Search results for "Molecule"

showing 10 items of 5162 documents

Studien zum Vorgang der Wasserstoffübertragung, 52. Zur Kenntnis der elektroreduktiven Spaltung der N - N-Bindung

1978

Am Beispiel von 35 Hydrazinderivaten wird die elektroreduktive Spaltung polarographisch und praparativ untersucht. Es wurde gefunden: 1) Beim mono-, tri- und tetrabenzoylierten Hydrazin 9, 11 bzw. 12 verschiebt sich das Potential proportional der Anzahl der Benzoylgruppen nach positiveren Werten. Beim symmetrischen 1,2-Dibenzoylhydrazin (10) wird das Halbstufenpotential E1/2 — bedingt durch H-Verbruckung und mesomere Stabilisierung — stark nach negativen Werten verschoben. — 2) Bei den cyclischen Hydrazinderivaten 14–16 werden die E1/2-Werte sowohl in Abhangigkeit von der Ringspaltung als auch durch cis-Fixierung der Benzoylgruppen noch zusatzlich nach positiveren Werten verlagert. — 3) Ube…

chemistry.chemical_compoundBicyclic moleculechemistryHydrogen bondStereochemistryOrganic ChemistryNegative potentialProtonationPhysical and Theoretical ChemistryAlkylationOniumBenzamideRing strainJustus Liebigs Annalen der Chemie
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Efficient Synthesis of 1,4,7-Triazacyclononane and 1,4,7-Triazacyclononane-Based Bifunctional Chelators for Bioconjugation

2014

The reaction of diethylenetriamine with chloroacetaldehyde yielded a bicyclic aminal intermediate for the synthesis of 1,4,7-triazacyclononane (TACN), a macrocyclic polyamine the derivatives of which find applications as catalysts, bleaching agents, and chelators for medical imaging. This new synthetic protocol outperforms the synthetic methods described so far because it does not involve any cyclization step. Moreover, this aminal intermediate allowed access to a new family of TACN derivatives functionalized on the carbon skeleton, for example, C-aminomethyl-TACN. This novel compound is a precursor of valuable bifunctional chelating agents for nuclear medicine, in particular, for the prepa…

chemistry.chemical_compoundBioconjugationchemistryBicyclic moleculeOrganic ChemistryDiethylenetriamineAminalOrganic chemistryChloroacetaldehydeChelationPhysical and Theoretical ChemistryBifunctionalCatalysisEuropean Journal of Organic Chemistry
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Macromolecules with groups of high reactivity

1960

Reactions on the reactive groups of macromolecular substances (e.g., cellulose) have long been known, even since before the structures of macromolecules were understood. H. Staudinger carried out numerous reactions with macromolecules, maintaining the degree of polymerization constant, in order to substantiate the macromolecular structure of the substances investigated (polymeric-analogous reactions). During the last fifteen years reactions with macromolecules have been investigated because it was desirable to compare the chemical diversity of low molecular weight compounds with the corresponding chemical diversity of macromolecular compounds. These endeavors bring forth materials which sup…

chemistry.chemical_compoundChemistryChemical diversityMacromolecular SubstancesOrganic chemistryReactivity (chemistry)Degree of polymerizationCelluloseMacromolecular CompoundsMacromoleculeGroup 2 organometallic chemistryJournal of Polymer Science
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Novel Applications of Dynamic NMR in Organic Chemistry

2004

Abstract This review article is oriented on NMR applications in studying various dynamic processes of organic molecules. The topic as a whole is too large to be covered exhaustively in one article or by one author. Therefore, the literature searches are limited mainly for the years 1999–2001. Further, many interesting branches joined essentially with organic chemistry such as supramolecular and organometallic chemistry are left outside this article because there exist recent reviews on these topics. Similarly, the theoretical background of dynamic NMR is not included. The nature of dynamic NMR itself is changing with the recent progress in computational possibilities to estimate the differe…

chemistry.chemical_compoundChemistryChemical shiftSupramolecular chemistryOrganic chemistryDensity functional theoryGeneral MedicineOrganometallic chemistryOrganic moleculesChemInform
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1,3-Di(hetero)aryl-7-substituted Pyrenes—An Undiscovered Area of Important Pyrene Derivatives

