作者: Hanze Ying , Jianjun Cheng
DOI: 10.1016/J.DYEPIG.2016.04.024
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摘要: Abstract One-step construction of the amino-substituted squaraine dye backbone was discovered unexpectedly in an amidation reaction. Under catalysis Mukaiyama's reagent, (4-dimethylamino)phenylacetic acid and bulky secondary amine 2,2,6,6-tetramethylpiperidine give reduced form aminosquaraine instead amide as major product. The can be oxidized to a dark-colored conjugated within seconds. method provides novel facile way functionalize four-membered core dye.