2008
DOI: 10.1021/cm801427s
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Supramolecular Network Conducting the Formation of Uniaxially Oriented Molecular Crystal of Cyano Substituted Oligo(p-phenylene vinylene) and Its Amplified Spontaneous Emission (ASE) Behavior

Abstract: The supramolecular interactions are of importance for inducing the molecular orientation and constructing functional materials with high performance. In this manuscript we report uniaxially oriented molecular crystal of a cyano substituted oligo(p-phenylene vinylene) 1,4-bis(R-cyano-4-diphenylaminostyryl)-2,5diphenylbenzene (CNDPASDB) with high luminescence under the driving force of the three-dimensional supramolecular interaction networks. Amplified spontaneous emission (ASE) with a low threshold value of 30… Show more

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Cited by 88 publications
(55 citation statements)
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References 55 publications
(85 reference statements)
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“…The torsional angles of the double bonds   (2,3,4,5) is 179.9° in the CNDSA crystal and 179.3° in the t-BUDSA (Table 2), larger than that of DSA (172.2°), resulting in relatively less twisted molecular structure. The torsional angles   (1,2,3,4) of CNDSA and t-BUDSA are 54.4° and 60.7°, larger than that of DSA (4.6°) and   (3,4,5,6) between the double bonds and the adjacent phenyl ring are 20.6° for CNDSA and 4.6° for t-BUDSA, smaller than that of DSA (75.0°) due to the effect of internal steric hindrance between the vinylene moieties and the substituents moieties (CN and t-BU). The analyses demonstrate that the two compounds have nonplanar conformation in their crystals.…”
Section: Resultsmentioning
confidence: 88%
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“…The torsional angles of the double bonds   (2,3,4,5) is 179.9° in the CNDSA crystal and 179.3° in the t-BUDSA (Table 2), larger than that of DSA (172.2°), resulting in relatively less twisted molecular structure. The torsional angles   (1,2,3,4) of CNDSA and t-BUDSA are 54.4° and 60.7°, larger than that of DSA (4.6°) and   (3,4,5,6) between the double bonds and the adjacent phenyl ring are 20.6° for CNDSA and 4.6° for t-BUDSA, smaller than that of DSA (75.0°) due to the effect of internal steric hindrance between the vinylene moieties and the substituents moieties (CN and t-BU). The analyses demonstrate that the two compounds have nonplanar conformation in their crystals.…”
Section: Resultsmentioning
confidence: 88%
“…Organic single crystals increasingly highlight their positions in material science and have attracted extensive attention [1][2][3] due to their unique properties, such as high thermostability and charge transport ability, low light propagation loss and reflecting mirror structure [4]. So they are prospectively applied in optical waveguides [5], solid-state laser [6], and many other high-tech areas [7,8].…”
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confidence: 99%
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“…Early in 1996, solid‐state organic lasing has been successfully demonstrated by Hide et al from an optically pumped thin‐film waveguide of MEH–PPV/polystyrene film, while Tessler et al made the first vertical microcavity laser based on conjugated polymers as gain materials. Subsequently, optically pumped lasers has been demonstrated in a broad range of conjugated polymers, oligomers, and evaporated small molecular films . Most recently, low threshold lasing under quasi continuous‐wave photoexcitation was reported by Adachi and coworkers Despite success in optically pumped lasing, the electrically pumped “injection laser” remains as a significant challenge.…”
mentioning
confidence: 99%