Diboron-containing fluorophores with extended ladder-type π-conjugated skeletons
Authors:
- 4 January 2011
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Dalton Transactions
- Vol. 40 (6) , 1279-1285
Abstract
A series of ladder type π-conjugated diboron complexes 1–4 have been designed and synthesized by a very simple synthetic procedure. Single crystals of complex 3 were grown and the molecular structure determined by X-ray diffraction analysis demonstrated that this type of diboron ladder has a rather planar skeleton. All complexes possess very high melting points (275–383 °C) and decomposition temperatures (Td5: 343–400 °C), indicative of their high thermal stabilities. The electrochemical and photophysical properties as well as theoretical calculations were investigated, suggesting the possibility of these boron complexes as efficient emitters in optoelectronics.Keywords
This publication has 51 references indexed in Scilit:
- Intramolecular Reductive Double Cyclization of o,o′-Bis(arylcarbonyl)diphenylacetylenes: Synthesis of Ladder π-Conjugated SkeletonsOrganic Letters, 2009
- The Larger Acenes: Versatile Organic SemiconductorsAngewandte Chemie International Edition, 2007
- Synthesis of Ladder-Type π-Conjugated Heteroacenes via Palladium-Catalyzed Double N-Arylation and Intramolecular O-ArylationThe Journal of Organic Chemistry, 2007
- Functionalized Acenes and Heteroacenes for Organic ElectronicsChemical Reviews, 2006
- Synthesis and characterization of novel conjugated bisindenocarbazolesTetrahedron, 2006
- Big Is Beautiful−“Aromaticity” Revisited from the Viewpoint of Macromolecular and Supramolecular Benzene ChemistryChemical Reviews, 2001
- Ladder-type materialsJournal of Materials Chemistry, 1999
- Electroluminescent Conjugated Polymers—Seeing Polymers in a New LightAngewandte Chemie International Edition, 1998
- Synthesis, Morphology, and Field-Effect Mobility of AnthradithiophenesJournal of the American Chemical Society, 1998
- Synthesis and properties of diethyl 5,10-dihetera-5,10-dihydroindeno[2,1-a]indene-2,7-dicarboxylatesThe Journal of Organic Chemistry, 1993