0000000000643191
AUTHOR
Elina Misina
Synthesis, optical, and thermal properties of glassy trityl group containing luminescent derivatives of 2-tert-butyl-6-methyl-4H-pyran-4-one
In this work we present simple preparation of original trityl group containing glassy luminescent 6-styryl substituted derivatives of 2-(2-tert-butyl-4H-pyran-4-ylidene)malononitrile (DWK-1TB), 2-(2-tert-butyl-4H-pyran-4-ylidene)-2- ethyl-2-cyanoacetate (KWK-1TB), 2-(2-tert-butyl-4H-pyran-4-ylidene)-1H-indene-1,3(2H)-dione (ZWK-1TB) and 5-(2-tert-butyl-4H-pyran-4-ylidene)pyrimidine-2,4,6(1H,3H,5H)-trione (JWK-1TB). Their optical properties have been investigated. The absorption maxima of synthesized glasses is in region from 425 nm to 515 nm and emission maxima is from 470 nm to 625 nm in solution of dichloromethane. But absorption maxima of their solid films is from 425 nm to 500 nm and em…
Glassy 2-(1-benzyl-2-styryl-6-methylpyridin-4(1H)-ylidene) fragment containing 1H-indene-1,3(2H)-dione and pyrimidine-2,4,6(1H,3H,5H)-trione derivatives with light-emitting and amplified spontaneous emission properties
A series of 2-(1-benzyl-2-(styryl)-6-methylpyridin-4(1H)-ylidene) fragment containing glassy organic compounds have been synthesized from relevant luminescent 4H-pyran-4-ylidene derivatives and investigated as potential solution processable emitters. Glass transition temperatures of synthesized 1H-pyridine compounds are above 100°C with thermal stabilities higher than 260°C. In the solutions of dichloromethane their absorption bands are in the range from 350 nm to 500 nm with photoluminescence from 500 nm to 650 nm. In a contrary to the 4H-pyran-4-ylidene derivatives, the incorporation of various electron acceptor fragments within the 1H-pyridine fragment containing molecules only slightly …
HAPPY Dyes as Light Amplification Media in Thin Films
A series of 1Hamorphous tri-phenyl pyridine (HAPPY) dyes have been synthesized from luminescent triphenyl-group-containing 2-methyl-6-styryl-substituted-4H-pyran-4-ylidene derivatives in reactions with benzylamine and investigated for suitability as solution-processable light-emitting medium components in thin films for amplified spontaneous emission (ASE). Conversion of a 4H-pyrane ring into a 1H-pyridine fragment enables aggregation-induced emission enhancement (AIEE) behavior in the target products and slightly increases thermal stability, glass transition temperatures, and ASE efficiency with PLQY up to 15% and ASE thresholds as low as 46 μJ/cm2 in neat spin-cast films, although thermal…
Solution processable 2-(trityloxy)ethyl and tert-butyl group containing amorphous molecular glasses of pyranylidene derivatives with light-emitting and amplified spontaneous emission properties
Abstract Small organic molecules with incorporated 4 H -pyran-4-ylidene (pyranylidene) fragment as the π-conjugation system which bonds the electron acceptor fragment (A) with electron donor part (D) in the molecule – also well known as derivatives of 4-(dicyano-methylene)-2-methyl-6-[p-(dimethylamino)styryl]-4H-pyran ( DCM ) laser dye-have attracted considerable attention of scientists as potential new generation materials for organic photonics and molecular electronics due to their low-cost fabrication possibility, flexibility and low-weight. Six glassy derivatives of 4 H -pyran-4-ylidene (pyranylidene) with attached bulky 2-(trityloxy)ethyl and tert -butyl groups are described in this re…