Sterically stabilized second-order nonlinear optical chromophores with improved stability and devices incorporating the same

• US 6,616,865 B1
• Filed: 04/11/2000
• Issued: 09/09/2003
• Est. Priority Date: 07/27/1998
• Status: Expired due to Term

• Current Assignee: MACOM Technology Solutions Holdings, Inc.
• Original Assignee: Pacific Wave Industries Incorporated
• Inventors: Zhang, Cheng, Fetterman, Harold R., Steier, William, Michael, Joseph
• Primary Examiner(s): TUCKER, PHILIP C
• Application Number:
  US09/546,930
• Time in Patent Office: 1,246 Days
• Field of Search: 252/582, 359/328
• US Class Current: 252/582
• CPC Class Codes: C08K 5/0041 Optical brightening agents, organic pigments
• CPC Class Codes: C09B 23/0066 the polymethine chain being part of a carbocyclic ring,(e.g. benzene, naphtalene, cyclohexene, cyclobutenene-quadratic acid)
• CPC Class Codes: C09B 23/0075 the polymethine chain being part of an heterocyclic ring
• CPC Class Codes: C09B 23/0091 having only one heterocyclic ring at one end of the methine chain, e.g. hemicyamines, hemioxonol styryl dyes see C09B23/14
• CPC Class Codes: C09B 23/145 the ethylene chain carrying an heterocyclic residue, e.g. heterocycle-CH=CH-C6H5
• CPC Class Codes: G02F 1/065 in an optical waveguide structure
• CPC Class Codes: G02F 1/212 Mach-Zehnder type
• CPC Class Codes: G02F 1/3611 containing Nitrogen
• CPC Class Codes: G02F 1/3612 Heterocycles having N as heteroatom
• CPC Class Codes: G02F 1/3613 containing Sulfur
• CPC Class Codes: G02F 1/3614 Heterocycles having S as heteroatom
• CPC Class Codes: G02F 1/3615 containing polymers

Abstract

Sterically stabilized second-order nonlinear optical chromophores and devices incorporating the same are embodied in a variety of chromophore materials. An exemplary preferred chromophore includes an electron donor group, an electron acceptor group and a ring-locked bridge structure therebetween, with the bridge structure being directly connected to the electron donor via a single bond. Another exemplary preferred chromophore includes an electron donor group, an electron acceptor group and a ring-locked bridge structure between the electron donor group and the electron acceptor group, with two free double bonds, one located between the donor and the bridge and the other located between the (fused) ring bridge and the acceptor. Another exemplary preferred chromophore includes an electron donor group, an electron acceptor group, and a bridge structure therebetween, with the chromophores having no carbon-carbon double bond between the donor and the (fused) ring bridge. In this class, there is only one unlocked carbon-carbon double bond between the (fused) ring bridge and the acceptor. Another exemplary preferred chromophore includes an electron donor group, an electron acceptor group, and a ring-locked bridge structure therebetween, with a built-in electron-withdrawing cyano group on the last ring of the (fused) bridge. Another exemplary preferred chromophore includes any electron donor group, an electron acceptor group including a linear conjugated triene bearing four cyano groups, and any bridge structure therebetween.

Claims

1. A nonlinear optical device comprising:

an active element including a chromophore formed as;

wherein D is an electron donor group;

wherein A is an electron acceptor group;

wherein R=H, F, or any perhalogenated, halogenated or non-halogenated aliphatic or aromatic group with 1-30 carbon atoms functionalized with zero or more of the following functional groups;

hydroxy, ether, ester, amino, silyl, and siloxy, and R groups at different positions are not necessarily the same.

2. The nonlinear optical device of claim 1 wherein the electron acceptor group is formed as:

3. The nonlinear optical device of claim 1 wherein the electron acceptor group is formed as:

24. The nonlinear optical device of any of claims 1-10 and 12-23 wherein the device is hermetically packaged in a container either vacuumed or vacuumed and then filled with an inert gas including one or more of:

nitrogen, helium, neon, argon, krypton and xenon.

25. The nonlinear optical device of claim 24 wherein the container is a metal case.

4. A nonlinear optical device comprising:

an active element formed from a chromophore including

an electron donor group,

an electron acceptor group, and

a π

-conjugate aliphatic fused-ring bridge structure between the electron donor group and the electron acceptor group;

wherein the electron donor group is directly connected to the bridge structure, with no carbon-carbon double bond between the electron donor group and the bridge structure;

wherein the electron acceptor group is connected to the fused ring of the bridge structure with a conjugated diene.

