Search results for "Azine"

showing 10 items of 1589 documents

Durability of a strach-based biodegradable polymer

2007

Abstract The photo-oxidation and the photo-stabilization of a commercial biodegradable polymer have been investigated in order to establish the possibility of using this polymer as raw material for films for agriculture. The degradation has been followed by measuring the mechanical properties as a function of photo-oxidation time and in particular by following the elongation at break. The virgin polymer, made from maize starch and a synthetic biodegradable polyester, shows poor resistance to the UV irradiation as observed by the fast decay of the elongation at break, but the presence of small amounts of conventional UV stabilizers strongly improves the durability of this polymer. The UV sta…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsStarchPolymerCondensed Matter PhysicsBiodegradable polymerAbsorbancechemistry.chemical_compoundchemistryChemical engineeringMechanics of MaterialsPolymer chemistryMaterials ChemistryBenzophenoneDegradation (geology)Polymer blendPolypropylenes Extrusion density polyethyleneTriazine
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Redox active polymers with phenothiazine moieties for nanoscale patterning via conductive scanning force microscopy

2011

Redox active polymers with phenothiazine moieties have been synthesized by Atomic Transfer Radical Polymerization (ATRP). These novel polymers reveal bistable behaviour upon application of a bias potential above the oxidation threshold value. Using conductive Scanning Force Microscopy, two distinguishable conductivity levels were induced on a nanoscale level. These levels were related to a high conducting “On” and a low conducting “Off” state. The “On” state is generated by the oxidation of the phenothiazine side chains to form stable phenothiazine radical cations. The formation and stability of the radical sites was examined by cyclic voltammetry, electron spin resonance and optical spectr…

chemistry.chemical_classificationMaterials scienceRadical polymerizationAnalytical chemistryChemiePolymerPhotochemistryRedoxlaw.inventionchemistry.chemical_compoundchemistrylawPhenothiazineSide chainGeneral Materials ScienceCyclic voltammetryThin filmElectron paramagnetic resonance
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Five-to-Six Membered Ring-rearrangements in the Reaction of 5-Perfluoroalkyl-1,2,4-oxadiazoles with Hydrazine and Methylhydrazine

2006

The hydrazinolysis reaction of 5-perfluoroalkyl-1,2,4-oxadiazoles with hydrazine or methylhydrazine as bidentate nucleophiles has been investigated. The reaction occurred through the addition of the bidentate nucleophile to the C(5)-N(4) double bond of the 1,2,4-oxadiazole followed by ring-opening and ring-closure (ANRORC) involving the second nucleophilic site of the reagent. This ring-closure step could involve either the original C(3) of the 1,2,4-oxadiazole (giving a five-to-five membered ring rearrangement) or an additional electrophilic center linked to it (exploiting a five-to-six membered ring rearrangement). An alternative initial nucleophilic attack may involve the additional elec…

chemistry.chemical_classificationMethylhydrazineKetoneDouble bondChemistryStereochemistryTRANSFORMATIONS15N-NMR SPECTROSCOPYCHEMICAL SHIFT CALCULATIONSOrganic ChemistryFLUORINATED HETEROCYCLIC-COMPOUNDSHydrazoneRegioselectivityBKR REARRANGEMENTRing (chemistry)EXPEDIENT ROUTEMOLECULAR-REARRANGEMENTSNucleophileAROMATICITY INDEXElectrophileATTACKFIVE TO SIX REAGGANGEMENT
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Fluorinated Heterocyclic Compounds. An Expedient Route to 5-Perfluoroalkyl-1,2,4-triazoles via an Unusual Hydrazinolysis of 5-Perfluoroalkyl-1,2,4-ox…

2003

The hydrazinolysis reaction of 5-perfluoroalkyl-1,2,4-oxadiazoles has been investigated. Nucleophilic addition of the reagent to the C(5)-N(4) double bond of the oxadiazole ring, followed by ring-opening and then ring-closure involving the beta-nitrogen atom of the hydrazino moiety and the C(3) of the oxadiazole ring, explains the formation of 5-perfluoroalkyl-1,2,4-triazoles as final products. Useful applications in synthesis of this uncommon hydrazinolysis can be claimed.

chemistry.chemical_classificationNucleophilic additionDouble bondOrganic ChemistryHydrazineOxadiazoleGeneral MedicineRing (chemistry)Medicinal chemistryChemical synthesischemistry.chemical_compoundchemistryReagentTriazole derivativesOrganic chemistryMoietyThe Journal of Organic Chemistry
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Macrocyclic (1,3)- and (1,4)-benzena-(1,4)-piperazinacyclophanes

1995

New large, up to 45-membered macrocycles were synthesised from piperazine and m- and p-2,6-bis(bromomethyl)xylene under high dilution conditions. X-ray structures of compounds 3a, 4a, 5a, and 8b were determined. Surprisingly, none of the macrocycles prepared showed any inclusion properties towards small guest molecules. Instead, the compounds were found to self-organize during the packing process into larger structures due to the complementary of the molecular skeletons. In the crystalline state 3a forms nets, where the macrocycles are bound by HCH…N interactions to each other. 4a exits in a dimeric structure, which, in turn, further extends to a sheet structure. The positively charged phan…

chemistry.chemical_classificationOrganic ChemistryXyleneSalt (chemistry)ProtonationGeneral ChemistryTurn (biochemistry)Piperazinechemistry.chemical_compoundCrystallographychemistrySheet structureMoleculeSelf-assemblyPhysical and Theoretical ChemistryLiebigs Annalen
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Phenothiazine-based dyes with bilateral extension of π-conjugation for efficient dye-sensitized solar cells

