IP Library Granted Patent US 9,229,006
Granted Patent B2
US 9,229,006 · App. 14/184,558 · Granted Jan 5, 2016

Small water-soluble quantum dots

Inventors: Paul R Selvin (Urbana, IL); Pinghua Ge (Urbana, IL)
Assignee: Board of Trustees of the University of Illinois
G01N33/587C09K11/00C09K11/0811C09K11/565G01N33/588Y10S977/74Y10S977/774Y10S977/883Y10S977/892
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Quick Facts
Patent No.
US 9,229,006
App. No.
14/184,558
Granted
Jan 5, 2016
Kind
B2
Abstract

Water-soluble, stable fluorescent PEGylated alkanethiol-coated quantum dots are made by contacting quantum dots with PEGylated alkanethiol in a non-oxidative, water-immiscible organic reaction solvent under a non-oxidative gas, wherein the reaction solvent is in contact with an aqueous phase, at elevated temperature and time sufficient to coat the dots with the PEGylated alkanethiol, wherein resultant water-soluble, stable fluorescent PEGylated alkanethiol-coated dots enter the aqueous phase.

Claims (28)

1. A method of making water-soluble, stable fluorescent PEGylated alkanethiol-coated quantum dots, the method comprising:

contacting quantum dots with PEGylated alkanethiol in a non-oxidative, water-immiscible organic reaction solvent under a non-oxidative gas, wherein the reaction solvent is in contact with an aqueous phase, at elevated temperature of 40-80° C. and time sufficient to coat the dots with the PEGylated alkanethiol, wherein resultant water-soluble, stable fluorescent PEGylated alkanethiol-coated dots enter the aqueous phase, wherein the PEGylated alkanethiol is in a mixture of the PEGylated alkanethiol and functionalized PEGylated alkanethiol.

2. The method of claim 1 wherein the elevated temperature is about 60 C and the time is about 4 hours.

3. The method of claim 1 wherein the gas comprises inert gas that is nitrogen.

4. The method of claim 1 wherein the reaction solvent comprises toluene, chlorobenzene, or octane.

5. The method of claim 1 wherein the aqueous phase comprises tetraethylammonium hydroxide (20% wt) in water.

6. The method of claim 1 wherein:

the elevated temperature is about 60 C and the time is about 4 hours;

the gas comprises inert gas that is nitrogen;

the reaction solvent comprises toluene; and

the aqueous phase comprises tetraethylammonium hydroxide (20% wt) in water.

7. The method of claim 1 wherein the dots comprise a nanocrystal metal core of CdSe, HgCdSe, CdTe, ZnTe, ZnS, CdS or InAs.

8. The method of claim 1 wherein the dots further comprise a shell of ZnS or CdS.

9. The method of claim 1 wherein the coated dots have a diameter less than 10 nm.

10. The method of claim 1 wherein:

the dots comprise a nanocrystal metal core of CdSe, CdTe, ZnTe, or ZnS;

the dots further comprise a shell of ZnS or CdS; and

the coated dots have a diameter less than 10 nm.

11. The method of claim 1 wherein the PEGylated alkanethiol is in a mixture of the PEGylated alkanethiol and functionalized PEGylated alkanethiol, wherein the functionalized PEGylated is 10% or less of the mixture.

12. The method of claim 1 wherein the PEGylated alkanethiol is in a mixture of the PEGylated alkanethiol and functionalized PEGylated alkanethiol, wherein the functionalized PEGylated alkanethiol is carboxyl PEGylated alkanethiol or amine PEGylated alkanethiol.

13. The method of claim 1 wherein the PEGylated alkanethiol is in a mixture of the PEGylated alkanethiol and functionalized PEGylated alkanethiol, wherein the functionalized PEGylated alkanethiol is a corresponding carboxyl PEGylated alkanethiol.

14. The method of claim 1 wherein the PEGylated alkanethiol is in a mixture of the PEGylated alkanethiol and functionalized PEGylated alkanethiol, wherein the functionalized PEGylated alkanethiol is a corresponding carboxyl PEGylated alkanethiol, wherein the mixture is HSC11(EG)4-OH/HSC11(EG)4-COOH (2.5%).

15. The method of claim 1 wherein the functionalized PEGylated alkanethiols of the coated dots are further functionalized with an affinity tag.

16. The method of claim 1 further comprising isolating the coated dots with anion exchange chromatography.

17. The method of claim 1 further comprising washing the aqueous phase containing the coated dots with a water-immiscible organic wash solvent and then isolating the coated dots with anion exchange chromatography.

18. The method of claim 1 further comprising isolating the coated dots and (a) storing the isolated dots in refrigeration for over one month, and/or (b) storing the isolated dots in a mixture comprising at least 50% ethylene glycol.

19. A composition comprising an organic phase comprising quantum dots and PEGylated alkanethiol, at elevated temperature of 40-80° C. under a non-oxidative gas, in contact with an aqueous phase comprising water-soluble, stable fluorescent corresponding PEGylated alkanethiol-coated quantum dots, wherein the PEGylated alkanethiol is in a mixture of the PEGylated alkanethiol and functionalized PEGylated alkanethiol.

20. The composition of claim 19 wherein the coated dots have a diameter less than 10 nm.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jan 9, 2015
From: UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 034747/0934 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 12, 2014
From: SELVIN, PAUL R.; GE, PINGHUA
To: THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS
Reel/Frame 032409/0879 →
Continuity (1)
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