5. The nonlinear optical device of claim 4 wherein the bridge structure includes one or more five-membered rings.

6. The nonlinear optical device of claim 4 wherein-the bridge structure includes one or more six-membered rings.

7. The nonlinear optical device of claim 4 wherein the bridge structure includes one or more seven-membered rings.

8. A nonlinear optical device comprising:

an active element including a chromophore formed as;

wherein D is an electron donor group;

wherein A is an electron acceptor group formed as;

wherein R=H, F, or any perhalogenated, halogenated or non-halogenated aliphatic or aromatic group with 1-30 carbon atoms functionalized with zero or more of the following functional groups;

hydroxy, ether, ester, amino, silyl, and siloxy, and R groups at different positions are not necessarily the same.

9. A nonlinear optical device comprising:

an active element including a chromophore formed as;

wherein D is an electron donor group;

wherein A is an electron acceptor group formed as;

wherein R=H, F, or any perhalogenated, halogenated or non-halogenated aliphatic or aromatic group with 1-30 carbon atoms functionalized with zero or more of the following functional groups;

hydroxy, ether, ester, amino, silyl, and siloxy, and R groups at different positions are not necessarily the same.

10. A nonlinear optical device comprising:

an active element including a chromophore formed as;

wherein D is an electron donor group;

wherein A is an electron acceptor group formed as;

wherein R=H, F, or any perhalogenated, halogenated or non-halogenated aliphatic or aromatic group with 1-30 carbon atoms functionalized with zero or more of the following functional groups;

hydroxy, ether, ester, amino, silyl, and siloxy, and R groups at different positions are not necessarily the same.

11. The nonlinear optical device of claim 8, 9, or 10 wherein one or more of the six-membered rings in the chromophore is/are replaced by one or more five-membered or seven-membered aliphatic rings.

12. A nonlinear optical device comprising:

an active element including a chromophore formed as;

wherein D is an electron donor group;

wherein A is a ring-locked tricyano electron acceptor group;

wherein R=H, F, or any perhalogenated, halogenated or non-halogenated aliphatic or aromatic group with 1-30 carbon atoms functionalized with zero or more of the following functional groups;

hydroxy, ether, ester, amino, silyl, and siloxy, and R groups at different positions are not necessarily the same.

13. The nonlinear optical device of claim 12 wherein the ring-locked tricyano electron acceptor is formed as:

14. A nonlinear optical device comprising:

an active element including a chromophore formed as;

wherein D is an electron donor group;

wherein A is an electron acceptor group formed as;

wherein R=H, F, or any perhalogenated, halogenated or non-halogenated aliphatic or aromatic group with 1-30 carbon atoms functionalized with zero or more of the following functional groups;

hydroxy, ether, ester, amino, silyl, and siloxy, and R groups at different positions are not necessarily the same.

15. A nonlinear optical device comprising:

an active element including a chromophore formed as;

wherein D is an electron donor group;

wherein A is an electron acceptor group;

wherein R=H, F, or any perhalogenated, halogenated or non-halogenated aliphatic or aromatic group with 1-30 carbon atoms functionalized with zero or more of the following functional groups;

hydroxy, ether, ester, amino, silyl, and siloxy, and R groups at different positions are not necessarily the same.

16. The nonlinear optical device of claim 15 wherein the electron donor group is formed as:

17. A nonlinear optical device comprising:

an active element formed from a chromophore including

an electron donor group,

an electron acceptor group, and

a bridge structure between the electron donor group and the electron acceptor group, the bridge structure including a ring double-bonded to the electron acceptor group, the ring including an electron withdrawing group.

18. The nonlinear optical device of claim 17 wherein the electron withdrawing group is a cyano group.

19. The nonlinear optical device of claim 17 wherein the bridge structure includes a five-membered ring.

20. The nonlinear optical device of claim 17 wherein the bridge structure includes a six-membered ring.

21. The nonlinear optical device of claim 17 wherein the bridge structure includes a seven-membered ring.

22. A nonlinear optical device comprising:

an active element including a chromophore formed as;

wherein D is an electron donor group;

wherein B is a n-conjugate bridge;

wherein A is an electron acceptor group;

wherein R=H, F, or any perhalogenated, halogenated or non-halogenated aliphatic or aromatic group with 1-30 carbon atoms functionalized with zero or more of the following functional groups;

hydroxy, ether, ester, amino, silyl, and siloxy, and R groups at different positions are not necessarily the same.

23. A nonlinear optical device comprising:

an active element formed from a chromophore including

an electron donor group,

an electron acceptor group including a linear conjugated triene bearing four cyano groups, and

a bridge structure between the electron donor group and the electron acceptor group;

wherein the linear conjugated triene is a linear extension of the conjugated system of the donor and the bridge.

26. An optical device comprising:

a nonlinear optical device having a nonlinear optical material which is polymeric, the nonlinear optical device being hermetically packaged in a container filled with an inert gas including one or more of nitrogen, neon and argon.