Preparing a nickel phosphorus ligand complex
US-9371346-B2 · Jun 21, 2016 · US
US11084839B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11084839-B2 |
| Application number | US-201816036932-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 16, 2018 |
| Priority date | Jul 14, 2017 |
| Publication date | Aug 10, 2021 |
| Grant date | Aug 10, 2021 |
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Provided herein are a symmetrical pincer metal and bimetallic complexes. The symmetrical pincer metal complex includes a structure according to Formula I:wherein M is a metal; each N and N′ is independently nitrogen or carbon; Z is selected from the group consisting of CH, C, and N; n is 0-3; each L is independently a neutral or charged ligand; and each R is independently an alkyl, Nx, CH2TMS. The symmetrical bimetallic complex includes a structure according to Formula II:wherein M is a metal; each N and N′ is independently nitrogen or carbon; Z is selected from the group consisting of CH, C, and N; n is 0-3; each L is independently a neutral or charged ligand; and wherein each R is independently an alkyl, Nx, CH2TMS. Also provided herein is a method of catalyzing a reaction including administering one or more of the compounds disclosed herein.
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What is claimed is: 1. A method of catalyzing reduction of CO 2 comprising administering a complex having a structure according to Formula I: wherein M is a transition metal; wherein each N and N′ is independently nitrogen; wherein Z is selected from the group consisting of CH, C, and N; wherein n is 0-3; wherein each L is independently a neutral or charged ligand; wherein each R is independently an alkyl, 3,3-dimethylbutyl (Nx), or CH 2 Si(CH 3 ) 3 (trimethylsilylmethyl); and wherein the dashed lines are independently a 6 membered ring including Z and the ortho C, N═CH, or HC═CH. 2. The method of claim 1 , wherein at least one L is selected from the group consisting of monodentate, bidentate, and tridentate ligands. 3. The method of claim 1 , wherein at least one L is selected from the group consisting of halogen, alkyl, aryl, biaryl, substituted aryl, aryloxy, acetate, trifluoroacetate, and alkoxy. 4. The method of claim 3 , wherein at least one L is a halogen. 5. The method of claim 3 , wherein the alkyl is selected from the group consisting of methyl, ethyl, propyl, butyl, pentyl, and hexyl. 6. The method of claim 3 , wherein the substituted aryl is a fluoro substituted aryl. 7. The method of claim 1 , wherein the alkyl of R is selected from the group consisting of methyl, ethyl, propyl, butyl, pentyl, and hexyl. 8. The method of claim 1 , wherein M is Ni. 9. The method of claim 8 , wherein the complex is selected from the group consisting of: 10. The method of claim 1 , wherein M is Pt. 11. The method of claim 10 , wherein the complex is selected from the group consisting of: 12. The method of claim 1 , wherein M is Pd. 13. The method of claim 12 , wherein the complex is selected from the group consisting of:
Electrolytic production of inorganic compounds or non-metals · CPC title
Nickel compounds · CPC title
Palladium compounds · CPC title
Platinum compounds · CPC title
from inorganic compounds · CPC title
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