2019

Despite the pyrene derivatives have been covered extensively by scientists during the last years, many interesting properties and applications of pyrene derivatives have been presented, nowadays there are still areas of pyrenes’ chemistry that need to be fulfilled. Most of the described in literature pyrenes are 1,3,6,8-tetrasubstituted followed by 4,5,9,10-tetrasubstituted, 2,7-, and 1,6-, and 1,8-disubstituted pyrene derivatives. In the case of 1,3-di(hetero)aryl-7-substituted, there are only a few examples of derivatives containing at position 7 - tert-butyl group. In this work, the necessity of synthesis of 1,3-di(hetero)aryl-7-substituted pyrenes is presented based on the results of th…

chemistry.chemical_compoundChemistryGroup (periodic table)ArylNitroMoleculePyreneDensity functional theoryAmine gas treatingCombinatorial chemistryBasis setThe 23rd International Electronic Conference on Synthetic Organic Chemistry
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Molecular Structure of the Phenylbiguanide Hydrochloride: C6H5.C2N5H6.HCl

2010

chemistry.chemical_compoundChemistryHydrochlorideMoleculeGeneral ChemistryPhenylbiguanideNuclear chemistryBulletin des Sociétés Chimiques Belges
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Discrete supramolecular donor-acceptor complexes

2009

The renewed interest in noncovalently associating electroactive molecules arises in part from the quest for new organic materials that convert solar energy into electrical/ chemical equivalents. In this context, the formation of charge-separated states is a key prerequisite. Charge-transfer events triggered by light have been studied in supramolecular donor–acceptor systems based on hydrogen bonds and coordinative metal bonds. Although many of the most widely utilized electroactive fragments feature large pconjugated surfaces, to date the use of p–p aromatic interactions has mainly been limited to the construction of semi-infinite ensembles of chromophores either to achieve charge transport…

chemistry.chemical_compoundChemistryHydrogen bondComputational chemistryTweezersSupramolecular chemistryMoleculePi interactionContext (language use)General ChemistryChromophoreCatalysisTetrathiafulvalene
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Bis[indanyl]- and bis[indenyl]arylmethanes: New molecular three-bladed propellers

1991

Proton-catalyzed arylmethylation of indan and indene derivatives with 4-methoxybenzaldehyde yield novel triarylmethanes bearing indan or indene substituents. According to Mislow's definition, these molecules belong to the class of molecular three-bladed propellers and exhibit an interesting stereochemistry.

chemistry.chemical_compoundChemistryMoleculeGeneral ChemistryIndeneMedicinal chemistryMonatshefte f�r Chemie Chemical Monthly
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ChemInform Abstract: Bis(indanyl)- and Bis(indenyl)arylmethanes: New Molecular Three-Bladed Propellers.

2010

Proton-catalyzed arylmethylation of indan and indene derivatives with 4-methoxybenzaldehyde yield novel triarylmethanes bearing indan or indene substituents. According to Mislow's definition, these molecules belong to the class of molecular three-bladed propellers and exhibit an interesting stereochemistry.

chemistry.chemical_compoundChemistryStereochemistryMoleculeGeneral MedicineIndeneChemInform
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Synthesis and Conformational Analysis of Saturated3,1,2-Benzoxazaphosphinine 2-Oxides

2005

N-Unsubstituted, N-methyl and N-benzyl cis- and trans-2(hydroxymethyl)cyclohexylamines were subjected to ring closure with phenylphosphonic dichloride, phenyl dichlorophosphate and bis(2-chloroethyl)phosphoramidic dichloride in order to synthesize P-epimeric diastereomers of the corresponding unsubsituted and N-substituted 2-phenyl-, 2phenoxy- and 2-[bis(2-chloroethyl)amino]octahydro-2H3,1,2-benzoxazaphosphinine 2-oxides. The stereochemistry and conformations of the prepared compounds were analyzed mainly by variable-temperature 1 H, 13 C and 31 P NMR spectroscopy. Geometry optimizations were performed for some trans-fused molecules by utilizing the B3LYP DFT method and a locally dense basi…

chemistry.chemical_compoundChemistryStereochemistryOrganic ChemistryDiastereomerMoleculeCyclohexylaminesHydroxymethylNuclear magnetic resonance spectroscopyPhysical and Theoretical ChemistryRing (chemistry)Phenyl dichlorophosphateBasis setEuropean Journal of Organic Chemistry
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