Highly Luminescent Ladderized Fluorene Copolymers Based on B-N Lewis Pair Functionalization

被引:36
作者
Alahmadi, Abdullah F. [1 ]
Lalancette, Roger A. [1 ]
Jakle, Frieder [1 ]
机构
[1] Rutgers Univ Newark, Dept Chem, 73 Warren St, Newark, NJ 07102 USA
基金
美国国家科学基金会;
关键词
conjugated polymers; isosterism; Lewis pairs; luminescent polymers; organoboranes; C-H BORYLATION; PI-CONJUGATED POLYMERS; HIGH ELECTRON-AFFINITY; ORGANIC SEMICONDUCTORS; PHOTOPHYSICAL PROPERTIES; BUILDING-BLOCKS; SOLAR-CELLS; BAND-GAP; BORON; SYSTEMS;
D O I
10.1002/marc.201800456
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A new B-N functionalized polyaromatic building block for conjugated hybrid polymers is developed. Bromine-functionalized dipyridylfluorene is first subjected to Lewis-base-directed electrophilic borylation and subsequently incorporated into conjugated polymers via transition-metal-catalyzed cross-coupling reactions. The borane monomer exhibits bright blue luminescence in solution, as a result of the rigid ladder-type structure generated upon electrophilic borylation. Yamamoto coupling gives rise to a homopolymer and Stille coupling to a vinylene-bridged copolymer. Polymerization of the BN-fused ladder molecules leads to large bathochromic shifts in absorption and emission, which are most pronounced for the vinylene-bridged copolymer. The polymers display strong luminescence in solution with quantum yields of 55% and 78% and sub-ns fluorescence lifetimes; the copolymer also exhibits bright yellow luminescence in the solid state when precipitated from solution.
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页数:5
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