Search results for "Self-condensation"

showing 10 items of 12 documents

Oligo(phenylenevinylene)s with reactive side chains: amine- and amide-bound alkoxysilanes

2002

Strongly luminescent oligo(phenylenevinylene) chromophores with monodisperse chain lengths are connected via short spacers containing a secondary amine or amide with di- and tri-ethoxysilane groups. The alkoxysilanes can be hydrolysed and condensed to cyclic and linear oligomers with high film forming capability and are also interesting functional units for hybrid materials for electro-optical applications. The luminescence properties in the solid state are influenced by hydrogen bonding of the amides resulting in strong hypsochromic shifts. The synthesis of the title compounds, their oligomerisation and the electronic spectra in the solution and solid state are presented.

Condensation polymerChemistryHydrogen bondMechanical EngineeringMetals and AlloysSelf-condensationCondensed Matter PhysicsElectronic Optical and Magnetic Materialschemistry.chemical_compoundMechanics of MaterialsAmidePolymer chemistryMaterials ChemistrySide chainAmine gas treatingHypsochromic shiftHybrid materialSynthetic Metals
researchProduct

Molecular parameters of hyperbranched polymers made by self-condensing vinyl polymerization. 1. Molecular weight distribution

1997

The molecular weight distribution (MWD) and its moments are calculated for hyperbranched polymers formed by self-condensing vinyl polymerization (SCVP) of monomers (“inimers”) with the general structure AB*, where A is a vinyl group and B* is an initiating group. The calculated MWD is extremely broad, the polydispersity index (PDI) being equal to the number-average degree of polymerization:  Pw/Pn = Pn. It is twice as broad as that for the polycondensation of AB2 type monomers. If the fraction of unreacted monomer is not taken into account, the MWD becomes somewhat narrower, P‘w/P‘n ≈ 0.40P‘n. The kinetics of the polymerization process are first order with respect to the concentration of vi…

Condensation polymerPolymers and PlasticsChemistryOrganic ChemistryDispersitySelf-condensationDegree of polymerizationInorganic ChemistryActive centerchemistry.chemical_compoundMonomerPolymerizationPolymer chemistryMaterials ChemistryMolar mass distribution
researchProduct

Polymerizable Well-Defined Oligo(thiophene amide)s and their ROMP Block Copolymers

2009

We report the synthesis of conjugated thiophene amide oligomers that constitute a new class of chromophores with potential for optoelectronic applications. The synthesis of defined norbornene-substituted oligothiophene amides using conventional coupling chemistry is described. Their electronic properties depend on the degree of oligomerization as UV/Vis and fluorescence spectroscopy demonstrate. A significant red shift in the spectra upon an increase in the oligomer length evidences conjugation of the thiophene rings via the amide linkages. ROMP of the norbornene-substituted oligomers gives homopolymers and block-copolymers with a solubilizing second block. The amphiphilic character of the …

Materials scienceCondensation polymerPolymers and PlasticsOrganic ChemistrySelf-condensationROMPConjugated systemOligomerchemistry.chemical_compoundchemistryAmidePolymer chemistryAmphiphileMaterials ChemistryThiopheneMacromolecular Rapid Communications
researchProduct

Synthesis of 6,12-Disubstituted Methanodibenzo[

2019

The preparation of unprecedented 6,12-disubstituted methanodibenzo[b,f][1,5]dioxocins from pyrrolidine catalyzed self-condensation of 2′-hydroxyacetophenones is herein described. This method provides easy access to this highly bridged complex core, resulting in construction of two C–O and two C–C bonds, a methylene bridge and two quaternary centers in a single step. The intricate methanodibenzo[b,f][1,5]dioxocin compounds were obtained in up to moderate yields after optimization of the reaction conditions concerning solvent, reaction times and the use of additives. Several halide substituted methanodibenzo[b,f][1,5]dioxocins could be prepared from correspondent 2′-hydroxyacetophenones.

Pyrrolidinesself-condensationMolecular StructureenamineAcetophenonesStereoisomerism15-dioxocin2′-hydroxyacetophenoneCatalysisArticleMolecules (Basel, Switzerland)
researchProduct

2019

The preparation of unprecedented 6,12-disubstituted methanodibenzo[b,f][1,5]dioxocins from pyrrolidine catalyzed self-condensation of 2′-hydroxyacetophenones is herein described. This method provides easy access to this highly bridged complex core, resulting in construction of two C–O and two C–C bonds, a methylene bridge and two quaternary centers in a single step. The intricate methanodibenzo[b,f][1,5]dioxocin compounds were obtained in up to moderate yields after optimization of the reaction conditions concerning solvent, reaction times and the use of additives. Several halide substituted methanodibenzo[b,f][1,5]dioxocins could be prepared from correspondent 2′-hydroxyacetophenones.

