2008
DOI: 10.1246/cl.2008.570
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Synthesis and Properties of 1-(4-Aminophenyl)-2,4-dicyano-3-diethylamino-9,9-diethylfluorenes: Potential Fluorescent Material

Abstract: Four new fluorenes bearing two electron donors and two electron acceptors were synthesized and found to emit blue fluorescence in both solution and solid states.

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Cited by 18 publications
(4 citation statements)
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“…5H),6.94 (d,J = 9.2 Hz,benzylidene)malononitrile (2b) 25 The compound was synthesized by the same procedure as described for 2a using 1b and malononitrile as starting materials. Yield: 89.55%.…”
Section: -(4-(diphenylamino)benzylidene)malononitrile (2a) 24mentioning
confidence: 99%
“…5H),6.94 (d,J = 9.2 Hz,benzylidene)malononitrile (2b) 25 The compound was synthesized by the same procedure as described for 2a using 1b and malononitrile as starting materials. Yield: 89.55%.…”
Section: -(4-(diphenylamino)benzylidene)malononitrile (2a) 24mentioning
confidence: 99%
“…3 In addition, the 2,6-dicyanoanilines type of A-D-A system constitutes a part of the molecular framework of many biological important compounds such as quinolines, isoquinolines, tetrahydroisoquinolines, fluorenes, 9-oxofluorenes, benzofurans, naphthalenes, steroids, quinazolines, phenoxazines and coumarins. [4][5][6][7][8][9][10][11][12][13][14][15][16][17] The most studied derivatives of 2,6-dicyanoanilines are 3,5-disubstituted-2,6-dicyanoanilines, and many synthetic procedures and catalyst systems have been used in the synthesis of 3,5-disubstituted-2,6-dicyanoanilines. 3 They are generally obtained from one-pot reaction process via multicomponent domino coupling reaction pathway by using appropriate aldehyde and ketone.…”
Section: Introductionmentioning
confidence: 99%
“…Aldehyde 6 was synthesized according to a previously reported method . Dicyanovinyl derivative 1 was synthesized by condensation of 6 with malonodinitrile . The reaction was carried out in ethanol at room temperature with triethylamine as catalyst and produced 1 in 80% yield (Scheme ).…”
Section: Resultsmentioning
confidence: 99%