SYNTHESIS AND PROPERTIES OF POLY(AROMATIC DIACETYLENE)S CONTAINING FLUORENE
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SYNTHESIS AND PROPERTIES OF POLY(AROMATIC DIACETYLENE)S CONTAINING FLUORENE
SYNTHESIS AND PROPERTIES OF POLY(AROMATIC DIACETYLENE)S CONTAINING FLUORENE
高分子科学(英文版)2008年26卷第2期 页码:195-201
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纸质出版:2008-03-20
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Han Peng a, Di Chang a, Ben-zhong Tang b. SYNTHESIS AND PROPERTIES OF POLY(AROMATIC DIACETYLENE)S CONTAINING FLUORENE[J]. 高分子科学(英文版), 2008,26(2):195-201.
Han Peng a, Di Chang a, Ben-zhong Tang b. SYNTHESIS AND PROPERTIES OF POLY(AROMATIC DIACETYLENE)S CONTAINING FLUORENE[J]. 2008, 26(2): 195-201.
Han Peng a, Di Chang a, Ben-zhong Tang b. SYNTHESIS AND PROPERTIES OF POLY(AROMATIC DIACETYLENE)S CONTAINING FLUORENE[J]. 高分子科学(英文版), 2008,26(2):195-201.DOI:
Han Peng a, Di Chang a, Ben-zhong Tang b. SYNTHESIS AND PROPERTIES OF POLY(AROMATIC DIACETYLENE)S CONTAINING FLUORENE[J]. 2008, 26(2): 195-201.DOI:
SYNTHESIS AND PROPERTIES OF POLY(AROMATIC DIACETYLENE)S CONTAINING FLUORENE
Novel fluorene-based poly(aromatic diacetylene)s have been synthesized by CuCl-catalyzed oxidative coupling of aromatic diynes. New aromatic diynes 2
7-diethynyl-9
9-bis(triphenylamine)fluorene (M1) is synthesized by multistep reactions. The structures and properties of the polymers are characterized and evaluated by IR
NMR
TGA
UV
photoluminescence (PL)
and cyclic voltammetry analyses. These polymers possess good thermal stability. All the polymers are completely soluble in common solvents such as toluene
THF
chloroform
and dichloromethane. The polymers exhibit strong blue photoluminescence in solution and green photoluminescence in the solid state. The polymer containing triphenylamine-substituted fluorene has lower oxidation potential (-5.45 eV) than the previous polyfluorenes (-5.80 eV).
Abstract
Novel fluorene-based poly(aromatic diacetylene)s have been synthesized by CuCl-catalyzed oxidative coupling of aromatic diynes. New aromatic diynes 2
7-diethynyl-9
9-bis(triphenylamine)fluorene (M1) is synthesized by multistep reactions. The structures and properties of the polymers are characterized and evaluated by IR
NMR
TGA
UV
photoluminescence (PL)
and cyclic voltammetry analyses. These polymers possess good thermal stability. All the polymers are completely soluble in common solvents such as toluene
THF
chloroform
and dichloromethane. The polymers exhibit strong blue photoluminescence in solution and green photoluminescence in the solid state. The polymer containing triphenylamine-substituted fluorene has lower oxidation potential (-5.45 eV) than the previous polyfluorenes (-5.80 eV).
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