Orthogonal 4,10 and 6,12 substitution of dibenzo[def,mno]chrysene polycyclic aromatic small molecules

Handle URI:
http://hdl.handle.net/10754/625805
Title:
Orthogonal 4,10 and 6,12 substitution of dibenzo[def,mno]chrysene polycyclic aromatic small molecules
Authors:
Koldemir, Unsal; Tinkham, Jonathan S.; Johnson, Robert; Lim, Bogyu ( 0000-0002-5524-3363 ) ; Yemam, Henok A.; Gagnon, Kevin J.; Parkin, Sean ( 0000-0001-5777-3918 ) ; Sellinger, Alan ( 0000-0001-6705-1548 )
Abstract:
A series of new polycyclic aromatic hydrocarbon compounds based on (4,10-disubstituted-dibenzo[def,mno]chrysene-6,12-dione) and 4,10 di-substituted 6,12-bis(triisopropylsilylethynyl)dibenzo[def,mno]chrysene are reported with tunable electronic properties through varied molecular architecture. Starting with an inexpensive commercially available textile dye known as Vat Orange #3, (4,10-dibromo-dibenzo[def,mno] chrysene-6,12-dione) we extended the conjugation at the 4- and 10-positions by the attachment of both electron rich and deficient hexylvinylphthalimide, thiophene, hexylthiophene, triphenylamine, and hexylbithiophene aromatic groups, and studied the resultant optoelectronic properties. By applying various synthetic metal-catalyzed reactions, soluble dibenzo[def,mno]chrysene and dibenzo[def,mno]chrysene-6,12-dione derivatives were achieved with optical edge band gaps between 2.30 eV and 1.65 eV.
Citation:
Koldemir U, Tinkham JS, Johnson R, Lim B, Yemam HA, et al. (2017) Orthogonal 4,10 and 6,12 substitution of dibenzo[def,mno]chrysene polycyclic aromatic small molecules. J Mater Chem C 5: 8723–8733. Available: http://dx.doi.org/10.1039/c7tc02528a.
Publisher:
Royal Society of Chemistry (RSC)
Journal:
J. Mater. Chem. C
KAUST Grant Number:
KUS-C1-015-21
Issue Date:
14-Jul-2017
DOI:
10.1039/c7tc02528a
Type:
Article
ISSN:
2050-7526; 2050-7534
Sponsors:
This work was partially supported by funds provided by the Global Climate and Energy Project (GCEP) award # 1138721 and by the Center for Advanced Molecular Photovoltaics (CAMP), award # KUS-C1-015-21 made by the King Abdullah University of Science and Technology (KAUST). Funding was also provided by the Research Corporation for Science Advancement (RCSA) through the Scialog Collaborative Innovation Award (#22355), and start up funds from the Colorado School of Mines (AS). We thank Prof. Alberto Salleo and Ms Camila Arantxa Cendra Guinassi from Stanford University, Department of Materials Science and Engineering for their help in testing these materials in organic field-effect transistors (OFETs). The Advanced Light Source is supported by the Director, Office of Science, Office of Basic Energy Sciences of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231. Crystallographic data for the structures reported in this paper have been deposited with the CCDC 1526927 and 1526928.
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Full metadata record

DC FieldValue Language
dc.contributor.authorKoldemir, Unsalen
dc.contributor.authorTinkham, Jonathan S.en
dc.contributor.authorJohnson, Roberten
dc.contributor.authorLim, Bogyuen
dc.contributor.authorYemam, Henok A.en
dc.contributor.authorGagnon, Kevin J.en
dc.contributor.authorParkin, Seanen
dc.contributor.authorSellinger, Alanen
dc.date.accessioned2017-10-04T14:59:17Z-
dc.date.available2017-10-04T14:59:17Z-
dc.date.issued2017-07-14en
dc.identifier.citationKoldemir U, Tinkham JS, Johnson R, Lim B, Yemam HA, et al. (2017) Orthogonal 4,10 and 6,12 substitution of dibenzo[def,mno]chrysene polycyclic aromatic small molecules. J Mater Chem C 5: 8723–8733. Available: http://dx.doi.org/10.1039/c7tc02528a.en
dc.identifier.issn2050-7526en
dc.identifier.issn2050-7534en
dc.identifier.doi10.1039/c7tc02528aen
dc.identifier.urihttp://hdl.handle.net/10754/625805-
dc.description.abstractA series of new polycyclic aromatic hydrocarbon compounds based on (4,10-disubstituted-dibenzo[def,mno]chrysene-6,12-dione) and 4,10 di-substituted 6,12-bis(triisopropylsilylethynyl)dibenzo[def,mno]chrysene are reported with tunable electronic properties through varied molecular architecture. Starting with an inexpensive commercially available textile dye known as Vat Orange #3, (4,10-dibromo-dibenzo[def,mno] chrysene-6,12-dione) we extended the conjugation at the 4- and 10-positions by the attachment of both electron rich and deficient hexylvinylphthalimide, thiophene, hexylthiophene, triphenylamine, and hexylbithiophene aromatic groups, and studied the resultant optoelectronic properties. By applying various synthetic metal-catalyzed reactions, soluble dibenzo[def,mno]chrysene and dibenzo[def,mno]chrysene-6,12-dione derivatives were achieved with optical edge band gaps between 2.30 eV and 1.65 eV.en
dc.description.sponsorshipThis work was partially supported by funds provided by the Global Climate and Energy Project (GCEP) award # 1138721 and by the Center for Advanced Molecular Photovoltaics (CAMP), award # KUS-C1-015-21 made by the King Abdullah University of Science and Technology (KAUST). Funding was also provided by the Research Corporation for Science Advancement (RCSA) through the Scialog Collaborative Innovation Award (#22355), and start up funds from the Colorado School of Mines (AS). We thank Prof. Alberto Salleo and Ms Camila Arantxa Cendra Guinassi from Stanford University, Department of Materials Science and Engineering for their help in testing these materials in organic field-effect transistors (OFETs). The Advanced Light Source is supported by the Director, Office of Science, Office of Basic Energy Sciences of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231. Crystallographic data for the structures reported in this paper have been deposited with the CCDC 1526927 and 1526928.en
dc.publisherRoyal Society of Chemistry (RSC)en
dc.titleOrthogonal 4,10 and 6,12 substitution of dibenzo[def,mno]chrysene polycyclic aromatic small moleculesen
dc.typeArticleen
dc.identifier.journalJ. Mater. Chem. Cen
dc.contributor.institutionDepartment of Chemistry, Colorado School of Mines, Golden, USAen
dc.contributor.institutionDepartment of Materials Science and Engineering, Stanford University, Stanford, USAen
dc.contributor.institutionAdvanced Light Source, LBNL, Berkeley, USAen
dc.contributor.institutionDepartment of Chemistry, University of Kentucky, Lexington, USAen
dc.contributor.institutionMaterials Science Programen
dc.contributor.institutionUSAen
dc.contributor.institutionGoldenen
dc.contributor.institutionColorado School of Minesen
dc.contributor.institutionDepartment of Chemistryen
kaust.grant.numberKUS-C1-015-21en
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