Basf Aktiengesellschaft

Basf Se Corporation

University of Michigan

Fraunhofer-gesellschaft Zur Foerderung Der Angewandten Forschung E.v.

Hermann Pütter

Ulrich Müller

Dieter Baumann

Heinz Hannebaum

Michael Hesse

Wolfgang Harder

Norbert Rieber

Omar M Yaghi

Marcus Guzmann

Markus Schubert

Georg Heinrich Grosch

Michael Schulz

Andreas Fischer

Franz Josef Brocker

Natalia Trukhan

Lars Wittenbecher

Ulrich Griesbach

Jürgen Huff

Andreas Weiper-Idelmann

Helge Wessel

Harald Winsel

Ingo Richter

The present invention relates to a process for preparing a porous metal organic framework comprising at least two organic compounds coordinated to at least one metal ion, which comprises the steps

Process for preparing porous metal organic frameworks

Process for preparing primary amines having a cyclopropyl unit and a primary amino group bound to an aliphatic or cycloaliphatic carbon atom (amine A) by cathodically reducing oximes having a cyclopropyl unit or oxime derivatives in which the hydrogen atom in the oxime group has been replaced by an alkyl or acyl group (oxime O) at a temperature of from 50 to 100&#xb0; C. in an essentially anhydrous electrolyte solution in a divided electrolysis cell.

Method for the production of primary amines comprising a primary amino group which bound to an aliphatic or cycloaliphatic C-atom, and a cyclopropyl unit

The present invention relates to a method of storing a liquefied gas in a container containing a metal-organic framework material, the container filled with such a gas, a process for filling container and the use of the container to release the gas.

Metal-organic framework materials for gaseous hydrocarbon storage

A process is provided for the preparation of trialkyl orthocarboxylates by the electrochemical oxidation of alpha, beta-diketones or alpha, beta-hydroxyketones, the keto group being present in the form of a ketal group derived from C- to C-alkylalcohols and the hydroxyl group optionally being present in the form of an ether group derived from C- to C-alkylalcohols (ketals K), in the presence of C- to C-alcohols (alcohols A), the molar ratio of the ketals K to the alcohols A in the electrolyte being 0.2:1 to 10:1.

Method for producing orthocarbonic acid trialkyl esters

A process for preparing butanetetracarboxylic acid derivatives as product of value I by coupled electrosynthesis which comprises cathodically reducing a compound selected from the group consisting of maleic esters, maleic ester derivatives, fumaric esters and fumaric ester derivatives where at least one hydrogen atom in positions 2 and 3 may be replaced by inert groups and obtaining a product of value II at the node.

Production of butane tetracarboxylic acid derivative by means of coupled electrosynthesis

Gauze catalyst based on titanium or vanadium zeolites and inert gauze

Electrolytic plate stack cell

Preparation of phthalides

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Neustadt, Germany

Hermann Pütter