Search results for "Catalysis"

showing 10 items of 5944 documents

Spin-State-Dependent Redox-Catalytic Activity of a Switchable Iron(II) Complex

2017

The spin state of catalytically active 3d metal centers plays a significant role for their activity in enzymatic processes and organometallic catalysis. Here we report on the catalytic activity of a Fe(II) coordination compound that can undergo a cooperative switch between low-spin (LS) and high-spin (HS) states. Catalytic measurements within 291 - 318 K temperature region reveal a drastic drop of the catalytic activity upon conversion of metallic centers from the LS to the HS form. For a thermoswitchable [Fe(NH2trz)3]Br2 complex (Tup = 305 K), an activation energy is found to be considerably lower for the LS state (158 kJ mol-1) comparing to the HS state (305 kJ mol-1). Mossbauer analysis …

chemistry.chemical_classificationSpin statesInorganic chemistry02 engineering and technologyActivation energy010402 general chemistry021001 nanoscience & nanotechnologyHeterogeneous catalysis01 natural sciencesRedox0104 chemical sciencesCoordination complexCatalysisInorganic ChemistryMetalCrystallographychemistrySpin crossovervisual_artvisual_art.visual_art_medium0210 nano-technologyEuropean Journal of Inorganic Chemistry
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Asymmetric Synthesis of Spiro Tetrahydrothiophene-indan-1,3-diones via a Squaramide-Catalyzed Sulfa-Michael/Aldol Domino Reaction

2016

Synthesis 48(08), 1131-1138(2016). doi:10.1055/s-0035-1560412

chemistry.chemical_classificationSpiro compound010405 organic chemistryOrganic ChemistrySquaramideEnantioselective synthesis540010402 general chemistry01 natural sciencesMedicinal chemistryCatalysisDomino0104 chemical scienceschemistry.chemical_compoundchemistryCascade reactionAldol reactionOrganocatalysisddc:540Organic chemistryTetrahydrothiophene
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Experimental Investigations and ab Initio Studies on Hexacoordinated Complexes of Dichlorosilane

1998

Dichlorosilane, SiH2Cl2, forms two different kinds of coordination compounds with pyridine and 3-picoline:  the simple adduct trans-SiH2Cl2(L)2 and the ionic complex [SiH2(L)4]Cl2·4CHCl3 (L = pyridine, 3-picoline). The adducts trans-SiH2Cl2(py)2, 1, and trans-SiH2Cl2(3pic)2, 2, form directly from the reaction of bis(dichlorosilyl)methylamine, NMe(SiHCl2)2 with pyridine (py), and 3-picoline (3pic). Reaction of 1 with an excess of pyridine in chloroform yielded [SiH2(py)4]Cl2·4CHCl3, 3. The molecular and crystal structures of 1−3 were investigated by single-crystal X-ray diffraction. The Si atoms of all three compounds are hexacoordinated and lie on centers of inversion. The basic structural …

chemistry.chemical_classificationStereochemistryAb initioDichlorosilaneGeneral ChemistryCrystal structureTriclinic crystal systemBiochemistryCatalysisCoordination complexAdductchemistry.chemical_compoundCrystallographyColloid and Surface ChemistrychemistryPyridineMonoclinic crystal systemJournal of the American Chemical Society
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Density functional theory study of the 5-pyrrolidin-2-yltetrazole-catalyzed aldol reaction

2005

Abstract The replacement of the carboxylic acid functionality with a tetrazolic acid in the proline-catalyzed asymmetric aldol reaction between acetone and trimethylacetaldehyde has been studied using DFT methods at the B3LYP/6-31G** computational level. For the C–C bond-formation step, four reactive channels corresponding to the syn and anti arrangement of the enamine and the re and si attack modes have been analyzed. The B3LYP/6-31G** results allowed us to explain the stereoselectivity and the increase in reactivity relative to the proline-catalyzed process in DMSO.

chemistry.chemical_classificationStereochemistryCarboxylic acidOrganic ChemistryCatalysisCatalysisEnamineInorganic Chemistrychemistry.chemical_compoundchemistryAldol reactionComputational chemistryAcetoneReactivity (chemistry)Density functional theoryStereoselectivityPhysical and Theoretical ChemistryTetrahedron: Asymmetry
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Catalytic triad of microsomal epoxide hydrolase: replacement of Glu404 with Asp leads to a strongly increased turnover rate

1998

Microsomal epoxide hydrolase (mEH) belongs to the superfamily of α/β-hydrolase fold enzymes. A catalytic triad in the active centre of the enzyme hydrolyses the substrate molecules in a two-step reaction via the intermediate formation of an enzyme-substrate ester. Here we show that the mEH catalytic triad is composed of Asp226, Glu404 and His431. Replacing either of these residues with non-functional amino acids results in a complete loss of activity of the enzyme recombinantly expressed in Saccharomyces cerevisiae. For Glu404 and His431 mutants, their structural integrity was demonstrated by their retained ability to form the substrate ester intermediate, indicating that the lack of enzymi…

chemistry.chemical_classificationStereochemistryCell BiologyBiochemistryAmino acidCatalysisResidue (chemistry)chemistry.chemical_compoundEnzymechemistryMicrosomal epoxide hydrolaseEpoxide HydrolasesCatalytic triadCyanogen bromideMolecular BiologyBiochemical Journal
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New Acylated Presenegenin Saponins from Two Species ofMuraltia

