2012
DOI: 10.1016/j.molstruc.2012.04.040
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Ordering the amorphous – Structures in PBD LED materials

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Cited by 5 publications
(3 citation statements)
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“…The crystal structure of the CAB-and PBD-functionalized CP 2 (Scheme 1) showed that the torsion angles between the central pentagon and phenyl groups at the 3,4-positions were 53° and 48° respectively due to the steric hindrance (see Figure S8). The corresponding angles for the PBD segment in this CP were 30°, 11° and 14° respectively, which were a little higher than the reported bare PBD single crystal results, namely 26°, 8° and 4° [45]. This suggests that the conjugation of the PBD moiety in the CP is somewhat reduced as compared with PBD.…”
Section: Synthesis and Structural Characterizationcontrasting
confidence: 54%
“…The crystal structure of the CAB-and PBD-functionalized CP 2 (Scheme 1) showed that the torsion angles between the central pentagon and phenyl groups at the 3,4-positions were 53° and 48° respectively due to the steric hindrance (see Figure S8). The corresponding angles for the PBD segment in this CP were 30°, 11° and 14° respectively, which were a little higher than the reported bare PBD single crystal results, namely 26°, 8° and 4° [45]. This suggests that the conjugation of the PBD moiety in the CP is somewhat reduced as compared with PBD.…”
Section: Synthesis and Structural Characterizationcontrasting
confidence: 54%
“…There are no hydrogen bondings; however, there is a weak intermolecular interaction N1…C1. An interesting comparison with the crystal structures of structurally related compounds NAXDIZ , IPODEX , and PEDQUM is presented in Figure . The methyl substituent in 7a causes only slight deviation from planarity, similar to the non‐substituted benzene ring in PEDQUM, but surprisingly not as twisted as in the meta‐substituted IPODEX.…”
Section: Resultsmentioning
confidence: 99%
“…Oxadiazole‐containing polymers and organic small molecules are a topic of interest because of their unique properties arising from the presence of nitrogen‐containing heterocyclic aromatic structure. Polymers containing 1,3,4‐oxadiazole rings present a great interest for high performance materials because of their high thermal stability and certain specific properties that are determined by the nature of oxadiazole unit that has a strong electron‐withdrawing character []. Poly(arylene‐oxadiazole)s give easily redox reactions, chemically or electrochemically, and the resulting materials are good candidates for electrochemical sensors or electroluminescent devices, to be used in optoelectronics, microelectronics, or other advanced fields [].…”
Section: Introductionmentioning
confidence: 99%