Search results for "Cyclooctene"

1972

The metathesis reaction of cyclooctene was investigated with respect to the solvent, the catalyst, and the ratio of its components. A necessary condition for an active metathesis catalyst appears to be the presence of two transition metal-carbon bonds in a complex of the transition metal compound with an aluminum halide. A structure for the active complex is proposed. Die Metathese-Reaktion von Cycloocten wurde unter dem Einflus verschiedener Losungsmittel, verschiedener Katalysatorsysteme und Verhaltnisse der Katalysatorkomponenten untersucht. Die Ergebnisse lassen darauf schliesen, das die aktiven Katalysatoren Komplexe besonderer Ubergangsmetallverbindungen mit Aluminiumhalogeniden darst…

CCDC 634268: Experimental Crystal Structure Determination

2007

Related Article: S.Dobis, D.Schollmeyer, Chunmei Gao, Derong Cao, H.Meier|2007|Eur.J.Org.Chem.|2007|2964|doi:10.1002/ejoc.200700140

CCDC 251049: Experimental Crystal Structure Determination

2005

Related Article: R.Herges, A.Papafilippopoulos, K.Hess, C.Chiappe, D.Lenoir, H.Detert|2005|Angew.Chem.,Int.Ed.|44|1412|doi:10.1002/anie.200461632

The Catalytic Effect of Fluoroalcohol Mixtures Depends on Domain Formation

2017

In the present contribution, we investigated catalytically active mixtures of 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) and aqueous H2O2 by molecular dynamics simulations. It is clearly observable that the HFIP molecule strongly binds to the H2O2, which is necessary for the desired catalytic reaction to occur. Upon the addition of the substrate cyclooctene to the solution, this interaction is enhanced, which suggests that the catalytic activity is increased by the presence of the hydrocarbon. We could clearly observe the microheterogeneous structure of the mixture, which is the result of the separation of the hydroxyl groups, water, and H2O2 from the fluorinated alkyl moiety in the form of l…

Model Pumices Supported Metal Catalysts

1997

The catalyzed, selective hydrogenation, in liquid phase, of 1,3-cyclooctadiene was studied on a series of Pd catalysts supported on natural pumice, model pumices (with variable content of alkali metal ions), silica, and sodium-doped silica. At constant pressure of H2(1 atm.) the reaction follows a zero-order kinetic for all the Pd catalysts. At low metal dispersion (Dx < 20%), Pd/pumice catalysts exhibit higher activity as compared to Pd/silica catalysts; the turnover frequency is maintained even at high metal dispersion in Pd/pumice but Pd/silica and Pd/model pumices without alkali ions show a decrease in activity. At increasingDx, the binding energy shift of Pd 3dlevel is negative in Pd/p…

Synthesis, Structure and Catalytic Properties of Dinuclear Mo-VI Complexes with Ditopic Diaminotetraphenols

2013

MoVI complexes with novel ditopic diaminotetraphenol ligands have been prepared by using a one-pot procedure in methanol or DMSO with [MoO2(acac)2] (acac = acetylacetonate) as the molybdenum source. The complexes were characterised with X-ray diffraction, NMR spectroscopic studies, elemental analysis and IR spectroscopy. In the solid state, the compounds represent either a rodlike molecular or oxido-bridged polymeric structure. The catalytic activity of the complexes was investigated by oxidising benzyl alcohol and 1-phenylethanol with hydrogen peroxide to the corresponding aldehyde and ketone, respectively. Furthermore, the catalytic activity was surveyed also in epoxidation of cyclooctene.

ChemInform Abstract: Synthesis of a Tetraazido-Substituted 2-Tetrazene from 1,5- Cyclooctadiene and Iodine Azide.

2010

In contrast to the addition of iodine azide to cyclooctene (1) or 1,3-cyclooctadiene (5), its reaction with 1,5-cyclooctadiene (12) leads mainly to the surprisingly stable tetraazido-substituted 2-tetrazene 14 The structure of this was established by 15N-NMR studies and an X-ray structural analysis. Treatment of 14 with hydrochloric acid yields the diazido-substituted 9-azabicyclo[3.3.1]nonane 20.

Evaluation of the inverse electron demand Diels-Alder reaction in rats using a scandium-44-labelled tetrazine for pretargeted PET imaging

2019

Background Pretargeted imaging allows the use of short-lived radionuclides when imaging the accumulation of slow clearing targeting agents such as antibodies. The biotin-(strept)avidin and the bispecific antibody-hapten interactions have been applied in clinical pretargeting studies; unfortunately, these systems led to immunogenic responses in patients. The inverse electron demand Diels-Alder (IEDDA) reaction between a radiolabelled tetrazine (Tz) and a trans-cyclooctene (TCO)-functionalized targeting vector is a promising alternative for clinical pretargeted imaging due to its fast reaction kinetics. This strategy was first applied in nuclear medicine using an 111In-labelled Tz to image TC…

Trans -Cyclooctene-Functionalized PeptoBrushes with Improved Reaction Kinetics of the Tetrazine Ligation for Pretargeted Nuclear Imaging

2020

Tumor targeting using agents with slow pharmacokinetics represents a major challenge in nuclear imaging and targeted radionuclide therapy as they most often result in low imaging contrast and high radiation dose to healthy tissue. To address this challenge, we developed a polymer-based targeting agent that can be used for pretargeted imaging and thus separates tumor accumulation from the imaging step in time. The developed targeting agent is based on polypeptide-graft-polypeptoid polymers (PeptoBrushes) functionalized with trans-cyclooctene (TCO). The complementary In-111-labeled imaging agent is a 1,2,4,5-tetrazine derivative, which can react with aforementioned TCO-modified PeptoBrushes i…