Methods of forming single source precursors, methods of forming polymeric single source precursors, and single source precursors formed by such methods

US9315529B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9315529-B2
Application numberUS-201414474602-A
CountryUS
Kind codeB2
Filing dateSep 2, 2014
Priority dateMar 13, 2008
Publication dateApr 19, 2016
Grant dateApr 19, 2016

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Abstract

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Methods of forming single source precursors (SSPs) include forming intermediate products having the empirical formula ½{L 2 N(μ-X) 2 M′X 2 } 2 , and reacting MER with the intermediate products to form SSPs of the formula L 2 N(μ-ER) 2 M′(ER) 2 , wherein L is a Lewis base, M is a Group IA atom, N is a Group IB atom, M′ is a Group IIIB atom, each E is a Group VIB atom, each X is a Group VIIA atom or a nitrate group, and each R group is an alkyl, aryl, vinyl, (per)fluoro alkyl, (per)fluoro aryl, silane, or carbamato group. Methods of forming polymeric or copolymeric SSPs include reacting at least one of HE 1 R 1 E 1 H and MER with one or more substances having the empirical formula L 2 N(μ-ER) 2 M′(ER) 2 or L 2 N(μ-X) 2 M′(X) 2 to form a polymeric or copolymeric SSP. New SSPs and intermediate products are formed by such methods.

First claim

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What is claimed is: 1. A method of forming a copolymeric single source precursor, comprising reacting a first single source precursor, a second single source precursor differing from the first single source precursor, and HE 1 R 1 E 1 H to form a copolymeric single source precursor having the empirical formula {[L 2 N 1 (ER) a (μ-E 1 R 1 E 1 ) b M′ 1 (ER) c (E 1 R 1 E 1 ) d ] m [L 2 N 2 (ER) e (μ-E 1 R 1 E 1 ) f M′ 2 (ER) g (E 1 R 1 E 1 ) h ] n } l , wherein L is a Lewis base, each N 1 and N 2 is individually selected from Group IB atoms, each M′ 1 and M′ 2 is individually selected from Group IIIA atoms, each E and E 1 is individually selected from Group VIA atoms, a is any number from zero (0) to two (2), b is the difference between two (2) and a, c is any number from zero (0) to two (2), d is the difference between two (2) and c, e is any number from zero (0) to two (2), f is the difference between two (2) and e, g is any number from zero (0) to two (2), h is the difference between two (2) and g, m is any number, n is any number, l is any number, each R is individually selected from the group consisting of alkyl, aryl, vinyl, (per)fluoro alkyl, (per)fluoro aryl, silane, and carbamato groups, and each R 1 is individually selected from the group consisting of α, ω-E 1 functionalized alkyl, aryl, vinyl, (per)fluoro alkyl, (per)fluoro aryl, silane, and carbamato groups. 2. A method of forming a copolymeric single source precursor, comprising reacting uME 1 R 1 E 1 M and vMER with a first substance having the empirical formula L 2 N 1 (μ-X) 2 M′ 1 (X) 2 and a second substance having the empirical formula L 2 N 2 (μ-X) 2 M′ 2 (X) 2 to form a copolymeric single source precursor having the empirical foimula {[L 2 N 1 (ER) a (μ-E 1 R 1 E 1 ) b M′ 1 (ER) c (E 1 R 1 E 1 ) d ] m [L 2 N 2 (ER) e (μ-E 1 R 1 E 1 ) f M′ 2 (ER) g (E 1 R 1 E 1 ) h ] n } l , wherein L is a Lewis base, each X is individually selected from Group VIIA atoms or a nitrate group, each N 1 and N 2 is individually selected from Group IB atoms, each M′ 1 and M′ 2 is individually selected from Group IIIA atoms, each E and E 1 is individually selected from Group VIA atoms, a is any number from zero (0) to two (2), b is the difference between two (2) and a, c is any number from zero (0) to two (2), d is the difference between two (2) and c, e is any number from zero (0) to two (2), f is the difference between two (2) and e, g is any number from zero (0) to two (2), h is the difference between two (2) and g, m is any number, n is any number, l is any number, u is any number from zero (0) to four (4), v is the difference between four (4) and u, each R is individually selected from the group consisting of alkyl, aryl, vinyl, (per)fluoro alkyl, (per)fluoro aryl, silane, and carbamato groups, and each R 1 is individually selected from the group consisting of α,ω-E 1 functionalized alkyl, aryl, vinyl, (per)fluoro alkyl, (per)fluoro aryl, silane, and carbamato groups. 3. The method of claim 1 , where at least two R 1 groups in the copolymeric single source precursor differ from one another. 4. The method of claim 1 , wherein at least two E 1 groups in the copolymeric single source precursor differ from one another. 5. The method of claim 1 , wherein the R 1 groups in the copolymeric single source precursor are the same. 6. The method of claim 1 , wherein the E 1 groups in the copolymeric single source precursor are the same. 7. The method of claim 1 , wherein m is between one and 20,000. 8. The method of claim 1 , wherein n is between one and 20,000. 9. The method of claim 1 , wherein l is between one and 20,000. 10. The method of claim 1 , wherein at least one of m, n, and l is greater than 20,000. 11. The method of claim 1 , further comprising selecting the first single source precursor to comprise a substance having the empirical formula L 2 N 1 (μ-X) 2 M′ 1 (X) 2 and selecting the second single source precursor to comprise a substance having the empirical formula L 2 N 2 (μ-X) 2 M′ 2 (X) 2 . 12. The method of claim 11 , wherein at least some N 1 atoms differ from at least some N 2 atoms in the copolymeric single source precursor. 13. The method of claim 11 , wherein at least some M′ 1 atoms differ from at least some M′ 2 atoms in the copolymeric single source precursor. 14. The method of claim 2 , where at least two R 1 groups in the copolymeric single source precursor differ from one another. 15. The method of claim 2 , wherein at least two E 1 groups in the copolymeric single source precursor differ from one another. 16. The method of claim 2 , wherein the E 1 groups in the copolymeric single source precursor are the same. 17. The method of claim 2 , wherein at least one of m, n, and l is between one and 20,000. 18. The method of claim 2 , wherein at least one of m, n, and l is greater than 20,000. 19. The method of claim 2 , wherein at least some N 1 atoms differ from at least some N 2 atoms in the copolymeric single source precursor. 20. The method of claim 2 , wherein at least some M′ 1 atoms differ from at least some M′ 2 atoms in the copolymeric single source precursor.

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Classifications

  • C07F9/5045Primary

    Complexes or chelates of phosphines with metallic compounds or metals · CPC title

  • without metal-C linkages · CPC title

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What does patent US9315529B2 cover?
Methods of forming single source precursors (SSPs) include forming intermediate products having the empirical formula ½{L 2 N(μ-X) 2 M′X 2 } 2 , and reacting MER with the intermediate products to form SSPs of the formula L 2 N(μ-ER) 2 M′(ER) 2 , wherein L is a Lewis base, M is a Group IA atom, N is a Group IB atom, M′ is a Group IIIB atom, each E is a Group VIB atom, each X is a Group VIIA atom…
Who is the assignee on this patent?
Battelle Energy Alliance Llc
What technology area does this patent fall under?
Primary CPC classification C07F9/5045. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Apr 19 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).