2004

Six new acylated bisdesmosidic triterpene glycosides 1–6 were isolated from the roots of Muraltia heisteria (L.) DC., as three inseparable mixtures 1/2, 3/4, and 5/6 of the (E)- and (Z)-3,4,5-trimethoxycinnamoyl derivatives. The compound pair 1/2 along with four known saponins were also isolated from the roots of Muraltia satureioides DC. Their structures were elucidated mainly by spectroscopic experiments including 2D-NMR techniques as 3-O-(β-D-glucopyranosyl)presenegenin 28-{O-β-D-apiofuranosyl-(13)-O-[β-D-xylopyranosyl-(14)]-O-α-L-rhamnopyranosyl-(12)-O-[6-O-acetyl-β-D-galactopyranosyl-(13)]-4-O-[(E)-3,4,5-trimethoxycinnamoyl]-β-D-fucopyranosyl} ester (1) and its (Z)-isomer 2, 3-O-(β-D-g…

chemistry.chemical_classificationStereochemistryChemistryOrganic ChemistryMuraltia heisteriaGlycosideBiochemistryPresenegeninCatalysisMuraltia satureioidesInorganic ChemistryTriterpeneDrug DiscoveryPhysical and Theoretical ChemistryHelvetica Chimica Acta
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Postsynthetic Approach for the Rational Design of Chiral Ferroelectric Metal–Organic Frameworks

2017

International audience; Ferroelectrics (FEs) are materials of paramount importance with a wide diversity of applications. Herein, we propose a postsynthetic methodology for the smart implementation of ferroelectricity in chiral metal−organic frameworks (MOFs): following a single-crystal to single-crystal cation metathesis, the Ca2+ counterions of a preformed chiral MOF of formula Ca6II{CuII24[(S,S)-hismox]12(OH2)3}·212H2O (1), where hismox is a chiral ligand derived from the natural amino acid l-histidine, are replaced by CH3NH3+. The resulting compound, (CH3NH3)12{CuII24[(S,S)-hismox]12(OH2)3}·178H2O (2), retains the polar space group of 1 and is ferroelectric below 260 K. These results op…

chemistry.chemical_classificationStereochemistryChiral ligandRational design02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyMetathesis01 natural sciencesBiochemistryFerroelectricityCatalysis0104 chemical sciencesCrystallographyColloid and Surface Chemistrychemistry[PHYS.COND.CM-MS]Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]Metal-organic frameworkCounterion0210 nano-technology
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High-Yield Synthesis of 20-, 24-, and 28-Membered Macropentolide, -hexolide, and -heptolide, Respectively, from (R)- or (S)-3-hydroxybutanoic acid un…

1988

The macrocyclic pentolide 1, hexolide 2, and heptolide 3 constitute ca. 80% of the oligomers formed in ca. 50% yield from enantiomerically pure 3-hydroxybutanoic acid under Yamaguchi's macrolactonization conditions. The FAB mass spectra of the MH+, M Na+, and MCs+ are reported (Figs. 2, 3, 5, and 6). No cyclic tetramer is detected. The 1H-NMR spectra of the cyclic oligomers, of the monomer, and of the polymer (PHB) are very similar (Fig. 4). Directed synthesis of the open-chain dimer and tetramer of 3-hydroxybutanoic acid and attempted cyclization do not lead to the isolation of the cyclic tetramer.

chemistry.chemical_classificationStereochemistryDimerOrganic ChemistryNuclear magnetic resonance spectroscopyBiochemistryOligomerCatalysisInorganic Chemistrychemistry.chemical_compoundMonomerchemistryTetramerYield (chemistry)Drug DiscoveryMass spectrumPhysical and Theoretical ChemistryLactoneHelvetica Chimica Acta
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Binding motif of ebselen in solution: Chalcogen and hydrogen bonds team up

2020

Ebselen (2-phenyl-1,2-benzoselenazol-3(2H)one), a glutathione peroxidase mimic, is active against several RNA viruses, among others the retrovirus responsible for the COVID-19 pandemic. In this paper 77Se and 1H NMR studies of ebselen are reported and they identify the chalcogen bond (ChB) and hydrogen bond (HB) that are central in the landscape of interactions formed by the compound in solution. The selenium atom and the hydrogen atom at the C7 carbon act as ChB and HB donors and the O and N atoms of neutral molecules function as acceptors. The ChB and HB give rise to a bifurcated supramolecular synthon, which fastens the interaction acceptor opposite to the N–Se covalent bond of the selen…

chemistry.chemical_classificationStereochemistryEbselenHydrogen bondSynthonSupramolecular chemistryGeneral ChemistryCatalysisdrugssupramolecular chemistrychemistry.chemical_compoundChalcogenchemistrycovid-19Covalent bondMaterials ChemistryThiolMoleculeselenium drugs covid-19 chalcogen bond supramolecular chemistryseleniumchalcogen bond
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Tri- and tetraurea piperazine cyclophanes: synthesis and complexation studies of preorganized and folded receptor molecules.

2010

A series of symmetrical tri- and tetrameric N-ethyl- and N-phenylurea-functionalized cyclophanes have been prepared in nearly quantitative yields (86-99 %) from the corresponding tri- and tetraamino-functionalized piperazine cyclophanes and ethyl or phenyl isocyanates. Their conformational and complexation properties have been studied by single-crystal X-ray diffraction, variable-temperature NMR spectroscopy, and ESI-MS analysis. The rigid 27-membered trimeric cyclophane skeleton assisted by a seam of intramolecular hydrogen bonds results in a preorganized ditopic recognition site with an all-syn conformation of the urea moieties that, complemented by a lipophilic cavity of the cyclophane, …

chemistry.chemical_classificationStereochemistryHydrogen bondOrganic ChemistryIodideSupramolecular chemistryGeneral ChemistryNuclear magnetic resonance spectroscopyCatalysisCrystallographychemistry.chemical_compoundPiperazinechemistryIntramolecular forceMoleculeCyclophaneChemistry (Weinheim an der Bergstrasse, Germany)
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