IP Library Granted Patent US 8,669,359
Granted Patent B2
US 8,669,359 · App. 12/552,187 · Granted Mar 11, 2014

Electrically conducting porphyrin and porphyrin-fullerene electropolymers

Inventors: John Devens Gust, Jr. (Mesa, AZ); Paul Anthony Liddell (Apache Junction, AZ); Miguel Andres Gervaldo (Cordoba, AR); James Ward Bridgewater (Mesa, AZ); Bradley James Brennan (Omaha, NE); Thomas Andrew Moore (Scottsdale, AZ); Ana Lorenzelli Moore (Scottsdale, AZ)
Assignee: Arizona Board of Regents for and on behalf of Arizona State University
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Quick Facts
Patent No.
US 8,669,359
App. No.
12/552,187
Granted
Mar 11, 2014
Kind
B2
Abstract

Compounds with aryl ring(s) at porphyrin meso position(s) bearing an amino group in position 4 relative to the porphyrin macrocycle, and at least one unsubstituted 5 (hydrogen-bearing) meso position with the 10-, 15-, and/or 20-relationship to the aryl ring bearing the amino group, and metal complexes thereof, feature broad spectral absorption throughout the visible region. These compounds are electropolymerized to form electrically conducting porphyrin and porphyrin-fullerene polymers that are useful in photovoltaic applications. The structure of one such electrically conducting porphyrin polymer is shown below.

Claims (14)

1. A porphyrin polymer having the formula:

wherein:

m is an integer greater than 2, wherein m indicates the number of porphyrin monomers in the porphyrin polymer,

each R 1 is independently —H, -alkyl, or -alkenyl, wherein R 1 is optionally substituted with one or more groups which are each independently R, or any two R 1 on adjacent carbon atoms form a fused phenyl group which is optionally substituted by one or more R groups,

and

R 3 is -halogen, -alkyl, -aryl, -cycloalkyl, -heterocyclyl, or -heteroaryl, wherein R 3 is optionally substituted with one or more R groups, and n is 0, 1, 2, 3, or 4,

each R is independently -halogen, -alkyl, -aryl, -cycloalkyl, -heterocyclyl, -heteroaryl, —OR 4 , —SR 4 , —N(R 4 ) 2 , —C(O)R 4 , —C(O)OR 4 , —C(O)N(R 4 ) 2 , —OC(O)R 4 , —OC(O)OR 4 , —OC(O)N(R 4 ) 2 , —N(R 4 )C(O)R 4 , —N(R 4 )C(O)OR 4 , —N(R 4 )C(O)N(R 4 ) 2 , —S(O) 2 R 4 , —S(O) 2 N(R 4 ) 2 , or —S(O) 2 OR 4 ,

each R′ is independently -halogen, -alkyl, -aryl, -cycloalkyl, -heterocyclyl, -heteroaryl, —SR 4 , —N(R 4 ) 2 , —C(O)R 4 , —C(O)OR 4 , —C(O)N(R 4 ) 2 , —OC(O)R 4 , —OC(O)OR 4 , —OC(O)N(R 4 ) 2 , —N(R 4 )C(O)R 4 , —N(R 4 )C(O)OR 4 , (R 4 )C(O)N(R 4 ) 2 , —S(O) 2 R 4 , —S(O) 2 N(R 4 ) 2 , —S(O) 2 OR 4 , or R F ,

R F is -L-cycloalkyl or -L-heterocyclyl, and wherein the cycloalkyl and heterocyclyl are optionally substituted with R 5 groups,

each R 4 is independently —H or -alkyl,

each R 5 is independently R, or two R 5 groups on adjacent carbon atoms form a fused aryl, -heteroaryl-, -heterocyclyl-, -cycloalkyl- or -fullerenyl-,

L is a bond, -L 1 -, -L 1 -alkyl-, or -L 1 -alkyl-L 1 -, wherein L 1 is —C(O)O—, —OC(O)—, —N(R 4 )C(O)—, —C(O)N(R 4 )—, —O—, —S—, —N(R 4 )—, —OC(O)O—, —OC(O)N(R 4 )—, —N(R 4 )C(O)O—, or —N(R 4 )C(O)N(R 4 )—, and

each p is independently 0, 1, 2, 3, 4, or 5.

2. The polymer according to claim 1 , wherein each p is independently 0, 1, 2, or 3, and each R′ is independently -halogen or -alkyl.

Assignments (2)
CONFIRMATORY LICENSE Recorded Oct 19, 2020
From: ARIZONA STATE UNIVERSITY-TEMPE CAMPUS
To: UNITED STATES DEPARTMENT OF ENERGY
Reel/Frame 054114/0982 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 19, 2009
From: GUST, JOHN DEVENS, JR; LIDDELL, PAUL ANTHONY; GERVALDO, MIGUEL ANDRES; BRIDGEWATER, JAMES WARD; BRENNAN, BRADLEY JAMES; MOORE, THOMAS ANDREW; MOORE, ANA LORENZELLI
To: ARIZONA BOARD OF REGENTS FOR AND ON BEHALF OF ARIZONA STATE UNIVERSITY
Reel/Frame 023547/0036 →
Continuity (3)
Continuation PCTUS2008055545 · Feb 29, 2008
Provisional Application 60892757 · Mar 2, 2007
Related Publication 20100065123A1 · Mar 18, 2010