IP Library Granted Patent US 9,447,107
Granted Patent B2
US 9,447,107 · App. 13/229,477 · Granted Sep 20, 2016

Broadly absorbing metalloporphyrin-based multichromophoric arrays for triplet harvesting

Inventors: Mark E. Thompson (Anaheim, CA); Matthew T. Whited (Northfield, MN); Peter I. Djurovich (Long Beach, CA)
Assignee: University of Southern California
C07D487/22C09B47/045C09B47/073C09B57/10C09K9/02C09K11/06H01L51/009C09K2211/1029C09K2211/1055C09K2211/185H01L51/008H01L51/0087Y02E10/549
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Quick Facts
Patent No.
US 9,447,107
App. No.
13/229,477
Granted
Sep 20, 2016
Kind
B2
Abstract

The present disclosure relates to multichromophoric assemblies comprising metalloporphyrin scaffolds. The present disclosure also relates, in part, to methods for generating electric-field-stabilized geminate polaron pairs comprising applying electric fields to the multichromophoric assemblies described herein, or alternatively, directly to the metalloporphyrins provided by the present disclosure. The present disclosure further relates, in part, to multichromophoric assemblies comprising metalloporphyrin scaffolds, which exhibit enhanced energy transfer properties.

Claims (24)

1. A multichromophoric assembly comprising a metalloporphyrin of Formula I

or salts or tautomers thereof, wherein:

Fl 1 , Fl 2 , Fl 3 and Fl 4 are each independently selected from the group consisting of 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene, fluorescein, and merocyanine-based dyes, wherein the Fl 1 , Fl 2 , Fl 3 , and Fl 4 are directly attached to the metalloporphyrin scaffold or are attached via a linker chosen from alkyl and phenylene;

R is selected from the group consisting of hydrogen, optionally substituted alkyl, optionally substituted aryl, optionally substituted heteroalkyl, and optionally substituted heteroaryl; or

one or more R groups may be connected to form a cycloalkyl or benzannulated ring system; and

M is selected from the group consisting of Y, La, Zr, Hf, Nb, Ta, Mo, W, Tc, Re, Ru, Os, Rh, Ir, Pd, Pt, Ag, Au, Cd, Hg, Ga, Ge, In, Sn, Sb, Ti, Pb, and Bi, which can be optionally bound to one or more additional neutral or anionic ligands, wherein the ligands are selected from the group consisting of pyridine, imidazole, pyrazine, furan, thiophene, halides, sulfonates and caboxylates.

2. The multichromophoric assembly according to claim 1 , wherein the sulfonates are trifluoromethanesulfonate groups and the carboxylates are acetate groups.

3. The multichromophoric assembly according to claim 1 , wherein adjacent R groups are connected to form a cyclohexene ring, benzene ring, or combination thereof.

4. The multichromophoric assembly according to claim 1 , wherein the cycloalkyl or benzannulated ring system comprise porphyrins.

5. The multichromophoric assembly according to claim 4 , wherein the porphyrins comprise benzoporphyrins, naphthoporphyrins, and anthracenoporphyrins.

6. The multichromophoric assembly according to claim 1 , wherein the metalloporphyrin of Formula I is

or salts or tautomers thereof.

7. The multichromophoric assembly according to claim 1 , further comprising at least one triplet forming dopant material.

8. The multichromophoric assembly according to claim 1 , wherein the Fl 1 , Fl 2 , Fl 3 , and Fl 4 exhibit a) strong absorption either at higher energy than the porphyrin Soret or at intermediate energy between the porphyrin Soret and Q band(s); or b) efficient transfer of energy from the photoexcited state to the metalloporphyrin scaffold core.

9. The multichromophoric assembly according to claim 1 , wherein M facilitates intersystem crossing such that photons absorbed by the Fl 1 , Fl 2 , Fl 3 , and Fl 4 are efficiently funneled to a porphryin-based triplet state.

10. The multichromophoric assembly according to claim 1 , comprising one platinum tetraphenyltetrabenzoporphyrin (Pt(TPBP)) core and four dimethyl boron dipyrrin Me 2 BODIPY moieties forming a shell in a core-shell arrangement, which exhibits energy transfer properties sufficient to funnel singlet to the core followed by triplet redistribution between the core and shell.

11. The multichromophoric assembly according to claim 1 , wherein there is energy transfer between at least one of the Fl 1 , Fl 2 , Fl 3 and Fl 4 and the metalloporphyrin, or any combination thereof.

12. The multichromophoric assembly according to claim 11 , wherein the energy transfer occurs via Förster resonant energy transfer (FRET).

13. A method for generating electric-field-stabilized geminate polaron pairs, comprising applying an electric field to a metalloporphyrin of Formula I

or salts or tautomers thereof, wherein:

Fl 1 , Fl 2 , Fl 3 and Fl 4 are each independently selected from the group consisting of 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene, fluorescein, and merocyanine-based dyes, wherein the Fl 1 , Fl 2 , Fl 3 , and Fl 4 are directly attached to the metalloporphyrin scaffold or are attached via a linker chosen from alkyl and phenylene;

R is selected from the group consisting of hydrogen, optionally substituted alkyl, optionally substituted aryl, optionally substituted heteroalkyl, and optionally substituted heteroaryl; or

one or more R groups may by connected to form a cycloalkyl or benzannulated ring system; and

M is selected from the group consisting of Y, La, Zr, Hf, Nb, Ta, Mo, W, Tc, Re, Ru, Os, Rh, Ir, Pd, Pt, Ag, Au, Cd, Hg, Ga, Ge, In, Sn, Sb, Ti, Pb, and Bi, which can be optionally bound to one or more additional neural or anionic ligands, wherein the ligands are selected from the group consisting of pyridine, imidazole, pyrazine, furan, thiophene, halides, sulfonates and caboxylates, and wherein charge separation to form geminate pairs are achieved without external dopants.

Assignments (2)
CONFIRMATORY LICENSE Recorded May 26, 2020
From: UNIVERSITY OF SOUTHERN CALIFORNIA
To: UNITED STATES DEPARTMENT OF ENERGY
Reel/Frame 052746/0701 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 1, 2012
From: THOMPSON, MARK E.; WHITED, MATTHEW T.; DJUROVICH, PETER I.
To: UNIVERSITY OF SOUTHERN CALIFORNIA
Reel/Frame 028694/0680 →
Continuity (3)
Provisional Application 61381819 · Sep 10, 2010
Provisional Application 61392457 · Oct 12, 2010
Related Publication 20120168697A1 · Jul 5, 2012