Patent classifications
C07F3/003
Hypergolic metal organic frameworks
A hypergolic metal organic framework material for producing a hypergol when combined with an oxidizer, comprising a general structure M1-L-M2, wherein L is an aromatic organic linker comprising one or more unsaturated substituents, and wherein M1 and M2 are same or different metal cations.
SYSTEM AND PROCESS FOR CONTINUOUS AND CONTROLLED PRODUCTION OF METAL-ORGANIC FRAMEWORKS AND METAL-ORGANIC FRAMEWORK COMPOSITES
A MOF production system and method of making are detailed for continuous and controlled synthesis of MOFs and MOF composites. The system can provide optimized yields of MOFs and MOF composites greater than or equal to 95%.
MATERIAL AND METHOD FOR CARBON DIOXIDE FIXATION
[Problem] To provide a new way for fixing carbon dioxide under mild conditions and with high efficiency.
[Solution] The material for carbon dioxide fixation according to the present invention contains a metal ion donor and an amine as a precursor of a bridging ligand. The amine is configured to react with a gaseous carbon dioxide to form the bridging ligand having at least one carbamate anion moiety. The bridging ligand is configured to react with the metal ion donor to form a coordination polymer in which a plurality of the metal ions is linked by the bridging ligand.
ZINC COMPLEXES AND THEIR USES
##STR00001##
A zinc complex of a compound where the zinc complex is either a complex of JBIR-141 and a zinc ion and has the chemical formula C.sub.31H.sub.48N.sub.6O.sub.11Zn, or when the zinc complex is a complex of JBIR-142 and a zinc ion and has the chemical formula C.sub.31H.sub.48N.sub.6O.sub.12Zn.
MULTIMETAL-METAL ORGANIC FRAMEWORK ADSORBENT
Mixed metal metal-organic frameworks (MM-MOFs) of copper-1,3,5-benzenetricarboxylate (BTC), M-Cu-BTC, wherein M is Zn(II), Ni(II), Co(II), and/or Fe(II) may be made using post-synthetic exchange (PSE) with metal ions. Such MM-MOFs may be used in H.sub.2 storage, especially Ni(II) and Co(II) MM-MOFs. Selected metal exchanged materials can provide gravimetric H.sub.2 uptake around 1.63 wt. % for Zn—Cu-BTC, around 1.61 wt. % for Ni—Cu-BTC, around 1.63 wt. % for Fe—Cu-BTC, and around 1.12 wt. % for Co—Cu-BTC.
Strontium precursor, method for preparing same, and method for forming thin film by using same
Disclosed herein is a novel strontium precursor containing a beta-diketonate compound. Being superior in thermal stability and volatility, the strontium precursor can form a quality strontium thin film.
FABRICATION OF METAL ORGANIC FRAMEWORK MATERIALS USING A LAYER-BY-LAYER SPIN COATING APPROACH
Embodiments describe a method of depositing an MOF, including depositing a metal solution onto a substrate, spinning the substrate sufficient to spread the metal solution, depositing an organic ligand solution onto the substrate and spinning the substrate sufficient to spread the organic ligand solution and form a MOF layer.
Bridged alkaline earth metal alkylphenates
A bridged alkaline earth metal alkylphenate having reduced monomeric alkylphenol is prepared by reacting (a) a 4-alkylphenol, unsubstituted at the ortho positions, (b) an alkaline earth metal oxide or hydroxide, (c) a bridging agent comprising sulfur or a carbonyl compound of 1 to about 6, or to 4 or to 2, carbon atoms, and (d) a 2,6-dialkylphenol. The amount of the 2,6-dialkylphenol is 0.05 to 3 moles per 1 mole of the 4-alkylphenol; if there is a molar excess of the 2,6-dialkylphenol, then the excess is added after initial reaction.
Zinc or Copper (II) Salt and Use Thereof as a Biocide
Zinc and copper (II) salts of the general formula CH.sub.2═C(R.sup.1)COO-M-OCOR.sup.2 are disclosed, wherein M-Zn or Cu, R.sup.1—H or CH.sub.3, R.sup.2—C.sub.2-C.sub.25 alkyl, or R.sup.2—CO—O— group is crotonate, or sorbate, or linoleate, excluding the compounds: CH.sub.2═C(CH.sub.3)—COO—Zn—O—CO—C.sub.2H.sub.5, CH.sub.2═CH—COO—Zn—O—CO—C.sub.2H.sub.5, CH.sub.2═CH—COO—Cu—O—CO—C.sub.2H.sub.5, CH.sub.2═C(CH.sub.3)—COO—Zn—O—CO—(CH.sub.2).sub.4—CH.sub.3, CH.sub.2═CH—COO—Zn—O—CO—(CH.sub.2).sub.4—CH.sub.3, CH.sub.2═CH—COO—Zn—O—CO—(CH.sub.2).sub.6—CH.sub.3, CH.sub.2═C(CH.sub.3)—COO—Zn—O—CO—(CH.sub.2).sub.6—CH.sub.3, CH.sub.2═CH—COO—Cu—O—CO—(CH.sub.2).sub.6—CH.sub.3, CH.sub.2═CH—COO—Zn—O—CO—(CH.sub.2).sub.14—CH.sub.3, CH.sub.2═C(CH.sub.3)—COO—Zn—O—CO—(CH.sub.2).sub.16—CH.sub.3, CH.sub.2═C(CH.sub.3)—COO—Zn—O—CO-iso-C.sub.17H.sub.35, CH.sub.2═CH—COO—Zn—O—CO-iso-C.sub.17H.sub.35, CH.sub.2═C(CH.sub.3)—COO—Zn—O—CO—(CH.sub.2).sub.17—CH.sub.3. Salts of the general formula wherein R.sup.2—C.sub.2-C.sub.25 alkyl, or R.sup.2—CO—O— group is crotonate, or sorbate, or linoleate, are applicable as biocides.
ALKALINE EARTH METAL SALTS
A composition may include an alkaline earth metal salt. The alkaline earth metal salt may have an angle of repose less than or equal to about 34. The alkaline earth salt may be used to form a tablet. The tablet may have a friability less than or equal to about 1%. A method of forming an alkaline earth metal salt may include providing a slurry that includes an alkaline earth metal and an organic polyatomic anion, and spray drying the slurry to form a spray dried alkaline earth metal salt. The slurry temperature may be greater than or equal to about 50° C. A method of forming a tablet may include tableting a non-agglomerated alkaline earth metal salt.