Patent classifications
C07F5/069
RECHARGEABLE BATTERY CELL
This disclosure relates to a rechargeable battery cell, comprising: an active metal; at least one positive electrode; at least one negative electrode comprising an active material selected from the group consisting of an insertion material made of carbon, an alloy-forming active material, an intercalation material which does not comprise carbon, and a conversion active material; an SO.sub.2 based electrolyte comprising a first conducting salt which has the formula (I),
##STR00001##
wherein: M is a metal selected from the group consisting of alkali metals, alkaline earth metals, metals of group 12 of the periodic table of the elements, and aluminum; x is an integer from 1 to 3; R.sup.1, R.sup.2, R.sup.3 and R.sup.4 are selected independently of one another from the group consisting of C.sub.1-C.sub.10 alkyl, C.sub.2-C.sub.10 alkenyl, C.sub.2-C.sub.10 alkynyl, C.sub.3-C.sub.10 cycloalkyl, C.sub.6-C.sub.14 aryl and C.sub.5-C.sub.14 heteroaryl; and Z is aluminum or boron.
RECHARGEABLE BATTERY CELL
This disclosure relates to a rechargeable battery cell having an active metal, at least one positive electrode, at least one negative electrode, a housing and an electrolyte, the positive electrode comprising at least one compound in the form of a layered oxide as an active material and the electrolyte being based on SO.sub.2 and comprising at least one first conducting salt which has the formula (I),
##STR00001##
M being a metal selected from the group formed by alkali metals, alkaline earth metals, metals of group 12 of the periodic table of the elements, and aluminum; x being an integer from 1 to 3; the substituents R.sup.1, R.sup.2, R.sup.3 and R.sup.4 being selected independently of one another from the group formed by C.sub.1-C.sub.10 alkyl, C.sub.2-C.sub.10 alkenyl, C.sub.2-C.sub.10 alkynyl, C.sub.3-C.sub.10 cycloalkyl, C.sub.6-C.sub.14 aryl and C.sub.5-C.sub.14 heteroaryl; and Z being aluminum or boron.
METHOD FOR MAKING MAGNESIUM SALT ELECTROLYTE AND ELECTROLYTE
An electrolyte and a method of making an electrolyte of the formula: Mg[Al(R).sub.4].sub.2, where R represents a compound selected from a deprotonated alcohol or thiol; an amine; or a mixture thereof. The method includes the steps of: combining a Mg(AlH.sub.4).sub.2 precursor with an alcohol, thiol or amine of the general formula R—H to create a reaction liquor containing Mg[Al(R).sub.4].sub.2; and washing the reaction liquor in an organic solvent.
Process For Producing Metal Organic Frameworks
The metal organic framework (MOF) MIL-100(Al) can be produced in a process in which aluminum nitrate and trimesic acid are brought to react with one another in an alcohol/water mixture under the action of NH.sub.3 and/or an NH.sub.3-releasing compound under mild conditions.
LOW TEMPERATURE PROCESS FOR THE SYNTHESIS OF MOF CARBOXYLATE NANOPARTICLES
The present invention relates to low temperature process for preparing nanoparticles of porous crystalline Fe-, Al- or Ti-based MOF carboxylate materials with low polydispersity index, and uses thereof, particularly as catalyst support for carrying out heterogeneously catalyzed chemical reactions, or as gas storage/separation/purification material, or as matrix for encapsulating active principles (medicine, cosmetics).
SYNTHESIS OF METAL COMPLEXES AND USES THEREOF
The present disclosure provides novel methods of making aluminum complexes with utility for promoting epoxide carbonylation reactions. Methods include reacting neutral metal carbonyl compounds with alkylaluminum complexes.
METAL-ORGANIC FRAMEWORK CATALYSTS, AND USES THEREOF
Provided herein are metal-organic frameworks having a repeating core structure that generally includes a linker coordinated to a secondary building unit through O-metal-O bonds. The linkers create a framework with a plurality of pores, where a cobalt carbonyl moiety occupies at least a portion of the plurality of pores. Provided are also methods of making such metal-organic frameworks via a solvothermal reaction. The metal-organic frameworks are suitable for use in carbonylation reactions, such as carbonylation of epoxides. The metal-organic frameworks may be used for producing acrylic acid from ethylene oxide and carbon monoxide on an industrial scale. The production may involve various unit operations, including for example a beta-propiolactone production system configured to produce beta-propiolactone from ethylene oxide and carbon monoxide; a polypropiolactone production system configured to produce polypropiolactone from beta-propiolactone; and an acrylic acid production system configured to produce acrylic acid with a high purity by thermolysis of polypropiolactone.
Multivariate and other metal-organic frameworks, and uses thereof
Compositions comprising multivariate metal-organic frameworks and other single-linker metal-organic frameworks are used for containing and storing a gas or fluid or for water harvesting or water purification applications.
MAIN GROUP METAL COMPLEX AND ITS PREPARATION METHOD AND USE
The present invention provides a main group metal complex, or pharmaceutically acceptable salt, solvate, non-covalent bond compound or prodrug thereof, which is composed of planar tetradentate Schiff base ligands and p-block main group metal ions. The main group metal complex can be conveniently prepared, and shows high cytotoxicity to a variety of cancer cell lines and has selective killing effect. The pharmaceutical compositions or pharmaceutical preparations prepared from the main group metal complex according to the present invention can be used for treatment of tumors. The main group metal complex also has fluorescent properties and can be used for fluorescent labeling.
TRANSITION METAL ORGANIC FRAMEWORK HAVING ANTIBACTERIAL PROPERTIES
The present invention relates to a transition metal organic framework, comprising: a transition metal oxide having antibacterial or antifungal properties; and an organic compound having at least one hydrophilic functional group, wherein the organic compound is bound to the transition metal oxide to surround the transition metal oxide and the hydrophilic functional group is placed toward the outside of the transition metal organic framework.