Functional hole transport materials for optoelectronic and/or electrochemical devices
US-2018190911-A1 · Jul 5, 2018 · US
US9443636B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9443636-B2 |
| Application number | US-201213526215-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 18, 2012 |
| Priority date | Jun 17, 2011 |
| Publication date | Sep 13, 2016 |
| Grant date | Sep 13, 2016 |
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Organic charge-transfer (CT) co-crystals in a crossed stack system are disclosed. The co-crystals exhibit bidirectional charge transfer interactions where one donor molecule shares electrons with two different acceptors, one acceptor face-to-face and the other edge-to-face. The assembly and charge transfer interaction results in a pleochroic material whereby the optical absorption continuously changes depending on the polarization angle of incident light.
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What is claimed is: 1. An organic charge-transfer (CT) co-crystal in a crossed stack lattice exhibiting bidirectional CT interactions, where one donor molecule shares electrons with two different acceptors; wherein one acceptor is face-to-face with the donor and a second acceptor is edge-to-face with the donor, and wherein the co-crystal exhibits visible pleochroism with RGB and CMYK colors, said organic CT co-crystal selected from the group consisting of and 2. The organic CT co-crystal according to claim 1 , wherein the acceptor is a diimide. 3. The organic CT co-crystal according to claim 1 , wherein the ionicity of and are ρ ms =0.53, ρ xs =0.47, and ρ ms =0.57, ρ xs , =0.42, respectively. 4. The organic CT co-crystal according to claim 1 , wherein the co-crystal violates the mutual exclusion rule of IR and Raman modes along a mixed stack axes and a crossed stack axes. 5. The organic CT co-crystal according to claim 1 , wherein absorption of light of the co-crystal is anisotropic. 6. The organic CT co-crystal according to claim 5 , wherein two distinct chromophores are observed. 7. The organic CT co-crystal according to claim 6 , wherein the two distinct chromophores absorb light at 53° and 95° with absorption maxima at 475 nm and 527 nm, respectively. 8. The organic CT co-crystal according to claim 6 , wherein the two distinct chromophores absorb light at 89° and 117° with absorption maxima at 490 nm and 595 nm, respectively.
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