IP Library Granted Patent US 9,443,636
Granted Patent B2
US 9,443,636 · App. 13/526,215 · Granted Sep 13, 2016

Supramolecular networks with electron transfer in two dimensions

Inventors: Samuel I. Stupp (Chicago, IL); J. Fraser Stoddart (Evanston, IL); Alexander K. Shveyd (Rochester, NY); Alok S. Tayi (Niskayuna, NY); Chi-Hau Sue (Berkley, CA); Ashwin Narayanan (Chicago, IL)
Assignee: Northwestern University
H01B1/121
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Quick Facts
Patent No.
US 9,443,636
App. No.
13/526,215
Granted
Sep 13, 2016
Kind
B2
Abstract

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.

Claims (11)

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.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 27, 2016
From: NARAYANAN, ASHWIN
To: NORTHWESTERN UNIVERSITY
Reel/Frame 039274/0561 →
CONFIRMATORY LICENSE Recorded Jun 6, 2014
From: NORTHWESTERN UNIVERSITY
To: ENERGY, UNITED STATES DEPARTMENT OF
Reel/Frame 033153/0262 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 7, 2013
From: STUPP, SAMUEL I.; STODDART, JAMES FRASER; SHVEYD, ALEX K.; TAYI, ALOK S.; SUE, CHI HAU
To: NORTHWESTERN UNIVERSITY
Reel/Frame 029579/0873 →
Continuity (2)
Provisional Application 61498262 · Jun 17, 2011
Related Publication 20120319058A1 · Dec 20, 2012