2004
DOI: 10.1039/b412762e
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Self-assembled zinc(ii) Schiff base polymers for applications in polymer light-emitting devices

Abstract: Thermally stable zinc(II) Schiff base polymers (decomposition temperature up to 461 degrees C; M(n)= 13580 to 20440) formed by self-assembly reactions of zinc(II) salts and salicylaldimine monomers exhibit blue to yellow PL with quantum yields up to 0.34 in DMF; PLEDs employing these polymers as emitters give green or orange EL with turn-on voltage at 5 and 6 V and maximum efficiency of 2.0 and 2.6 cd A(-1) respectively.

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Cited by 58 publications
(10 citation statements)
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“…Polymers P1 − P3 were fabricated into four-layer PLED devices, respectively, with a configuration of ITO/PEDOT:PSS(40−50 nm)/polymer ( P1 − P3 ) (50−60 nm)/BCP(10 nm)/Alq 3 (30 nm)/LiF(1 nm)/Al(150 nm) using standard procedures of spin-coating and vacuum deposition methods, where polymers P1 − P3 were used as the emission layer and PEDOT: PSS as the hole transporter. Besides, either BCP or ALQ was used as an electron transporter 19c. The EL properties are listed in Table .…”
Section: Resultsmentioning
confidence: 99%
“…Polymers P1 − P3 were fabricated into four-layer PLED devices, respectively, with a configuration of ITO/PEDOT:PSS(40−50 nm)/polymer ( P1 − P3 ) (50−60 nm)/BCP(10 nm)/Alq 3 (30 nm)/LiF(1 nm)/Al(150 nm) using standard procedures of spin-coating and vacuum deposition methods, where polymers P1 − P3 were used as the emission layer and PEDOT: PSS as the hole transporter. Besides, either BCP or ALQ was used as an electron transporter 19c. The EL properties are listed in Table .…”
Section: Resultsmentioning
confidence: 99%
“…16, H 5.42, N, 11.89; found for 1Z, 1E: C 78. 13, 78.10, H 5.49, 5.50, N 11.70, 11.68 4,111.0,111.9,112.2,122.7,127.0,130.4,134.8,136.0,142.6,155.4,162.9 (N=CH) 21.0,104.5,110.9,111.2,111.8,125.3,126.9,130.4,134.6,135.9,142.7,155.1,162.4 (N=CH) A mixture of 2-hydroxy-4-(di-p-tolylamino)benzaldehyde (635 mg, 2.0 mmol), ZnA C H T U N G T R E N N U N G (OAc) 2 ·2H 2 O (327 mg, 1.5 mmol) and diaminomaleonitrile (108 mg, 1.0 mmol) was stirred in MeOH/THF (10 mL/20 mL) overnight at room temperature. Then the solvent was removed under vacuum.…”
Section: Methodsmentioning
confidence: 98%
“…[4] Of particular interest are salen ligands functionalized by an electron-donor (D)/electron-acceptor (A) pair having intramolecular charge-transfer (ICT) properties, such that the associated complexes may have nonlinear optical (NLO) properties. [5,6] To enhance the strength of ICT, the salen ligands are generally anchored by a strongly electron withdrawing moiety such as a cyano group (A) on diamines and dialkylamino substituents (D) at the conjugated position of the diamines.…”
Section: Introductionmentioning
confidence: 99%
“…Unsymmetrical Schiff base complexes, where the metal atom is in an unsymmetrical ligand environment play an important role in many biological systems [20]. These compounds may be used as catalysts for various organic transformations, as promising materials for optoelectronic applications [21][22][23]. They can potentially serve as photoactive materials [4].…”
Section: Introductionmentioning
confidence: 99%