Determination of explosives including RDX

• US 7,666,684 B2
• Filed: 10/16/2006
• Issued: 02/23/2010
• Est. Priority Date: 10/11/2006
• Status: Expired due to Fees

• Current Assignee: Massachusetts Institute of Technology
• Original Assignee: Massachusetts Institute of Technology
• Inventors: Bouffard, Jean, Thomas, Samuel W., Swager, Timothy M., Andrew, Trisha L.
• Primary Examiner(s): Gakh; Yelena G
• Assistant Examiner(s): WEISZ, DAVID G
• Application Number:
  US11/581,777
• Publication Number:
  US 20100022011A1
• Time in Patent Office: 1,226 Days
• Field of Search: None
• US Class Current: 436/106
• CPC Class Codes: G01N 2021/6432 Quenching
• CPC Class Codes: G01N 2021/6441 with two or more labels
• CPC Class Codes: G01N 2021/7786 Fluorescence
• CPC Class Codes: G01N 21/643 non-biological material
• CPC Class Codes: G01N 33/22 Fuels; Explosives
• CPC Class Codes: Y10T 436/145555 Hetero-N
• CPC Class Codes: Y10T 436/17 Nitrogen containing
• CPC Class Codes: Y10T 436/200833 Carbonyl, ether, aldehyde or ketone containing

Abstract

The present invention provides sensors and methods for determination of an analyte. The analytes may be determined by monitoring, for example, a change in an optical signal of an emissive material upon exposure to an analyte. In some embodiments, the analyte and the emissive material may interact via a chemical reaction, or other chemical, biochemical or biological interaction (e.g., recognition), to form a new emissive species. In some cases, the present invention may be used for the detection of analytes such as explosives (e.g., RDX, PETN). Methods of the present invention may be advantageous in that the high sensitivity of luminescence (e.g., fluorescence) spectroscopy can allow for the reliable detection of small changes in luminescence intensity.

Claims

1. A method for determination of an analyte, comprising:

exposing a compound having a luminescence emission to a sample suspected of containing an analyte, wherein the analyte, if present, interacts with the compound to accept a hydride equivalent from the compound, causing a change in the luminescence emission of the compound;

wherein the compound has the structure,

2. A method as in claim 1, further comprising exposing the compound and the analyte, if present, to a source of energy applicable to the compound to cause the compound to transfer an electron to the analyte, if present.

3. A method as in claim 2, wherein, upon exposure to the source of energy, the analyte interacts with the compound via an electron-proton-electron transfer reaction.

4. A method as in claim 3, wherein the electron-proton-electron transfer reaction comprises transfer of a proton and at least one electron from the compound to the analyte.

5. A method as in claim 3, wherein the electron-proton-electron transfer reaction comprises transfer of a proton and two electrons from the compound to the analyte.

6. A method as in claim 1, wherein the change comprises a change in the wavelength of the luminescence.

7. A method as in claim 1, wherein the change comprises a decrease in luminescence intensity.

8. A method as in claim 1, wherein the change comprises an increase in luminescence intensity.

9. A method as in claim 1, wherein M is Co or Zn.

10. A method as in claim 1, wherein M is Zn.

11. A method as in claim 1, wherein L¹ and L² are halide, methanol, or L¹ and L² are joined together to form ethylenediamine or a substituted derivative thereof.

12. A method as in claim 1, wherein L¹ and L² are joined together to form a ligand having the structure,

13. A method as in claim 1, wherein the compound is in solution.

14. A method as in claim 1, further comprising a support material, wherein the compound is dispersed within the support material.

15. A method as in claim 14, wherein the support material is a polymer.

16. A method as in claim 15, wherein the polymer is poly(methyl methacrylate), polyethylene, polypropylene, poly(vinyl chloride), poly(vinyl benzoate), poly(vinyl acetate), cellulose, corn starch, poly(vinyl pyrrolidinone), polyacrylamide, epoxy, silicone, poly(vinyl butyral), polyurethane, nylon, polacetal, polycarbonate, polyester, polyether, polybutadiene, or combinations thereof.

17. A method as in claim 15, wherein the polymer is poly(methylmethacrylate), poly(vinylpyrrolidinone), or poly(4-vinylpyridine).

18. A method as in claim 15, wherein the polymer is poly(methylmethacrylate).

19. A method as in claim 15, wherein the polymer is poly(vinylpyrrolidinone).

20. A method as in claim 1, further comprising a source of energy applicable to the compound to cause the compound to transfer an electron to an analyte.

21. A method as in claim 1, wherein the source of energy, when applied to the compound, causes an emission of radiation and causes the compound to transfer an electron to an analyte.

22. A method as in claim 1, wherein the source of energy is an electric, magnetic, optical, acoustic, electromagnetic, or mechanical field.

23. A method as in claim 1, wherein the source of energy is electromagnetic radiation.

24. A method as in claim 1, wherein the analyte is 2,4,6-hexahydro-1,3,5-triazinane (RDX), 2,3-dimethyl-2,3-dinitrobutane (DMNB), 2,2-bis[(nitrooxy)-methyl]-1,3-propanediol dinitrate ester (PETN), or 1,3,5,7-tetranitroperhydro-1,3,5,7-tetrazocine (HMX).

25. A method as in claim 1, wherein the analyte is 2,4,6-hexahydro-1,3,5-triazinane (RDX).

26. A method as in claim 1, wherein the analyte is 22,2-bis[(nitrooxy)-methyl]-1,3-propanediol dinitrate ester (PETN).