Reaction conditions010405 organic chemistryChemistryOrganic ChemistryPharmaceutical ScienceHalideMethylene bridgeSelf-condensation010402 general chemistry01 natural sciencesMedicinal chemistryPyrrolidine0104 chemical sciencesAnalytical ChemistryCatalysisEnamineSolventchemistry.chemical_compoundChemistry (miscellaneous)Drug DiscoveryMolecular MedicinePhysical and Theoretical ChemistryMolecules
researchProduct

Synthesis of the New Ring System Bispyrido[4',3':4,5]pyrrolo [1,2-a:1',2'-d]pyrazine and Its Deaza Analogue

2014

Derivatives of the new ring systems bispyrido[4',3':4,5]pyrrolo[1,2-a:1',2'-d] pyrazine-6,13-dione and its deaza analogue pyrido[4'',3'':4',5']pyrrolo-[1',2':4,5]pyrazino [1,2-a]indole-6,13-dione were conveniently synthesized through a four-step sequence. Symmetrical derivatives of the former ring system were obtained through self condensation. On the other hand, condensation of 6-azaindole carboxylic acid with indole 2-carboxylic acid afforded the deaza analogue ring system. Derivatives of the title ring system were tested by the National Cancer Institute (Bethesda, MD, USA) and four of them exhibited modest activity against MCF7 (a breast cancer cell line) and/or UO-31 (a renal cancer cel…

antiproliferative activitydiketopiperazines; plinabulin A; bispyrido-pyrrolo-pyrazine; pyrido-pyrrolopyrazino- indole; antiproliferative activityPyrazineStereochemistrypyrido-pyrrolo-pyrazino-indoleCarboxylic acidpyrido-pyrrolopyrazino- indoleCarboxylic AcidsPharmaceutical ScienceAntineoplastic AgentsRing (chemistry)ArticleAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryBreast cancer cell lineHeterocyclic Compoundsdiketopiperazines; plinabulin A; bispyrido-pyrrolo-pyrazine; pyrido-pyrrolo-pyrazino-indole; antiproliferative activityDrug DiscoveryHumansPyrrolesPhysical and Theoretical Chemistrybispyrido-pyrrolo-pyrazinechemistry.chemical_classificationIndole testplinabulin AOrganic ChemistrydiketopiperazineSelf-condensationSettore CHIM/08 - Chimica FarmaceuticadiketopiperazineschemistryChemistry (miscellaneous)PyrazinesMCF-7 CellsMolecular MedicineDrug Screening Assays AntitumorCancer cell linesMolecules
researchProduct

Long-chain branched ROMP polymers

2009

This article describes the construction of branched ROMP-polymer architectures via polycondensation of ABn-type macromonomers. For this convergent strategy, a polymer was synthesized that carries several hydroxyl-groups along the polymer chain and one carboxylic acid group at the chain end. An esterification reaction between these functional groups yielded long-chain branched polymers. The polymers were analyzed by NMR and SEC to monitor the condensation reaction. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2009

chemistry.chemical_classificationCondensation polymerPolymers and PlasticsCarboxylic acidOrganic ChemistryROMPSelf-condensationPolymerCondensation reactionRing-opening polymerizationEnd-groupchemistryPolymer chemistryMaterials ChemistryOrganic chemistryJournal of Polymer Science Part A: Polymer Chemistry
researchProduct

Molecular Parameters of Hyperbranched Polymers Made by Self-Condensing Vinyl Polymerization. 2. Degree of Branching

1997

Using a modified definition, the average degree of branching, , the fraction of branchpoints, , as well as the fractions of various structural units are calculated as a function of conversion of double bonds for hyperbranched polymers formed by self-condensing vinyl polymerization (SCVP) of monomers (or “inimers”) with the general structure AB*, where A is a vinyl group and B* is an initiating group. The results are compared to those for the polycondensation of AB2-type monomers. At full conversion, is somewhat smaller for SCVP ( ∞ ≈ 0.465) than for AB2 systems ( ∞ = 0.5). There are two kinds of linear groups in SCVP whereas there is only one kind in AB2 systems. Since there are two differe…

chemistry.chemical_classificationCondensation polymerPolymers and PlasticsDouble bondOrganic ChemistryHyperbranched polymersSelf-condensationBranching (polymer chemistry)Inorganic Chemistrychemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryMaterials ChemistryMoleculeMacromolecules
researchProduct

Molecular Weight Distribution of Hyperbranched Polymers Generated by Self-Condensing Vinyl Polymerization in Presence of a Multifunctional Initiator

1999

The molecular weight distribution (MWD) is derived for polymers generated by self-condensing vinyl polymerization (SCVP) of a monomer having a vinyl and an initiator group (“inimer”) in the presence of a multifunctional initiator. If the monomer is added slowly to the initiator solution (semi-batch process), this leads to hyperbranched polymers with a multifunctional core. If monomer and initiator are mixed simultaneously (batch process), even at vinyl group conversions as high as 99%, the total MWD consists of polymers which have grown via reactions between inimer molecules (i.e., the normal SCVP process) and those which have reacted with the initiator. Consequently, the weight distributio…

chemistry.chemical_classificationPolymers and PlasticsBulk polymerizationOrganic ChemistryPolymerSelf-condensationInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryWeight distributionMaterials ChemistryMolar mass distributionMoleculeMacromolecules
researchProduct

Hyperbranched methacrylates by self-condensing group transfer polymerization

1997

The synthesis of hyperbranched methacrylates was achieved by self-condensing group transfer polymerization of 2-(2-methyl-1-triethylsiloxy-1-propenyloxy)ethyl methacrylate (1). “Back-biting” is shown to be the predominant side reaction. In spite of this, the compact nature of the hyperbranched molecules was demonstrated through SEC-viscosity measurements and comparison with a linear analogue. The degree of branching can be controlled by copolymerization with conventional monomers, e.g. MMA, and the living polymers can be used as macroinitiators for star-shaped polymers.

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistrySide reactionPolymerSelf-condensationBranching (polymer chemistry)Methacrylatechemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerMacromolecular Rapid Communications
researchProduct