Title:
Hydroxy cruciforms and bis(hydroxystyryl)benzenes: synthesis, structure, and photophysical properties of novel π-systems

dc.contributor.advisor Bunz, Uwe H. F.
dc.contributor.author McGrier, Psaras Lamar en_US
dc.contributor.committeeMember Collard, David
dc.contributor.committeeMember El-Sayed, Mostafa A.
dc.contributor.committeeMember Griffin, Anselm
dc.contributor.committeeMember Tolbert, Laren
dc.contributor.department Chemistry and Biochemistry en_US
dc.date.accessioned 2011-03-04T20:21:02Z
dc.date.available 2011-03-04T20:21:02Z
dc.date.issued 2010-06-15 en_US
dc.description.abstract This thesis examines the synthesis, photophysical properties, and sensory responses of hydroxy-substituted 1,4-distyryl-2,5-bis(arylethynyl)benzenes (Cruciforms, XFs). These two-dimensional cross-conjugated materials possess spatially separated frontier molecular orbitals (FMOs). This spatial separation allows the HOMO and LUMO to be addressed independently by analytes, which leads to significant changes in their absorption and emission. These properties allow XFs to be utilized for the detection of various analytes. These studies highlight the benefits of utilizing XFs for the development of advanced functional solid state materials for sensory applications. en_US
dc.description.degree Ph.D. en_US
dc.identifier.uri http://hdl.handle.net/1853/37185
dc.publisher Georgia Institute of Technology en_US
dc.subject Cruciforms en_US
dc.subject Novel Pi systems en_US
dc.subject Amine sensing en_US
dc.subject Bis(hydroxystyryl)benzenes en_US
dc.subject Spatially separated FMOs en_US
dc.subject.lcsh Amines
dc.subject.lcsh Semiconductors
dc.subject.lcsh Fluorescent polymers
dc.title Hydroxy cruciforms and bis(hydroxystyryl)benzenes: synthesis, structure, and photophysical properties of novel π-systems en_US
dc.type Text
dc.type.genre Dissertation
dspace.entity.type Publication
local.contributor.corporatename School of Chemistry and Biochemistry
local.contributor.corporatename College of Sciences
relation.isOrgUnitOfPublication f1725b93-3ab8-4c47-a4c3-3596c03d6f1e
relation.isOrgUnitOfPublication 85042be6-2d68-4e07-b384-e1f908fae48a
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