.chemical_compound0302 clinical medicineantiradical activityPharmacology (medical)anti-inflammatory activityanalgesic activityOriginal ResearchPharmacologyResidue (complex analysis)biologyTraditional medicine010405 organic chemistryRosmarinic acidbiology.organism_classificationAcute toxicity0104 chemical scienceschemistryherbPolyphenol030220 oncology & carcinogenesispostdistillation wasteLamiaceaeTherapeutics. PharmacologyFrontiers in Pharmacology
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Combined effect of low-molecular-weight organic acids and creosote on phosphatase activities in sandy soil

2018

This paper assesses the impact of creosote and low-molecular-weight organic acids (LMWOAs) on the activity of acid phosphomonoesterase, alkaline phosphomonoesterase, phosphotriesterase, and inorganic pyrophosphatase in soil. The experiment was carried out on loamy sand samples with organic carbon content of 8.71 g · kg -1 , with the following variable factors: dosages of creosote: 0, 0.5%, and 2.5%; type of LMWOAs: oxalic acid, tartaric acid, and citric acid in the amount of 50 mmol · kg -1 of soil; days of experiment: 1, 7, 14, 28, 56, 112. Obtained results showed that contamination with creosote caused decrease in the activity of soil phosphatases. The observed effect did not always incre…

sandy loamOxalic acidPhosphataseSoil Science010501 environmental sciences01 natural sciencesoxalic acidlaw.inventionchemistry.chemical_compoundlawcreosotephosphatases0105 earth and related environmental sciencesEarth-Surface ProcessesTotal organic carbonEcology04 agricultural and veterinary sciencescitric acidSoil contaminationCreosotechemistrytartaric acidLoamEnvironmental chemistry040103 agronomy & agricultureTartaric acid0401 agriculture forestry and fisheriesCitric acidPolish Journal of Soil Science
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