C07F17/02

Redox-active compounds and uses thereof

Ferrocene based redox-active compounds have a total number of cyclopentadienyl substituents that is three or greater per ferrocene core. The cyclopentadienyl substituents generally have a linker and a solubilizing group. An aqueous solution of the redox-active compound and a salt may be used as an electrolyte. Aqueous compositions including the redox-active compounds may be used in electrodialysis systems.

METHOD FOR DEGRADING ANTIBIOTICS BY AQUEOUS PHASE TRANSFER CATALYSIS USING AN ANIONIC LIQUID AND HYDROGEN PEROXIDE

Disclosed is a method for degrading antibiotics by aqueous phase transfer catalysis using an anionic liquid and hydrogen peroxide, including: adding hydrogen peroxide to a wastewater containing the antibiotics to obtain a first mixture, and adjusting a pH of the first mixture to 3-4 to form an aqueous phase, and adding a catalyst to a water-insoluble ionic liquid to obtain a second mixture, and stirring the second mixture to form an ionic liquid phase, wherein the catalyst is selected from the group consisting of ferrocene, iron dodecyl sulfonate, ferrous dodecyl sulfonate, and copper dodecyl sulfonate; and mixing the aqueous phase and the ionic liquid phase in a volume ratio of (8-11):1 to obtain a mixed phase, and stirring the mixed phase to degrade the antibiotics.

METHOD FOR DEGRADING ANTIBIOTICS BY AQUEOUS PHASE TRANSFER CATALYSIS USING AN ANIONIC LIQUID AND HYDROGEN PEROXIDE

Disclosed is a method for degrading antibiotics by aqueous phase transfer catalysis using an anionic liquid and hydrogen peroxide, including: adding hydrogen peroxide to a wastewater containing the antibiotics to obtain a first mixture, and adjusting a pH of the first mixture to 3-4 to form an aqueous phase, and adding a catalyst to a water-insoluble ionic liquid to obtain a second mixture, and stirring the second mixture to form an ionic liquid phase, wherein the catalyst is selected from the group consisting of ferrocene, iron dodecyl sulfonate, ferrous dodecyl sulfonate, and copper dodecyl sulfonate; and mixing the aqueous phase and the ionic liquid phase in a volume ratio of (8-11):1 to obtain a mixed phase, and stirring the mixed phase to degrade the antibiotics.

METALLOCENE COMPOUND, AND PREPARATION METHOD THEREFOR AND APPLICATION THEREOF

A metallocene compound having a structure shown by formula (I). A functional group connected to a bridging atom of the metallocene compound is an amine-substituted group and/or a metallocene-substituted group and/or a substituted metallocene group. A metallocene catalyst containing the metallocene compound has high catalytic activity, and can synthesize metallocene polypropylene having high isotacticity.


R.sup.IR.sup.IIZ(Cp.sup.III).sub.n(E).sub.2-nML.sup.IVL.sup.V   (I)

METALLOCENE COMPOUND, AND PREPARATION METHOD THEREFOR AND APPLICATION THEREOF

A metallocene compound having a structure shown by formula (I). A functional group connected to a bridging atom of the metallocene compound is an amine-substituted group and/or a metallocene-substituted group and/or a substituted metallocene group. A metallocene catalyst containing the metallocene compound has high catalytic activity, and can synthesize metallocene polypropylene having high isotacticity.


R.sup.IR.sup.IIZ(Cp.sup.III).sub.n(E).sub.2-nML.sup.IVL.sup.V   (I)

COMPLEXES
20220356200 · 2022-11-10 ·

A compound of formula (I) wherein M is Pd(II) or Ni(II); X is a halide; R.sub.1 and R.sub.2 are independently organic groups having 1-20 carbon atoms, or R.sub.1 and R.sub.2 are linked to form a ring structure with the phosphorus atom; R.sub.3 is an organic group having 1-20 carbon atoms; provided that R.sub.1, R.sub.2, R.sub.3 are not each phenyl.

##STR00001##

COMPLEXES
20220356200 · 2022-11-10 ·

A compound of formula (I) wherein M is Pd(II) or Ni(II); X is a halide; R.sub.1 and R.sub.2 are independently organic groups having 1-20 carbon atoms, or R.sub.1 and R.sub.2 are linked to form a ring structure with the phosphorus atom; R.sub.3 is an organic group having 1-20 carbon atoms; provided that R.sub.1, R.sub.2, R.sub.3 are not each phenyl.

##STR00001##

FERROCENE DERIVATIVE, PREPARATION METHOD THEREFOR AND USE THEREOF
20220356199 · 2022-11-10 ·

A ferrocene derivative has the formula (I), In formula (I), Z is selected from O, NH and S; R.sub.1 is selected from hydrogen, methyl and halogen; R.sub.2 is selected from hydrogen, halogen, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 alkoxy, C.sub.1-C.sub.6 haloalkyl, C.sub.1-C.sub.6 haloalkoxy and nitro; and n is an integer from 0 to 5, and R.sub.2 may be the same or different groups. The ferrocene derivative, a salt thereof, as well as a solvate thereof have anti-tumor activity, and can be used as candidate drugs or lead compounds for treating diseases such as tumor and cancer.

##STR00001##

FERROCENE DERIVATIVE, PREPARATION METHOD THEREFOR AND USE THEREOF
20220356199 · 2022-11-10 ·

A ferrocene derivative has the formula (I), In formula (I), Z is selected from O, NH and S; R.sub.1 is selected from hydrogen, methyl and halogen; R.sub.2 is selected from hydrogen, halogen, C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 alkoxy, C.sub.1-C.sub.6 haloalkyl, C.sub.1-C.sub.6 haloalkoxy and nitro; and n is an integer from 0 to 5, and R.sub.2 may be the same or different groups. The ferrocene derivative, a salt thereof, as well as a solvate thereof have anti-tumor activity, and can be used as candidate drugs or lead compounds for treating diseases such as tumor and cancer.

##STR00001##

Bladder cancer photodynamic therapeutic agents with off-on magnetic resonance imaging enhancement

Provided herein are porphyrinato-lanthanide complexes useful as theranostic agents and methods of preparation and use thereof. The porphyrinato-lanthanide complexes are useful in the treatment and imaging of cancer.