2013

Four novel organic photo-sensitizers based on phenothiazine were designed, synthesized and characterized for efficient dye-sensitized solar cells. Anisole, octyloxybenzene and dodecyloxybenzene were incorporated into the phenothiazine by an Ullmann reaction. An additional octyloxybenzene was incorporated into one dye unit through a Suzuki coupling reaction. The modified phenothiazine moiety acts as an electron donor and cyanoacrylic acid acts as an electron acceptor and anchoring unit. The photophysical, electrochemical and sensitizing characteristics of the new dyes were evaluated. The bis(octyloxybenzene) substituted dye delivered the best performance with its sensitized solar cell displa…

chemistry.chemical_classificationProcess Chemistry and TechnologyGeneral Chemical EngineeringElectron donorElectron acceptorPhotochemistryUllmann reactionlaw.inventionchemistry.chemical_compoundDye-sensitized solar cellSuzuki reactionchemistrylawPhenothiazineSolar cellMoietyDyes and Pigments
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Magneto-structural versatility of copper(II)-3-phenylpropionate coordination polymers with N-donor coligands.

2015

A novel series of copper(II) coordination polymers [Cu2(O2CC8H9)4(pyz)]n (1), [Cu2(O2CC8H9)4(dps)]n (2), {[Cu(O2CC8H9)2(dps)(H2O)]·H2O}n (3), {[NaCu(O2CC8H9)2(bpm)(NO3)]·H2O}n (4), and [Cu4(O2CC8H9)6(OH)2(bpp)2]n (5) [O2CC8H9− = 3-phenylpropionate anion, pyz = pyrazine, dps = di(4-pyridyl)sulfide, bpm = 2,2′-bipyrimidine, and bpp = 1,3-bis(4-pyridyl)propane] have been synthesized and magneto-structurally investigated. Compounds 1 and 2 belong to a large group of copper(II) carboxylates where bis-monodentate pyz (1) and dps (2) ligands connect the paddle-wheel [CuII2(μ-O2CC8H9)4] units leading to alternating copper(II) chains. The structure of 3 consists of uniform chains of trans-[CuII(O2CC…

chemistry.chemical_classificationPyrazine010405 organic chemistryLigandStereochemistrychemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciencesCopper0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryFerromagnetismAntiferromagnetismNon-covalent interactionsCarboxylateDalton transactions (Cambridge, England : 2003)
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Electrochemical study of dinuclear ruthenium(II)—arene compounds: Electrogeneration of Ru(II)—Ru(I) species

1987

Abstract The preparation and characterization of Ru(II)—arene compounds [{RuCl2(p-cym)}2(μ-L-L)] where p-cym = p-MeC6H4CHMe2; and L-L = diphenylphosphinomethane (I), 1,1′-bisdiphenylphosphinoferrocene (II), pyrazine (III) and 4,4′-bipyridine (IV), are described. Electrochemical data for these compounds obtained by cyclic voltammetry and coulometry are reported. The electrochemical reduction of compounds I or II yields ruthenium(O) species. However, compounds III or IV containing ligands with delocalized Π orbitals undergo one-electron reduction. The ESR signal detected during the electrolysis of compounds III or IV is consistent with one delocalized electron through the whole dinuclear unit.

chemistry.chemical_classificationPyrazineInorganic chemistrychemistry.chemical_elementElectrochemistryMedicinal chemistryRutheniumInorganic ChemistryCoulometrychemistry.chemical_compoundDelocalized electronHydrocarbonchemistryMaterials ChemistryPhysical and Theoretical ChemistryCyclic voltammetryMetallocenePolyhedron
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Bistetrazine-Cyanines as Double-Clicking Fluorogenic Two-Point Binder or Crosslinker Probes

2018

Fluorogenic probes can be used to minimize the background fluorescence of unreacted and nonspecifically adsorbed reagents. The preceding years have brought substantial developments in the design and synthesis of bioorthogonally applicable fluorogenic systems mainly based on the quenching effects of azide and tetrazine moieties. The modulation power exerted by these bioorthogonal motifs typically becomes less efficient on more conjugated systems; that is, on probes with redshifted emission wavelength. To reach efficient quenching, that is, fluorogenicity, even in the red range of the spectrum, we present the synthesis, fluorogenic, and conjugation characterization of bistetrazine-cyanine pro…

chemistry.chemical_classificationQuenching (fluorescence)010405 organic chemistryChemistryOrganic ChemistryPeptideGeneral ChemistryConjugated system010402 general chemistry01 natural sciencesFluorescenceCombinatorial chemistryCatalysis0104 chemical sciencesTetrazinechemistry.chemical_compoundCovalent bondAzideBioorthogonal chemistryChemistry - A European Journal
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Chiral synthetic pseudopeptidic derivatives as triplet excited state quenchers

2009

The behavior of 6 pseudopeptidic models, synthesized by connecting different protected amino acids (Trp, Tyr, Phe, and Lys) with various diamino spacers, as quenchers of the triplet excited state of tiaprofenic acid (and its methyl ester), has been investigated. A series of quenching constants have been determined, which depend on the nature of the quencher and on the stereochemistry of the excited drug. A significant degree of stereodifferentiation has been found for the peptidomimetic synthesized with Phe and Tyr linked by a piperazine bridge. The obtained results support the utility of laser flash photolysis (LFP) as a tool to investigate the interactions between photoexcited drugs and s…

chemistry.chemical_classificationQuenching (fluorescence)010405 organic chemistryPeptidomimeticStereochemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryPhotochemistryOrganic ChemistryLaser flash photolysis010402 general chemistry01 natural sciencesBiochemistry3. Good health0104 chemical sciencesAmino acidPiperazinechemistry.chemical_compoundchemistryExcited stateQuenchingDrug DiscoveryTriplet excited stateFlash photolysisBinding site
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