Surface bonded Rh-bis(diarylphosphine) on magnetic nanoparticles as a recyclable catalyst for hydroformylation of olefins

Patent metadata

Field	Value
Publication number	US-9480978-B1
Application number	US-201614989219-A
Country	US
Kind code	B1
Filing date	Jan 6, 2016
Priority date	Jan 6, 2016
Publication date	Nov 1, 2016
Grant date	Nov 1, 2016

Abstract

A functionalized nanomaterial having an average particles size of less than 10 nm comprising an iron oxide nanoparticle core and a bis(diarylphosphinomethyl) dopamine based ligand layer anchored to the iron oxide nanoparticle core is disclosed. In addition, a catalyst composition for use in a variety of chemical transformations wherein the bisphosphine groups of the functionalized nanomaterial chelate a catalytic metal is disclosed. In addition, a method for producing the functionalized nanomaterial and a method for the hydroformylation of olefins to aldehydes employing the functionalized nanomaterial with high conversion percentage and high selectivity are disclosed.

First claim

The invention claimed is:

1. A functionalized nanomaterial, comprising;
an iron oxide nanoparticle core, and
a bis(diarylphosphinomethyl) dopamine ligand
wherein the bis(diarylphosphinomethyl) dopamine ligand is anchored to a surface of the iron oxide nanoparticle core by phenolic hydroxide groups to form a bis(diarylphosphinomethyl) dopamine ligand layer, and
wherein the bisphosphine groups of the bis(diarylphosphinomethyl) dopamine ligand chelate a catalytic metal.

2. The functionalized nanomaterial of claim 1 , which is in the form of particles having a spherical morphology and an average diameter of 1-20 nm.

3. The functionalized nanomaterial of claim 1 , which has a phosphine content of 0.2-1.0 mmol per gram of functionalized nanomaterial.

4. The functionalized nanomaterial of claim 1 , wherein the average thickness of the bis(diarylphosphinomethyl) dopamine ligand layer is less than 5 nm.

5. The functionalized nanomaterial of claim 1 , wherein the bis(diarylphosphinomethyl) dopamine ligand layer covers greater than 70% of the surface of the iron oxide nanoparticle core.

6. The functionalized nanomaterial of claim 1 , wherein the iron oxide nanoparticle core comprises magnetite, Fe 3 O 4 .

7. The functionalized nanomaterial of claim 1 , wherein the bis(diarylphosphinomethyl) dopamine ligand is bis(diphenylphosphinomethyl) dopamine.

8. The functionalized nanomaterial of claim 1 , which loses less than 1% of its total weight after heating at a temperature of 200° C. and less than 10% of its total weight after heating at a temperature of 500° C.

9. A process for producing the functionalized nanomaterial of claim 1 , comprising;
reacting paraformaldehyde with a phosphine to produce a phosphinomethanol,
reacting the phosphinomethanol with a dopamine salt to form the bis(diarylphosphinomethyl) dopamine ligand,
mixing the bis(diarylphosphinomethyl) dopamine ligand with the iron oxide nanoparticle core to form the functionalized nanomaterial.

10. The process of claim 9 , wherein the iron oxide nanoparticle core is formed by precipitating an iron salt under alkaline conditions.

11. A method for hydroformylating an olefin to a corresponding aldehyde, comprising;
mixing the functionalized nanomaterial of claim 1 with the olefin,
adding a rhodium salt as source of the catalytic metal, then
hydroformylating the olefin in the presence of carbon monoxide or a carbon monoxide surrogate to form the corresponding aldehyde.

12. The method of claim 11 , further comprising recovering and reusing the functionalized nanomaterial in at least 2 reaction iterations.

13. The method of claim 11 , wherein the rhodium salt comprises rhodium (III) chloride, RhCl 3 or 2,5-norbornadiene-rhodium (I) chloride dimer, [Rh(NBD)Cl] 2 .

14. The method of claim 11 , wherein the olefin is a styrene.

15. The method of claim 11 , wherein a percent conversion from the olefin to the corresponding aldehyde is greater than 90%.

16. The method of claim 11 , wherein the mixing involves no more than 50 mg of functionalized nanomaterial per 1.0 mmol of olefin.

17. The method of claim 11 , wherein the corresponding aldehyde has a linear aldehyde form and a branched aldehyde form and the ratio of the linear aldehyde form to the branched aldehyde form is greater than or equal to 1.

18. A catalyst composition comprising the functionalized nanomaterial of claim 1 and a catalytic metal, wherein the bisphosphine groups of the bis(diarylphosphinomethyl) dopamine ligand of the functionalized nanomaterial chelate the catalytic metal.

19. The catalyst composition of claim 18 , wherein the catalytic metal is at least one selected from the group consisting of nickel, platinum, palladium, rhodium, iron, gold, silver, ruthenium and iridium.

20. The catalyst composition of claim 18 , wherein the catalyst composition is employed in at least one chemical transformation selected from the group consisting of hydrogenations, palladium-catalyzed coupling reactions and selective oxidations.

Assignees

• Univ King Fahd Pet & Minerals

Inventors

• Shaikh Mohammed Nasiruzzaman
• Yamani Zain Hassan

Classifications

• B01J2235/10

  Infrared [IR] · CPC title

• B01J2235/05

  Nuclear magnetic resonance [NMR] · CPC title

• B01J2235/30

  Scanning electron microscopy; Transmission electron microscopy · CPC title

• B01J35/45

  Nanoparticles · CPC title

• B01J2235/15

  X-ray diffraction · CPC title